Browse by Current Cardiff authors

Ali, Nabila M.H, Chawner, Samuel, Kushan-Wells, Leila, Bearden, Carrie, Mulle, Jennifer Gladys, Pollak, Rebecca, Gur, Raquel, Ghung, Wendy, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2025. Comparison of autism domains across thirty rare variant genotypes. EBioMedicine 112 , 105521. 10.1016/j.ebiom.2024.105521

Panagiotaropoulou, Georgia, Hellberg, Kajsa-Lotta Georgii, Coleman, Jonathan R. I., Seok, Darsol, Kalman, Janos, Bipolar Disorder Working Group of the Psychiatric Genomics Conso, Major Depressive Disorder Working Group of the Psychiatric Genom, iPSYCH Study Consortium, Mitchell, Philip B., Schofield, Peter R., Forstner, Andreas J., Bauer, Michael, Scott, Laura J., Pato, Carlos N., Pato, Michele T., Li, Qingqin S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Landén, Mikael, Jonsson, Lina, Müller-Myhsok, Bertram, Smoller, Jordan W., Binder, Elisabeth B., Brückl, Tanja M., Czamara, Darina, Van der Auwera, Sandra, Grabe, Hans J., Homuth, Georg, Schmidt, Carsten O., Potash, James B., DePaulo, J.Raymond, Goes, Fernando S., MacKinnon, Dean F., Mondimore, Francis M., Weissman, Myrna M., Shi, Jianxin, Frye, Mark A., Biernacka, Joanna M., Reif, Andreas, Witt, Stephanie H., Kahn, René R., Boks, Marco M., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Gordon-Smith, Katherine, Mitchell, Brittany L., Martin, Nicholas G., Medland, Sarah E., Jones, Lisa., Knowles, James A., Levinson, Douglas F., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Lewis, Cathryn M., Breen, Gerome, Werge, Thomas, Schork, Andrew J., Ophoff, Roel A., Ripke, Stephan and Olde Loohuis, Loes 2025. Identifying genetic differences between bipolar disorder and major depression through multiple genome-wide association analyses. The British Journal of Psychiatry 10.1192/bjp.2024.125

Woolway, Grace E., Legge, Sophie E., Lynham, Amy J., Smart, Sophie E. ORCID: https://orcid.org/0000-0002-6709-5425, Hubbard, Leon, Daniel, Ellie R., Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, O’Donovan, Michael C., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian R. and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2024. Assessing the validity of a self-reported clinical diagnosis of schizophrenia. Schizophrenia 10 (1) , 99. 10.1038/s41537-024-00526-5

Benger, Lauren, LINC Consortium, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Mon-Williams, Mark, Katzourou, Ioanna and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2024. Adverse childhood experiences and multimorbidity of internalising and cardiometabolic conditions in an older-age population. Presented at: International Population Data Linkage Conference, Chicago, USA, 15-18 September 2025. Conference Proceedings for International Population Data Linkage Conference. International Journal of Population Data Science. , vol.9 (5) Swansea University, p. 133. 10.23889/ijpds.v9i5.2617

Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Cardno, Alastair G., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael J. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2024. Genetic and phenotypic features of Schizophrenia in the UK Biobank. JAMA Psychiatry 81 , pp. 681-690. 10.1001/jamapsychiatry.2024.0200

Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura, Andlauer, Till, von Scheidt, Moritz, Schizophrenia Working Group of the Psychiatric Genomics Consorti, Budde, Monika, Heilbronner, Urs, Papiol, Sergei, Teumer, Alexander, Homouth, Georg, Falkai, Peter, Volzke, Henry, Dorr, Marcus, Schulze, Thomas, Gagneur, Julien, Iorio, Francesco, Müller-Myhsok, Bertram, Schunkert, Heribert, Ziller, Michael, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Kavanagh, David, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Legge, Sophie, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Richards, Alexander L., Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412 2024. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications 15 , 5534. 10.1038/s41467-024-49338-2

Hall, Jessica H., Chawner, Samuel J. R. A., Wolstencroft, Jeanne, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14 (1) , 259. 10.1038/s41398-024-02975-z

Stevenson-Hoare, Joshua, Legge, Sophie E., Simmonds, Emily, Han, Jun, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2024. Severe psychiatric disorders are associated with increased risk of dementia. BMJ Mental Health 27 (1) , e301097. 10.1136/bmjment-2024-301097

Haddon, Josephine E. ORCID: https://orcid.org/0000-0001-5975-813X, Titherage, Daniel, Heckenast, Julia R., Carter, Jennifer, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124 and Jones, Matthew W. 2024. Linking haploinsufficiency of the autism- and schizophrenia-associated gene Cyfip1 with striatal-limbic-cortical network dysfunction and cognitive inflexibility. Translational Psychiatry 14 (1) , 256. 10.1038/s41398-024-02969-x

Cabezas De La Fuente, Daniel, Tamburini, Claudia, Stonelake, Emily, Andrews, Robert, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Li, Meng ORCID: https://orcid.org/0000-0002-4803-4643 2024. Impaired oxysterol-liver X receptor signaling underlies aberrant cortical neurogenesis in a human stem cell model of neurodevelopmental disorder. Cell Reports 43 (3) , 113946. 10.1016/j.celrep.2024.113946

Kopal, Jakub, Kumar, Kuldeep, Shafighi, Kimia, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Douard, Elise, Jizi, Khadije, Beauchamp-Chatel, Alexis, Kushan, Leila, Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Zatorre, Robert, Jacquemont, Sébastien and Bzdok, Danilo 2024. Using rare genetic mutations to revisit structural brain asymmetry. Nature Communications 15 (1) , 2639. 10.1038/s41467-024-46784-w

Kappel, Djenifer, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Fenner, Eilidh, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 2024. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology 80 , pp. 47-54. 10.1016/j.euroneuro.2023.12.007

Tandon, Rajiv, Nasrallah, Henry, Akbarian, Schahram, Carpenter, William T., DeLisi, Lynn E., Gaebel, Wolfgang, Green, Michael F., Gur, Raquel E., Heckers, Stephan, Kane, John M., Malaspina, Dolores, Meyer-Lindenberg, Andreas, Murray, Robin, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Smoller, Jordan W., Yassin, Walid and Keshavan, Matcheri 2024. The schizophrenia syndrome, circa 2024: What we know and how that informs its nature. Schizophrenia Research 264 , pp. 1-28. 10.1016/j.schres.2023.11.015

Doherty, Joanne L., Cunningham, Adam C., Chawner, Samuel J. R. A., Moss, Hayley M., Dima, Diana C. ORCID: https://orcid.org/0000-0002-9612-5574, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 and Singh, Krish D. ORCID: https://orcid.org/0000-0002-3094-2475 2024. Atypical cortical networks in children at high-genetic risk of psychiatric and eurodevelopmental disorders. Neuropsychopharmacology 49 , pp. 368-376. 10.1038/s41386-023-01628-x

Boen, Rune, Kaufmann, Tobias, van der Meer, Dennis, Frei, Oleksandr, Agartz, Ingrid, Ames, David, Andersson, Micael, Armstrong, Nicola J., Artiges, Eric, Atkins, Joshua R., Bauer, Jochen, Benedetti, Francesco, Boomsma, Dorret I., Brodaty, Henry, Brosch, Katharina, Buckner, Randy L., Cairns, Murray J., Calhoun, Vince, Caspers, Svenja, Cichon, Sven, Corvin, Aiden P., Facorro, Benedicto Crespo, Dannlowski, Udo, David, Friederike S., de Geus, Eco J.C., de Zubicaray, Greig I., Desrivières, Sylvane, Doherty, Joanne L., Donohoe, Gary, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fisher, Simon E., Forstner, Andreas J., Uyà, Lidia Fortaner, Frouin, Vincent, Fukunaga, Masaki, Ge, Tian, Glahn, David C., Goltermann, Janik, Grabe, Hans J., Green, Melissa J., Groenewold, Nynke A., Grotegerd, Dominik, Hahn, Tim, Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Henskens, Frans A., Holmes, Avram J., Haberg, Asta K., Haavik, Jan, Jacquemont, Sebastien, Jansen, Andreas, Jockwitz, Christiane, Jonsson, Erik G., Kikuchi, Masataka, Kircher, Tilo, Kumar, Kuldeep, Le Hellard, Stephanie, Leu, Costin, Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Liu, Jingyu, Loughnan, Robert, Mather, Karen A., McMahon, Katie L., McRae, Allan F., Medland, Sarah E., Meinert, Susanne, Moreau, Clara A., Morris, Derek W., Mowry, Bryan J., Muhleisen, Thomas W., Nenadi?, Igor, Nöthen, Markus M., Nyberg, Lars, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paolini, Marco, Paus, Tomas, Pausova, Zdenka, Persson, Karin, Quidé, Yann, Marques, Tiago Reis, Sachdev, Perminder S., Sando, Sigrid B., Schall, Ulrich, Scott, Rodney J., Selbæk, Geir, Shumskaya, Elena, Silva, Ana I., Sisodiya, Sanjay M., Stein, Frederike, Stein, Dan J., Straube, Benjamin, Streit, Fabian, Strike, Lachlan T., Teumer, Alexander, Teutenberg, Lea, Thalamuthu, Anbupalam, Tooney, Paul A., Tordesillas-Gutierrez, Diana, Trollor, Julian N., Ent, Dennis van 't, van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254, van Haren, Neeltje E.M., Vazquez-Bourgon, Javier, Volzke, Henry, Wen, Wei, Wittfeld, Katharina, Ching, Christopher R.K., Westlye, Lars T., Thompson, Paul M., Bearden, Carrie E., Selmer, Kaja K., Alnæs, Dag, Andreassen, Ole A. and Sonderby, Ida E. 2024. Beyond the global brain differences: Intra-individual variability differences in 1q21.1 distal and 15q11.2 BP1-BP2 deletion carriers. Biological Psychiatry 95 (2) , pp. 147-160. 10.1016/j.biopsych.2023.08.018

Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2024. Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes. Nature Reviews Neurology 20 (1) , pp. 7-21. 10.1038/s41582-023-00896-x

Ge, Ruiyang, Ching, Christopher R. K., Bassett, Anne S., Kushan, Leila, Antshel, Kevin M., van Amelsvoort, Therese, Bakker, Geor, Butcher, Nancy J., Campbell, Linda E., Chow, Eva W. C., Craig, Michael, Crossley, Nicolas A., Cunningham, Adam, Daly, Eileen, Doherty, Joanne L., Durdle, Courtney A., Emanuel, Beverly S., Fiksinski, Ania, Forsyth, Jennifer K., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Gur, Raquel E., Jalbrzikowski, Maria, Kates, Wendy R., Lin, Amy, Linden, David E. J., McCabe, Kathryn L., McDonald‐McGinn, Donna, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Villalon‐Reina, Julio E., Repetto, Gabriela M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Schuite‐Koops, Sanne, Angkustsiri, Kathleen, Sun, Daqiang, Vajdi, Ariana, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Vorstman, Jacob, Thompson, Paul M., Vila‐Rodriguez, Fidel and Bearden, Carrie E. 2024. Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping 45 (1) , e26553. 10.1002/hbm.26553

O'Connell, Kevin, Koromina, Maria, van der Veen, Tracey, Boltz, Toni, David, Friederike, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412 and Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889 2024. Genomics yields biological and phenotypic insights into bipolar disorder. Biological Psychiatry Item availability restricted.

Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2024. The genetics of cognition in schizophrenia. Genomic Psychiatry 10.61373/gp024i.0040

Wang, Sheng, Wang, Belinda, Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Tourette International Collaborative Genetics (TIC Genetics), Bal, Vanessa, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Hoekstra, Pieter, Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary, Tischfield, Jay, Fernandez, Thomas, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, State, Matthew and Willsey, Jeremy 2023. Rare X-linked variants carry predominantly male risk in Autism, Tourette Syndrome, and ADHD. Nature Communications 14 , 8077. 10.1038/s41467-023-43776-0

Chilvers, Clair and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2023. Mental Health Research, shared goals. Journal of Mental Health 32 , 1017. 10.1080/09638237.2021.1898562

Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Legge, Sophie, Bracher-Smith, Matthew, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2023. Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance. Biological Psychiatry: Global Open Science 3 (4) , pp. 902-911. 10.1016/j.bpsgos.2022.10.006

Lock, Siobhan K., Legge, Sophie E., Kappel, Djenifer B., Willcocks, Isabella R. ORCID: https://orcid.org/0000-0002-3568-5236, Helthius, Marinka, Jansen, John, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590 2023. Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count. Schizophrenia 9 , 74. 10.1038/s41537-023-00404-6

Doherty, Anna, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Hamshere, Marian ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2023. Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors. The American Journal of Psychiatry 180 (10) , pp. 723-738. 10.1176/appi.ajp.21121266

Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Legge, Sophie, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2023. Genomic findings in schizophrenia and their implications. Molecular Psychiatry 28 , pp. 3638-3647. 10.1038/s41380-023-02293-8

Kumar, Kuldeep, Modenato, Claudia, Moreau, Clara, Ching, Christopher R.K., Harvey, Annabelle, Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Douard, Elise, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurélie, Kushan, Leila, Isaev, Dmitry, Alpert, Kathryn, Ragothaman, Anjani, Turner, Jessica A., Wang, Lei, Ho, Tiffany C., Schmaal, Lianne, Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E.J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Lippé, Sarah, Dumas, Guillaume, Draganski, Bogdan, Gutman, Boris A., Sønderby, Ida E., Andreassen, Ole A., Schultz, Laura M., Almasy, Laura, Glahn, David C., Bearden, Carrie E., Thompson, Paul M. and Jacquemont, Sébastien 2023. Subcortical brain alterations in carriers of genomic copy number variants. The American Journal of Psychiatry 180 (9) , pp. 685-698. 10.1176/appi.ajp.20220304

Le Guen, Yann, Luo, Guo, Ambati, Aditya, Damotte, Vincent, Jansen, Iris, Yu, Eric, Nicolas, Aude, de Rojas, Itziar, Peixoto Leal, Thiago, Miyashita, Akinori, Bellenguez, Céline, Lian, Michelle Mulan, Parveen, Kayenat, Morizono, Takashi, Park, Hyeonseul, Grenier-Boley, Benjamin, Naito, Tatsuhiko, Küçükali, Fahri, Talyansky, Seth D., Yogeshwar, Selina Maria, Sempere, Vicente, Satake, Wataru, Alvarez, Victoria, Arosio, Beatrice, Belloy, Michael E., Benussi, Luisa, Boland, Anne, Borroni, Barbara, Bullido, María J., Caffarra, Paolo, Clarimon, Jordi, Daniele, Antonio, Darling, Daniel, Debette, Stéphanie, Deleuze, Jean-François, Dichgans, Martin, Dufouil, Carole, During, Emmanuel, Düzel, Emrah, Galimberti, Daniela, Garcia-Ribas, Guillermo, García-Alberca, José María, García-González, Pablo, Giedraitis, Vilmantas, Goldhardt, Oliver, Graff, Caroline, Grünblatt, Edna, Hanon, Olivier, Hausner, Lucrezia, Heilmann-Heimbach, Stefanie, Holstege, Henne, Hort, Jakub, Jung, Yoo Jin, Jürgen, Deckert, Kern, Silke, Kuulasmaa, Teemu, Lee, Kun Ho, Lin, Ling, Masullo, Carlo, Mecocci, Patrizia, Mehrabian, Shima, de Mendonça, Alexandre, Boada, Mercè, Mir, Pablo, Moebus, Susanne, Moreno, Fermin, Nacmias, Benedetta, Nicolas, Gael, Niida, Shumpei, Nordestgaard, Børge G., Papenberg, Goran, Papma, Janne, Parnetti, Lucilla, Pasquier, Florence, Pastor, Pau, Peters, Oliver, Pijnenburg, Yolande A. L., Piñol-Ripoll, Gerard, Popp, Julius, Porcel, Laura Molina, Puerta, Raquel, Pérez-Tur, Jordi, Rainero, Innocenzo, Ramakers, Inez, Real, Luis M., Riedel-Heller, Steffi, Rodriguez-Rodriguez, Eloy, Ross, Owen A., Luís Royo, Jose, Rujescu, Dan, Scarmeas, Nikolaos, Scheltens, Philip, Scherbaum, Norbert, Schneider, Anja, Seripa, Davide, Skoog, Ingmar, Solfrizzi, Vincenzo, Spalletta, Gianfranco, Squassina, Alessio, van Swieten, John, Sánchez-Valle, Raquel, Tan, Eng-King, Tegos, Thomas, Teunissen, Charlotte, Thomassen, Jesper Qvist, Tremolizzo, Lucio, Vyhnalek, Martin, Verhey, Frans, Waern, Margda, Wiltfang, Jens, Zhang, Jing, Zetterberg, Henrik, Blennow, Kaj, He, Zihuai, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Amouyel, Philippe, Jessen, Frank, Kehoe, Patrick G., Andreassen, Ole A., Van Duin, Cornelia, Tsolaki, Magda, Sánchez-Juan, Pascual, Frikke-Schmidt, Ruth, Sleegers, Kristel, Toda, Tatsushi, Zettergren, Anna, Ingelsson, Martin, Okada, Yukinori, Rossi, Giacomina, Hiltunen, Mikko, Gim, Jungsoo, Ozaki, Kouichi, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Foo, Jia Nee, van der Flier, Wiesje, Ikeuchi, Takeshi, Ramirez, Alfredo, Mata, Ignacio, Ruiz, Agustín, Gan-Or, Ziv, Lambert, Jean-Charles, Greicius, Michael D., Mignot, Emmanuel, Bellenguez, Céline, Küçükali, Fahri, Jansen, Iris, Andrade, Victor, Moreno-Grau, Sonia, Amin, Najaf, Grenier-Boley, Benjamin, Campos-Martin, Rafael, Holmans, Peter A., Boland, Anne, Kleineidam, Luca, Damotte, Vincent, van der Lee, Sven J., Kuulasmaa, Teemu, de Rojas, Itziar, Yaqub, Amber, Prokic, Ivana, Costa, Marcos R, Chapuis, Julien, Ahmad, Shahzad, Giedraitis, Vilmantas, Aarsland, Dag, Garcia-Gonzalez, Pablo, Abdelnour, Carla, Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Álvarez, Victoria, Armstrong, Nicola J., Anthoula, Tsolaki, Appollonio, Ildebrando, Arcaro, Marina, Archetti, Silvana, Arias Pastor, Alfonso, Arosio, Beatrice, Athanasiu, Lavinia, Bailly, Henri, Banaj, Nerisa, Baquero, Miquel, Belén Pastor, Ana, Benussi, Luisa, Berr, Claudine, Besse, Céline, Bessi, Valentina, Binetti, Giuliano, Bizarro, Alessandra, Blesa, Rafael, Boada, Mercè, Borroni, Barbara, Boschi, Silvia, Bossù, Paola, Bråthen, Geir, Bresner, Catherine, Brodaty, Henry, Brookes, Keeley J., Ignacio Brusco, Luis, Buiza-Rueda, Dolores, BÛrger, Katharina, Burholt, Vanessa, Calero, Miguel, Chene, Geneviève, Carracedo, Ángel, Cecchetti, Roberta, Cervera-Carles, Laura, Charbonnier, Camille, Chillotti, Caterina, Ciccone, Simona, Claassen, Jurgen A.H.R., Clarimon, Jordi, Clark, Christopher, Conti, Elisa, Corma-Gómez, Anaïs, Costantini, Emanuele, Custodero, Carlo, Daian, Delphine, Dalmasso, Maria Carolina, Daniele, Antonio, Dardiotis, Efthimios, Dartigues, Jean-François, de Deyn, Peter Paul, Debette, Stéphanie, Deckert, Jürgen, del Ser, Teodoro, Denning, Nicola, Dichgans, Martin, Diehl-Schmid, Janine, Diez-Fairen, Mónica, Dionigi Rossi, Paolo, Djurovic, Srdjan, Duron, Emmanuelle, 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Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Yang, Jessica M. K. ORCID: https://orcid.org/0000-0002-3685-4126, Crawford, Karen, Bergink, Veerle, Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Gordon-Smith, Katherine, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889 2021. Post-partum psychosis and its association with bipolar disorder in the UK: a case-control study using polygenic risk scores. The Lancet Psychiatry 8 (12) , pp. 1045-1052. 10.1016/S2215-0366(21)00253-4

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Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Legge, Sophie, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Cardno, Alastair, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2021. Risk factors, clinical features, and polygenic risk scores in schizophrenia and schizoaffective disorder depressive-type. Schizophrenia Bulletin 47 (5) , pp. 1375-1384. 10.1093/schbul/sbab036

Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Collado-Torres, Leonardo, Burke, Emily E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Janet C., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Weinberger, Daniel R., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Jaffe, Andrew E. and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2021. Developmental profile of psychiatric risk associated with voltage-gated cation channel activity. Biological Psychiatry 90 (6) 10.1016/j.biopsych.2021.03.009

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Creeth, Hugo, Hwo, Hai-Gwo, Chen, Wei J., Tsuang, Ming, Glatt, Stephen J., Rey, Romain, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2021. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications 12 , 5353. 10.1038/s41467-021-25532-4

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Forsyth, Jennifer K., Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R. K., Villalon-Reina, Julio E., Thompson, Paul M., Bearden, Carrie E., Cunningham, Adam, Doherty, Joanne L., Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 31 (7) , pp. 3285-3298. 10.1093/cercor/bhab008

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Glanville, Kylie P., Coleman, Jonathan R.I., Hanscombe, Ken B., Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L., Breen, Gerome, Air, Tracy M., Andlauer, Till F.M., Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H.R., Boomsma, Dorret I., Buttenschøn, Henriette N., Colodro-Conde, Lucía, Dannlowski, Udo, Direk, Nese, Dunn, Erin C., Forstner, Andreas J., de Geus, Eco J.C., Grabe, Hans J., Hamilton, Steven P., Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A., Knowles, James A., Kutalik, Zoltán, Levinson, Douglas F., Lewis, Glyn, Lind, Penelope A., Lucae, Susanne, Magnusson, Patrik K., McGuffin, Peter, McIntosh, Andrew M., Milaneschi, Yuri, Mors, Ole, Mostafavi, Sara, Müller-Myhsok, Bertram, Pedersen, Nancy L., Penninx, Brenda W.J.H., Potash, James B., Preisig, Martin, Ripke, Stephan, Shi, Jianxin, Shyn, Stanley I., Smoller, Jordan W., Streit, Fabian, Sullivan, Patrick F., Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Weissman, Myrna M., O'Reilly, Paul F., Lewis, Cathryn M., Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F.M., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan T.F., Bigdeli, Tim B., Binder, Elisabeth B., Bryois, Julien, Buttenschøn, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan R.I., Colodro-Conde, Lucía, Couvy-Duchesne, Baptiste, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Crawford, Gregory E., Davies, Gail, Deary, Ian J., Degenhardt, Franziska, Derks, Eske M., Direk, Nese, Dolan, Conor V., Dunn, Erin C., Eley, Thalia C., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Hassan Kiadeh, Farnush Farhadi, Finucane, Hilary K., Foo, Jerome C., Forstner, Andreas J., Frank, Josef, Gaspar, Héléna A., Gill, Michael, Goes, Fernando S., Gordon, Scott D., Grove, Jakob, Hall, Lynsey, Hansen, Christine Søholm, Hansen, Thomas F., Herms, Stefan, Hickie, Ian B., Hoffmann, Per, Homuth, Georg, Horn, Carsten, Hottenga, Jouke-Jan, Hougaard, David M., Howard, David M., Ising, Marcus, Jansen, Rick, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A., Jorgenson, Eric, Knowles, James A., Kohane, Isaac S., Kraft, Julia, Kretzschmar, Warren W., Kutalik, Zoltán, Li, Yihan, Lind, Penelope A., MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Maier, Wolfgang, Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, McGuffin, Peter, Medland, Sarah E., Mehta, Divya, Middeldorp, Christel M., Mihailov, Evelin, Milaneschi, Yuri, Milani, Lili, Mondimore, Francis M., Montgomery, Grant W., Mostafavi, Sara, Mullins, Niamh, Nauck, Matthias, Ng, Bernard, Nivard, Michel G., Nyholt, Dale R., O'Reilly, Paul F., Oskarsson, Hogni, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, Painter, Jodie N., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Peterson, Roseann E., Pettersson, Erik, Peyrot, Wouter J., Pistis, Giorgio, Posthuma, Danielle, Quiroz, Jorge A., Qvist, Per, Rice, John P., Riley, Brien P., Rivera, Margarita, Mirza, Saira Saeed, Schoevers, Robert, Schulte, Eva C., Shen, Ling, Shi, Jianxin, Shyn, Stanley I., Sigurdsson, Engilbert, Sinnamon, Grant C.B., Smit, Johannes H., Smith, Daniel J., Stefansson, Hreinn, Steinberg, Stacy, Streit, Fabian, Strohmaier, Jana, Tansey, Katherine E., Teismann, Henning, Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Traylor, Matthew, Treutlein, Jens, Trubetskoy, Vassily, Uitterlinden, Andrés G., Umbricht, Daniel, Van der Auwera, Sandra, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Webb, Bradley T., Weinsheimer, Shantel Marie, Wellmann, Jürgen, Willemsen, Gonneke, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Arolt, Volker, Baune, Bernhard T., Berger, Klaus, Boomsma, Dorret I., Cichon, Sven, Dannlowski, Udo, de Geus, E.J.C., DePaulo, J. Raymond, Domenici, Enrico, Domschke, Katharina, Esko, Tõnu, Grabe, Hans J., Hamilton, Steven P., Hayward, Caroline, Heath, Andrew C., Kendler, Kenneth S., Kloiber, Stefan, Lewis, Glyn, Li, Qingqin S., Lucae, Susanne, Madden, Pamela AF., Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Nordentoft, Merete, Nöthen, Markus M., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Paciga, Sara A., Pedersen, Nancy L., Penninx, Brenda W.J.H., Perlis, Roy H., Porteous, David J., Potash, James B., Preisig, Martin, Rietschel, Marcella, Schaefer, Catherine, Schulze, Thomas G., Smoller, Jordan W., Stefansson, Kari, Tiemeier, Henning, Uher, Rudolf, Völzke, Henry, Weissman, Myrna M., Werge, Thomas, Lewis, Cathryn, Levinson, Douglas F., Breen, Gerome, Børglum, Anders D., Sullivan, Patrick F. and Wray, Naomi 2020. 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Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, GROUP Investigators, Han, Jun, Morgan, Joanne, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2

Morrison, Sinead, Chawner, Samuel J. R. A., van Amelsvoort, Therese A. M. J., Swillen, Ann, Vingerhoets, Claudia, Vergaelen, Elfi, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Linden, Stefanie ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2020. Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology. Translational Psychiatry 10 , 53. 10.1038/s41398-020-0736-7

Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. A developmental perspective on the convergence of genetic risk factors for neuropsychiatric disorders. Biological Psychiatry 87 (2) , pp. 98-99. 10.1016/j.biopsych.2019.09.010

Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E., Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong and Zwick, Michael 2020. Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects. American Journal of Human Genetics 106 (1) , pp. 26-40. 10.1016/j.ajhg.2019.11.010

Hall, Lynsey S, Medway, Christopher W ORCID: https://orcid.org/0000-0002-1764-0587, Pain, Oliver, Pardinas, Antonio F ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott G ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Bray, Nicholas J ORCID: https://orcid.org/0000-0002-4357-574X, Holmans, Peter A ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T R ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2020. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 29 (1) , pp. 159-167. 10.1093/hmg/ddz253

Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Bracher-Smith, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508

Lee, Phil H., Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A., Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M., Nivard, Michel G., Grotzinger, Andrew D., Posthuma, Danielle, Wang, Meg M.-J., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K. ORCID: https://orcid.org/0000-0002-6980-4053, Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X, Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H., Coppola, Giovanni, Derks, Eske M., Hoekstra, Pieter J., Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kranzler, Henry R., Luykx, Jurjen J., Rohde, Luis A., Zai, Clement C., Agerbo, Esben, Arranz, M.J., Asherson, Philip, Bækvad-Hansen, Marie, Baldursson, Gísli, Bellgrove, Mark, Belliveau, Richard A., Buitelaar, Jan, Burton, Christie L., Bybjerg-Grauholm, Jonas, Casas, Miquel, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Cormand, Bru, Crosbie, Jennifer, Dalsgaard, Søren, Demontis, Ditte, Doyle, Alysa E., Dumont, Ashley, Elia, Josephine, Grove, Jakob, Gudmundsson, Olafur O., Haavik, Jan, Hakonarson, Hakon, Hansen, Christine S., Hartman, Catharina A., Hawi, Ziarih, Hervás, Amaia, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Kuntsi, Jonna, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Lesch, Klaus-Peter, Leung, Patrick W.L., Loo, Sandra K., Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Martin, Alicia R. ORCID: https://orcid.org/0000-0002-8911-3479, McGough, James J., Medland, Sarah E., Moran, Jennifer L., Mors, Ole, Mortensen, Preben B., Oades, Robert D., Palmer, Duncan S., Pedersen, Carsten B., Pedersen, Marianne G., Peters, Triinu, Poterba, Timothy, Poulsen, Jesper B., Ramos-Quiroga, Josep Antoni, Reif, Andreas, Ribasés, Marta, Rothenberger, Aribert, Rovira, Paula, Sánchez-Mora, Cristina, Satterstrom, F. Kyle, Schachar, Russell, Artigas, Maria Soler, Steinberg, Stacy, Stefansson, Hreinn, Turley, Patrick, Walters, G. Bragi ORCID: https://orcid.org/0000-0002-6980-4053, Werge, Thomas, Zayats, Tetyana, Arking, Dan E., Bettella, Francesco, Buxbaum, Joseph D., Christensen, Jane H., Collins, Ryan L., Coon, Hilary, De Rubeis, Silvia, Delorme, Richard, Grice, Dorothy E., Hansen, Thomas F., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hope, Sigrun, Hultman, Christina M., Klei, Lambertus, Ladd-Acosta, Christine, Magnusson, Pall, Nærland, Terje, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Roeder, Kathryn, Rouleau, Guy A., Saemundsen, Evald, Sanders, Stephan J., Sandin, Sven, St Pourcain, Beate, Stefansson, Kari, Sutcliffe, James S., Talkowski, Michael E., Weiss, Lauren A., Willsey, A. Jeremy, Agartz, Ingrid, Akil, Huda, Albani, Diego, Alda, Martin, Als, Thomas D., Anjorin, Adebayo, Backlund, Lena, Bass, Nicholas, Bauer, Michael, Baune, Bernhard T., Bellivier, Frank, Bergen, Sarah E., Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H.R., Bøen, Erlend, Budde, Monika, Bunney, William, Burmeister, Margit, Byerley, William, Byrne, Enda M., Cichon, Sven, Clarke, Toni-Kim, Coleman, Jonathan R.I., Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Curtis, David, Czerski, Piotr M., Dale, Anders M., Dalkner, Nina, Dannlowski, Udo, Degenhardt, Franziska, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Elvsåshagen, Torbjørn, Etain, Bruno, Fischer, Sascha B., Forstner, Andreas J., Forty, Liz, Frank, Josef, Frye, Mark, Fullerton, Janice M., Gade, Katrin, Gaspar, Héléna A., Gershon, Elliot S., Gill, Michael, Goes, Fernando S., Gordon, Scott D., Gordon-Smith, Katherine, Green, Melissa J., Greenwood, Tiffany A., Grigoroiu-Serbanescu, Maria, Guzman-Parra, José, Hauser, Joanna, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hoffmann, Per, Holland, Dominic, Jamain, Stéphane, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A. ORCID: https://orcid.org/0000-0001-5821-5889, Kandaswamy, Radhika, Kelsoe, John R., Kennedy, James L., Joachim, Oedegaard Ketil, Kittel-Schneider, Sarah, Kogevinas, Manolis, Koller, Anna C., Lavebratt, Catharina, Lewis, Cathryn M., Li, Qingqin S., Lissowska, Jolanta, Loohuis, Loes M.O., Lucae, Susanne, Maaser, Anna, Malt, Ulrik F., Martin, Nicholas G. ORCID: https://orcid.org/0000-0002-8911-3479, Martinsson, Lina, McElroy, Susan L., McMahon, Francis J., McQuillin, Andrew, Melle, Ingrid, Metspalu, Andres, Millischer, Vincent, Mitchell, Philip B., Montgomery, Grant W., Morken, Gunnar, Morris, Derek W., Müller-Myhsok, Bertram, Mullins, Niamh, Myers, Richard M., Nievergelt, Caroline M., Nordentoft, Merete, Adolfsson, Annelie Nordin, Nöthen, Markus M., Ophoff, Roel A., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paciga, Sara A., Pato, Carlos N., Pato, Michele T., Perlis, Roy H., Perry, Amy, Potash, James B., Reinbold, Céline S., Rietschel, Marcella, Rivera, Margarita, Roberson, Mary, Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Scott, Laura J., Serretti, Alessandro, Sigurdsson, Engilbert, Smeland, Olav B., Stordal, Eystein, Streit, Fabian, Strohmaier, Jana, Thorgeirsson, Thorgeir E., Treutlein, Jens, Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Wang, Yunpeng, Witt, Stephanie H., Zandi, Peter, Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Aschauer, Harald, Baker, Jessica H., Bencko, Vladimir, Bergen, Andrew W., Birgegård, Andreas, Perica, Vesna Boraska, Brandt, Harry, Burghardt, Roland, Carlberg, Laura, Cassina, Matteo, Clementi, Maurizio, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James J., Danner, Unna N., Davis, Oliver S.P., Degortes, Daniela, DeSocio, Janiece E., Dick, Danielle M., Dina, Christian, Docampo, Elisa, Egberts, Karin, Ehrlich, Stefan, Espeseth, Thomas, Fernández-Aranda, Fernando, Fichter, Manfred M., Foretova, Lenka, Forzan, Monica, Gambaro, Giovanni, Giegling, Ina, Gonidakis, Fragiskos, Gorwood, Philip, Mayora, Monica Gratacos, Guo, Yiran, Halmi, Katherine A., Hatzikotoulas, Konstantinos, Hebebrand, Johannes, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hinney, Anke, Imgart, Hartmut, Jiménez-Murcia, Susana, Johnson, Craig, Jordan, Jennifer, Julià, Antonio, Kaminská, Deborah, Karhunen, Leila, Karwautz, Andreas, Kas, Martien J.H., Kaye, Walter H., Kennedy, Martin A., Kim, Youl-Ri, Klareskog, Lars, Klump, Kelly L., Knudsen, Gun Peggy S., Landén, Mikael, Le Hellard, Stephanie, Levitan, Robert D., Li, Dong, Lichtenstein, Paul, Maj, Mario, Marsal, Sara, McDevitt, Sara, Mitchell, James, Monteleone, Palmiero, Monteleone, Alessio Maria, Munn-Chernoff, Melissa A., Nacmias, Benedetta, Navratilova, Marie, O'Toole, Julie K., Padyukov, Leonid, Pantel, Jacques, Papezova, Hana, Rabionet, Raquel, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ricca, Valdo, Roberts, Marion, Rujescu, Dan, Rybakowski, Filip, Scherag, André, Schmidt, Ulrike, Seitz, Jochen, Slachtova, Lenka, Slof-Opt Landt, Margarita C.T., Slopien, Agnieszka, Sorbi, Sandro, Southam, Lorraine, Strober, Michael, Tortorella, Alfonso, Tozzi, Federica, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., Wade, Tracey D., Wagner, Gudrun, Walton, Esther, Watson, Hunna J., Wichmann, H-Erich, Woodside, D. Blake, Zeggini, Eleftheria, Zerwas, Stephanie, Zipfel, Stephan, Adams, Mark J., Andlauer, Till F.M., Berger, Klaus, Binder, Elisabeth B., Boomsma, Dorret I., Castelao, Enrique, Colodro-Conde, Lucía, Direk, Nese, Docherty, Anna R., Domenici, Enrico, Domschke, Katharina, Dunn, Erin C., Foo, Jerome C., de. Geus, E.J.C., Grabe, Hans J., Hamilton, Steven P., Horn, Carsten, Hottenga, Jouke-Jan, Howard, David, Ising, Marcus, Kloiber, Stefan, Levinson, Douglas F., Lewis, Glyn, Magnusson, Patrik K.E., Mbarek, Hamdi, Middeldorp, Christel M., Mostafavi, Sara, Nyholt, Dale R., Penninx, Brenda WJH., Peterson, Roseann E., Pistis, Giorgio, Porteous, David J., Preisig, Martin, Quiroz, Jorge A., Schaefer, Catherine, Schulte, Eva C., Shi, Jianxin, Smith, Daniel J., Thomson, Pippa A., Tiemeier, Henning, Uher, Rudolf, van der Auwera, Sandra, Weissman, Myrna M., Alexander, Madeline, Begemann, Martin, Bramon, Elvira, Buccola, Nancy G., Cairns, Murray J., Campion, Dominique, Carr, Vaughan J., Cloninger, C. 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Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Helthuis, Marinka, Jansen, John A., Jollie, Karel, Knapper, Steven ORCID: https://orcid.org/0000-0002-6405-4441, MacCabe, James H., Rujescu, Dan, Collier, David A., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2019. A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia. Molecular Psychiatry 24 , pp. 328-337. 10.1038/s41380-018-0335-7

Kunkle, Brian W., Grenier-Boley, Benjamin, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Bis, Joshua C., Damotte, Vincent, Naj, Adam C., Boland, Anne, Vronskaya, Maria, van der Lee, Sven J., Amlie-Wolf, Alexandre, Bellenguez, Céline, Frizatti, Aura, Chouraki, Vincent, Martin, Eden R., Sleegers, Kristel, Badarinarayan, Nandini ORCID: https://orcid.org/0000-0002-6944-748X, Jakobsdottir, Johanna, Hamilton-Nelson, Kara L., Moreno-Grau, Sonia, Olaso, Robert, Raybould, Rachel, Chen, Yuning, Kuzma, Amanda B., Hiltunen, Mikko, Morgan, Taniesha, Ahmad, Shahzad, Vardarajan, Badri N., Epelbaum, Jacques, Hoffmann, Per, Boada, Merce, Beecham, Gary W., Garnier, Jean-Guillaume, Harold, Denise, Fitzpatrick, Annette L., Valladares, Otto, Moutet, Marie-Laure, Gerrish, Amy, Smith, Albert V., Qu, Liming, Bacq, Delphine, Denning, Nicola, Jian, Xueqiu, Zhao, Yi, Del Zompo, Maria, Fox, Nick C., Choi, Seung-Hoan, Mateo, Ignacio, Hughes, Joseph T., Adams, Hieab H., Malamon, John, Sanchez-Garcia, Florentino, Patel, Yogen, Brody, Jennifer A., Dombroski, Beth A., Naranjo, Maria Candida Deniz, Daniilidou, Makrina, Eiriksdottir, Gudny, Mukherjee, Shubhabrata, Wallon, David, Uphill, James, Aspelund, Thor, Cantwell, Laura B., Garzia, Fabienne, Galimberti, Daniela, Hofer, Edith, Butkiewicz, Mariusz, Fin, Bertrand, Scarpini, Elio, Sarnowski, Chloe, Bush, Will S., Meslage, Stéphane, Kornhuber, Johannes, White, Charles C., Song, Yuenjoo, Barber, Robert C., Engelborghs, Sebastiaan, Sordon, Sabrina, Voijnovic, Dina, Adams, Perrie M., Vandenberghe, Rik, Mayhaus, Manuel, Cupples, L. 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Chawner, Samuel, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Raymond, Lucy, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2019. Genotype-phenotype relationships in children with copy number variants associated with high neuropsychiatric risk: Findings from the Intellectual Disability & Mental Health: Assessing the Genomic Impact on Neurodevelopment (IMAGINE-ID) study. [Online]. BioRxiv. Available at: https://doi.org/10.1101/535708

Richards, Alexander, Horwood, John, Boden, Joseph, Kennedy, Martin, Sellers, Ruth, Riglin, Lucy, Mistry, Sumit, Jones, Hannah, Smith, Daniel J., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Harold, Gordon T. 2019. Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a New Zealand longitudinal population cohort study. British Journal of Psychiatry 214 (2) , pp. 96-102. 10.1192/bjp.2018.227

Drakesmith, Mark ORCID: https://orcid.org/0000-0001-8574-9560, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049 and Linden, David E. J. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) , 102. 10.1038/s41398-019-0440-7

Crawford, Karen, Bracher-Smith, Matthew, Owen, David ORCID: https://orcid.org/0000-0003-4798-0862, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Pardinas, Antonio F., Einon, Mark ORCID: https://orcid.org/0000-0003-3797-7352, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2019. Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank. Journal of Medical Genetics 56 , pp. 131-138. 10.1136/jmedgenet-2018-105477

Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Hannon, Eilis ORCID: https://orcid.org/0000-0001-6840-072X, Harwood, Janet C., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Thomas, Kerrie L. ORCID: https://orcid.org/0000-0003-3355-9583, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2019. Dynamic expression of genes associated with schizophrenia and bipolar disorder across development. Translational Psychiatry 9 , 74. 10.1038/s41398-019-0405-x

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Chawner, Samuel, Fiksinski, Ania, Vorstman, Jacob A.S., Maeder, Johanna, Schneider, Maude, Eliez, Stephan, Armando, Marco, Pontillo, Maria, Vicari, Stefano, McDonald-McGinn, Donna M., Emanuel, Beverly, Zackai, Elaine, Bearden, Carrie E., Shashi, Vandana, Hooper, Stephen R., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Gur, Raquel A., Wray, Naomi R., van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2019. Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome. Schizophrenia Research 204 , pp. 320-325. 10.1016/j.schres.2018.07.044

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Chawner, Samuel J.R.A., Doherty, Joanne L., Maillard, Anne M., Jacquemont, Sbastien, Chung, Wendy K., Green-Snyder, LeeAnne, Bernier, Raphael A., Goin-Kochel, Robin P., Hanson, Ellen, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Linden, Stefanie C. ORCID: https://orcid.org/0000-0002-5638-9292, Raymond, F. Lucy, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2019. Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry 10.1038/s41398-018-0339-8

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Bracher-Smith, Matthew, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2019. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank. Journal of Molecular Psychiatry , -. 10.1038/s41380-018-0328-6 Item availability restricted.

Vivian-Griffiths, Timothy, Baker, Emily, Schmidt, Karl M. ORCID: https://orcid.org/0000-0002-0227-3024, Bracher-Smith, Matthew, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Artemiou, Andreas ORCID: https://orcid.org/0000-0002-7501-4090, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2019. Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 (1) , pp. 80-85. 10.1002/ajmg.b.32705

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Byrne, Enda, Trzaskowski, Maciej, Sidorenko, Julia, Kemper, Kathryn, McGrath, John J., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Wray, Naomi R. 2019. Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Translational Psychiatry 10 , 51. 10.1038/s41398-020-0688-y

Brieva, Jorge, Lepore, Natasha, Romero, Eduardo, Cunningham, Adam C., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Schmitt, Eric, Gur, Raquel E., Roalf, David, Ruparel, Kosha, McDonald-McGinn, Donna, Emanuel, Beverly, Craig, Michael, Murphy, Declan, Murphy, Clodaph, Gudbrandsen, Maria, Daly, Eileen, Kates, Wendy R., Bakker, Geor, van Amelsvoort, Therese, Jonas, Rachel, Hansen, Laura, Lin, Amy, Nir, Talia, Sun, Daqiang V., Kothapalli, Deydeep, Ching, Christopher R., Thompson, Paul M., Bearden, Carrie E., Jahanshad, Neda, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E., Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Doherty, Joanne, Durdle, Courtney A., McCabe, Kathryn L., Campbell, Linda E., Fremont, Wanda, Antshel, Kevin M., Jalbrzikowski, Maria, Vajdi, Ariana V., Kushan, Leila V., Forsyth, Jennifer K. and Villalón-Reina, Julio 2018. Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome. Presented at: 14th International Symposium on Medical Information Processing and Analysis,, Mazatlán, Mexico, 24-26 October 2018. Published in: Romero, Eduardo, Lepore, Natasha and Brieva, Jorge eds. 14th International Symposium on Medical Information Processing and Analysis. Proceedings of SPIE , vol.10975 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788

Arnau-Soler, Aleix, Adams, Mark J., Hayward, Caroline, Thomson, Pippa A., Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, M J ORCID: https://orcid.org/0000-0003-4798-0862, Tansey, Katherine and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2018. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PLoS ONE 13 (12) , e0209160. 10.1371/journal.pone.0209160

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Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Hubbard, Leon, Tansey, Katherine, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Legge, Sophie, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2018. Examining cognition across the bipolar / schizophrenia diagnostic spectrum. Journal of Psychiatry and Neuroscience 43 (3) , 170076. 10.1503/jpn.170076

Cosgrove, Donna, Mothersill, David O., Whitton, Laura, Harold, Denise, Kelly, Sinead, Holleran, Laurena, Holland, Jessica, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Richards, Alexander, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Gill, Michael, Corvin, Aiden, Morris, Derek W. and Donohoe, Gary 2018. Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (3) , pp. 369-376. 10.1002/ajmg.b.32620

Morrison, Sinead, Chawner, Samuel, van Amelsvoort, Therese, Swillen, Ann, Vergaelen, Elfi, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2018. Vulnerable periods for cognitive development in individuals at high genomic risk of schizophrenia [Conference Abstract]. Schizophrenia Bulletin 44 (suppl) , S86. 10.1093/schbul/sby015.214

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Corbin, L, Tan, V, Wade, K, Paul, D, Tansey, Katherine E., Butcher, F, Dudbridge, F, Howson, J, Jallow, M, John, C, Kingston, N, Lindgren, C, O' Donavan, Michael, O’Rahilly, S, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Palmer, C, Pearson, E, Scott, R, van Heel, D, Whittaker, J, Frayling, T, Tobin, M, Wain, L, Smith, G, Evans, D, Karpe, F, McCarthy, M, Danesh, J, Franks, P and Timpson, N 2018. Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference. Nature Communications 9 , 711. 10.1038/s41467-018-03109-y

Cunningham, Adam C., Delport, Sue ORCID: https://orcid.org/0000-0001-8065-5493, Cumines, Wendy, Busse, Monica, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2018. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome. British Journal of Psychiatry 212 (1) , pp. 27-33. 10.1192/bjp.2017.6

Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Hamshere, Marian ORCID: https://orcid.org/0000-0002-8990-0958, Pardiñas, Antonio F., Forty, Liz, Knott, Sarah, Gordon-Smith, Katherine, Porteous, David J., Haywood, Caroline, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, McIntosh, Andrew M., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2018. Association between schizophrenia-related polygenic liability and the occurrence and level of mood-incongruent psychotic symptoms in bipolar disorder. JAMA Psychiatry 75 (1) , pp. 28-35. 10.1001/jamapsychiatry.2017.3485

Green, Elaine K., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Forty, Liz, Gordon-Smith, Katherine, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Fraser, Christine, Richards, Alexander L., Moran, Jennifer L., Purcell, Shaun, Sklar, Pamela, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889 and Jones, Ian R. ORCID: https://orcid.org/0000-0001-5821-5889 2017. Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 (8) , pp. 767-771. 10.1002/ajmg.b.32572

Cosgrove, Donna, Mothersill, Omar, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Konte, Bettina, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Giegling, Ina, Hartmann, Annette, Richards, Alexander, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Gill, Michael, Rujescu, Dan, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Corvin, Aiden, Morris, Derek W. and Donohoe, Gary 2017. Cognitive characterization of schizophrenia risk variants involved in synaptic transmission: evidence of CACNA1C's role in working memory. Neuropsychopharmacology 42 , pp. 2612-2622. 10.1038/npp.2017.123

Bassett, Anne S., Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Repetto, Gabriela M., Simon, Tony, Boot, Erik, Heung, Tracy, Evers, Rens, Vingerhoets, Claudia, van Duin, Esther, Zackai, Elaine, Vergaelen, Elfi, Devriendt, Koen, Vermeesch, Joris, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Clodagh, Michaelovosky, Elena, Kushan, Leila, Schneider, Maude, Fremont, Wanda, Busa, Tiffany, Hooper, Stephen, McCabe, Kathryn, Duijff, Sasja, Isaev, Karin, Pellecchia, Giovanna, Wei, John, Gazzellone, Matthew J., Scherer, Stephen W., Emanuel, Beverly S., Guo, Tingwei, Morrow, Bernice E., Marshall, Christian R. and International 22q11.2DS Brain and Behavior Consortium 2017. Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome. American Journal of Psychiatry 174 (11) , pp. 1054-1063. 10.1176/appi.ajp.2017.16121417

Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Richards, Alexander L., Walters, James T. ORCID: https://orcid.org/0000-0002-6980-4053, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Chambert, Kimberly, Al Eissa, Mariam M., Sharp, Sally I., O'Brien, Niamh L., Curtis, David, Bass, Nicholas J., McQuillin, Andrew, Hultman, Christina, Moran, Jennifer L., McCarroll, Steven A., Sklar, Pamela, Neale, Benjamin M., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Sullivan, Patrick F. and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2017. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 (7) , pp. 724-731. 10.1002/ajmg.b.32560

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Schneider, Maude, Debbané, Martin, Bassett, Anne S., Chow, Eva W.C., Fung, Wai Lun Alan, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W.J., Swillen, Ann, Gothelf, Doron, Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J. and Eliez, Stephan 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: Results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. American Journal of Psychiatry 171 (6) , pp. 627-639. 10.1176/appi.ajp.2013.13070864

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Liu, Guiyou, Yao, Lifen, Liu, Jiafeng, Jiang, Yongshuai, Ma, Guoda, Chen, Zugen, Zhao, Bin, Li, Keshen, Chapman, Jade, Denning, Nicola, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Gerrish, Amy, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2014. Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies. Neurobiology of Aging 35 (4) , pp. 786-92. 10.1016/j.neurobiolaging.2013.10.084

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Monks, Stephen, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Davies, Aimee, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 and Murphy, Kieran 2014. Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome. Schizophrenia Research 153 (1-3) , pp. 231-236. 10.1016/j.schres.2014.01.020

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van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Miller, Gregory, Mansell, Elizabeth, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Flinter, Frances and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2013. The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS). European Journal of Medical Genetics 56 (8) , pp. 439-441. 10.1016/j.ejmg.2013.05.001

Power, Robert A., Lecky-Thompson, Lucy, Fisher, Helen L., Cohen-Woods, Sarah, Hosang, Georgina M., Uher, Rudolf, Powell-Smith, Georgia, Keers, Robert, Tropeano, Maria, Korszun, Ania, Jones, Lisa, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Craig, Ian W., Farmer, Anne E. and McGuffin, Peter 2013. The interaction between child maltreatment, adult stressful life events and the 5-HTTLPR in major depression. Journal of Psychiatric Research 47 (8) , pp. 1032-1035. 10.1016/j.jpsychires.2013.03.017

Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Cross, William, Newsway, Victoria, Dillman, Allissa, Vandrovcova, Jana, Morris, Christopher M., Nalls, Michael A., Ferrucci, Luigi, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Cookson, Mark R., Singleton, Andrew B., de Silva, Rohan and Morris, Huw R. 2013. Variation in tau isoform expression in different brain regions and disease states. Neurobiology of Aging 34 (7) , 1922.e7-1922.e12. 10.1016/j.neurobiolaging.2013.01.017

Yang, Li, Neale, Benjamin M., Liu, Lu, Lee, S. Hong, Wray, Naomi R., Ji, Ning, Li, Haimei, Qian, Qiujin, Wang, Dongliang, Li, Jun, Faraone, Stephen V., Wang, Yufeng, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2013. Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (5) , pp. 419-430. 10.1002/ajmg.b.32169

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Smith, Rhodri, Richards, Alexander, Green, Elaine Karen, Grozeva, Detelina Valentinova ORCID: https://orcid.org/0000-0003-3239-8415, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Forty, Elizabeth, Jones, L. ORCID: https://orcid.org/0000-0001-5821-5889, Gordon-Smith, Katherine, Riley, B., O'Neill, T., Kendler, K. S., Sklar, P., Purcell, S, Kranz, J., Morris, D., Gill, M., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Corvin, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2013. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Molecular Psychiatry 18 (6) , pp. 708-712. 10.1038/mp.2012.67

Zou, Fanggeng, Belbin, Olivia, Carrasquillo, Minerva M., Culley, Oliver J., Hunter, Talisha A., Ma, Li, Bisceglio, Gina D., Allen, Mariet, Dickson, Dennis W., Graff-Radford, Neill R., Petersen, Ronald C., Morgan, Kevin, Younkin, Steven G., Chapman, Jade, Denning, Nicola, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Gerrish, Amy, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pahwa, Jaspreet, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Thomas, Charlene and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2013. Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's Disease pathology. PLoS ONE 8 (5) , e64802. 10.1371/journal.pone.0064802

Kavanagh, Davd, Dwyer, Sarah, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2013. The ENCODE project: implications for psychiatric genetics. Molecular Psychiatry 18 (5) , pp. 540-542. 10.1038/mp.2013.13

Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Lewis, Glyn, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 2013. Defective processing speed and nonclinical psychotic experiences in children: longitudinal analyses in a large birth cohort. American Journal of Psychiatry 170 (5) , pp. 550-557. 10.1176/appi.ajp.2012.12060792

Lambert, J. C., Grenier-Boley, B., Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Zelenika, D., Chouraki, V., Kamatani, Y., Sleegers, K., Ikram, M. A., Hiltunen, M., Reitz, C., Mateo, I., Feulner, T., Bullido, M., Galimberti, D., Concari, L., Alvarez, V., Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Gerrish, Amy, Chapman, Jade Alice, Deniz-Naranjo, C., Solfrizzi, V., Sorbi, S., Arosio, B., Spalletta, G., Siciliano, G., Epelbaum, J., Hannequin, D., Dartigues, J. F., Tzourio, C., Berr, C., Schrijvers, E. M. C., Rogers, R., Tosto, G., Pasquier, F., Bettens, K., Van Cauwenberghe, C., Fratiglioni, L., Graff, C., Delepine, M., Ferri, R., Reynolds, C. A., Lannfelt, L., Ingelsson, M., Prince, J. A., Chillotti, C., Pilotto, A., Seripa, D., Boland, A., Mancuso, M., Bossù, P., Annoni, G., Nacmias, B., Bosco, P., Panza, F., Sanchez-Garcia, F., Del Zompo, M., Coto, E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Valdivieso, F., Caffara, P., Scarpini, E., Combarros, O., Buée, L., Campion, D., Soininen, H., Breteler, M., Riemenschneider, M., Van Broeckhoven, C., Alpérovitch, A., Lathrop, M., Trégouët, D. A., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Amouyel, P. 2013. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease [Correction]. Molecular Psychiatry 18 (4) , p. 521. 10.1038/mp.2012.75

Kronenberg, Florian, Huertas-Vazquez, Adriana, Nelson, Christopher P., Guo, Xiuqing, Reinier, Kyndaron, Uy-Evanado, Audrey, Teodorescu, Carmen, Ayala, Jo, Jerger, Katherine, Chugh, Harpriya, WTCCC+, Braund, Peter S., Deloukas, Panos, Hall, Alistair S., Balmforth, Anthony J., Jones, Michelle, Taylor, Kent D., Pulit, Sara L., Newton-Cheh, Christopher, Gunson, Karen, Jui, Jonathan, Rotter, Jerome I., Albert, Christine M., Samani, Nilesh J., Chugh, Sumeet S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Dunajewski, Katherine, Forty, Elizabeth, Green, Elaine, Grozeva, Detelina, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2013. Novel Loci Associated with Increased Risk of Sudden Cardiac Death in the Context of Coronary Artery Disease [Article]. PLoS ONE 8 (4) , e59905. 10.1371/journal.pone.0059905

Terwisscha van Scheltinga, Afke F., Bakker, Steven C., van Haren, Neeltje E.M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B.M., Cahn, Wiepke, Hulshoff Pol, Hilleke E., Ripke, Stephan, Ophoff, Roel A., Kahn, René S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Dwyer, Sarah, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ruderfer, Doug, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2013. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological Psychiatry 73 (6) , pp. 525-531. 10.1016/j.biopsych.2012.08.017

Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S. and Morrow, Bernice E. 2013. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics 92 (3) , pp. 439-447. 10.1016/j.ajhg.2013.01.018

Guha, Saurav, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Darvasi, Ariel, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K., Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M., Moran, Jennifer L., Chambert, Kimberly D., Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill,, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M., Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lencz, Todd and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2013. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 70 (3) , pp. 253-260. 10.1001/2013.jamapsychiatry.71

Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Monks, Stephen, Murphy, Kieran C., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2013. Schizophrenia two-hit hypothesis in velo-cardio facial syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (2) , pp. 177-182. 10.1002/ajmg.b.32129

Donohoe, G., Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Hargreaves, A., Rose, E. J., Morris, D. W., Fahey, C., Bellini, S., Cummins, E., Giegling, I., Hartmann, A. M., Möller, H.-J., Muglia, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Tropea, D., Rujescu, D. and Corvin, A. 2013. Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. Genes, Brain and Behavior 12 (2) , pp. 203-209. 10.1111/gbb.12016

Chapman, J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Harold, Denise, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Gerrish, Amy, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Hollingworth, P, Stretton, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476

Rucker, J. J. H., Breen, G., Pinto, D., Pedroso, I., Lewis, C. M., Cohen-Woods, S., Uher, R., Schosser, A., Rivera, M., Aitchison, K. J., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, L., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Korszun, A., Muglia, P., Barnes, M. R., Preisig, M., Mors, O., Gill, M., Maier, W., Rice, J., Rietschel, M., Holsboer, F., Farmer, A. E., Craig, I. W., Scherer, S. W. and McGuffin, P. 2013. Genome-wide association analysis of copy number variation in recurrent depressive disorder. Molecular Psychiatry 18 , pp. 183-189. 10.1038/mp.2011.144

Fisher, Helen L., Cohen-Woods, Sarah, Hosang, Georgina M., Korszun, Ania, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Craig, Ian W., Farmer, Anne E., McGuffin, Peter and Uher, Rudolf 2013. Interaction between specific forms of childhood maltreatment and the serotonin transporter gene (5-HTT) in recurrent depressive disorder. Journal of Affective Disorders 145 (1) , pp. 136-141. 10.1016/j.jad.2012.05.032

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Russo, Giancarlo, Vedernikov, Alexey, Sharma, Manu, Saad, Mohamad, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Bras, Jose M., Bettella, Francesco, Keller, Margaux F., Nicolaou, Nayia, Simón-Sánchez, Javier, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Peter, Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael Conlon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Morris, Huw and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2013. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurology 70 (10) , pp. 1268-1276. 10.1001/jamaneurol.2013.448

Kim, Y., Ripke, Stephan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Sklar, Pamela, Purcell, Shaun M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Sullivan, Patrick F. 2013. Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophrenia Research 143 (1) , pp. 11-17. 10.1016/j.schres.2012.11.002

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Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, Farmer, A., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L., McGuffin, P., Moran, J. L., Purcell, S., Sklar, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2013. Association at SYNE1 in both bipolar disorder and recurrent major depression. Molecular Psychiatry 18 , pp. 614-617. 10.1038/mp.2012.48

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Håvik, Bjarte, Degenhardt, Franziska A., Johansson, Stefan, Fernandes, Carla P. D., Hinney, Anke, Scherag, André, Lybæk, Helle, Djurovic, Srdjan, Christoforou, Andrea, Ersland, Kari M., Giddaluru, Sudheer, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Mühleisen, Thomas W., Mattheisen, Manuel, Schimmelmann, Benno G., Renner, Tobias, Warnke, Andreas, Herpertz-Dahlmann, Beate, Sinzig, Judith, Albayrak, Özgür, Rietschel, Marcella, Nöthen, Markus M., Bramham, Clive R., Werge, Thomas, Hebebrand, Johannes, Haavik, Jan, Andreassen, Ole A., Cichon, Sven, Steen, Vidar M. and Le Hellard, Stéphanie 2012. DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS ONE 7 (4) , e35424. 10.1371/journal.pone.0035424

Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Conrad, Donald F., Barnes, Chris P., Hurles, Matthew, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2012. Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia. Schizophrenia Research 135 (1-3) , pp. 1-7. 10.1016/j.schres.2011.11.004

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Economou, Alexis, Grey, Michelle, McGregor, Joanna, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Lyons, Ronan A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Price, Vaughn, Thomson, Sue, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 and Lloyd, Keith 2012. The health informatics cohort enhancement project (HICE): using routinely collected primary care data to identify people with a lifetime diagnosis of psychotic disorder. BMC Research Notes 5 (1) , pp. 95-100. 10.1186/1756-0500-5-95

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Jia, P., Wang, L., Fanous, A. H., Chen, X., Kendler, K. S., Zhao, Z., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Georgieva, Lyudmila, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ruderfer, D.M., Williams, H. and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2012. A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics 49 (2) , pp. 96-103. 10.1136/jmedgenet-2011-100397

Richards, Alexander, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell, S., Visscher, P. M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2012. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry 17 (2) , pp. 193-201. 10.1038/mp.2011.11

Stergiakouli, Evangelia, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Zaharieva, Irina, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2012. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry 169 (2) , pp. 186-194. 10.1176/appi.ajp.2011.11040551

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Franke, Barbara, Mick, Eric, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Freitag, Christine M., Gill, Michael, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter and Faraone, Stephen V. 2012. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry 169 (2) , pp. 195-204. 10.1176/appi.ajp.2011.11060822

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Sullivan, P, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2012. Don't give up on GWAS [Letter]. Molecular Psychiatry 17 (1) , pp. 2-3. 10.1038/mp.2011.94

Proitsi, Petroula, Lupton, Michelle K., Reeves, Suzanne J., Hamilton, Gillian, Archer, Nicola, Martin, Belinda M., Iyegbe, Conrad, Hollingworth, Paul, Lawlor, Brian, Gill, Michael, Brayne, Carol, Rubinsztein, David C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Lovestone, Simon and Powell, John F. 2012. Association of serotonin and dopamine gene pathways with behavioral subphenotypes in dementia. Neurobiology of Aging 33 (4) , pp. 791-803. 10.1016/j.neurobiolaging.2010.06.011

Fisher, Helen L., Cohen-Woods, Sarah, Hosang, Georgina M., Uher, Rudolf, Powell-Smith, Georgia, Keers, Robert, Tropeano, Maria, Korszun, Ania, Jones, Lisa, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Craig, Ian W., Farmer, Anne E. and McGuffin, Peter 2012. Stressful life events and the serotonin transporter gene (5-HTT) in recurrent clinical depression. Journal of Affective Disorders 136 (1-2) , pp. 189-193. 10.1016/j.jad.2011.09.016

Doherty, Joanne L., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2012. Recent genomic advances in schizophrenia. Clinical Genetics 81 (2) , pp. 103-109. 10.1111/j.1399-0004.2011.01773.x

Baig, Shabnam, Palmer, Laura E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Kehoe, Patrick G. and Love, Seth 2012. Clusterin mRNA and protein in Alzheimer's disease. Journal of Alzheimer's Disease 28 (2) , pp. 337-344. 10.3233/JAD-2011-110473

Hinney, Anke, Scherag, André, Jarick, Ivonne, Albayrak, Özgür, Pütter, Carolin, Pechlivanis, Sonali, Dauvermann, Maria R., Beck, Sebastian, Weber, Heike, Scherag, Susann, Nguyen, Trang T., Volckmar, Anna-Lena, Knoll, Nadja, Faraone, Stephen V., Neale, Benjamin M., Franke, Barbara, Cichon, Sven, Hoffmann, Per, Nöthen, Markus M., Schreiber, Stefan, Jöckel, Karl-Heinz, Wichmann, H.-Erich, Freitag, Christine, Lempp, Thomas, Meyer, Jobst, Gilsbach, Susanne, Herpertz-Dahlmann, Beate, Sinzig, Judith, Lehmkuhl, Gerd, Renner, Tobias J., Warnke, Andreas, Romanos, Marcel, Lesch, Klaus-Peter, Reif, Andreas, Schimmelmann, Benno G., Hebebrand, Johannes, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2011. Genome-wide association study in German patients with attention deficit/hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 888-897. 10.1002/ajmg.b.31246

Cardno, A. G., Holmans, Peter Andrew ORCID: https://orcid.org/0000-0003-0870-9412, Rees, M. I., Jones, L. A., McCarthy, G. M., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Williams, H. J., Fenton, I., Murphy, K. C., Sanders, R. D., Gray, M. Y., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. A genomewide linkage study of age at onset in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (8) , pp. 929-940. 10.1002/ajmg.1404

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2011. De novo rates and selection of schizophrenia-associated copy number variants. Biological Psychiatry 70 (12) , pp. 1109-1114. 10.1016/j.biopsych.2011.07.011

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Zuliani, Riccardo, Moorhead, T. William J., Bastin, Mark E., Johnstone, Eve C., Lawrie, Stephen M., Brambilla, Paolo, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy and McIntosh, Andrew M. 2011. Genetic variants in the ErbB4 gene are associated with white matter integrity. Psychiatry Research: Neuroimaging 191 (2) , pp. 133-137. 10.1016/j.pscychresns.2010.11.001

Reilly, Muredach P, Li, Mingyao, He, Jing, Ferguson, Jane F, Stylianou, Ioannis M, Mehta, Nehal N, Burnett, Mary Susan, Devaney, Joseph M, Knouff, Christopher W, Thompson, John R, Horne, Benjamin D, Stewart, Alexandre FR, Assimes, Themistocles L, Wild, Philipp S, Allayee, Hooman, Nitschke, Patrick Linsel, Patel, Riyaz S, Martinelli, Nicola, Girelli, Domenico, Quyyumi, Arshed A, Anderson, Jeffrey L, Erdmann, Jeanette, Hall, Alistair S, Schunkert, Heribert, Quertermous, Thomas, Blankenberg, Stefan, Hazen, Stanley L, Roberts, Robert, Kathiresan, Sekar, Samani, Nilesh J, Epstein, Stephen E, Rader, Daniel J, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. The Lancet 377 (9763) , pp. 383-392. 10.1016/S0140-6736(10)61996-4

Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Russo, Giancarlo, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dwyer, Sarah Lynne, Smith, Rhodri L., Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2011. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Human Molecular Genetics 20 (2) , pp. 387-391. 10.1093/hmg/ddq471

Bridges, Michael, Heron, Elizabeth A., O'Dushlaine, Colm, Segurado, Ricardo, Morris, Derek, Corvin, Aiden, Gill, Michael, Pinto, Carlos, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Toncheva, Draga, Milanova, Vihra and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Green, Elaine Karen, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, Anne, McGuffin, Peter, Sklar, P., Purcell, S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2011. Polygenic dissection of the bipolar phenotype. British Journal of Psychiatry 198 (4) , pp. 284-288. 10.1192/bjp.bp.110.087866

Schosser, A., Ng, M.Y., Butler, A.W., Cohen-Woods, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craig, I., Farmer, A.E., Lewis, C.M. and McGuffin, P. 2011. P02-217 - COMT in major depression - UK candidate gene association study [Meeting Abstract]. European Psychiatry 26 , p. 813. 10.1016/S0924-9338(11)72518-4

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2011. Structural variations in attention-deficit hyperactivity disorder - Authors' reply [Letter]. The Lancet 377 (9763) , p. 378. 10.1016/S0140-6736(11)60121-9

Reitz, Christine, Cheung, Rong, Rogaeva, Ekaterina, Lee, Joseph H., Tokuhiro, Shinya, Zou, Fanggeng, Bettens, Karolien, Sleegers, Kristel, Tan, Eng King, Kimura, Ryo, Shibata, Nobuto, Arai, Heii, Kamboh, Ilyas, Prince, Jonathan A., Maier, Wolfgang, Riemenschneider, Matthias, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Hollingworth, Paul, Cellini, Elena, Sorbi, Sandro, Nacmias, Benedetta, Takeda, Masatoshi, Pericak-Vance, Margaret A., Haines, Jonathan L., Younkin, Steven, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, van Broeckhoven, Christine, Farrer, Lindsay, St George-Hyslop, Peter and Mayeux, Richard 2011. Meta-analysis of the association between variants in SORL1 and Alzheimer Disease. Archives of Neurology 68 (1) , pp. 99-106. 10.1001/archneurol.2010.346

Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Raybould, Rachel, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, St. Clair, D., Young, A.H., Ferrier, I.N., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2011. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (4) , pp. 490-492. 10.1002/ajmg.b.31187

Smith, Rhodri L., Knight, Deborah, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Dwyer, Sarah Lynne, Richards, Alexander, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Analysis of neurogranin (NRGN) in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (5) , pp. 532-535. 10.1002/ajmg.b.31191

Schosser, A., Gaysina, D., Cohen-Woods, S., Domenici, E., Perry, J., Tozzi, F., Korszun, A., Gunasinghe, C., Gray, J., Jones, L., Binder, E. B., Holsboer, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craig, I. W., Farmer, A. E., Muglia, P. and McGuffin, P. 2011. A follow-up case-control association study of tractable (druggable) genes in recurrent major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (6) , pp. 640-650. 10.1002/ajmg.b.31204

Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Dwyer, Sarah Lynne, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade Alice, Denning, Nicola, Abraham, Richard Alun, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Pahwa, Jaspreet Singh, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dowzell, Kimberley Frances, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 764-771. 10.1002/ajmg.b.31216

Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Smith, Rhodri L., Dwyer, Sarah Lynne, Russo, Giancarlo, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2011. Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 781-784. 10.1002/ajmg.b.31219

Carroll, Liam Stuart, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 844-849. 10.1002/ajmg.b.31231

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, McGuffin, Peter, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Cardno, Alastair G. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 929-940. 10.1002/ajmg.b.31240

Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Waite, Adrian James, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Morris, Huw Rees 2011. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Movement Disorders 26 (10) , pp. 1939-1942. 10.1002/mds.23791

Boot, Erik, Booij, Jan, Zinkstok, Janneke R., Baas, Frank, Swillen, Ann, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Declan G., Murphy, Kieran C., Linszen, Don H. and Van Amelsvoort, Thérèse A. 2011. COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome. Synapse 65 (9) , pp. 967-970. 10.1002/syn.20932

Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miró, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, René, Schmäl, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H.-Erich, Schreiber, Stefan, Müller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Reif, Andreas, Sasse, Johanna, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Mitchell, Philip B., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Gustafsson, Omar, Andreassen, Ole, Djurovic, Srdjan, Sigurdsson, Engilbert, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Kapur-Pojskic, Lejla, Oruc, Liliana, Rivas, Fabio, Mayoral, Fermín, Chuchalin, Alexander, Babadjanova, Gulja, Tiganov, Alexander S., Pantelejeva, Galina, Abramova, Lilia I., Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C., Czerski, Piotr M., Hauser, Joanna, Zimmer, Andreas, Lathrop, Mark, Schulze, Thomas G., Wienker, Thomas F., Schumacher, Johannes, Maier, Wolfgang, Propping, Peter, Rietschel, Marcella and Nöthen, Markus M. 2011. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics 88 (3) , pp. 372-381. 10.1016/j.ajhg.2011.01.017

Hansen, Thomas, Ingason, Andrés, Djurovic, Srdjan, Melle, Ingrid, Fenger, Mogens, Gustafsson, Omar, Jakobsen, Klaus D., Rasmussen, Henrik B., Tosato, Sarah, Rietschel, Marcella, Frank, Josef, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Bonetto, Chiara, Suvisaari, Jaana, Thygesen, Johan Hilge, Pétursson, Hannes, Lönnqvist, Jouko, Sigurdsson, Engilbert, Giegling, Ina, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Ruggeri, Mirella, Cichon, Sven, Ophoff, Roel A., Pietiläinen, Olli, Peltonen, Leena, Nöthen, Markus M., Rujescu, Dan, St. Clair, David, Collier, David A., Andreassen, Ole A. and Werge, Thomas 2011. At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biological Psychiatry 70 (1) , pp. 59-63. 10.1016/j.biopsych.2011.01.031

Donohoe, Gary, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Morris, Derek W., Da Costa, Andreia, Rose, Emma, Hargreaves, April, Maher, Katie, Hayes, Eimear, Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Muglia, Pierandrea, Moskvina, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Gill, Michael, Corvin, Aiden and Rujescu, Dan 2011. A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809 [Letter]. Schizophrenia Research 125 (2-3) , pp. 304-306. 10.1016/j.schres.2010.10.019

Proitsi, P., Hamilton, G., Tsolaki, M., Lupton, M., Daniilidou, M., Hollingworth, Paul, Archer, N., Foy, C., Stylios, F., McGuinness, B., Todd, S., Lawlor, B., Gill, M., Brayne, C., Rubinsztein, D.C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, John David, Craig, D., Passmore, P., Lovestone, S. and Powell, J. F. 2011. A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD). Neurobiology of Aging 32 (3) , pp. 434-442. 10.1016/j.neurobiolaging.2009.03.005

Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T., Borglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietilainen, O. P. H., Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N., Tuulio-Henriksson, A., Suvisaari, J., Lonnqvist, J., Paunio, T., Agartz, I., Melle, I., Djurovic, S., Strengman, E., Jurgens, G., Glenthoj, B., Terenius, L., Hougaard, D, Orntoft, T., Wiuf, C., Didriksen, M., Hollegaard, M. V., Nordentoft, M., van Winkel, R., Kenis, G., Abramova, L., Kaleda, V., Arrojo, M., Sanjuan, J., Arango, C., Sperling, S., Rossner, M., Ribolsi, M., Magni, V., Siracusano, A., Christiansen, C., Kiemeney, L. A., Veldink, J., van den Berg, L., Ingason, A., Muglia, P., Murray, R., Nothen, M. M., Sigurdsson, E., Petursson, H., Thorsteinsdottir, U., Kong, A., Rubino, I. A., De Hert, M., Rethelyi, J. M., Bitter, I., Jonsson, E. G., Golimbet, V., Carracedo, A., Ehrenreich, H., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Ruggeri, M., Tosato, S., Peltonen, L., Ophoff, R. A., Collier, D. A., St Clair, D., Rietschel, M., Cichon, S., Stefansson, H., Rujescu, D. and Stefansson, K. 2011. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics 20 (20) , pp. 4076-4081. 10.1093/hmg/ddr325

Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Kamatani, Y., Kamatani, N., Stoianov, D., Vazharova, R., Karachanak, S., Zaharieva, I., Dimova, I., Hadjidekova, S., Milanova, V., Madjirova, N., Gerdjikov, I., Tolev, T., Poryazova, N., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Toncheva, D. and Nakamura, Y. 2011. Genome-wide association study on bipolar disorder in the Bulgarian population. Genes, Brain and Behavior 10 (7) , pp. 789-797. 10.1111/j.1601-183X.2011.00721.x

Samaan, Zainab, Gaysina, Daria, Cohen-Woods, Sarah, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Lisa, Korszun, Ania, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mente, Andrew, McGuffin, Peter and Farmer, Anne 2011. Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis. BMC Neurology 11 , pp. 66-74. 10.1186/1471-2377-11-66

Breen, Gerome, Webb, Bradley Todd, Butler, Amy W., van den Oord, Edwin J. C. G., Tozzi, Federica, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, Mike, Korszun, Ania, Maier, Wolfgang, Middleton, Lefkos, Mors, Ole, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Cohen-Woods, Sarah, Perry, Julia, Galwey, Nicholas W., Upmanyu, Ruchi, Craig, Ian, Lewis, Cathryn M., Ng, Mandy, Brewster, Shyama, Preisig, Martin, Rietschel, Marcella, Jones, Lisa, Knight, Jo, Rice, John, Muglia, Pierandrea, Farmer, Anne E. and McGuffin, Peter 2011. A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. American Journal of Psychiatry 168 (8) , pp. 840-847. 10.1176/appi.ajp.2011.10091342

Schosser, Alexandra, Butler, Amy W., Ising, Marcus, Perroud, Nader, Uher, Rudolf, Ng, Mandy Y., Cohen-Woods, Sarah, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Korszun, Ania, Jones, Lisa, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Gill, Michael, Rice, John P., Maier, Wolfgang, Mors, Ole, Rietschel, Marcella, Lucae, Susanne, Binder, Elisabeth B., Preisig, Martin, Perry, Julia, Tozzi, Federica, Muglia, Pierandrea, Aitchison, Katherine J., Breen, Gerome, Craig, Ian W., Farmer, Anne E., Müller-Myhsok, Bertram, McGuffin, Peter and Lewis, Cathryn M. 2011. Genomewide association scan of suicidal thoughts and behaviour in major depression. PLoS ONE 6 (7) , e20690. 10.1371/journal.pone.0020690

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2011. Neurodevelopmental hypothesis of schizophrenia. British Journal of Psychiatry 198 (3) , pp. 173-175. 10.1192/bjp.bp.110.084384

Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5) , pp. 398-403.

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Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Jones, L, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Nikolov, Ivan, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Vukcevic, D., Caesar, S., Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen Elizabeth, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Donnelly, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype. Molecular Psychiatry 15 (2) , pp. 146-153. 10.1038/mp.2008.66

Ikeda, Masashi, Tomita, Yasuyuki, Mouri, Akihiro, Koga, Minori, Okochi, Tomo, Yoshimura, Reiji, Yamanouchi, Yoshio, Kinoshita, Yoko, Hashimoto, Ryota, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Takeda, Masatoshi, Nakamura, Jun, Nabeshima, Toshitaka, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Honda, Hiroyuki, Arinami, Tadao, Ozaki, Norio and Iwata, Nakao 2010. Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches. Biological psychiatry 67 (3) , pp. 263-269. 10.1016/j.biopsych.2009.08.030

Ikeda, Masashi, Aleksic, Branko, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kinoshita, Yoko, Yamanouchi, Yoshio, Kitajima, Tsuyoshi, Kawashima, Kunihiro, Okochi, Tomo, Kishi, Taro, Zaharieva, Irina Takova, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Ozaki, Norio and Iwata, Nakao 2010. Copy number variation in schizophrenia in the Japanese population. Biological Psychiatry 67 (3) , pp. 283-286. 10.1016/j.biopsych.2009.08.034

Schosser, A., Ng, M. Y., Butler, A. W., Uher, R., Cohen-Woods, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Aitchison, K. J., Breen, G., Craig, I., Farmer, A. E., Lewis, C. M. and McGuffin, P. 2010. Genome wide association scan of co-morbid anxiety in major depressive disorder (MDD) [Abstract]. International Journal of Psychiatry in Clinical Practice 14 (S1) , p. 37.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2010. Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia. Archives of General Psychiatry 67 (7) , pp. 667-673. 10.1001/archgenpsychiatry.2010.69

Ikeda, Masashi, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Smith, Rhodri, Monks, Stephen, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2010. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 980-982. 10.1002/ajmg.b.31060

Cohen-Woods, Sarah, Craig, Ian, Gaysina, Darya, Gray, Joanna, Gunasinghe, Cerisse, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Elkin, Amanda, Jones, Lisa, Kennedy, James, King, Nicole, Korszun, Ania, Knight, Jo, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Parikh, Sagar, Strauss, John, Sterne, Abram, Tozzi, Federica, Perry, Julia, Muglia, Pierandrea, Vincent, John, McGuffin, Peter and Farmer, Anne 2010. The Bipolar Association Case-Control Study (BACCS) and meta-analysis: No association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7) , pp. 1298-1304. 10.1002/ajmg.b.31101

Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa, Forty, Elizabeth, Caesar, Sian, Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen, St Clair, David, Young, Allan H., Ferrier, Nicol, Farmer, Anne, McGuffin, Peter, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2010. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7) , pp. 1347-1349. 10.1002/ajmg.b.31108

Dwyer, Sarah Lynne, Williams, Hywel ORCID: https://orcid.org/0000-0001-7758-0312, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2010. No evidence that rare coding variants in ZNF804A confer risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1411-1416. 10.1002/ajmg.b.31117

Talkowski, Michael E., McCann, Kathleen L., Chen, Michael, McClain, Lora, Bamne, Mikhil, Wood, Joel, Chowdari, Kodavali V., Watson, Annie, Prasad, Konasale M., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Georgieva, Lyudmila, Toncheva, Draga, Mansour, Hader, Lewis, David A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Papasaikas, Panagiotis, Sullivan, Patrick, Ruderfer, Douglas, Yao, Jeffrey K., Leonard, Sherry, Thomas, Pramod, Miyajima, Fabio, Quinn, John, Lopez, A. Javier and Nimgaonkar, Vishwajit L. 2010. Fine-mapping reveals novel alternative splicing of the dopamine transporter. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1434-1447. 10.1002/ajmg.b.31125

Butler, Amy W., Breen, Gerome, Tozzi, Federica, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, Mike, Korszun, Ania, Maier, Wolfgang, Middleton, Lefkos T., Mors, Ole, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Perry, Julia, Preisig, Martin, Rice, John P., Rietschel, Marcella, Jones, Lisa, Farmer, Anne E., Lewis, Cathryn M. and McGuffin, Peter 2010. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1465-1473. 10.1002/ajmg.b.31127

Hollingworth, Paul, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2010. Alzheimer's disease genetics: current knowledge and future challenges. International Journal of Geriatric Psychiatry 26 (8) , pp. 793-802. 10.1002/gps.2628

Lupton, Michelle K, Stahl, Daniel, Archer, Nicola, Foy, Catherine, Poppe, Michaela, Lovestone, Simon, Hollingworth, Paul, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Dowzell, Kimberley Frances, Abraham, Richard Alun, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Brayne, Carol, Rubinsztein, David, Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn and Powell, John F 2010. Education, occupation and retirement age effects on the age of onset of Alzheimer's disease. International Journal of Geriatric Psychiatry 25 (1) , pp. 30-36. 10.1002/gps.2294

Neale, Benjamin M., Medland, Sarah E., Ripke, Stephan, Asherson, Philip, Franke, Barbara, Lesch, Klaus-Peter, Faraone, Stephen V., Nguyen, Thuy Trang, Schäfer, Helmut, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Daly, Mark, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Walitza, Susanne, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Buitelaar, Jan, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Gill, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Kent, Lindsey, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric, Biederman, Joseph, Doyle, Alysa, Smalley, Susan, Loo, Sandra, Hakonarson, Hakon, Elia, Josephine, Todorov, Alexandre, Ana, Miranda, Mulas, Fernando, Ebstein, Richard P., Rothenberger, Aribert, Banaschewski, Tobias, Oades, Richard D., Sonuga-Barke, Edmund, McGough, James, Nisenbaum, Laura, Middleton, Frank, Hu, Xiaolan and Nelson, Stan 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 884-897. 10.1016/j.jaac.2010.06.008

Blake, Derek J., Forrest, Marc, Chapman, Ria M., Tinsley, Caroline L., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. TCF4, Schizophrenia, and Pitt-Hopkins Syndrome. Schizophrenia Bulletin 36 (3) , pp. 443-447. 10.1093/schbul/sbq035

Liu, Y., Blackwood, D. H., Caesar, S., de Geus, E. J. C., Farmer, A., Ferreira, M. A. R., Ferrier, I. N., Fraser, Christine, Gordon-Smith, K., Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Gurling, H. M., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Heutink, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hoogendijk, W. J., Hottenga, J. J., Jones, L., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lin, D., McGuffin, P., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Nolen, W. A., Perlis, R. H., Posthuma, D., Scolnick, E. M., Smit, A. B., Smit, J. H., Smoller, J. W., St Clair, D., van Dyck, R., Verhage, M., Willemsen, G., Young, A. H., Zandbelt, T., Boomsma, D. I., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Penninx, B. W. J. H., Purcell, S., Sklar, P. and Sullivan, P. F. 2010. Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder [Letter]. Molecular Psychiatry 16 (1) , pp. 2-4. 10.1038/mp.2009.107

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Authors' reply:. British Journal of Psychiatry 196 (6) , pp. 495-496. 10.1192/bjp.196.6.495a

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Molecular genetics and the relationship between epilepsy and psychosis [Letter]. British Journal of Psychiatry 197 (1) , pp. 75-76. 10.1192/bjp.197.1.75a

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Data and clinical utility should be the drivers of changes to psychiatric classification [Letter]. British Journal of Psychiatry 197 (2) , p. 158. 10.1192/bjp.197.2.158

Lewis, Cathryn M., Ng, Mandy Y., Butler, Amy W., Cohen-Woods, Sarah, Uher, Rudolf, Pirlo, Katrina, Weale, Michael E., Schosser, Alexandra, Paredes, Ursula M, Rivera, Margarita, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Lisa, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Korszun, Ania, Aitchison, Katherine J., Shi, Jianxin, Quinn, John P., MacKenzie, Alasdair, Vollenweider, Peter, Waeber, Gerard, Heath, Simon, Lathrop, Mark, Muglia, Pierandrea, Barnes, Michael R., Whittaker, John C., Tozzi, Frederica, Holsboer, Florian, Preisig, Martin, Farmer, Anne E., Breen, Gerome, Craig, Ian W. and McGuffin, Peter 2010. Genome-wide association study of major recurrent depression in the U.K. population. American Journal of Psychiatry 167 (8) , pp. 949-957. 10.1176/appi.ajp.2010.09091380

Cruchaga, Carlos, Kauwe, John S. K., Mayo, Kevin, Spiegel, Noah, Bertelsen, Sarah, Nowotny, Petra, Shah, Aarti R., Abraham, Richard, Hollingworth, Paul, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Lovestone, Simon, Peskind, Elaine R., Li, Ge, Leverenz, James B., Galasko, Douglas, Morris, John C., Fagan, Anne M., Holtzman, David M. and Goate, Alison M. 2010. SNPS associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease. PLoS Genetics 6 (9) , e1001101. 10.1371/journal.pgen.1001101

Baig, Shabnam, Joseph, Sally A., Tayler, Hannah, Abraham, Richard Alun, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Kehoe, Patrick G. and Love, Seth 2010. Distribution and expression of picalm in alzheimer disease. Journal of Neuropathology and Experimental Neurology 69 (10) , pp. 1071-1077. 10.1097/NEN.0b013e3181f52e01

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. The Kraepelinian dichotomy - going, going... but still not gone (Reappraisal). British Journal of Psychiatry 196 (2) , pp. 92-95. 10.1192/bjp.bp.109.073429

Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., van den Oord, E., Sullivan, P. F., Shi, J., Levinson, D. F., Gejman, P. V., Sanders, A., Duan, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Blackman, Janet, Lewis, D., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Qin, W., Schwab, S., Wildenauer, D., Chowdari, K., Nimgaonkar, V., Straub, R. E., Weinberger, D. R., O'Neill, F. A., Walsh, D., Bronstein, M., Darvasi, A., Lencz, T., Malhotra, A. K., Rujescu, D., Giegling, I., Werge, T., Hansen, T., Ingason, A., Nöethen, M. M., Rietschel, M., Cichon, S., Djurovic, S., Andreassen, O. A., Cantor, R. M., Ophoff, R., Corvin, A., Morris, D. W., Gill, M., Pato, C. N., Pato, M. T., Macedo, A., Gurling, H. M. D., McQuillin, A., Pimm, J., Hultman, C., Lichtenstein, P., Sklar, P., Purcell, S. M., Scolnick, E., St Clair, D., Blackwood, D. H. R. and Kendler, K. S. 2010. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry 16 (11) , pp. 1117-1129. 10.1038/mp.2010.96

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Molecular genetics and the kraepelinian dichotomy: one disorder, two disorders, or do we need to start thinking afresh? Psychiatric Annals 40 (2) , pp. 88-91. 10.3928/00485718-20100127-04

Fowler, Tom Alan, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Ross, Kenny, Wilkinson, Lawrence Stephen ORCID: https://orcid.org/0000-0002-9337-6124, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2009. Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatric Genetics 19 (6) , pp. 312-319. 10.1097/YPG.0b013e3283328df4

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Hollingworth, Paul, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dowzell, Kimberley, Moore, Pamela J., Foy, Catherine, Archer, Nicola, Lynch, Aoibhinn, Lovestone, Simon, Brayne, Carol, Rubinsztein, David C., Lawlor, Brian, Gill, Mike, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2006. Four Components Describe Behavioral Symptoms in 1,120 Individuals with Late-Onset Alzheimer's Disease. Journal of the American Geriatrics Society 54 (9) , pp. 1348-1354. 10.1111/j.1532-5415.2006.00854.x

Li, Yonghong, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Brayne, Carol, Rowland, Charles, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Morris, John C and Maxwell, Taylor J 2006. DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. Human Molecular Genetics 15 (17) , pp. 2560-2568. 10.1093/hmg/ddl178

Georgieva, Lyudmila, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Peirce, Timothy Rowan, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Macgregor, Stuart, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Wilkinson, Jennifer Camilla, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Nikolov, Ivan, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Davis, Kenneth L., Haroutunian, Vahram, Buxbaum, Joseph D., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America (PNAS) ISSN 1091-6490 103 (33) , pp. 12469-12474. 10.1073/pnas.0603029103

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2006. Genes and behavior: nature-nurture interplay explained. British Journal of Psychiatry 189 (2) , pp. 192-193. 10.1192/bjp.189.2.192

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2006. Refining the attention deficit hyperactivity disorder phenotype for molecular genetic studies. Molecular Psychiatry 11 (8) , pp. 714-20. 10.1038/sj.mp.4001831

Li, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Sham, Pak C and Lin, He 2006. Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD). Human Molecular Genetics 15 (14) , pp. 2276-2284. 10.1093/hmg/ddl152

Talkowski, Michael E., Seltman, Howard, Bassett, Anne S., Brzustowicz, Linda M., Chen, Xiangning, Chowdari, Kodavali V., Collier, David A., Cordeiro, Quirino, Corvin, Aiden P., Deshpande, Smita N., Egan, Michael F., Gill, Michael, Kendler, Kenneth S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Richard, Christian, Semwal, Prachi, Sobell, Janet L., St Clair, David, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Wood, Joel, Zhang, Feng, Devlin, Bernie and Nimgaonkar, Vishwajit L. 2006. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological psychiatry 60 (2) , pp. 152-162. 10.1016/j.biopsych.2006.02.015

Rees, Mark I., Harvey, Kirsten, Pearce, Brian R., Chung, Seo-Kyung, Duguid, Ian C, Thomas, Philip, Beatty, Sarah, Graham, Gail E., Armstrong, Linlea, Shiang, Rita, Abbott, Kim J., Zuberi, Sameer M., Stephenson, John B. P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Tijssen, Marina A. J., Maagdenberg, Arn M. J. M. van den, Smart, Trevor G., Supplisson, Stéphane and Harvey, Robert J. 2006. Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nature genetics 38 (7) , pp. 801-806. 10.1038/ng1814

Hamilton, Gillian, Samedi, Farzana, Knight, Jo, Archer, Nicola, Foy, Catherine, Walter, Sarah, Turic, Dragana, Jehu, Luke, Moore, Pamela, Hollingworth, Paul, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lovestone, Simon and Powell, John F. 2006. Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease. Neuroscience Letters 401 (1-2) , pp. 77-80. 10.1016/j.neulet.2006.03.021

Paylor, R., Glaser, B., Mupo, A., Ataliotis, P., Spencer, C., Sobotka, A., Sparks, C., Choi, C.-H., Oghalai, J., Curran, S., Murphy, K. C., Monks, S., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Scambler, P. J. and Lindsay, E. 2006. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome. Proceedings of the National Academy of Sciences of the United States of America 103 (20) , pp. 7729-7734. 10.1073/pnas.0600206103

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Green, Elaine Karen, Dwyer, Sarah Lynne, Macgregor, Stuart, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Raybould, Rachel, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Lisa Anne, Cardno, Alastair George, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2006. Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of General Psychiatry 63 (4) , pp. 366-373. 10.1001/archpsyc.63.4.366

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. Effects of differential genotyping error rate on the Type 1 error probability of case-control studies. Human heredity 61 (1) , pp. 55-64. 10.1159/000092553

Norton, Nadine, Williams, Hywel J and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2006. An update on the genetics of schizophrenia. Current Opinion in Psychiatry 19 (2) , pp. 158-164. 10.1097/01.yco.0000214341.52249.59

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Nikolov, Ivan, Georgieva, Lyudmila, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. Pooled DNA genotyping on Affymetrix SNP genotyping arrays. BMC Genomics 7 (1) , pp. 27-37. 10.1186/1471-2164-7-27

Harold, Denise, Macgregor, S., Patterson, C. E., Hollingworth, P., Moore, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Passmore, P., McIlroy, S. and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2006. A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease. Pharmacogenetics and genomics 16 (2) , pp. 75-77.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2006. Chromosome 22 deletion syndrome and schizophrenia. International Review of Neurobiology 73 , pp. 1-27. 10.1016/S0074-7742(06)73001-X

Smemo, S1, Nowotny, P., Hinrichs, A. L., Kauwe, J. S., Cherny, S., Erickson, K, Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Morris, C. M., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, J. and Goate, A. 2006. Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease. Annals of Neurology 59 (1) , pp. 21-26. 10.1002/ana.20673

Grupe, Andrew, Li, Yonghong, Rowland, Charles, Nowotny, Petra, Hinrichs, Anthony L., Smemo, Scott, Kauwe, John S. K., Maxwell, Taylor J., Cherny, Sara, Doil, Lisa, Tacey, Kristina, Luchene, Ryan van, Myers, Amanda, Wavrant-De Vrièze, Fabienne, Kaleem, Mona, Hollingworth, Paul, Jehu, Luke, Foy, Catherine, Archer, Nicola, Hamilton, Gillian, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Morris, Chris M., Catanese, Joseph, Sninsky, John, White, Thomas J., Powell, John, Hardy, John, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lovestone, Simon, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Morris, John C., Thal, Leon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Goate, Alison 2006. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. The American Journal of Human Genetics 78 (1) , pp. 78-88.

Peirce, Timothy Rowan, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Preece, Anna Charlotte, Haroutunian, Vahram, Buxbaum, Joseph D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of general psychiatry 63 (1) , pp. 18-24. 10.1001/archpsyc.63.1.18

Peirce, TR, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Preece, Anna, Haroutunian, V, Buxbaum, JD, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. Convergent evidence for 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of General Psychiatry 63 (1) , pp. 18-24.

Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Morris, Derek W., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Preece, Anna Charlotte, Dwyer, Sarah, Wilkinson, Jennifer C., Spurlock, Gillian, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Buckland, Paul Robert, Waddington, John L., Gill, Michael, Corvin, Aiden P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael John ORCID: https://orcid.org/0000-0001-7073-2379 2006. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (1) , pp. 96-101. 10.1002/ajmg.b.30236

Lambert, D., Middle, F., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Segurado, R., Raybould, Rachel, Corvin, A., Green, E., O'Mahony, E., Nikolov, I., Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, N., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lendon, C, Jones, L, Jones, I, Holmans, P, Gill, M and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2006. Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22 - Corrigendum. Molecular Psychiatry 11 (12) , pp. 1140-1143. 10.1038/sj.mp.4001917

Green, E. K., Norton, N., Peirce, T., Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2006. Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation. Molecular Psychiatry 11 (9) , pp. 798-799. 10.1038/sj.mp.4001853

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, H., Cardno, Alastair G., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, L. A., Murphy, K. C., Sanders, Rebecca, McCarthy, G., Gray, M. Y., Jones, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2006. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. Journal of Medical Genetics 43 (7) , pp. 563-567. 10.1136/jmg.2005.035345

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons. Molecular Psychiatry 11 (5) , pp. 446-458. 10.1038/sj.mp.4001808

Blair, I. P., Chetcuti, A. F., Badenhop, R. F., Scimone, A., Moses, M. J., Adams, L. J., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Green, E., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kwok, J. B. J., Donald, J. A., Mitchell, P. B. and Schofield, P. R. 2006. Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele. Molecular Psychiatry 11 (4) , pp. 372-383. 10.1038/sj.mp.4001784

Green, Elaine K., Baybould, Rachel, MacGregor, Stuart, Hyde, Sally, Young, Allan H., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Lisa, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2006. Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder: case-control study of over 3000 individuals from the UK. British Journal of Psychiatry 188 (1) , pp. 21-25. 10.1192/bjp.bp.105.009969

Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Turic, D., Peirce, T. R., Mills, S., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2005. No support for association between the dopamine transporter (DAT1) gene and ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 139B (1) , pp. 7-10. 10.1002/ajmg.b.30206

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Kraepelinian dichotomy - Author's reply. British Journal of Psychiatry 187 , pp. 485-486.

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Fowler, Tom, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Turic, Darko, Whittinger, Naureen, Aggleton, John Patrick ORCID: https://orcid.org/0000-0002-5573-1308, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder. Archives of General Psychiatry 62 (11) , pp. 1275-1278. 10.1001/archpsyc.62.11.1275

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. The genetics of attention deficit hyperactivity disorder. Human Molecular Genetics 14 (2) , pp. 275-282. 10.1093/hmg/ddi263

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia? Schizophrenia Bulletin 31 (4) , pp. 800-805. 10.1093/schbul/sbi061

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Bennett, Philip, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Segurado, Ricardo, Cardno, Alastair George, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Lambert, David, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Corvin, Aiden, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Gill, Michael, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Archives of general psychiatry 62 (10) , pp. 1081-1088. 10.1001/archpsyc.62.10.1081

Li, Y., Rowland, C., Tacey, K., Catanese, J., Sninsky, J., Hardy, J., Powell, J., Lovestone, S., Morris, J. C., Thal, L., Goate, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Grupe, A. 2005. The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. Molecular Psychiatry 10 (9) , pp. 809-810. 10.1038/sj.mp.4001702

Williams, H. J., Glaser, B., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, MacGregor, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. No association between schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry 162 (9) , pp. 1736-1738. 10.1176/appi.ajp.162.9.1736

Ahuja, Alka, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Genetics of mental retardation. Indian Journal of Medical Sciences 59 (9) , pp. 407-417. 10.4103/0019-5359.16820

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Tredget, John, John, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lazarus, J. H. 2005. A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients. Journal of affective disorders 87 (2-3) , pp. 313-317. 10.1016/j.jad.2005.03.010

Glaser, B1, Schumacher, J., Williams, H. J., Jamra, R. A., Ianakiev, N., Milev, R., Ohlraun, S., Schulze, T. G., Czerski, P. M., Hauser, J., Jonsson, E. G., Sedvall, G. C., Klopp, N., Illig, T., Becker, T., Propping, P., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cichon, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rietschel, M., Murphy, K. C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Nothen, M. M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological psychiatry 58 (1) , pp. 78-80.

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Finding schizophrenia genes. The Journal of Clinical Investigation 115 (6) , pp. 1440-1448. 10.1172/JCI24759

Turic, D., Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Williams, H., Norton, N., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder. Biological psychiatry 57 (11) , pp. 1461-1466. 10.1016/j.biopsych.2005.03.025

Green, Elaine Karen, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine Mary, Heron, Jess, Hyde, Sally, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Archives of general psychiatry 62 (6) , pp. 642-648. 10.1001/archpsyc.62.6.642

Norton, Nadine, Williams, Hywel, Dwyer, Sarah, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Preece, Anna, Gerrish, Amy, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Yerassimou, P., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 5 , 23. 10.1186/1471-244X-5-23

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Hollingworth, P., Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Tunstall, N., Jones, S., Moore, P., Wavrant DeVrieze, F., Myers, A., Crook, R., Compton, D., Marshall, H., Meyer, D., Shears, S., Booth, J., Ramic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1) , pp. 24-32. 10.1002/ajmg.b.30114

Lambert, D., Middle, F., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Segurado, Ricardo, Raybould, Rachel, Corvin, A., Green, Elaine Karen, O'Mahony, E., Nikolov, Ivan, Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lendon, C., Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Gill, M. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular psychiatry 10 (9) , pp. 831-841. 10.1038/sj.mp.4001684

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Preece, Anna Charlotte, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Human Molecular Genetics 14 (14) , pp. 1947-1954. 10.1093/hmg/ddi199

Cope, Natalie Alexandra, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Hill, Gary Trevor, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Stevenson, Jim, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2005. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics 76 (4) , pp. 581-591. 10.1086/429131

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Streamlined analysis of pooled genotype data in SNP-based association studies. Genetic Epidemiology 28 (3) , pp. 273-282. 10.1002/gepi.20062

Li, Y., Hollingworth, P., Moore, P., Foy, C., Archer, N., Powell, J., Nowotny, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Tacey, K., Doil, L., van Luchene, R., Garcia, V., Rowland, V., Lau, K., Cantanese, J., Sninsky, J., Hardy, J., Thal, L., Morris, J. C., Goate, A., Lovestone, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Grupe, A. 2005. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation 25 (3) , pp. 270-277. 10.1002/humu.20138

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Linkage studies in schizophrenia: New findings promise new insights. European Psychiatry 20 (1) , S36-S36.

Cope, N. A., Hill, G., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Harold, D., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Green, E. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia. Molecular Psychiatry 10 (3) , pp. 237-238. 10.1038/sj.mp.4001596

Turic, D., Williams, Hywel, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 133B (1) , pp. 64-67. 10.1002/ajmg.b.30123

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Harrison, P. J. 2005. Schizophrenia: a genetic disorder of the synapse? British Medical Journal (BMJ) 330 (7484) , pp. 158-159. 10.1136/bmj.330.7484.158

Glaser, B., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Green, E., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 132B (1) , pp. 38-45. 10.1002/ajmg.b.30081

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Genomic approaches to schizophrenia. Clinical Therapeutics 27 (A) , S2-S7.

Dimitrova, A., Milanova, V., Krastev, S., Nikolov, I., Toncheva, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2005. Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment. The Pharmacogenomics Journal 5 (1) , pp. 35-41. 10.1038/sj.tpj.6500273

Norton, N. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. HTR2A: association and expression studies in neuropsychiatric genetics. Annals of Medicine 37 (2) , pp. 121-129.

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology. Schizophrenia Bulletin 32 (1) , pp. 9-16. 10.1093/schbul/sbj033

McGuffin, Peter, Knight, Jo, Breen, Gerome, Brewster, Shyama, Boyd, Peter R., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, Mike, Korszun, Ania, Maier, Wolfgang, Middleton, Lefkos, Mors, Ole, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Perry, Julia, Preisig, Martin, Reich, Theodore, Rice, John, Rietschel, Marcella, Jones, Lisa, Sham, Pak and Farmer, Anne E. 2005. Whole genome linkage scan of recurrent depressive disorder from the depression network study. Human Molecular Genetics 14 (22) , pp. 3337-3345. 10.1093/hmg/ddi363

Kent, L., Green, Elaine, Hawi, Z., Kirley, A., Dudbridge, F., Lowe, N., Raybould, Rachel, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Fitzgerald, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Gill, M., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular Psychiatry 10 (10) , pp. 939-943. 10.1038/sj.mp.4001696

Glaser, B., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Green, E., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Identification of a potential Bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4. Molecular Psychiatry 10 (10) , pp. 920-927. 10.1038/sj.mp.4001689

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Schizophrenia: genes at last? Trends in Genetics 21 (9) , pp. 518-525. 10.1016/j.tig.2005.06.011

Raybould, Rachel, Green, Elaine K., MacGregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Caesar, Sian, Nikolov, Ivan, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, Lisa, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological psychiatry 57 (7) , pp. 696-701. 10.1016/j.biopsych.2005.01.018

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. The genetics of schizophrenia and bipolar disorder: dissecting psychosis. Journal of Medical Genetics 42 (3) , pp. 193-204. 10.1136/jmg.2005.030718

Green, E., Elvidge, G., Jacobsen, N., Glaser, B., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23-q24 region in two pedigrees with bipolar disorder and Darier's disease. American Journal of Psychiatry 162 (1) , pp. 35-42. 10.1176/appi.ajp.162.1.35

Farmer, A., Breen, G., Brewster, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, M., Korszun, A., Maier, W., Middleton, L., Mors, O., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Perry, J., Preisig, M., Rietschel, M., Reich, T., Jones, L. ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889 and McGuffin, P. 2004. The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study. BMC Psychiatry 4 , 42. 10.1186/1471-244X-4-42

Jones, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Genetics: The implications for forensic psychiatry. Journal of Forensic Psychiatry & Psychology 15 (4) , pp. 696-704. 10.1080/14789940410001729509

Li, Yonghong, Nowotny, Petra, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Smemo, Scott, Kauwe, John S. K., Hinrichs, Anthony L., Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Gogic, Goran, Chan, Joanne, Cravchik, Anibal, Ross, David, Lau, Kit, Kwok, Shirley, Chang, Sheng-Yung, Catanese, Joseph, Sninsky, John, White, Thomas J., Hardy, John, Powell, John, Lovestone, Simon, Morris, John C., Thal, Leon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, Alison and Grupe, Andrew 2004. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences 101 (44) , pp. 15688-15693. 10.1073/pnas.0403535101

van Amelsvoort, T., Daly, E., Henry, J., Robertson, D., Ng, V., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. 2004. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. Archives of General Psychiatry 61 (11) , pp. 1085-1096. 10.1001/archpsyc.61.11.1085

van Amelsvoort, T, Henry, J, Morris, R, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Linszen, D, Murphy, K and Murphy, D 2004. Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome. Schizophrenia Research 70 (2-3) , pp. 223-232. 10.1016/j.schres.2003.10.004

Fowler, T. A., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Turic, Dragana, Whittinger, N., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Aggleton, John Patrick ORCID: https://orcid.org/0000-0002-5573-1308, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Early onset antisocial behaviour in children with ADHD is associated with a functional variant in the catechol-O-methyltransferase (COMT) gene [Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 98. 10.1002/ajmg.b.30101

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Preece, Anna, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, HJ, Norton, N, Wilkinson, J, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Allelic variation in the expression of neuropsychiatric candidate genes [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 25.

Peirce, T. R., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Haroutunian, V., Buxbaum, J., Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 81. 10.1002/ajmg.b.30101

Farbrother, Jane Elizabeth, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Guggenheim, Jeremy Andrew ORCID: https://orcid.org/0000-0001-5164-340X 2004. Family aggregation of high myopia: estimation of the sibling recurrence risk ratio. Investigative Ophthalmology and Visual Science 45 (9) , pp. 2873-2878. 10.1167/iovs.03-1155

Farbrother, Jane Elizabeth, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pong-Wong, Ricardo, Haley, Chris S. and Guggenheim, Jeremy Andrew ORCID: https://orcid.org/0000-0001-5164-340X 2004. Linkage analysis of the genetic loci for high myopia on chromosomes 18p, 12q and 17q in 51 UK families. Investigative Ophthalmology and Visual Science 45 (9) , pp. 2879-2885. 10.1167/iovs.03-1156

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jehu, Luke, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Buckland, Paul Robert, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Allelic expression of APOE in brain [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 61.

Norton, N, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Morris, DW, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, HJ, Preece, Anna, Dwyer, SL, Wilkinson, JC, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Buckland, Paul Robert, Waddington, JL, Gill, M, Corvin, AP, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 18.

Li, Yonghong, Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Lau, Kit, Catanese, Joe, Sninsky, John, Nowotny, Petra, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hardy, John, Powell, John, Lovestone, Simon, Thal, Leon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie, Goate, Alison and Grupe, Andrew 2004. Association of ABCA1 with late-onset Alzheimer?s disease is not observed in a case-control study. Neuroscience Letters 366 (3) , pp. 268-271. 10.1016/j.neulet.2004.05.047

Mowry, B J, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Pulver, A E, Gejman, P V, Riley, B, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Laurent, C, Schwab, S G, Wildenauer, D B, Bauché, S, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wormley, B, Sanders, A R, Nestadt, G, Liang, K Y, Duan, J, Ribble, R, Norton, N, Soubigou, S, Maier, W, Ewen-White, K R, deMarchi, N, Carpenter, B, Walsh, D, Williams, H, Jay, M, Albus, M, Nertney, D A, Papadimitriou, G, O'Neill, A, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Deleuze, J-F, Lerer, F B, Dikeos, D, Kendler, K S, Mallet, J, Silverman, J M, Crowe, R R and Levinson, D F 2004. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry 9 (8) , pp. 784-795. 10.1038/sj.mp.4001481

Morris, D.W., Ivanov, D. ORCID: https://orcid.org/0000-0001-6271-6301, Robinson, L., Williams, N. ORCID: https://orcid.org/0000-0003-1177-6931, Stevenson, J., Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Williams, J. and O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 2004. Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability. American Journal Of Medical Genetics Part A 129B (1) , pp. 97-103. 10.1002/ajmg.b.30033

Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Gaynor, Jones, Susan J., Norton, Nadine, Sanders, Robert D., Milham, Charis, McCarthy, Geraldine M., Jones, Lisa A., Cardno, Alastair G., Gray, Marion, Murphy, Kieran C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophrenia. American Journal of Medical Genetics 128B (1) , pp. 19-20. 10.1002/ajmg.b.30021

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jehu, Luke, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. P4-101 Allelic expression of APOE in brain [Conference Abstract]. Neurobiology of Aging 25 , S503-S503. 10.1016/S0197-4580(04)81659-2

Harvey, Kirsten, Duguid, Ian C, Alldred, Melissa J., Beatty, Sarah E., Ward, Hamish, Keep, Nicholas H., Lingenfelter, Sue E., Pearce, Brian R., Lundgren, Johan, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Smart, Trevor G., Lüscher, Bernhard, Rees, Mark I. and Harvey, Robert J. 2004. The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. Journal of neuroscience 24 (25) , pp. 5816-5826. 10.1523/JNEUROSCI.1184-04.2004

Reid, Suzanne J., van Roon-Mom, Willeke M.C., Wood, Phil C., Rees, Mark I., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Faull, Richard L.M., Dragunow, Mike and Snell, Russell G. 2004. TBP, a polyglutamine tract containing protein, accumulates in Alzheimer's disease. Molecular Brain Research 125 (1-2) , pp. 120-128. 10.1016/j.molbrainres.2004.03.018

Mills, Sophie, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Street, Eddy, Turic, Darko, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2004. No evidence of association between Catechol-O-Methyltransferase (COMT) Val(158)Met genotype and performance on neuropsychological tasks in children with ADHD: A case-control study. BMC Psychiatry 4 , p. 15. 10.1186/1471-244X-4-15

Plomin, R, Turic, D M, Hill, L, Turic, D E, Stephens, M, Williams, J, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability. Molecular Psychiatry 9 (6) , pp. 582-586. 10.1038/sj.mp.4001441

Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Allebeck, P, Dalman, C, Lundberg, I, Hemmingson, T, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lewis, G 2004. Parental age difference and schizophrenia - Reply. British Journal of Psychiatry 184 , pp. 540-541.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Genetic abnormalities of chromosome 22 and the development of psychosis. Current Psychiatry Reports 6 (3) , pp. 176-182. 10.1007/s11920-004-0062-4

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Nikolov, Ivan, Milev, Radoi, Koleva, Svetlinka, Dimitrova, Albena, Toncheva, Draga, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biological psychiatry 55 (10) , pp. 971-975. 10.1016/j.biopsych.2004.01.025

Turic, D., Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Direct analysis of the genes encoding G proteins G alpha T2, G alpha o, G alpha Z in ADHD. American Journal of Medical Genetics 127B (1) , pp. 68-72. 10.1002/ajmg.b.20173

Korszun, Ania, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Brewster, Shyama, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Ferrero, Francois, Gill, Michael, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa Anne, Maier, Wolfgang, Mors, Ole, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Preisig, Martin, Reich, Theodore, Rietschel, Marcella, Farmer, Anne Elizabeth and McGuffin, Peter 2004. Familiarity of symptom dimensions in depression. Archives of General Psychiatry 61 (5) , pp. 468-474. 10.1001/archpsyc.61.5.468

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Dysbindin-1 and schizophrenia: from genetics to neuropathology. The Journal of Clinical Investigation 113 (9) , pp. 1255-1257. 10.1172/JCI200421470

Fekadu, Abebaw, Shibre, Teshome, Alem, Atalay, Kebede, Derge, Kebreab, Samuel, Negash, Alemayehu and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Bipolar disorder among an isolated island community in Ethiopia. Journal of affective disorders 80 (1) , pp. 1-10. 10.1016/S0165-0327(02)00345-2

Murphy, K.C., Williams, H.J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. What can velo-cardio-facial syndrome tell us about the genetics of schizophrenia? European Psychiatry 19 (Supp1) , 96S-96S.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna, Mortis, DW, Spurlock, Gillian, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Stephens, M, Norton, N, Williams, H, Clement, M, Dwyer, S, Curran, C, Wilkinson, J, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Waddington, JL, Gill, M, Corvin, AP, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Archives of General Psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Cook, Lynnette J., Ho, Luk W., Taylor, Alison E., Brayne, Carol, Evans, John Grimley, Xuereb, John, Cairns, Nigel J., Pritchard, Antonia, Lemmon, Helen, Mann, David, St Clair, David, Turic, Dragana, Hollingworth, Paul, Moore, Pamela J., Jehu, Luke, Archer, Nicola, Walter, Sarah, Foy, Catherine, Edmondson, Amanda, Powell, John, Lovestone, Simon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Lendon, Corinne and Rubinsztein, David C. 2004. Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease. Neuroscience Letters 358 (2) , pp. 142-146. 10.1016/j.neulet.2004.01.016

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Spurlock, Gillian, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, McCreadie, Robin G, Buckland, Paul Robert, Sharkey, Val, Chowdari, Kodavali V., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Nimgaonkar, Vishwajit, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Support for RGS4 as a susceptibility gene for schizophrenia. Biological Psychiatry 55 (2) , pp. 192-195. 10.1016/j.biopsych.2003.11.002

Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Marshall, Lucy, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Thomas, Hollie Victoria, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2004. Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD. American Journal of Psychiatry 161 (1) , pp. 133-138. 10.1176/appi.ajp.161.1.133

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Morris, D. W., Spurlock, Gillian, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Stephens, Mark Keith, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Clement, Mathew ORCID: https://orcid.org/0000-0002-9280-5281, Dwyer, Sarah Lynne, Curran, Catherine, Wilkinson, Jennifer Camilla, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Waddington, J. L., Gill, M., Corvin, A. P., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Identification in two independent samples of a novel schizophrenia risk haplotype of the dystobrevin binding protein gene (DTNBP1). Archives of general psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. The molecular genetics of schizophrenia: new findings promise new insights. Molecular Psychiatry 9 (1) , pp. 14-27. 10.1038/sj.mp.4001444

Myers, Amanda J., Marshall, Helen, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Compton, Danielle, Crook, Richard J.P., Mander, Adrian P., Nowotny, Petra, Smemo, Scott, Dunstan, Melanie ORCID: https://orcid.org/0000-0003-3817-2142, Jehu, Luke, Wang, Jen C., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Morris, John C., Norton, Joanne, Chakraventy, Sumi, Tunstall, Nigel, Lovestone, Simon, Petersen, Ronald, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, John and Goate, Alison 2004. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics 124B (1) , pp. 29-37. 10.1002/ajmg.b.20036

Norton, Nadine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. DNA pooling as a tool for large-scale association studies in complex traits. Annals of Medicine 36 (2) , pp. 146-152. 10.1080/07853890310021724

Busby, Victoria, Goossens, Steven, Nowotny, Petra, Hamilton, Gillian, Smemo, Scott, Harold, Denise, Turic, Dragana, Jehu, Luke, Myers, Amanda, Womick, Meredith, Woo, Daniel, Compton, Danielle, Doil, Lisa M., Tacey, Kristina M., Lau, Kit F., Al-Saraj, Safa, Killick, Richard, Pickering-Brown, Stuart, Moore, Pamela, Hollingworth, Paul, Archer, Nicola, Foy, Catherine, Walter, Sarah, Lovestone, Simon, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2004. Alpha-T-Catenin Is Expressed in Human Brain and Interacts With the Wnt Signaling Pathway But Is Not Responsible for Linkage to Chromosome 10 in Alzheimer's Disease. Neuromolecular Medicine 5 (2) , pp. 133-146. 10.1385/NMM:5:2:133

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Buckland, Paul Robert, Hall, H., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain. Molecular Psychiatry 9 (1) , pp. 109-114. 10.1038/sj.mp.4001366

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jehu, Luke, Moskvina, Vanentina, Buxbaum, Joseph D., Dracheva, Stella, Haroutunian, Vahram, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes. Human Molecular Genetics 13 (22) , pp. 2885-2892. 10.1093/hmg/ddh299

Cichon, Sven, Buervenich, Silvia, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Akula, Nirmala, Dimitrova, Albena, Green, Elaine, Schumacher, Johannes, Klopp, Norman, Becker, Tim, Ohlraun, Stephanie, Schulze, Thomas G, Tullius, Monja, Gross, Magdalena M, Jones, Lisa, Krastev, Stefan, Nikolov, Ivan, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Czerski, Piotr M., Leszczynska-Rodziewicz, Anna, Kapelski, Pawel, Van Den Bogaert, Ann, Illig, Thomas, Hauser, Joanna, Maier, Wolfgang, Berrettini, Wade, Byerley, William, Coryell, William, Gershon, Elliot S., Kelsoe, John R., McInnis, Melvin G., Murphy, Dennis L., Nurnberger, John I., Reich, Theodore, Scheftner, William, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Propping, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Rietschel, Marcella, Nöthen, Markus M., McMahon, Francis J. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2004. Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin. Nature Genetics 36 (8) , pp. 783-784. 10.1038/ng0804-783

Turic, Dragana, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Mills, S., Stephens, M., Lawson, D., Govan, Catherine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Kent, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2004. Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD. Molecular Psychiatry 9 (2) , pp. 169-173. 10.1038/sj.mp.4001387

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Ekholm, B., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Lindblom, Y., Chowdari, K. V., Cardno, Alastair George, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Lisa Anne, Murphy, Kieran Christopher, Sanders, Robert David, McCarthy, Geraldine MaryTeresa, Gray, Marion Yvonne, Jones, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Nimgaonkar, V., Adolfson, R., Osby, U., Terenius, L., Sedvall, G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. The American journal of human genetics 73 (6) , pp. 1355-1367. 10.1086/380206

Marchbanks, R.M., Ryan, Margaret, Day, I.N.M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Whatley, S.A. 2003. A mitochondrial DNA sequence variant associated with schizophrenia and oxidative stress. Schizophrenia Research 65 (1) , pp. 33-38. 10.1016/S0920-9964(03)00011-2

Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Nikolov, Ivan, Tzwetkova, R., Stambolova, S. M., Murphy, Kieran Christopher, Toncheva, Draga, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis: Molecular genetic study. The British Journal of Psychiatry 183 (5) , pp. 409-413. 10.1192/bjp.183.5.409

Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Allebeck, P., Dalman, C., Lundberg, I., Hemmingson, T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lewis, G. 2003. Paternal age and risk for schizophrenia. British Journal of Psychiatry 183 (5) , pp. 405-408. 10.1192/bjp.183.5.405

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Marshall, L., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Thomas, Hollie Victoria, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. ADHD children with and without the dopamine D4 receptor 7-repeat allele: Evidence of differences in performance on neuropsychological tests. Behavior Genetics 33 (6) , p. 721.

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Recent advances in the genetics of schizophrenia. Human Molecular Genetics 12 (suppl) , R125-R133. 10.1093/hmg/ddg302

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Georgieva, Lyudmila, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Nikolov, Ivan, Norton, Nadine, Toncheva, Draga, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Variation in the protocadherin - A gene cluster? Genomics 82 (4) , pp. 433-440. 10.1016/S0888-7543(03)00167-8

Payton, A., Turic, D., Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Mills, S., Lawson, D.C., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2003. No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder. Psychiatric Genetics 13 (3) , pp. 183-185.

Harold, Denise, Peirce, Timothy, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Lovestone, Simon, Powell, John, Foy, Catherine, Archer, Nicola, Walter, Sarah, Edmonson, Amanda, McIlroy, Stephen, Craig, David, Passmore, Peter A., Goate, Alison, Hardy, John, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Liddell, Malcolm, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Myers, Amanda, Jones, Susan, Hollingworth, Paul and Moore, Pamela 2003. Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Human Genetics 113 (3) , pp. 258-267. 10.1007/s00439-003-0960-2

Rees, Mark I., Harvey, Kirsten, Ward, Hamish, White, Julia H., Evans, Luc, Duguid, Ian C., Hsu, Cynthia C.-H., Coleman, Sharon Louise, Miller, Jan, Baer, Kristin, Waldvogel, Henry J., Gibbon, Francis, Smart, Trevor G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Harvey, Robert J. and Snell, Russell G. 2003. Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia. Journal of Biological Chemistry 278 (27) , pp. 24688-24696. 10.1074/jbc.M301070200

Norton, N., Williams, H.J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G., Jones, S., Owen, R., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Mutation screening of the Homer gene family and association analysis in schizophrenia. American Journal of Medical Genetics 120B (1) , pp. 18-21. 10.1002/ajmg.b.20032

Williams, H.J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Norton, N., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia. American Journal of Medical Genetics 120B (1) , pp. 42-46. 10.1002/ajmg.b.20049

Williams, H. J., Williams, N. ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Norton, N., Ivanov, D. ORCID: https://orcid.org/0000-0001-6271-6301, McCreadie, R. G., Preece, A., Sharkey, V., Jones, S., Zammit, S. ORCID: https://orcid.org/0000-0002-2647-9211, Nikolov, I., Kehaiov, I., Thapar, A. ORCID: https://orcid.org/0000-0002-3689-737X, Murphy, K. C., Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 2003. Association between PRODH and schizophrenia is not confirmed. Molecular Psychiatry 8 (7) , pp. 644-645. 10.1038/sj.mp.4001276

Lewis, Cathryn M., Levinson, Douglas F., Wise, Lesley H., DeLisi, Lynn E., Straub, Richard E., Hovatta, Iiris, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Schwab, Sibylle G., Pulver, Ann E., Faraone, Stephen V., Brzustowicz, Linda M., Kaufmann, Charles A., Garver, David L., Gurling, Hugh M.D., Lindholm, Eva, Coon, Hilary, Moises, Hans W., Byerley, William, Shaw, Sarah H., Mesen, Andrea, Sherrington, Robin, O'Neill, F. Anthony, Walsh, Dermot, Kendler, Kenneth S., Ekelund, Jesper, Paunio, Tiina, Lönnqvist, Jouko, Peltonen, Leena, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wildenauer, Dieter B., Maier, Wolfgang, Nestadt, Gerald, Blouin, Jean-Louis, Antonarakis, Stylianos E., Mowry, Bryan J., Silverman, Jeremy M., Crowe, Raymond R., Cloninger, C. Robert, Tsuang, Ming T., Malaspina, Dolores, Harkavy-Friedman, Jill M., Svrakic, Dragan M., Bassett, Anne S., Holcomb, Jennifer, Kalsi, Gursharan, McQuillin, Andrew, Brynjolfson, Jon, Sigmundsson, Thordur, Petursson, Hannes, Jazin, Elena, Zoëga, Tomas and Helgason, Tomas 2003. Genome scan meta-analysis of schizophrenia and bipolar disorder, Part II: schizophrenia. American Journal of Human Genetics 73 (1) , pp. 34-48. 10.1086/376549

Bray, Nicholas Bray ORCID: https://orcid.org/0000-0002-4357-574X, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. Cis-acting variation in the expression of a high proportion of genes in human brain. Human Genetics 113 (2) , pp. 149-153. 10.1007/s00439-003-0956-y

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Buckland, Paul Robert, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. The American Journal of Human Genetics 73 (1) , pp. 152-161. 10.1086/376578

Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Payton, Antony, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Pay, Helen M., Lawson, Deborah C., Turic, Darko, Ollier, William, Worthington, Jane, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2003. No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorder. Psychiatric Genetics 13 (2) , pp. 107-110. 10.1097/01.ypg.0000056177.32550.a5

Edwards, Deborah ORCID: https://orcid.org/0000-0003-1885-9297, Burnard, Philip, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hannigan, Ben ORCID: https://orcid.org/0000-0002-2512-6721, Fothergill, A. and Coyle, D. 2003. A systematic review of the effectiveness of stress-management interventions for mental health professionals. Journal of Psychiatric and Mental Health Nursing 10 (3) , pp. 370-371. 10.1046/j.1365-2850.2003.00606.x

Reid, Suzanne J., Rees, Mark I., van Roon-Mom, Willeke M.C., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, MacDonald, Marcy E., Sutherland, Greg, During, Matthew J., Faull, Richard L.M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Dragunow, Mike and Snell, Russell G. 2003. Molecular investigation of TBP allele length:. Neurobiology of Disease 13 (1) , pp. 37-45. 10.1016/S0969-9961(03)00014-7

Georgieva, Lyudmila, Nikolov, Ivan, Poriazova, Nadezhda, Jones, Gaynor, Toncheva, Draga, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Genetic variation in the seven-pass transmembrane cadherin CELSR1. Psychiatric Genetics 13 (2) , pp. 103-106. 10.1097/01.ypg.0000057486.14812.03

Jönsson, Erik G., Norton, Nadine, Forslund, Kaj, Mattila-Evenden, Marja, Rylander, Gunnar, Åsberg, Marie, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, Göran C. 2003. Association between a promoter variant in the monoamine oxidase A gene and schizophrenia. Schizophrenia Research 61 (1) , pp. 31-37. 10.1016/S0920-9964(02)00224-4

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, A, Spurlock, G, Norton, N, Williams, H J, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia. Molecular Psychiatry 8 (5) , pp. 485-487. 10.1038/sj.mp.4001348

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Georgieva, Lyudmila, Nikolov, Ivan, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Gaynor, Poriazova, Nadezhda, Tolev, Todor, Owen, Richard, Jones, Sue and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Association analysis of the HOPA12bp polymorphism in schizophrenia and manic depressive illness. American Journal of Medical Genetics 118B (1) , pp. 16-19. 10.1002/ajmg.b.10065

Jordan, Nicola, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Gregory, John Welbourn ORCID: https://orcid.org/0000-0001-5189-3812, Evans, C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Ludgate, Marian Elizabeth 2003. The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population. Journal of Clinical Endocrinology & Metabolism 88 (3) , pp. 1002-5. 10.1210/jc.2002-021301

Harrison, Paul J and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Genes for schizophrenia? Recent findings and their pathophysiological implications. The Lancet 361 (9355) , pp. 417-419. 10.1016/S0140-6736(03)12379-3

Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Abraham, Richard, Rudrasingham, Varuni, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2003. Memory for new information as a cognitive marker of liability to Alzheimer's disease in a high risk group: a research note. International Journal of Geriatric Psychiatry 18 (2) , pp. 155-160. 10.1002/gps.808

Turic, D, Robinson, L, Duke, M, Morris, D W, Webb, V, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Milham, C, Hopkin, E, Pound, K, Fernando, S, Grierson, A, Easton, M, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Chowdhury, R, Gruen, J, Stevenson, J, Krawczak, M, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2003. Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22. Molecular Psychiatry 8 (2) , pp. 176-185. 10.1038/sj.mp.4001216

Lawson, Deborah C., Turic, Darko, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Pay, Helen M., Govan, Catherine F., Norton, Nadine, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2003. Association analysis of monoamine oxidase a and attention deficit hyperactivity disorder. American Journal of Medical Genetics 116B (1) , pp. 84-89. 10.1002/ajmg.b.10002

van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. The future of psychiatric genetics. Annals of Medicine 35 (2) , pp. 122-134. 10.1080/07853890310010023

Farbrother, Jane Elizabeth, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Guggenheim, Jeremy Andrew ORCID: https://orcid.org/0000-0001-5164-340X 2003. Linkage analysis of 18p, 12q and 17q high myopia loci in 51 UK families. Investigative ophthalmology & visual science 44 (E-Abst)

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Genetic findings in psychotic disorders. Soares, Jair C. and Gershon, Samuel, eds. Handbook of Medical Psychiatry, New York: Marcel Dekker, pp. 417-432.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. Schizophrenia and genetics. Plomin, R., DeFries, J. C., Craig, I. C. and McGuffin, P., eds. Behavioral Genetics in the Postgenomic Era, Washington, DC: APA Books, pp. 463-480. (10.1037/10480-023)

Green, Elaine K., Elvidge, Gareth P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2003. Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: phenylalanine hydroxylase and human LIM-homeobox LHX5. Psychiatric Genetics 13 (2) , pp. 97-101. 10.1097/01.ypg.0000057882.80011.9e

Børglum, A.D., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Mors, O., Muir, W., Murray, V., McKee, I., Collier, D.A., Ewald, H., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Blackwood, D. and Kruse, T. A. 2003. Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. American Journal of Medical Genetics 117B (1) , pp. 18-22. 10.1002/ajmg.b.10030

Heron, J., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Jones, L. 2003. Self-reported schizotypy and bipolar disorder: demonstration of a lack of specificity of the Kings Schizotypy Questionnaire. Schizophrenia Research 65 (2-3) , pp. 153-158. 10.1016/S0920-9964(03)00004-5

Levinson, D.F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Laurent, C., Mallet, J., Riley, B., Kendler, K.S., Pulver, A.E., Gejman, P.V., Sanders, A.R., Schwab, S.G., Wildenauer, D.B., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Mowry, B.J. 2002. Is schizophrenia linked to chromosome 1q? Response. Science 298 (5602) , pp. 2277-2279.

Sham, Pak, Bader, Joel S., Craig, Ian, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. DNA Pooling: a tool for large-scale association studies. Nature Reviews Genetics 3 (11) , pp. 862-871. 10.1038/nrg930

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, RJ, Jacobsen, NJ, Georgieva, Lyudmila, Williams, HJ, Norton, N, Spurlock, Gillian, Jones, S, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Screening the protocadherin 8 (PCDH8) gene in schizophrenia [Conference Abstract]. American Journal of Medical Genetics 114 (7) , p. 844.

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Buckland, Paul Robert, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2002. Detection of cis-acting polymorphisms and epigenetic modification affecting gene expression [Conference Abstracts]. American Journal of Medical Genetics 114 (7) , p. 750. 10.1002/ajmg.10971

Dimitrova, Albena, Georgieva, Lyudmila, Nikolov, Ivan, Poriazova, Nadejda, Krastev, Stefan, Toncheva, Draga, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2002. Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies. Psychiatric Genetics 12 (3) , pp. 137-141. 10.1097/00041444-200209000-00004

Richards, A. J., Morgan, J., Bearcroft, P. W. P., Pickering, E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Tysoe, C., Pope, F. M., Snaed, M. P. and Hughes, H. 2002. Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule. Journal of Medical Genetics 39 (9) , pp. 661-665. 10.1136/jmg.39.9.661

Wickham, Harvey, Walsh, Cathy, Asherson, Philip, Gill, Mike, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, Peter, Murray, Robin and Sham, Pak 2002. Familiality of clinical characteristics in schizophrenia. Journal of Psychiatric Research 36 (5) , pp. 325-329. 10.1016/S0022-3956(02)00008-0

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, R. J., Jacobsen, N. J., Georgieva, Lyudmila, Williams, H. J., Norton, N., Spurlock, Gillian, Jones, S., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Screening the human protocadherin 8 (PCDH8) gene in schizophrenia. Genes, Brain and Behavior 1 (3) , pp. 187-191. 10.1034/j.1601-183X.2002.10307.x

Norton, Nadine, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Gaynor, Jones, Susan, Owen, Richard, Krawczak, Michael, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Schizophrenia and functional polymorphisms in the MAOA and COMT genes: No evidence for association or epistasis. American Journal Of Medical Genetics Part A 114 (5) , pp. 491-496. 10.1002/ajmg.10517

Walter, S., Archer, N., Foy, C., Lovestone, Simon, Davis, G., Hollingsworth, P., Jones, S., Moore, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2002. The retained ability to display affection and emotion in Alzheimer's disease. Neurobiology of Aging 23 (1) , S44-S45.

Archer, N., Foy, C., Walter, S., Lovestone, Simon, Davis, G., Hollingworth, Paul, Jones, S., Moore, P, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2002. Delusions in dementia - An investigation into their persistence and predictive value. Neurobiology of Aging 23 (1) , S156-S156.

Vrieze, F. W. D., Hardy, J., Rudrasingham, V., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lahiri, D. 2002. APP promotor variability as a risk factor for AD. Neurobiology of Aging 23 (1) , S299-S299.

Georgieva, Lyudmila, Dimitrova, A., Nikolov, I., Koleva, S., Tsvetkova, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Toncheva, D. and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2002. Dopamine transporter gene (DAT1) VNTR polymorphism in major psychiatric disorders: family-based association study in the Bulgarian population. Acta Psychiatrica Scandinavica 105 (5) , pp. 396-399. 10.1034/j.1600-0447.2002.1o174.x

Sedvall, O., Adolfsson, R., Agartz, I., Arnborg, S., Ekholm, B., Hall, H., Jonsson, E., McNeil, T.F., Okugawa, G., Osby, U., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Terenius, L. 2002. The Swedish HUBIN Project on Schizophrenia. European Psychiatry 17 (1) , 4S-5S. 10.1016/S0924-9338(02)80018-9

Jönsson, E.G., Norton, N., Forslund, K., Mattila-Evenden, M., Rylander, G., Åsberg, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. 2002. Association between a functional promoter MAOA variant and schizophrenia. European Psychiatry 17 (1) , 182S-182S. 10.1016/S0924-9338(02)80781-7

Norton, Nadine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel J., Spurlock, Gillian, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Morris, Derek W., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2002. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Human Genetics 110 (5) , pp. 471-478. 10.1007/s00439-002-0706-6

Levinson, Douglas. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Laurent, Claudine, Riley, Brien, Pulver, Ann E., Gejman, Pablo V., Schwab, Sibylle G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wildenauer, Dieter B., Sanders, Alan R., Nestadt, Gerald, Mowry, Brian J., Wormley, Brandon, Bauche, Stephanie, Soubigou, Stephane, Ribble, Robert, Nertney, Deborah A., Liang, Kung Yee, Martinolich, Laura, Maier, Wolfgang, Norton, Nadine, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Albus, Margot, Carpenter, Eric B., DeMarchi, Nicola, Ewen-White, Kelly R., Walsh, Dermot, Jay, Maurice, Deleuze, Jean-Francois, O'Neill, Anthony F., Papadimitriou, George, Weilbaecher, Ann, Lerer, Bernard, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Dikeos, Dimitris, Silverman, Jeremy M., Kendler, Kenneth S., Mallet, Jacques, Crowe, Raymond R. and Walters, Marilyn 2002. No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science 296 (5568) , pp. 739-741. 10.1126/science.1069914

Myers, Amanda, Wavrant De-Vrieze, Fabienne, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Giles, Peter ORCID: https://orcid.org/0000-0003-3143-6854, Tunstall, Nigel, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Lovestone, Simon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, John and Goate, Alison 2002. Full genome screen for Alzheimer disease: Stage II analysis. American Journal Of Medical Genetics Part A 114 (2) , pp. 235-244. 10.1002/ajmg.10183

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Genome scans and microarrays: converging on genes for schizophrenia? Genome Biology 3 (4) , Reviews1011-Reviews1011.5.

Garpenstrand, Hakan, Norton, Nadine, Damberg, Mattias, Rylander, Gunnar, Forslund, Kaj, Mattila-Evenden, Marja, Gustavsson, J. Petter, Ekblom, Jonas, Oreland, Lars, Bergman, Hans, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Jönsson, Erik G. 2002. A regulatory monoamine oxidase a promoter polymorphism and personality traits. Neuropsychobiology 46 (4) , pp. 190-193. 10.1159/000067804

Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jacobsen, N, Green, Elaine Karen, Elvidge, G. P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2002. Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease. Molecular Psychiatry 7 (4) , pp. 424-427.

Henry, J. C., van Amelsvoort, T, Morris, R. G, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, D. G. M. and Murphy, K. C. 2002. An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS). Neuropsychologia 40 (5) , pp. 471-478. 10.1016/S0028-3932(01)00136-1

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Rees, Mark I., Bryan, E., Spurlock, Gillian, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Cardno, Alastair George, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, S., Jones, G., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Smith, K. J., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Coleman, Sharon Louise, Guy, Carol, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Buckland, Paul Robert 2002. Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular psychiatry 7 (5) , pp. 493-502. 10.1038/sj.mp.4001003

Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jacobsen, Nicholas James Olaf, Green, Elaine Karen, Elvidge, G. P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2002. Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's disease. Molecular psychiatry 7 (4) , pp. 424-427. 10.1038/sj.mp.4000989

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Krawczak, Michael, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Nikolov, Ivan, Georgieva, Lyudmila, Jones, S., Cardno, Alastair George, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. Molecular Psychiatry 7 (10) , pp. 1092-1100. 10.1038/sj.mp.4001188

Rees, Mark I., Lewis, Trevor M., Kwok, John B. J., Mortier, Geert R., Govaert, Paul, Snell, Russell G., Schofield, Peter R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Hyperekplexia associated with compound heterozygote mutations in the β-subunit of the human inhibitory glycine receptor (GLRB). Human Molecular Genetics 11 (7) , pp. 853-860. 10.1093/hmg/11.7.853

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Spurlock, Gillian, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2002. Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor. Molecular Psychiatry 7 (5) , pp. 508-514. 10.1038/sj.mp.4001030

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Scourfield, Jane 2002. Childhood disorders. McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gottesman, Irving I., eds. Psychiatric Genetics and Genomics, Oxford Medical Publications, Oxford: Oxford University Press, pp. 147-181.

Scourfield, Jane and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Genetic counselling. McGuffin, P., Owen, M. J. and Gottesman, I. I., eds. Psychiatric Genetics and Genomics, Oxford Medical Publications, Oxford: Oxford University Press, pp. 415-424.

Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Neurogenetics of schizophrenia. D'haenen, H., den Boer, J. A. and Willner, P., eds. Biological Psychiatry, Chichester: Wiley, pp. 663-671. (10.1002/0470854871.chxvii9)

Tsuang, M. T. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Molecular and population genetics of schizophrenia. Davis, K. L., Charney, D., Coyle, J. T. and Nemeroff, C., eds. Neuropsychopharmacology - 5th Generation of Progress, Philadelphia, PA: Lippincott, Williams and Wilkins, pp. 671-687.

West, A., Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Kent, L., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2002. Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios. Molecular Psychiatry 7 (9) , pp. 962-966. 10.1038/sj.mp.4001129

Sklar, P., Gabriel, S. B., McInnis, M. G., Bennett, P., Lim, Y-M, Tsan, G., Schaffner, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, DePaulo, J. R. and Lander, E. S. 2002. Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Molecular Psychiatry 7 (6) , p. 579. 10.1038/sj.mp.4001058

Bennett, P., Segurado, R., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Bort, S., McCandless, F., Lambert, D., Heron, J., Comerford, C., Middle, F., Corvin, A., Pelios, G., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Larsen, B., Mulcahy, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Connell, R., O'Mahony, E., Payne, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Gill, M. 2002. The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Molecular Psychiatry 7 (2) , pp. 189-200. 10.1038/sj.mp.4000957

Holmes, Jane, Payton, Antony, Barrett, Jennifer, Harrington, Richard, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, William, Worthington, Jane, Gill, Michael, Kirley, Aiveen, Hawi, Ziarih, Fitzgerald, Michael, Asherson, Philip, Curran, Sarah, Mill, John, Gould, Alison, Taylor, Eric, Kent, Lyndsey, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2002. Association of DRD4 in children with ADHD and comorbid conduct problems. American Journal of Medical Genetics 114 (2) , pp. 150-153. 10.1002/ajmg.10149

Hawi, Z, Dring, M, Kirley, A, Foley, D, Kent, L, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Asherson, P, Curran, S, Gould, A, Richards, S, Lawson, D, Pay, H, Turic, D, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Fitzgerald, M and Gill, M 2002. Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Molecular Psychiatry 7 (7) , pp. 718-725. 10.1038/sj.mp.4001048

Payton, A., Holmes, J., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2001. Susceptibility genes for a trait measure of attention deficit hyperactivity disorder: a pilot study in a non-clinical sample of twins. Psychiatry Research 105 (3) , 273 -278. 10.1016/S0165-1781(01)00342-0

Jurewicz, I, Owen, R.J, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Searching for susceptibility genes in schizophrenia. European Neuropsychopharmacology 11 (6) , pp. 395-398. 10.1016/S0924-977X(01)00116-X

Abraham, Richard, Myers, Amanda, Wavrant-DeVrieze, Fabienne, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Thomas, Hollie Victoria, Marshall, Helen, Compton, Danielle, Spurlock, Gillian, Turic, Dragana, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Kwon, Jennifer M., Petersen, Ronald C., Tangalos, Eric, Norton, Joanne, Morris, John C., Bullock, Roger, Liolitsa, Danae, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2001. Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. Human Genetics 109 (6) , pp. 646-652. 10.1007/s00439-001-0614-1

Plomin, R., Hill, L., Craig, I. W., McGuffin, P., Purcell, S., Sham, P., Lubinski, D., Thompson, L. A., Fisher, P. J., Turic, D. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups. Behaviour Genetics 31 (6) , pp. 497-509. 10.1023/A:1013385125887

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. British Journal of Psychiatry 179 (5) , pp. 397-402. 10.1192/bjp.179.5.397

Jones, R. G., Morley-Canellas, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murphy, K. C. 2001. Chromosome 22q11 deletions and severe learning disability [comment]. The British Journal of Psychiatry 179 (5) , pp. 466-467. 10.1192/bjp.179.5.466-a

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lowry, C. A., Stephens, M., Oldfield, S., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lightman, S. L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder. Molecular Psychiatry 6 (6) , pp. 671-677. 10.1038/sj.mp.4000899

Stephens, M, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. ADARB1, a brain specific member of the RNA-specific adenosine deaminase family and bipolar affective disorder. American Journal of Medical Genetics 105 (7) , p. 622.

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Stehens, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Screening of three candidate genes in the bipolar candidate region on chromosome 21q22.3. American Journal of Medical Genetics 105 (7) , p. 612.

Green, Elaine Karen, Elvidge, G., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2001. Mutational analysis of 2 positional candidate susceptibility genes for bipolar disorder: PAH and LHX5. American Journal of Medical Genetics 105 (7) , pp. 610-611.

Williams, H., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Meyer, J., Lesch, K. P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Further analysis of KIAA0027 in schizophrenic patients. American Journal of Medical Genetics 105 (7) , p. 561.

Reid, S. J., Rees, M. I., van Roon-Mom, W. M. C., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, McDonald, M. E., Sutherland, G. T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Dragunow, M. and Snell, R. G. 2001. Expression and population studies of the TATA-box binding protein polyglutamine region at normal and expanded lengths. American Journal of Human Genetics 69 (4) , p. 424.

Hamshere, Marian Linsday ORCID: https://orcid.org/0000-0002-8990-0958, Giles, Peter ORCID: https://orcid.org/0000-0003-3143-6854, Krawczak, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Statistical analysis of genotypic association data with HAPMAXII. AMERICAN JOURNAL OF HUMAN GENETICS 69 (4) , p. 390.

Rees, M. I., Baer, K., Ward, H., Coleman, Sharon Louise, Evans, I. L., Miller, J., Waldvogel, H., Faull, R. L. M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Snell, R. G. 2001. A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. American Journal of Human Genetics 69 (4) , p. 627.

Jones, Gaynor, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Jones, S. J., Milham, C., Sanders, R. D., McCarthy, G. M., Jones, L. A., Cardno, Alastair G., Gray, M., Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype. British Journal of Psychiatry 179 (4) , pp. 351-355. 10.1192/bjp.179.4.351

Rees, M. I., Lewis, T. M., Vafa, B., Ferrie, C., Corry, P., Muntoni, F, Jungbluth, H., Stephenson, J. B., Kerr, Michael Patrick, Snell, R. G., Schofield, P.R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Hum Genet 109 (3) , pp. 267-270.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Simple and complex genetics of Alzheimer's disease. Journal of Medical Genetics 38 , S29-S29.

2001. Evidence of association between DRD4 and ADHD with conduct disturbance. Presented at: Behavior Genetics Association Meeting, Cambridge, 11 July 2001. Published in: Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Holmes, J., Payton, A., Barrett, J., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Gill, M., Kirley, A., Hawi, Z., Fitzgerald, M., Asherson, P., Curran, S., Mill, J., Gould, A., Taylor, E., Kent, L., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Worthingon, J. eds. Behavior Genetics. Behavior Genetics Association Meeting Abstracts , vol.31 (5) Springer Verlag, pp. 470-471.

Campbell, L. E., Stevens, A. F., Morris, R., Karmiloff-Smith, A., Siminoff, E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, D. G. M. and Murphy, K. C. 2001. Neuropsychological profile of children with Velo-cardio-facial syndrome (VCFS). Journal of Medical Genetics 38 , S39-S39.

Liddell, M., Lovestone, S. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Advising relatives of risk of Alzheimer's disease - Authors' reply. British Journal of Psychiatry 179 (1) , pp. 73-74. 10.1192/bjp.179.1.73

Payton, A., Holmes, J., Barrett, J. H., Hever, T., Fitzpatrick, H., Trumper, A. L., Harrington, R., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2001. Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study. Neuroscience Letters 105 (5) , pp. 464-470. 10.1002/ajmg.1407

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Spurlock, G., Wittekindt, O. H., Morris-Rosendahl, D. J., Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Brzustowicz, L., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G, Sanders, Rebecca, Jones, L. A., McCarthy, G., Jones, S., Bassett, A., Cardno, A. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2001. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation [Letter]. Molecular Psychiatry 6 (3) , pp. 259-260. 10.1038/sj.mp.4000128

van Amelsvoort, T., Daly, E., Robertson, D., Suckling, J., Ng, V., Critchley, H., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Henry, J., Murphy, K. C. and Murphy, D. G. 2001. Structural brain abnormalities associated with deletion at chromosome 22q11. British Journal of Psychiatry (178) , pp. 412-419. 10.1192/bjp.178.5.412

Wang, Edward Chung Yern ORCID: https://orcid.org/0000-0002-2243-4964, Thern, Anette, Denzel, Angela, Kitson, Jeremy, Farrow, Stuart N. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. DR3 regulates negative selection during thymocyte development. Molecular and cellular biology 21 (10) , pp. 3451-61. 10.1128/MCB.21.10.3451-3461.2001

Williams, H. J., Murphy, K. C., Spurlock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. No association between a promoter polymorphism of the UFD1L gene and schizophrenia in individuals with or without velo-cardio-facial syndrome (VCFS). Schizophrenia Research 49 , p. 81.

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Searching for schizophrenia genes. Trends in Molecular Medicine 7 (4) , pp. 169-174.

Jones, L. A., Cardno, A. G., Sanders, R. D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2001. Sustained and selective attention as measures of genetic liability to schizophrenia. Schizophrenia Research 48 (2-3) , pp. 263-267.

Wickham, H., Walsh, C., Asherson, P., Taylor, C., Sigmundson, T., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P., Murray, R. and Sham, P. 2001. Familiality of symptom dimensions in schizophrenia. Schizophrenia Research 47 (2-3) , pp. 223-232. 10.1016/S0920-9964(00)00098-0

Turic, D., Fisher, P. J., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. No association between apolipoprotein E polymorphisms and general cognitive ability in children. Neuroscience Letters 299 (1-2) , pp. 97-100. 10.1016/S0304-3940(00)01789-4

Wang, Edward Chung Yern ORCID: https://orcid.org/0000-0002-2243-4964, Kitson, Jeremy, Thern, Anette, Williamson, Jill, Farrow, Stuart N. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Genomic structure, expression, and chromosome mapping of the mouse homologue for the WSL-1 (DR3, Apo3, TRAMP, LARD, TR3, TNFRSF12) gene. Immunogenetics 53 (1) , pp. 59-63. 10.1007/s002510000290

Liddell, M. B., Lovestone, S. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Genetic risk of Alzheimer's disease: advising relatives. British Journal of Psychiatry 178 (1) , pp. 7-11. 10.1192/bjp.178.1.7

Jacobsen, Nick J. O., Elvidge, Gareth, Franks, Emily K. E., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. CUX2, a potential regulator of NCAM expression: Genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder. American Journal of Medical Genetics 105 (3) , pp. 295-300. 10.1002/ajmg.1325

Elvidge, Gareth, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, Fiona, Asherson, Phil, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2001. Allelic variation of aBalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: Results of analysis and meta-analysis. American Journal of Medical Genetics 105 (4) , pp. 307-311. 10.1002/ajmg.1353

Jacobsen, N. J. O., Franks, E. K. E., Elvidge, G., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2001. Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Molecular Psychiatry 6 (1) , pp. 92-97. 10.1038/sj.mp.4000774

Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Spurlock, G., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Norton, N., Davis, K.L., Buxbaum, J.D., Haroutunian, V., Saunders, R., Cardno, A.G., McCarthy, G., O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 2001. Screening of candidate genes related to myelination for mutations associated with schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 105 (7) , p. 589.

Myers, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Abraham, R., Tunstall, N., Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Lovestone, S., Perez-Tur, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, J. and Goate, A. M. 2000. Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290 (5500) , pp. 2304-2305. 10.1126/science.290.5500.2304

Vincent, John B., Qiu-Ping, Yuan, Schalling, Martin, Adolfsson, R., Azevedo, M. Helena, Macedo, Antonio, Bauer, Amy, Dalla Torre, Camille, Medeiros, Helena M., Pato, Carlos N., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Paterson, Andrew D., Petronis, Arturas and Kennedy, James L. 2000. Long repeat tracts at SCA8 in major psychosis. American Journal of Medical Genetics 96 (6) , pp. 873-876. 10.1002/1096-8628(20001204)96:6<873::AID-AJMG37>3.0.CO;2-9

Sham, P. C., Sterne, A., Purcell, S., Cherny, S., Webster, M., Rijsdijk, F., Asherson, P., Ball, D., Craig, I., Eley, T., Goldberg, D., Gray, J., Mann, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Plomin, R. 2000. GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. Twin Research 3 (4) , pp. 316-322. 10.1375/136905200320565292

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Ashworth, Lindsay, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Guy, Carol, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, Fiona, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder. Bipolar Disorders 2 (4) , pp. 328-331. 10.1034/j.1399-5618.2000.020406.x

Deb, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Apolipoprotein E, Alzheimer's disease and Down's syndrome - Reply. British Journal of Psychiatry 177 , pp. 469-470.

Jones, L. A., Cardno, A. G., Murphy, K. C., Sanders, R. D., Gray, M. Y., McCarthy, G., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2000. The kings schizotypy questionnaire as a quantitative measure of schizophrenia liability. Schizophrenia Research 45 (3) , pp. 213-221. 10.1016/S0920-9964(99)00183-8

Snell, R. G., Miller, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Rees, M. I. 2000. Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes. American Journal of Human Genetics 67 (4) , p. 385.

Rees, M. I., Lewis, T. M., Mortier, G., Snell, R. G., Schofield, P. R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). American Journal of Human Genetics 67 (4) , p. 391.

Austin, J., Buckland, Paul Robert, Cardno, Alastair G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G., Sanders, R., Jones, L., McCarthy, G., Jones, S., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry 5 (5) , pp. 552-557. 10.1038/sj.mp.4000761

Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

van Amelsvoort, T., Daly, E., Critchley, H., Robertson, D., Henry, J. C., Suckling, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. M. 2000. Brain abnormalities associated with deletions at 22q11: Implications for psychosis. Journal of Medical Genetics 37 , S26-S26.

Holmes, J., Payton, A., Barrett, J. H., Hever, T., Fitzpatrick, H., Trumper, A. L., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2000. A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder. Molecular Psychiatry 5 (5) , pp. 523-530. 10.1038/sj.mp.4000751

Levinson, D. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Straub, R. E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Schwab, S. G., Lerer, B., Mowry, B. J., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. F. and Mallet, J. 2000. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics 67 (3) , pp. 652-663. 10.1086/303041

Williams, H.J. ORCID: https://orcid.org/0000-0001-7758-0312, Murphy, K.C., Spurlock, G., O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 2000. No association of the -277A variant allele of the UFD1L promoter polymorphism and schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4) , pp. 533-534.

Van Amelsvoort, T., Daly, E., Critchley, H., Robertson, D., Henry, D., Suckling, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. M. 2000. Brain abnormalities associated with deletions at 22q11: Implicatons for psychosis. American Journal of Medical Genetics 96 (4) , p. 551.

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Stephens, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Examining the 4p16 region for association with bipolar disorder using DNA pooling. American Journal of Medical Genetics 96 (4) , p. 548.

Walters, S. E., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Sanders, R. D., McCarthy, G. M., Cardno, A. G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia. American Journal of Medical Genetics 96 (4) , p. 535.

Payton, A., Holmes, J., Barrett, J., Hever, T., Fitzpatrick, H., Trumper, A., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2000. A family based candidate gene association study of Attention Deficit Hyperactivity Disorder. American Journal of Medical Genetics 96 (4) , p. 489.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Evidence for association between polymorphisms of the catechol-O-methyltransferase (COMT) and monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. American Journal of Medical Genetics 96 (4) , p. 476.

Henry, J. C., van Amelsvoort, T., Morris, R. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. M. 2000. The neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS). American Journal of Medical Genetics 96 (4) , p. 474.

McCarthy, G. M., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Investigating familiality of subtypes in schizophrenia. American Journal of Medical Genetics 96 (4) , pp. 473-474.

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jacobsen, N., Spurlock, Gillian, Austin, Jehanine, Williams, Hywel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. A functional and positional candidate gene for schizophrenia. American Journal of Medical Genetics 96 (4) , pp. 461-462.

Elvidge, G. P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2000. Mutational analysis of purinergic receptor, P2X4: A positional candidate susceptibility gene for bipolar disorder. American Journal of Medical Genetics 96 (4) , p. 493.

Jacobsen, N. J., Franks, E. K., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Genomic characterisation and mutational analysis of CUX2, a potential regulator of NCAM expression, mapping to chromosome 12q23-q24.1. American Journal of Medical Genetics 96 (4) , pp. 493-494.

Fitzpatrick, E., Spurlock, G., Coleman, Sharon Louise, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Buckland, Paul Robert 2000. Association studies of polymorphisms in the promoter region of the dopamine D4 receptor and the D2 receptor [Abstract]. American Journal of Medical Genetics 96 (4) , p. 530. 10.1002/1096-8628(20000807)96:4<515::AID-AJMG6>3.0.CO;2-U

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Cardno, A. G., Gray, M., Jones, L. A., Murphy, K. C., Sanders, R., Spurlock, G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics 10 (2) , pp. 83-86. 10.1097/00041444-200010020-00005

Jonsson, E. G., Norton, N., Gustavsson, J. P., Oreland, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. C. 2000. A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers. Journal of Psychiatric Research 34 (3) , pp. 239-244. 10.1016/S0022-3956(00)00013-3

Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. APOE epsilon 4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome. British Journal of Psychiatry 176 , pp. 468-472. 10.1192/bjp.176.5.468

Middle, F., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Barrett, T., Khanim, F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lendon, C. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2000. Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene. American Journal of Medical Genetics 96 (2) , pp. 154-157. 10.1002/(sici)1096-8628(20000403)96:2%3C154::aid-ajmg5%3E3.0.co;2-f

Morris, D. W., Robinson, L., Turic, D., Duke, M., Webb, V., Milham, C., Hopkin, E., Pound, K., Fernando, S., Easton, M., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2000. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Human Molecular Genetics 9 (5) , pp. 843-848. 10.1093/hmg/9.5.843

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Molecular genetic studies of schizophrenia. Brain research. Brain research reviews 31 (2-3) , pp. 179-186. 10.1016/S0165-0173(99)00035-1

Austin, J., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Buckland, Paul Robert, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Middle, F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Association analysis of the proneurotensin gene and bipolar disorder. Psychiatric Genetics 10 (1) , pp. 51-54. 10.1097/00041444-200010010-00009

Austin, J., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Buckland, Paul Robert, Speight, G., Cardno, A., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Sanders, R., Jones, L., Murphy, Kevin, McCarthy, G., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2) , pp. 208-212. 10.1038/sj.mp.4000693

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Cardno, A. G., Vincent, J. B., Kennedy, J. L., Jones, L. A., Gray, M, Sanders, Rhys, McCarthy, G, Murphy, K. C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatric Genetics 10 (1) , pp. 33-37. 10.1097/00041444-200010010-00006

Farmer, A. E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 2000. Bioethics and genetic research in psychiatry. British Journal of Psychiatry 176 , pp. 105-108. 10.1192/bjp.176.2.105

Rees, M. I., Watts, P., Fenton, I., Clarke, A., Snell, R. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gray, J. 2000. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). Human Genetics 106 (2) , pp. 206-209. 10.1007/s004390051029

Tunstall, N., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Carty, S., Lillystone, S., Fraser, L., Kehoe, P., Neill, D., Rudrasingham, V., Sham, P. and Lovestone, S. 2000. Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. British Journal of Psychiatry 176 , pp. 156-159. 10.1192/bjp.176.2.156

Buckland, J., Pennington, D. J., Bruno, L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Co-ordination of the expression of the protein tyrosine kinase p56(lck) with the pre-T cell receptor during thymocyte development. European Journal of Immunology 30 (1) , pp. 8-18. 10.1002/1521-4141(200001)30:1<8::AID-IMMU8>3.0.CO;2-8

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Cardno, A. G. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Psychiatric genetics: back to the future. Molecular Psychiatry 5 (1) , pp. 22-31. 10.1038/sj.mp.4000702

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Stephens, M., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples. Balkan Journal of Medical Genetics 3 , pp. 23-28.

Cardno, A. G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Genetic risk factors for schizophrenia. International Journal of Mental Health 29 (3) , pp. 13-38.

Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Presence of the Apolipoprotein E e4 allele is associated with the manifestation of Alzheimer dementia in adults with Down syndrome. Journal of Intellectual Disability Research 44 , p. 259.

Murphy, K.C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. No association between polymorphisms of catechol-o-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Schizophrenia Research 41 (1) , p. 96. 10.1016/S0920-9964(00)90531-0

Murphy, K.C., Jones, L.A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS). Schizophrenia Research 41 (1) , p. 29. 10.1016/S0920-9964(00)90364-5

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Sham, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1) , pp. 105-115.

Speight, G., Turic, Dragana, Austin, Jehannine, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Cardno, Alistair, Jones, L., Murphy, K. C., Sanders, R., McCarthy, G., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., McGuffin, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Buckland, Paul Robert and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder. Molecular Psychiatry 5 (3) , pp. 327-331. 10.1038/sj.mp.4000717

Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5) , pp. 488-493. 10.1007/s004390000397

Watts, Patrick, Rees, Mark I., Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286, Beck, Lyn, Lane, Carol M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gray, Jonathon 2000. Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13. Eye 14 (2) , pp. 172-175. 10.1038/eye.2000.48

Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Bowen, T. ORCID: https://orcid.org/0000-0001-6050-0435, Spurlock, G., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Norton, N., Austin, J., Walters, A., Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 2000. Identification and characterisation of SNPs in candidate genes for schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4) , p. 462.

Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Spurlock, G., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Norton, N., Walters, A., Saunders, R., Cardno, A.G., McCarthy, G., O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 2000. Linkage disequilibrium mapping and candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4) , p. 475.

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Norton, N., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder. International Journal of Neuropsychopharmacology 2 (4) , pp. 293-298. 10.1017/s1461145799001601

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5. Molecular Psychiatry 4 (6) , pp. 558-565.

Willliams, Hywel, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Murphy, K. C., Cardno, A. G., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No evidence for allelic association between schizophrenia and a functional variant of the human dopamine beta-hydroxylase gene (DBH). American Journal Of Medical Genetics Part A 88 (5) , pp. 557-559. 10.1002/(SICI)1096-8628(19991015)88:5<557::AID-AJMG22>3.0.CO;2-F

Murphy, K. C., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Archives of General Psychiatry 56 (10) , pp. 940-945. 10.1001/archpsyc.56.10.940

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Identification of new microsatellite markers on chromosome 4p16. American Journal of Human Genetics 65 (4) , A257-A257.

Murphy, K. C., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. High rates of schizophrenia in velo-cardio-facial syndrome. American Journal of Human Genetics 65 (4) , A336-A336.

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Gill, M., Spurlock, Gillian, Vallada, H. P., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Linkage studies of bipolar disorder with chromosome 18 markers. American Journal of Medical Genetics 15 (88) , pp. 503-509. 10.1002/(SICI)1096-8628(19991015)88:5<503::AID-AJMG13>3.0.CO;2-U

McCarthy, G., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Intra-pair correlations of symptom dimensions in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , S26-S27.

Fisher, P. J., Hill, L., Turic, D., Asherson, P., Benbow, C., Chorney, K., Chorney, M., Craig, I., Lubinski, D., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Plomin, R. 1999. A high resolution genome scan made possible with DNA pooling. Molecular Psychiatry 4 (1) , S10-S10.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Evidence of novel loci in late onset Alzheimer's disease. Molecular Psychiatry 4 (1) , S9-S9.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No association between polymorphisms of catechol-O-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Journal of Medical Genetics 36 , S78-S78.

Murphy, K., Thompson, P. W., Davies, S. J., Groves, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Stuart, G. 1999. The prevalence of chromosome 22q11 deletions in an adult congenital heart disease population. Journal of Medical Genetics 36 , S59-S59.

Jones, L. A., Sanders, R. D., Cardno, A. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 1999. Sustained and selective attention as quantitative measures of schizophrenia liability. Molecular Psychiatry 4 , S117-S117.

Emilien, Gérard, Maloteaux, Jean-Marie, Geurts, Muriel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Dopamine receptors and schizophrenia: contribution of molecular genetics and clinical neuropsychology. The International Journal of Neuropsychopharmacology 2 (3) , p. 197. 10.1017/S1461145799001479

Williams, H. J., McCarthy, G. M., Saunders, R. D., Cardno, A. G., Gray, M. Y., Murphy, K. C., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Characterization, mutational analysis, and association of the human proline oxidase gene: A candidate gene for schizophrenia. Molecular Psychiatry 4 , S115-S115.

Sanders, R. D., Norton, Nadine, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Pre-pulse inhibition in the functional psychoses. Molecular Psychiatry 4 , S121-S121.

Hill, L., Chorney, M. J., Chorney, K., Craig, I., Fisher, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1999. IGF2R and cognitive ability. Molecular Psychiatry 4 , S108-S108.

Jonsson, E. G., Norton, N., Gustavsson, J. P., Oreland, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. C. 1999. Monoamine oxidase a promoter polymorphism and relationships to monoamine metabolite concentrations in CSF. Molecular Psychiatry 4 , S97-S98.

Norton, N., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. C., Murphy, K. C., Jones, L. A., Sanders, R. D., McCarthy, G., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , S96-S96.

Middle, F. A., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, MacCandless, F., Khanim, F., Barrett, T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lendon, C. L. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Association studies between bipolar disorder and a polymorphism in the Wolfram gene. Molecular Psychiatry 4 , S76-S76.

Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Further evidence of familial cosegregation of major affective disorder and Darier's disease. Molecular Psychiatry 4 , S73-S73.

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Payton, T., Holmes, J., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Poulton, K., Barrett, I., Ollier, W. and Worthington, J. 1999. A quantitative trait loci study of attention deficit hyperactivity disorder. Molecular Psychiatry 4 , S52-S53.

McCarthy, G., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Familial aggregation of clinical variables in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , S121-S121.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Rees, M. I., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Human Molecular Genetics 8 (9) , pp. 1729-1739. 10.1093/hmg/8.9.1729

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Candidate-gene association studies of schizophrenia. American Journal of Human Genetics 65 (3) , pp. 587-592. 10.1086/302560

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Cardno, A. G., Fitzpatrick, E. R., Buckland, Paul Robert and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Embryonic NCAM and schizophrenia: Genetic analysis of regulatory enzymes. Molecular Psychiatry 4 , S32-S32.

Jacobsen, N. J., Lyons, I., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Burge, S., Kwok, P. Y., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes. Human Molecular Genetics 8 (9) , pp. 1631-1636. 10.1093/hmg/8.9.1631

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, M., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Bipolar disorder and the serotonin transporter gene: a family-based association study. Psychological Medicine -London- 29 (5) , pp. 1249-1254. 10.1017/s003329179900882x

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, H., Hoogendorn, B., Asherson, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1) , S42-S42.

Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1999. CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder. Neurobiology of Disease 6 (4) , pp. 302-307. 10.1006/nbdi.1999.0249

Wavrant-De Vrieze, F., Crook, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kehoe, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Roehl, K., Laliiri, D. K., Shears, S., Booth, J., Wu, W., Goate, A., Chartier-Harlin, M. C., Hardy, J. and Perez-Tur, J. 1999. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters 269 (2) , pp. 67-70.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Cardno, A. G. 1999. Psychiatric genetics: progress, problems, and potential. The Lancet 354 (1) , SI11-SI14. 10.1016/S0140-6736(99)90242-8

Rees, M. I., Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A., Asherson, P., Spurlock, G., Vallada, H., Dawson, E., Li, M. W., Collier, D. A., Powell, J. F., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521

Cardno, Alastair G., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Jones, Lisa A., McCarthy, Geraldine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Murphy, Kieran C., Spurlock, Gillian, Gray, Marion, Sanders, Rebecca, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1999. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia. Biological Psychiatry 45 (12) , pp. 1592-1596. 10.1016/s0006-3223(99)00033-5

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Kehoe, P. G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Case-control study of presenelin-1 intronic polymorphism. Journal of Neurology, Neurosurgery & Psychiatry 66 (6) , p. 702. 10.1136/jnnp.66.6.702

Fisher, P. J., Turic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Asherson, P., Ball, D., Craig, I., Eley, T., Hill, L., Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Human Molecular Genetics 8 (5) , pp. 915-922. 10.1093/hmg/8.5.915

Jacobsen, N. J., Franks, E. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder. Molecular Psychiatry 4 (3) , pp. 274-279. 10.1038/sj.mp.4000476

Amelsvoort, T. V., Daly, E., Critchley, H., Robertson, D., Murphy, K., Simmons, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Henry, J. and Murphy, D. G. M. 1999. An MRI and fMRI study on the effect of deletions on chromosome 22 on brain. Biological psychiatry 45 (8) , 110S-111S.

Hill, L., Craig, I. W., Asherson, P., Ball, D., Eley, T., Ninomiya, T., Fisher, P. J., Turic, D., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Thompson, L. A. and Plomin, R. 1999. DNA pooling and dense marker maps: a systematic search for genes for cognitive ability. NeuroReport 10 (4) , pp. 843-848. 10.1097/00001756-199903170-00032

Wavrant-DeVrieze, F., Rudrasingham, V., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Perez-Tur, J., Frigard, B., Morric, J. C., Carty, S., Cottel, D., Tunstall, N., Lovestone, S., Petersen, R. C., Chartier-Harlin, M. C., Goate, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Hardy, J. 1999. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters 262 (2) , pp. 137-139. 10.1016/S0304-3940(99)00035-X

Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C. S., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Kucherlapati, R., Rees, J. L., Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Lathrop, G. M., Monaco, A. P., Strachan, T. and Hovnanian, A. 1999. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nature Genetics 21 (3) , pp. 271-277.

Franks, Emily, Guy, Carol, Jacobsen, N., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder. American Journal of Medical Genetics 88 (1) , pp. 67-70. 10.1002/(SICI)1096-8628(19990205)88:1<67::AID-AJMG12>3.0.CO;2-#

Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, I. R., McCandless, F, McGuffin, P, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1999. No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder. American Journal of Medical Genetics 88 (1) , pp. 57-60. 10.1002/(sici)1096-8628(19990205)88:1%3C57::aid-ajmg10%3E3.0.co;2-6

Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, A., Hardy, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237

Kehoe, P., Krawczak, M., Harper, P. S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 1999. Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length. Journal of Medical Genetics 36 (2) , pp. 108-111. 10.1136/jmg.36.2.108

Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1) , pp. 71-72. 10.1038/5009

Kerwin, R and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Genetics of novel therapeutic targets in schizophrenia. The British journal of psychiatry. Supplement. 38 , pp. 1-4.

Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Oefner, P. J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Austin, J. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1999. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Human Genetics 104 (1) , pp. 89-93. 10.1007/s004390050915

Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1999. Dimensions of psychosis in affected sibling pairs. Schizophrenia Bulletin 25 (4) , pp. 841-850.

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, I., McCandless, F. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Tryptophan hydroxylase gene and manic-depressive illness [letter]. Archives of General Psychiatry 56 (1) , pp. 98-99. 10.1001/archpsyc.56.1.98

Kehoe, P. G., Williams, H., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wilcock, G., Cairns, N. J., Neal, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Journal of Medical Genetics 35 (12) , pp. 1034-1035. 10.1136/jmg.35.12.1034

Spurlock, Gillian, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics 81 (6) , pp. 525-526.

Poulton, K., Holmes, J., Hever, T., Trumper, A., Fitzpatrick, H., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Worthington, J., Ollier, W., Harrington, R. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 1998. A molecular genetic study of hyperkinetic disorder/attention deficit hyperactivity disorder. American Journal of Medical Genetics 81 (6) , p. 458.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Fenton, I. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects. American Journal of Medical Genetics 81 (6) , pp. 463-464.

Fisher, P. J., Turic, D., Asherson, P., Ball, D., Benbow, C., Chorney, M., Chorney, K., Craig, I., Eley, T., Hill, L., Lubinski, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. DNA pooling for genomic scanning - Application to an association study. American Journal of Medical Genetics 81 (6) , p. 469.

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Family-based association studies of candidate genes in bipolar disorder. American Journal of Medical Genetics 81 (6) , pp. 476-477.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder. American Journal of Medical Genetics 81 (6) , p. 486.

Bennett, P., Mulcahy, T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Gill, M. 1998. The Wellcome Trust UK-Irish Bipolar Sib-pair Study: Chromosome 21. American Journal of Medical Genetics 81 (6) , p. 541.

Hill, L., Asherson, P., Ball, D., Craig, I., Daniels, J., Eley, T., Freeman, B., Ninomiya, T., Fisher, P., Turic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Chorney, M., Chorney, K., Lubinski, D., Benbow, C., Thompson, L. A., Detterman, D. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1998. QTLs for general cognitive ability in children: DNA pooling for chromosome 22. American Journal of Medical Genetics 81 (6) , p. 486.

Spurlock, G., Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Williams, H.J. ORCID: https://orcid.org/0000-0001-7758-0312 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polymorphism screening of the human type 1 Sigma (σ) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics - Neuropsychiatric Genetics 81 (6) , pp. 525-526.

Deb, S., Braganza, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kehoe, P., Williams, H. and Norton, N. 1998. No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome. Alzheimers Reports 1 (6) , pp. 365-368.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Chromosome 22qII deletions and aggressive behaviour. British Journal of Psychiatry 173 , pp. 353-354. 10.1192/bjp.173.4.353b

Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Hutton, M., Hardy, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619

Straub, R. E., Vallada, H., Curtis, D., Sham, P., Kunugi, H., Zhao, J. H., Murray, R., McGuffin, P., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., Collier, D. A., Antonarakis, S., Housman, D., Kazazian, H., Nestadt, G., Pulver, A. E., MacLean, C. J., Walsh, D., Kendler, K. S., DeLisi, L., Polymeropoulos, M., Coon, H., Byerley, W., Lofthouse, R., Gershon, E., Goldin, L., Freedman, R., Laurent, C., Bodeau-Pean, S., d'Amato, T., Jay, M., Campion, D., Mallet, J., Wildenauer, D. B., Lerer, B., Albus, M., Ackenheil, M., Ebstein, R. P., Hallmayer, J., Maier, W., Gurling, H., Curtis, D., Kalsi, G., Brynjolfsson, J., Sigmundson, T., Petursson, H., Blackwood, D., Muri, W., StClair, D., He, L., Maguire, S., Moises, H. W., Hwu, H. G., Yang, L., Wiese, C., Kristbjarnarson, H., Levinson, D. F., Mowry, B. J., Donis-Keller, H., Hayward, N. K., Crowe, R. R., Silverman, J. M., Nancarrow, D. J. and Read, C. M. 1998. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22. Schizophrenia Research 32 (2) , pp. 115-121. 10.1016/S0920-9964(98)00048-6

Wright, P., Dawson, E., Donaldson, P. T., Underhill, J. A., Sham, P. C., Zhao, J., Gill, M., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Murray, R. M. 1998. A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia. Schizophrenia Research 32 (2) , pp. 75-80. 10.1016/S0920-9964(98)00050-4

Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1998. Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables. Psychological Medicine 28 (4) , pp. 815-823. 10.1017/S0033291798006783

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1998. Chromosome 11 workshop. Psychiatric Genetics 8 (2) , pp. 89-92.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1998. The programmed alliance of two disciplines. La Recherche 311 , pp. 38-39.

Asherson, P., Mant, R., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A., Jones, L., Murphy, Kevin, Collier, D. A., Nanko, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Morris, S., Muir, W., Blackwood, B., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder. Molecular Psychiatry 3 (4) , pp. 310-320. 10.1038/sj.mp.4000399

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Murphy, K. C., Arranz, M. J., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Kunugi, H., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1998. Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Molecular Psychiatry 3 (4) , pp. 342-345. 10.1038/sj.mp.4000385

Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5) , pp. 1189-1197. 10.1086/301816

Chorney, M.J., Chorney, K., Seese, N., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Daniels, J., McGuffin, P., Thompson, L.A., Detterman, D.K., Benbow, C., Lubinski, D., Eley, T. and Plomin, R. 1998. A Quantitative Trait Locus Associated With Cognitive Ability in Children. Psychological Science 9 (3) , pp. 159-166. 10.1111/1467-9280.00032

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Cardno, A. G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Murphy, K. C., Jones, L. A., Gray, M., Sanders, Rebecca, McCarthy, G, Chandy, K. G., Fantino, E, Kalman, K, Gutman, G. A., Gargus, J. J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3) , pp. 266-269. 10.1038/sj.mp.4000400

Daniels, J., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Plomin, R. 1998. Molecular genetic studies of cognitive ability. Human Biology 70 (2) , pp. 281-296.

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Spurlock, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Mant, R., Murphy, K., Jones, L., Cardno, A., Asherson, P., Blackwood, D., Muir, W., Meszaros, K., Aschauer, H., Mallet, J., Laurent, C., Pekkarinen, P., Seppala, J., Stefanis, C. N., Papadimitriou, G. N., Macciardi, F., Verga, M., Pato, C., Azevedo, H., Crocq, M. A., Gurling, H. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2) , pp. 141-149.

Spurlock, G., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Aschauer, H. N., Lenzinger, E., Fuchs, K., Sieghart, W. C., Meszaros, K., Fathi, N., Laurent, C., Mallet, J., Macciardi, F., Pedrini, S., Gill, M., Hawi, Z., Gibson, S., Jazin, E. E., Yang, H. T., Adolfsson, R., Pato, C. N., Dourado, A. M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics 81 (1) , pp. 24-28. 10.1002/(SICI)1096-8628(19980207)81:1<24::AID-AJMG5>3.0.CO;2-N

Cardno, A. G., Murphy, K. C., Jones, L. A., Cobb, A. M., Gray, J., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polydactyly and psychosis. Five cases of co-occurrence. British Journal of Psychiatry 172 , pp. 184-185. 10.1192/bjp.172.2.184

Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability. British Journal of Psychiatry 172 , pp. 180-183. 10.1192/bjp.172.2.180

Ball, D., Hill, L., Eley, T. C., Chorney, M. J., Chorney, K., Thompson, L. A., Detterman, D. K., Benbow, C., Lubinski, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1998. Dopamine markers and general cognitive ability. NeuroReport 9 (2) , pp. 347-349. 10.1097/00001756-199801260-00031

Arranz, M. J., Munro, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Spurlock, G., Sham, P. C., Zhao, J., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Collier, D. A. and Kerwin, R. W. 1998. Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine. Molecular Psychiatry 3 (1) , pp. 61-66. 10.1038/sj.mp.4000348

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Psychiatric disorders in Wolfram syndrome heterozygotes. Molecular Psychiatry 3 (1) , pp. 12-13.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. The behavioural phenotype in velo-cardio-facial syndrome. Schizophrenia Research 29 (1-2) , p. 132.

Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2) , pp. 131-132. 10.1016/S0920-9964(97)88632-X

Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Chromosome 22q11 deletions - An under-recognized cause of idiopathic learning disability? Schizophrenia Research 29 (1-2) , p. 132. 10.1016/S0920-9964(97)88634-3

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Norton, N, Jacobsen, N. J., Guy, Carol, Daniels, J. K., Sanders, Rebecca, Cardno, A. G., Jones, L. A., Murphy, Kevin, McGuffin, P, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Molecular Psychiatry 3 (1) , pp. 67-71. 10.1038/sj.mp.4000293

Spurlock, G., Heils, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, J., D'Souza, U. M., Cardno, A., Murphy, K. C., Jones, L., Buckland, Paul Robert, McGuffin, P., Lesch, K. .P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Molecular Psychiatry 3 (1) , pp. 42-49. 10.1038/sj.mp.4000342

Cardno, A. G., McCandless, F., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Jones, L. A., Murphy, Kevin, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1998. Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification [comparative study]. Psychiatric Genetics 8 (1) , pp. 29-32. 10.1097/00041444-199800810-00005

Vallada, H. P., Vasques, L., Curtis, D, Zatz, M., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lauriano, V., Gentil, V., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Collier, D. A. 1998. Linkage analysis between bipolar affective disorder and markers on chromosome X. Psychiatric Genetics 8 (3) , pp. 183-186. 10.1097/00041444-199800830-00008

Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Middle, F., Guy, Carol, Spurlock, G., Cairns, N. J., McGuffin, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia. Molecular Psychiatry 2 (6) , pp. 478-482. 10.1038/sj.mp.4000297

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Nothen, . and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. A meta analysis of association between the 5-HT2a receptor, T102C polymorphism and schizophrenia. American Journal of Medical Genetics 74 (6) , p. 612.

Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Chromosome 22q11 deletions: An underrecognized cause of idiopathic learning disability? American Journal of Medical Genetics 74 (6) , p. 567.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. The behavioral phenotype in velo-cardio-facial syndrome. American Journal of Medical Genetics 74 (6) , p. 660.

Vallada, H. P., Vasques, L., Curtis, D., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Gentil, V., Zatz, M., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Collier, D. A. 1997. Linkage studies in bipolar affective disorder with markers on chromosome Xq25-27. American Journal of Medical Genetics 74 (6) , pp. 679-680.

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McKeon, P., Moorhead, S., Guy, Carol, Harrison, D., Mynett-Johnson, L., Claffey, E., Feldman, E., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. Expanded CAG/CTG repeats in bipolar disorder: no correlation with phenotypic measures of illness severity. Biological psychiatry 42 (10) , pp. 876-881. 10.1016/s0006-3223(96)00516-1

Kunugi, H., Vallada, H. P., Sham, P. C., Hoda, F., Arranz, M. J., Li, T., Nanko, S., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Collier, D. A. 1997. Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families. Psychiatric Genetics 7 (3) , pp. 97-101. 10.1097/00041444-199723000-00001

Davies, S. J., Norton, N., Daniels, J. K. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Parietal foramina and multiple exostoses - familial inheritance of a molecular deletion. American Journal of Human Genetics 61 (4) , A95-A95.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1997. Genetics and psychiatry. British Journal of Psychiatry 171 , pp. 201-202. 10.1192/bjp.171.3.201

Rees, M., Norton, N., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Scourfield, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Moorhead, S., Feldman, E., Sadler, S., Cole, T., Redman, K., Farmer, A., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1997. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT). Molecular Psychiatry 2 (5) , pp. 398-402. 10.1038/sj.mp.4000256

Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Daniels, J. K., Speight, G., McKeon, P., Mynett-Johnson, L., Claffey, E., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder. American Journal of Psychiatry 154 (8) , pp. 1146-1147.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Murphy, K. C., Jones, L. A., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Psychiatric Genetics 7 (2) , pp. 83-85. 10.1097/00041444-199722000-00005

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and McGuffin, P. 1997. Association studies in psychiatric genetics. Molecular Psychiatry 2 (4) , pp. 270-273. 10.1038/sj.mp.4000292

Daniels, J. K., Spurlock, G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3) , pp. 319-323. 10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, Peter, Nothen, Markus and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia. The Lancet 349 (9060) , p. 1221. 10.1016/S0140-6736(05)62413-0

Speight, G., Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Asherson, P., McGuffin, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia. American Journal of Medical Genetics 74 (2) , pp. 204-206. 10.1002/(SICI)1096-8628(19970418)74:2<204::AID-AJMG19>3.0.CO;2-M

Spurlock, Gillian, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, Peter, Mallet, Jacques, Nöthen, Markus, Gill, Michael, Aschauer, Harald, Adlfsson, Rolf, Macciardi, Fabio and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene. Schizophrenia Research 24 (1-2) , p. 91. 10.1016/S0920-9964(97)82247-5

Arranz, M.J., Munro, J., Sham, P., Zhao, J., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Sodhi, M., Spurlock, G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Collier, D.A. and Kerwin, R. 1997. Polymorphisms in the 5-HT2A receptor gene and promoter region associated with clozapine response. Schizophrenia Research 24 (1-2) , p. 90. 10.1016/S0920-9964(97)82243-8

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, L. A., Murphy, K. C., Cardno, A. G., Asherson, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. American Journal of Medical Genetics 74 (1) , pp. 37-39. 10.1002/(SICI)1096-8628(19970221)74:1<37::AID-AJMG8>3.0.CO;2-S

Andrew, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Hyperekplexia: abnormal startle response due to glycine receptor mutations. British Journal of Psychiatry 170 , pp. 106-108. 10.1192/bjp.170.2.106

Petrill, S. A., Plomin, R., McClearn, G. E., Smith, D. L., Vignetti, S., Chorney, M. J., Chorney, K., Thompson, L. A., Detterman, D. K., Benbow, C., Lubinski, D., Daniels, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1997. No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene. Behavior Genetics 27 (1) , pp. 29-31. 10.1023/A:1025659124405

Jonsson, E. G., Goldman, D., Spurlock, G., Gustavsson, J. P., Nielsen, D. A., Linnoila, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. C. 1997. Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers. European Archives of Psychiatry and Clinical Neuroscience 247 (6) , pp. 297-230. 10.1007/BF02922258

Thomas, Nicholas Stuart Tudor, Davies, K., Webb, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Price, W., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pereira, J., Kerr, A., Anvret, M., Hanefeld, E. and Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286 1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1) , p. 94.

Petrill, Stephen A., Ball, David, Eley, Thalia, Hill, Linzy, Plomin, Robert, Mcclearn, Gerald E., Smith, Deborah L., Chorney, Karen, Chorney, Michael, Hershz, Milton S., Detterman, Douglas K., Thompson, Lee A., Benbow, Camilla, Lubinski, David, Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1997. Failure to replicate a QTL association between a DNA marker identified by EST00083 and IQ. Intelligence 25 (3) , pp. 179-184. 10.1016/S0160-2896(97)90041-6

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Introducing Selfcite 2.0--career enhancing software. BMJ 313 (7072) , pp. 1659-1660. 10.1136/bmj.313.7072.1659

Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Scott, L. C., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1996. Factor analysis of schizophrenic symptoms using the OPCRIT checklist. Schizophrenia Research 22 (3) , pp. 233-239. 10.1016/S0920-9964(96)00060-6

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Candidate gene association studies in psychiatric genetics: a SERTain future? Molecular Psychiatry 1 (6) , pp. 434-436.

Cardno, A. G., Murphy, K. C., Jones, L. A., Guy, C. A., Asherson, P., De Azevedo, M. H., Coelho, I. M., de Macedo e Santos, A. J., Pato, C. N., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1996. Expanded CAG/CTG repeats in schizophrenia. A study of clinical correlates. British Journal of Psychiatry 169 (6) , pp. 766-771. 10.1192/bjp.169.6.766

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Guy, Carol, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Involvement of expanded trinucleotide repeats in common diseases. The Lancet 348 (9043) , pp. 1739-1740. 10.1016/s0140-6736(05)65870-9

Vallada, H., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Vasques, L., Curtis, D., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lauriano, V., Gentil, V., Passos-Beuno, R., Murray, R. M., Zatz, M., McGuffin, P., Powell, J. F., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. A. 1996. Linkage studies in bipolar affective disorder with markers on chromosome 21. Journal of affective disorders 41 (3) , pp. 217-221. 10.1016/s0165-0327(96)00055-9

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, McKeon, P., Macedo, A., Maier, W., Wildenauer, D., Aschauer, H. N., Sorbi, S., Feldman, E., Mynett-Johnson, L., Claffey, E., Nacmias, B., Valente, J., Dourado, A., Grassi, E., Lenzinger, E., Heiden, A. M., Moorhead, S., Harrison, D., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder. Psychological Medicine -London- 26 (6) , pp. 1145-1153. 10.1017/s0033291700035868

Levinson, D. F., Wildenauer, D. B., Schwab, S. G., Albus, M., Hallmayer, J., Lerer, B., Maier, W., Blackwood, D., Muir, W., StClair, D., Morris, S., Moises, H. W., Yang, L., Kristbjarnarson, H., Helgason, T., Wiese, C., Collier, D. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Daniels, J., Rees, M., Asherson, P., Roberts, Q., Cardno, A., Arranz, M. J., Vallada, H., McGuffin, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pulver, A. E., Antonarakis, S. E., Babb, R., Blouin, J. L., DeMarchi, N., Dombroski, B., Housman, D., Karayiorgou, M., Ott, J., Kasch, L., Kazazian, H., Lasseter, V. K., Loetscher, E., Luebbert, H., Nestadt, G., Ton, C., Wolyniec, P. S., Laurent, C., deChaldee, M., Thibaut, F., Jay, M., Samolyk, D., Petit, M., Campion, D., Mallet, J., Straub, R. E., MacLean, C. J., Easter, S. M., ONeill, F. A., Walsh, D., Kendler, K. S., Gejman, P. V., Cao, Q. H., Gershon, E., Badner, J., Beshah, E., Zhang, J., Riley, B. P., Rajagopalan, S., MogudiCarter, M., Jenkins, T., Williamson, R., DeLisi, L. E., Garner, C., Kelly, M., LeDuc, C., Cardon, L., Lichter, J., Harris, T., Loftus, J., Shields, G., Comasi, M., Vita, A., Smith, A., Dann, J., Joslyn, G., Gurling, H., Kalsi, G., Brynjolfsson, J., Curtis, D., Sigmundsson, T., Butler, R., Read, T., Murphy, P., Chen, A. C. H., Petursson, H., Byerley, B., Hoff, M., Holik, J., Nancarrow, D. J., Crowe, R. R., Andreasen, N., Silverman, J. M., Mohs, R. C., Siever, L. J., Endicott, J., Sharpe, L., Walters, M. K., Lennon, D. P., Hayward, N. K., Sandkuijl, L. A., Mowry, B. J., Aschauer, H. N., Meszaros, K., Lenzinger, E., Fuchs, K., Heiden, A. M., Kruglyak, L., Daly, M. J. and Matise, T. C. 1996. Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. American Journal of Medical Genetics 67 (6) , pp. 580-594. 10.1002/(SICI)1096-8628(19961122)67:6<580::AID-AJMG11>3.0.CO;2-P

Petrill, Stephen A., Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Thompson, Lee A., Detterman, Douglas K., Benbow, Camilla, Lubinski, David, Daniels, Joanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1996. DNA markers associated with general and specific cognitive abilities. Intelligence 23 (3) , p. 191. 10.1016/S0160-2896(96)90003-3

Kunugi, H., Curtis, D., Vallada, H. P., Nanko, S., Powell, J. F., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Collier, D. A. 1996. A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families. Schizophrenia Research 22 (1) , pp. 61-68. 10.1016/0920-9964(96)00048-5

Daniels, J., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Molecular genetic research on IQ: can it be done? Should it be done? Journal of Biosocial Science 28 (4) , pp. 491-507. 10.1017/S0021932000022550

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Speight, G., Jones, L., Cardno, A., Murphy, Kevin, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1996. Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set. American Journal of Human Genetics 59 (4) , pp. 912-917.

Kehoe, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Liddell, M., Lovestone, S., Holmes, C., Powell, J., Neal, J., Wilcock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. NeuroReport 7 (13) , pp. 2155-2158. 10.1097/00001756-199609020-00019

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kehoe, P. and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 1996. Presenilin-1 polymorphism and Alzheimer's disease. The Lancet 348 (9024) , p. 414. 10.1016/S0140-6736(05)65041-6

Farmer, A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Genomics: the next psychiatric revolution? British Journal of Psychiatry 169 (2) , pp. 135-138. 10.1192/bjp.169.2.135

Ashworth, A., Abusaad, I., Walsh, C., Nanko, S., Murray, R. M., Asherson, P., McGuffin, P., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. A. 1996. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat. Psychiatric Genetics 6 (2) , pp. 81-86. 10.1097/00041444-199622000-00008

Parfitt, E., Asherson, P., Roberts, E., Mant, R., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19. Human Heredity 46 (4) , pp. 191-196. 10.1159/000154352

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, J., McGuffin, P. and Farmer, A. E. 1996. Concurrent validity of the OPCRIT diagnostic system. Comparison of OPCRIT diagnoses with consensus best-estimate lifetime diagnoses. British Journal of Psychiatry 169 (1) , pp. 58-63. 10.1192/bjp.169.1.58

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Modern molecular genetic approaches to psychiatric disease. British Medical Bulletin 52 (3) , pp. 434-452. 10.1093/oxfordjournals.bmb.a011558

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Spurlock, G., McGuffin, P., Mallet, J., Nothen, M. M., Gill, M., Aschauer, H., Nylander, P. O., Macciardi, F. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. The Lancet 347 (9011) , pp. 1294-1296. 10.1016/S0140-6736(96)90939-3

Asherson, P., Mant, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Cardno, A., Murphy, K., Jones, L., Collier, D., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 1 (2) , pp. 125-132.

Kehoe, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Lovestone, S., Wilcock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Presenilin-1 polymorphism and Alzheimer's disease. The UK Alzheimer's Disease Collaborative Group. The Lancet 347 (9009) , p. 1185.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Schizophrenia, CATCH 22 and FISH. British Journal of Psychiatry 168 (4) , pp. 397-398.

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs. Molecular Psychiatry 1 (1) , pp. 59-64.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1996. Modern molecular genetic approaches to complex traits: implications for psychiatric disorders [review]. Molecular Psychiatry 1 (1) , pp. 21-26.

Lim, Lionel C. C., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Sham, Pak, Nothen, Markus M., Korner, Judith, Rietschel, Marcella, Fimmer, Rolf, Propping, Peter, McGuffin, Peter, Murray, Robin and Gill, Michael 1996. Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees. Behavior Genetics 26 (2) , pp. 113-122. 10.1007/bf02359889

Gill, M., Vallada, H., Collier, D., Sham, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Murray, R., McGuffin, P., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Antonarakis, S., Housman, D., Kazazian, H., Nestadt, G., Pulver, A. E., Straub, R. E., MacLean, C. J., Walsh, D., Kendler, K. S., DeLisi, L., Polymeropoulos, M., Coon, H., Byerley, W., Lofthouse, R., Gershon, E. and Read, C. M. 1996. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics 67 (1) , pp. 40-45. 10.1002/(SICI)1096-8628(19960216)67:1<40::AID-AJMG6>3.0.CO;2-W

Cardno, Alastair, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Harvey, I., Williams, M. B., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1996. Factor-derived subsyndromes of schizophrenia and familial morbid risks. Schizophrenia Research 18 (2-3) , IVA2-IVA2.

Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Minor physical anomalies and their relationship to the aetiology of schizophrenia. British Journal of Psychiatry 168 (2) , pp. 139-142. 10.1192/bjp.168.2.139

Daniels, J. K., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Jones, L. A., Cardno, A. G., Murphy, K. C., Spurlock, G., Riley, B., Scambler, P., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. American Journal of Psychiatry 153 (2) , pp. 268-270. 10.1176/ajp.153.2.268

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Dynamic mutations and psychiatric genetics. Psychological Medicine 26 (1) , pp. 1-6. 10.1017/S0033291700033663

Lin, M. W., Curtis, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Powell, J. F. 1996. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Cytogenetics and Cell Genetics 75 , pp. 2-3.

Jacobsen, N., Daniels, J., Moorhead, S., Harrison, D., Feldman, E., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1996. Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1. Psychiatric Genetics 6 (4) , pp. 195-199. 10.1097/00041444-199624000-00005

Roberts, A. G., Whatley, S. D., Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thompson, P., Long, C. and Elder, G. H. 1995. Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Human Molecular Genetics 4 (12) , pp. 2387-2390. 10.1093/hmg/4.12.2387

Arranz, M., Sharma, T., Sham, P., Kerwin, R., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Collier, D. 1995. Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families. American Journal of Medical Genetics 60 (5) , pp. 377-381. 10.1002/ajmg.1320600506

Dawson, E., Powell, J. F., Sham, P., Shaikh, S., Taylor, C., Clements, A., Asherson, P., Sargeant, M., Collier, D., Nanko, S., Whatley, S., Murray, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1995. Systematic search for major genes in schizophrenia: methodological issues and results from chromosome 12. American Journal of Medical Genetics 60 (5) , pp. 424-433. 10.1002/ajmg.1320600513

Okoro, C., Bell, R., Sham, P., Nanko, S., Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., McGuffin, P., Murray, R. M. and Collier, D. 1995. No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia. American Journal of Medical Genetics 60 (5) , pp. 461-464. 10.1002/ajmg.1320600520

Lin, M. W., Curtis, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1995. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatric Genetics 5 (3) , pp. 117-126. 10.1097/00041444-199505030-00004

Vallada, H., Curtis, D., Sham, P. C., Murray, R. M., McGuffin, P., Nanko, S., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. 1995. Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia. Psychiatric Genetics 5 (3) , pp. 127-130. 10.1097/00041444-199505030-00005

McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Farmer, A. E. 1995. Genetic basis of schizophrenia. The Lancet 346 (8976) , pp. 678-682. 10.1016/S0140-6736(95)92285-7

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, J., Roberts, E., Rees, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms. American Journal of Medical Genetics 60 (4) , pp. 322-324. 10.1002/ajmg.1320600412

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Murphy, Kevin, Cardno, Alastair G., Jones, L. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1995. Expanded CAG repeats in schizophrenia and bipolar disorder [letter]. Nature Genetics 10 (4) , pp. 380-381. 10.1038/ng0895-380

Skuder, Patricia, Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Kasarda, Steven, Thompson, Lee A., Detterman, Douglas K., Petrill, Stephen A., Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1995. A polymorphism in mitochondrial DNA associated with IQ? Intelligence 21 (1) , pp. 1-11. 10.1016/0160-2896(95)90035-7

Liddell, M. B., Bayer, Antony James ORCID: https://orcid.org/0000-0002-7514-248X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease. Human Molecular Genetics 4 (5) , pp. 853-858. 10.1093/hmg/4.5.853

Vallada, H. P., Gill, M., Sham, P., Lim, L. C., Nanko, S., Asherson, P., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. 1995. Linkage studies on chromosome 22 in familial schizophrenia. American Journal of Medical Genetics 60 (2) , pp. 139-146. 10.1002/ajmg.1320600210

Dawson, E., Parfitt, E., Roberts, Q., Daniels, J., Lim, L., Sham, P., Nothen, M., Propping, P., Lanczik, M., Maier, W., Reuner, U., Weissenbach, J., Gill, M., Powell, J., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1995. Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. American Journal of Medical Genetics 60 (2) , pp. 94-102. 10.1002/ajmg.1320600203

Mullan, M., Bennett, C., Figueredo, C., Hughes, D., Mant, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Warren, A., McInnis, M., Marshall, A., Lantos, P., Collinge, J., Goate, A. M., Houlden, H. and Crawford, F. 1995. Clinical features of early onset, familial Alzheimer's disease linked to chromosome 14. American Journal of Medical Genetics 60 (1) , pp. 44-52. 10.1002/ajmg.1320600109

Daniels, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Asherson, P, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. No association between schizophrenia and polymorphisms within the genes for debrisoquine 4-hydroxylase (CYP2D6) and the dopamine transporter (DAT). American Journal of Medical Genetics 60 (1) , pp. 85-87. 10.1002/ajmg.1320600115

Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Skuder, Patricia, Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Kasarda, Steven, Thompson, Lee A., Detterman, Douglas K., Petrill, Stephen A., Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1995. Allelic associations between 100 DNA markers and high versus low IQ. Intelligence 21 (1) , p. 31. 10.1016/0160-2896(95)90037-3

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Roberts, Q., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. Association study of bipolar disorder using a functional polymorphism (Ser311-->Cys) in the dopamine D2 receptor gene. Psychiatric Genetics 5 (2) , pp. 63-65.

Rees, M. I., Andrew, M., Jawad, S. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. Human Molecular Genetics 3 (12) , pp. 2175-2179. 10.1093/hmg/3.12.2175

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Is there an inverse relationship between Down's syndrome and bipolar affective disorder? literature review and genetic implications [Review]. Journal of Intellectual Disability Research 38 (6) , pp. 613-620. 10.1111/j.1365-2788.1994.tb00462.x

McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Asherson, P. and Farmer, A. E. 1994. Genetics, chance and dysmorphogenesis in schizophrenia. British Journal of Psychiatry 165 , pp. 694-695. 10.1192/bjp.165.5.693b

Daniels, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Mant, R., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Repeat length variation in the dopamine D4 receptor gene shows no evidence of association with schizophrenia. American Journal of Medical Genetics 54 (3) , pp. 256-258. 10.1002/ajmg.1320540313

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Darier's disease cosegregating with affective disorder [letter]. British Journal of Psychiatry 165 (2) , p. 272. 10.1192/bjp.165.2.272a

Plomin, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1994. The genetic basis of complex human behaviors. Science 264 (5166) , pp. 1733-1739. 10.1126/science.8209254

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, Jo, McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Variation at the fragile X locus does not influence susceptibility to bipolar disorder. American Journal of Medical Genetics 54 (2) , pp. 141-143. 10.1002/ajmg.1320540209

Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Gottesman, I. I., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, P. 1994. The genetics of mental retardation. The British Journal of Psychiatry 164 (6) , p. 747. 10.1192/bjp.164.6.747

James, C. M., Daniels, J., Wiles, Charles Mark and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Debrisoquine hydroxylase gene polymorphism in motor-neuron disease. Neurodegeneration 3 (2) , pp. 149-152.

McGuffin, P, Asherson, P, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Farmer, A 1994. The strength of the genetic effect. Is there room for an environmental influence in the aetiology of schizophrenia? British Journal of Psychiatry 164 (5) , pp. 593-599. 10.1192/bjp.164.5.593

Asherson, P., Walsh, C., Williams, J., Sargeant, M., Taylor, C., Clements, A., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1994. Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia? The British Journal of Psychiatry 164 (5) , pp. 619-624. 10.1192/bjp.164.5.619

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Chromosomal aberrations and bipolar affective disorder [review]. British Journal of Psychiatry 164 (4) , pp. 507-512. 10.1192/bjp.164.4.507

Asherson, P, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Roberts, E, McGuffin, M and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. DRD2 Ser311/Cys311 polymorphism in schizophrenia. The Lancet 343 (8904) , p. 1045.

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Brockington, I., Mant, R., Parfitt, E., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Bipolar affective puerperal psychosis associated with consanguinity. British Journal of Psychiatry 164 (3) , pp. 359-364. 10.1192/bjp.164.3.359

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Burge, S., Kurian, B., Thomas, P. and McGuffin, P. 1994. Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis). British Journal of Psychiatry 164 (3) , pp. 355-358. 10.1192/bjp.164.3.355

Pulver, Ann E., Karayiorgou, Maria, Lasseter, Virginia K., Wolyniec, Paula, Kasch, Laura, Antonarakis, Stylianos, Housman, David, Kazazian, Haig H., Meyers, Deborah, Nestadt, Gerald, Ott, Jurg, Liang, Kung-Yee, Lamacz, Malgorzata, Thomas, Marion, Childs, Barton, Diehl, Scott R., Wang, Shengbiao, Murphy, Bernadette, Sun, Cui-E, O'Neill, F. Anthony, Nie, Li, Sham, Pak, Burke, John, Duke, Betty W., Duke, Fiona, Kipps, Barbara R., Bray, Joseph, Hunt, Wanda, Shinkwin, Rosmarie, Nuallain, Maurin Ni, Su, Ying, Maclean, Charles J., Walsh, Dermot, Kendler, Kenneth S., Gill, Michael, Vallada, Homero, Mant, Rebecca, Asherson, Philip, Collier, David, Parfitt, Elizabeth, Roberts, Enriquetta, Nanko, Shin, Walsh, Cathy, Daniels, Johanna, Murray, Robin, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Laurent, Claudine, Dumas, Jean-Baptiste, d'Amato, Thierry, Jay, Maurice, Martinez, Maria, Campion, Dominique and Mallet, Jacques 1994. Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2. American Journal of Medical Genetics 54 (1) , pp. 44-50. 10.1002/ajmg.1320540109

Shaikh, S., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Asherson, P., McGuffin, P., Nanko, S., Murray, R. M. and Collier, D. A. 1994. Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. American Journal of Medical Genetics 54 (1) , pp. 8-11. 10.1002/ajmg.1320540104

Mant, R., Williams, J., Asherson, P., Parfitt, E., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia. American Journal of Medical Genetics 54 (1) , pp. 21-26. 10.1002/ajmg.1320540106

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Liddell, M and McGuffin, P 1994. Alzheimer's disease. British Medical Journal (BMJ) 308 (6930) , pp. 672-673. 10.1136/bmj.308.6930.672

Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Venditti, Charles P., Kasarda, Steven, Thompson, Lee A., Detterman, Douglas K., Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1994. DNA markers associated with high versus low IQ: The IQ quantitative trait loci (QTL) project. Behavior Genetics 24 (2) , pp. 107-118. 10.1007/BF01067815

Liddell, Malcolm Brandon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Bayer, Antony James ORCID: https://orcid.org/0000-0002-7514-248X, Kaiser, F. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease. Journal of Medical Genetics 31 (3) , pp. 197-200. 10.1136/jmg.31.3.197

Asherson, P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Anticipation in mental illness. The American Journal of Human Genetics 54 (2) , pp. 386-387.

Parfitt, E., Burge, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Roberts, E., McLean, W. H., Weissenbach, J., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. The gene for Darier's disease maps between D12S78 and D12S79. Human Molecular Genetics 3 (1) , pp. 35-38. 10.1093/hmg/3.1.35

Vallada, H, Gill, M, Nanko, S, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murray, R.M and Collier, C 1994. Is there a major gene for schizophrenia on chromosome-22. Schizophrenia Research 11 (2) , p. 147.

Korner, J., Rietschel, M., Hunt, N., Castle, D., Gill, M., Nothen, M. M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Fimmers, R., Fritze, J., Moller, H. -J. and Propping, P. 1994. Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls. Psychiatric Genetics 4 (3) , pp. 167-175. 10.1097/00041444-199400430-00007

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. The molecular genetics of Alzheimer's disease. Molecular and Cell Biology of Human Diseases Series 1994 (4) , pp. 92-109.

McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlan ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Gottesman, Irving I. 1994. Seminars in psychiatric genetics. Gaskell, Royal College of Psychiatrists.

Daniels, J.K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, Peter, Thompson, Lee, Detterman, Douglas K., Chorney, Michael, Chorney, Karen, Smith, Deborah, Skuder, Patricia, Vignetti, Sylvia, McClearn, Gerald E. and Plomin, Robert 1994. IQ and variation in the number of fragile X CGG repeats: No association in a normal sample. Intelligence 19 (1) , pp. 45-50. 10.1016/0160-2896(94)90052-3

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Dawson, Elisabeth, Burge, Susan, Parfitt, Liz, Mant, Becky, Roberts, Queta, Daniels, Jo, Gill, Mike, McGuffin, Peter, Powell, John and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. The gene for Darier's disease maps to chromosome 12q23-q24.1. Human Molecular Genetics 2 (11) , pp. 1941-1943. 10.1093/hmg/2.11.1941

McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Molecular-genetics and schizophrenia - the current picture. Behavior Genetics 23 (6) , p. 558.

Saudino, K. J., Chorney, M., McClern, G. E., McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Smith, D., Detterman, D., Thompson, L. and Plomin, R. 1993. Applying a QTL association approach to temperament. Behavior Genetics 23 (6) , p. 564.

Asherson, P., Mant, R., Taylor, C., Sargeant, M., Collier, D., Clements, A., Nanko, S., Whatley, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Failure to find linkage between schizophrenia and genetic markers on chromosome 21. American Journal of Medical Genetics 48 (3) , pp. 161-165. 10.1002/ajmg.1320480310

Mant, R., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Asherson, P., Parfitt, E., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Susceptibility to schizophrenia and the dopamine d3 receptor gene. American Journal of Human Genetics 53 (3) , p. 1654.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P 1993. Association and linkage: complementary strategies for complex disorders. Journal of Medical Genetics 30 (8) , pp. 638-639. 10.1136/jmg.30.8.638

Shaikh, S., Ball, D., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Castle, D., Hunt, N., Mant, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Collier, D. and Gill, M. 1993. The dopamine D3 receptor gene: no association with bipolar affective disorder. Journal of Medical Genetics 30 (4) , pp. 308-309. 10.1136/jmg.30.4.308

Gill, M., McGuffin, P., Parfitt, E., Mant, R., Asherson, P., Vallada, H., Collier, D., Powell, J., Taylor, C., Sargeant, M., Clements, A., Nanko, S., Whatley, S., Murray, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. A linkage study of schizophrenia with DNA markers from the long arm of chromosome 11. Psychological Medicine 23 (1) , pp. 27-44. 10.1017/S0033291700038824

Jones, P. B., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lewis, S. W. and Murray, R. M. 1993. A case-control study of family history and cerebral cortical abnormalities in schizophrenia. Acta Psychiatrica Scandinavica 87 (1) , pp. 6-12. 10.1111/j.1600-0447.1993.tb03322.x

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Burge, S., Parfitt, L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Linkage is excluded between Darier's disease and the Duffy blood group locus in five British families. Annales de Genetique 36 (4) , pp. 211-213.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Liddell, M 1992. Role of amyloid beta-protein in Alzheimer's disease. The Lancet 340 (8823) , p. 851.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1992. The molecular genetics of schizophrenia. British Medical Journal (BMJ) 305 (6855) , pp. 664-665. 10.1136/bmj.305.6855.664

Mant, R., Asherson, P., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. Schizophrenia scepticism. Nature Genetics 2 (1) , p. 12. 10.1038/ng0992-12

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mant, R., Parfitt, E., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Asherson, P., O'Mahoney, G., Van Os, J., Llewellyn, D., Collier, D., Gill, M. and McGuffin, P. 1992. No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia. Human Genetics 90 (1-2) , pp. 131-132. 10.1007/BF00210756

Vallada, Homero, Collier, David, Dawson, Elisabeth, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Nanko, Shin, Murray, Robin and Gill, Mike 1992. Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophrenia. The Lancet 340 (8812) , pp. 181-182. 10.1016/0140-6736(92)93266-P

Asherson, Philip, Parfitt, E., Sargeant, M., Tidmarsh, Simon, Buckland, Paul Robert, Taylor, C., Clements, A., Gill, M., McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. No evidence for a pseudoautosomal locus for schizophrenia. Linkage analysis of multiply affected families. British Journal of Psychiatry 161 (1) , pp. 63-68. 10.1192/bjp.161.1.63

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. Advances and Retreats in the Molecular Genetics of Major Mental Illness. Annals of Medicine 24 (3) , pp. 171-177. 10.3109/07853899209147816

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. Christmas disease and major affective disorder [letter]. British Journal of Psychiatry 160 , p. 715. 10.1192/bjp.160.5.715a

Nanko, Shinichiro, Gill, Michael, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Takazawa, Noboru, Moridaira, Junko and Kazamatsuri, Hajime 1992. Linkage Study of Schizophrenia with Markers on Chromosome 11 in Two Japanese Pedigrees. Psychiatry and Clinical Neurosciences 46 (1) , pp. 155-159. 10.1111/j.1440-1819.1992.tb00828.x

Shaikh, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1992. DRD2 (TGn) repeat polymorphism in a large family data set. Schizophrenia Research 6 (2) , p. 91. 10.1016/0920-9964(92)90088-M

Dawson, E., Shaikh, S., Vallada, H., Powell, J., Collier, D., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1992. Genetic linkage analysis of schizophrenia using microsatellite repeat polymorphisms on chromosome 12. Schizophrenia Research 6 (2) , p. 90. 10.1016/0920-9964(92)90086-K

Collier, DavidA., Gill, Michael, Nanko, Shen, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Vallada, Homero 1992. Linkage analysis of schizophrenia on chromosome 22. Schizophrenia Research 6 (2) , pp. 89-90. 10.1016/0920-9964(92)90085-J

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and GILL, M. 1992. Looking for genes in schizophrenia. Clinical Neuropharmacology 15 (Suppl1) , 222A-223A. 10.1097/00002826-199201001-00116

Upadhyaya, M, Lunt, P W, Sarfarazi, M, Broadhead, W, Daniels, J, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Harper, P S 1991. A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q. Journal of Medical Genetics 28 (10) , pp. 665-671. 10.1136/jmg.28.10.665

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Parfitt, E., Sargeant, M., Asherson, P., McGuffin, P., Taylor, C., Collier, D., Powell, J., Murray, R. and Gill, M. 1991. Linkage studies of schizophrenia with markers of chromosome-11q. American Journal of Human Genetics 49 (4) , p. 354.

Mant, R., Parfitt, E., Hardy, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1991. Mononucleotide repeat polymorphism in the APP gene. Nucleic Acids Research 19 (16) , p. 4572. 10.1093/nar/19.16.4572-a

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Goate, A.M. and Hardy, J.A. 1991. A polymorphic microsatellite repeat sequence on chromosome 21 (D21S80). Nucleic Acids Research 19 (16) , pp. 4574-4571. 10.1093/nar/19.16.4574

Foerster, A., Lewis, S. W., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murray, R. M. 1991. Low birth weight and a family history of schizophrenia predict poor premorbid functioning in psychosis. Schizophrenia Research 5 (1) , pp. 13-20. 10.1016/0920-9964(91)90049-W

Goate, Alison, Chartier-Harlin, Marie-Christine, Mullan, Mike, Brown, Jeremy, Crawford, Fiona, Fidani, Liana, Giuffra, Luis, Haynes, Andrew, Irving, Nick, James, Louise, Mant, Rebecca, Newton, Phillippa, Rooke, Karen, Roques, Penelope, Talbot, Chris, Pericak-Vance, Margaret, Roses, Alien, Williamson, Robert, Rossor, Martin, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Hardy, John 1991. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349 (6311) , pp. 704-706. 10.1038/349704a0

Foerster, A., Lewis, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murray, R. 1991. Pre-morbid adjustment and personality in psychosis. Effects of sex and diagnosis. British Journal of Psychiatry 158 (2) , pp. 171-176. 10.1192/bjp.158.2.171

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1991. DNA-and classical genetic markers in schizophrenia. European Archives of Psychiatry and Clinical Neuroscience 240 (3) , pp. 197-203. 10.1007/BF02190764

McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1991. The molecular genetics of schizophrenia: An overview and forward view. European Archives of Psychiatry and Clinical Neuroscience 240 (3) , pp. 169-173. 10.1007/BF02190759

Mant, R, Asherson, P, Sargeant, M, Hicks, A, Darlison, M, Johnstone, K, Sander, T, Taylor, C, Murray, R, Whatley, S, Gill, M, McGuffin, P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1991. Exclusion of close linkage between GABA a receptor subunit 1a gene and schizophrenia using a microsatellite repeat marker. Cytogenetics and Cell Genetics 58 (3-4) , pp. 1900-1991.

Upadhyaya, M., Lunt, P.W., Sarfarazi, M., Broadhead, W., Daniels, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Harper, P.S. 1990. DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease. The Lancet 336 (8726) , pp. 1320-1321. 10.1016/0140-6736(90)93005-A

St George-Hyslop, P. H., Haines, J. L., Farrer, L. A., Polinsky, R., Broeckhoven, C. Van, Goate, A., McLachlan, D. R. Crapper, Orr, H., Bruni, A. C., Sorbi, S., Rainero, I., Foncin, J.-F., Pollen, D., Cantu, J-M., Tupler, R., Voskresenskaya, N., Mayeux, R., Growdon, J., Fried, V. A., Myers, R. H., Nee, L., Backhovens, H., Martin, J-J., Rossor, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mullan, M., Percy, M. E., Karlinsky, H., Rich, S., Heston, L., Montesi, M., Mortilla, M., Nacmias, N., Gusella, J. F. and Hardy, J. A. 1990. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature 347 (6289) , pp. 194-197. 10.1038/347194a0

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, Peter and Andrews, R.C.Richardson 1990. Obstetric complications and schizophrenia. The Lancet 336 (8707) , p. 122. 10.1016/0140-6736(90)91643-O

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craufurd, D. and St Clair, D. 1990. Localisation of a susceptibility locus for schizophrenia on chromosome 5. British Journal of Psychiatry 157 (1) , pp. 123-127. 10.1192/bjp.157.1.123

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, James, L.A., Hardy, J.A., Williamson, R and Goate, A.M. 1990. Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21. American Journal of Human Genetics 46 (2) , pp. 316-322.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Mullan, Michael J. 1990. Molecular genetic studies of manic-depression and schizophrenia. Trends in Neurosciences 13 (1) , pp. 29-31. 10.1016/0166-2236(90)90059-J

Goate, A.M., Hardy, J.A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Haynes, A., James, L., Farrell, M., Mullan, M.J., Roques, P. and Rossor, M.N. 1990. Genetics of Alzheimer's disease. Advances in Neurology -New York- Raven Press- 51 , pp. 197-198.

Hardy, John, Goate, Alison, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Rossor, Martin 1989. Presenile dementia associated with mosaic trisomy 21 in a patient with a down syndrome child. The Lancet 334 (8665) , p. 743. 10.1016/S0140-6736(89)90805-2

Hardy, J.A., Goate, A.M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mullan, M.J., Rossor, M.N. and Pearson, R.C.A. 1989. Modelling the occurrence and pathology of Alzheimer's disease. Neurobiology of Aging 10 (5) , pp. 429-431. 10.1016/0197-4580(89)90084-5

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lewis, S. W. and Murray, R. M. 1989. Family history and cerebral ventricular enlargement in schizophrenia. A case control study. British Journal of Psychiatry 154 (5) , pp. 629-634. 10.1192/bjp.154.5.629

Goate, AlisonM., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, James, LouiseA., Mullan, MichaelJ., Rossor, MartinN., Haynes, AndrewR., Farrall, Martin, Lai, LawrenceY.C., Roques, Penelope, Williamson, Robert and Hardy, JohnA. 1989. Predisposing locus for Alzheimer's disease on chromosome 21. The Lancet 333 (8634) , pp. 352-355. 10.1016/S0140-6736(89)91725-X

HARDY, J. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, GOATE, A. M., JAMES, L. A., HAYNES, A. R., ROSSOR, M. N., ROQUES, P. and MULLAN, M. J. 1989. Molecular genetics of Alzheimer's disease. Biochemical Society Transactions 17 (1) , pp. 75-76. 10.1042/bst0170075

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murray, R.M. 1988. Blue genes. British Medical Journal (BMJ) 297 (6653) , pp. 871-872.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lewis, S. W. 1988. Risk factors in schizophrenia. British Journal of Psychiatry 153 (3) , p. 407. 10.1192/bjp.153.3.407a

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Whatley, S.A. 1988. Polymorphic DNA markers and mental disease. Psychological Medicine 18 (3) , pp. 529-533.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lewis, Shôn W. and Murray, Robin M. 1988. Obstetric complications and schizophrenia: a computed tomographic study. Psychological Medicine 18 (02) , pp. 331-339. 10.1017/S003329170000787X

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Nimgaonkar, V.L. 1987. The continuum of psychosis and the gene. British Journal of Psychiatry 150 , pp. 566-567.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lweis, S.W. 1986. Lateral ventricular size in schizophrenia. The Lancet 2 (8500) , pp. 223-224.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1984. Does amnesia after transection of the fornix in monkeys reflect abnormal sensitivity to proactive interference? Behavioural Brain Research 14 (3) , pp. 183-192.

Gaffan, D, Saunders, RC, Gaffan, EA, Harrison, S, Shields, C and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1984. Effects of fornix transection upon associative memory in monkeys: role of the hippocampus in learned action. Quarterly Journal of Experimental Psychology 36 (3) , pp. 173-221.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1981. Amnesia after transection of the fornix in monkeys: Long-term memory impaired, short-term memory intact. Behavioural Brain Research 3 (1) , pp. 115-123. 10.1016/0166-4328(81)90032-2

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1980. Effects of fornix lesions on recognition memory in the monkey. Journal of Anatomy 131 (DEC) , p. 771.

Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1980. The effects of fornix lesions on latent learning in the rat. Physiology & Behavior 24 (5) , pp. 817-822. 10.1016/0031-9384(80)90133-X