Browse by Current Cardiff authors

Richards, Alexander L., Fenner, Eilidh, Clifton, Nicholas E., Cameron, Darren, Tume, Claire E., Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X, Legge, Sophie E., Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter A. 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 2025. Effects of shared and nonshared schizophrenia and bipolar disorder alleles on cognition and educational attainment in the UK Biobank. Biological Society: Global Open Science 5 (6) , 100601. 10.1016/j.bpsgos.2025.100601

Smart, Sophie E. ORCID: https://orcid.org/0000-0002-6709-5425, Legge, Sophie E., Fenner, Eilidh, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Escott‐Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Wilkinson, Lawrence ORCID: https://orcid.org/0000-0002-9337-6124, 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 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2025. The role of SLC39A8.p.( Ala391Thr ) in schizophrenia symptom severity and cognitive ability: cross‐sectional studies of schizophrenia and the general UK population. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 198 (7) , pp. 135-146. 10.1002/ajmg.b.33037

Rodriguez, Victoria, Alameda, Luis, Aas, Monica, Gayer-Anderson, Charlotte, Trotta, Giulia, Spinazzola, Edoardo, Quattrone, Diego, Tripoli, Giada, Jongsma, Hannah E., Stilo, Simona, La Cascia, Caterina, Ferraro, Laura, La Barbera, Daniele, Lasalvia, Antonio, Tosato, Sarah, Tarricone, Ilaria, Bonora, Elena, Jamain, Stéphane, Selten, Jean-Paul, Velthorst, Eva, de Haan, Lieuwe, Llorca, Pierre-Michel, Arrojo, Manuel, Bobes, Julio, Bernardo, Miguel, Arango, Celso, Kirkbride, James, Jones, Peter B., Rutten, Bart P, Richards, Alexander, Sham, Pak C., O’Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Van Os, Jim, Morgan, Craig, Di Forti, Marta, Murray, Robin M. and Vassos, Evangelos 2025. Polygenic and polyenvironment interplay in schizophrenia-spectrum disorder and affective psychosis; the EUGEI first episode study. Schizophrenia Bulletin: The Journal of Psychoses and Related Disorders 51 (5) , pp. 1254-1265. 10.1093/schbul/sbae207

Uffelmann, Emil, Lewis, Cathryn M., McIntosh, Andrew M., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Price, Alkes L., Posthuma, Danielle and Peyrot, Wouter J. 2025. Estimating disorder probability based on polygenic prediction using the BPC approach. Nature Communications 16 (1) , 8443. 10.1038/s41467-025-62929-x

Shakeshaft, Amy ORCID: https://orcid.org/0000-0003-1412-5413, Farhat, Luis C., Dennison, Charlotte A. ORCID: https://orcid.org/0000-0002-7493-2041, Eyre, Olga, Oginni, Olakunle, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Stringaris, Argyris, Leibenluft, Ellen, Polanczyk, Guilherme V., Riglin, Lucy and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2025. Mapping phenotypic and genetic relationships among irritability, depression and ADHD in adolescence using network analysis. Journal of Child Psychology and Psychiatry , jcpp.70040. 10.1111/jcpp.70040

Agrawal, Arpana, Bulik, Cynthia M., Abebe, Dawit Shawel, Andreassen, Ole A., Atkinson, Elizabeth G., Choi, Karmel W., Corvin, Aiden, Davies, Helena L., Davies, Lea K., Docherty, Anna R., Edenberg, Howard J., Franke, Barbara, Gelernter, Joel, Giusti - Rodriquez, Paola, Hettema, John M., Hjerling - Leffler, Jens, Huang, Hailiang, Johnson, Emma C., Lewis, Cathryn M., Lu, Yi, Lynall, Mary-Ellen, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, McIntosh, Andrew M., Montalvo-Ortiz, Janitza L., Mullins, Niamh, Nievergelt, Caroline M., O'Connell, Kevin S., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Okewole, Adeniran, Peterson, Roseann E., Posthuma, Danielle, Sebat, Jonathan, Smoller, Jordan W., Sud, Reeteka, Viswanath, Biju, Walters, James T.R., Won, Hyejung, Wray, Naomi R. and Sullivan, Patrick F. 2025. The Psychiatric Genomics Consortium: discoveries and directions. The Lancet Psychiatry 12 (8) , pp. 600-610. 10.1016/S2215-0366(25)00124-5 Item availability restricted.

Chick, Sophie L., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Cameron, Darren, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 and Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 2025. Whole-exome sequencing analysis identifies risk genes for schizophrenia. Nature Communications 16 (1) , 7102. 10.1038/s41467-025-62429-y

Koromina, Maria, Ravi, Ashvin, Panagiotaropoulou, Georgia, Schilder, Brian M., Humphrey, Jack, Braun, Alice, Bidgeli, Tim, Chatzinakos, Chris, Coombes, Brandon J., Kim, Jaeyoung, Liu, Xiaoxi, Terao, Chikashi, O'Connell, Kevin S., Adams, Mark J., Adolfsson, Rolf, Alda, Martin, Alfredsson, Lars, Andlauer, Till F. M., Andreassen, Ole A., Antoniou, Anastasia, Baune, Bernhard T., Bengesser, Susanne, Biernacka, Joanna, Boehnke, Michael, Bosch, Rosa, Cairns, Murray J., Carr, Vaughan J., Casas, Miquel, Catts, Stanley, Cichon, Sven, Corvin, Aiden, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Dafnas, Konstantinos, Dalkner, Nina, Dannlowski, Udo, Degenhardt, Franziska, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Dikeos, Dimitris, Fellendorf, Frederike Tabea, Ferentinos, Panagiotis, Forstner, Andreas J., Forty, Liz, Frye, Mark, Fullerton, Janice M., Gawlik, Micha, Gizer, Ian R., Gordon-Smith, Katherine, Green, Melissa J., Grigoroiu-Serbanescu, Maria, Guzman-Parra, José, Hahn, Tim, Henskens, Frans, Hillert, Jan, Jablensky, Assen V., Jones, Lisa, Jones, Ian, Jonsson, Lina, Kelsoe, John R., Kircher, Tilo, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kittel-Schneider, Sarah, Kogevinas, Manolis, Landén, Mikael, Leboyer, Marion, Lenger, Melanie, Lissowska, Jolanta, Lochner, Christine, Loughland, Carmel, MacIntyre, Donald J., Martin, Nicholas G., Maratou, Eirini, Mathews, Carol A., Mayoral, Fermin, McElroy, Susan L., McGregor, Nathaniel W., McIntosh, Andrew, McQuillin, Andrew, Michie, Patricia, Mitchell, Philip B., Moutsatsou, Paraskevi, Mowry, Bryan, Müller-Myhsok, Bertram, Myers, Richard M., Nenadi, Igor, Nievergelt, Caroline M., Nöthen, Markus M., Nurnberger, John, O'Donovan, Michael O. ORCID: https://orcid.org/0000-0001-7073-2379, O'Donovan, Claire O., Ophoff, Roel A., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pantelis, Christos, Pato, Carlos, Pato, Michele T., Patrinos, George P., Pawlak, Joanna M., Perlis, Roy H., Porichi, Evgenia, Posthuma, Danielle, Ramos-Quiroga, Josep Antoni, Reif, Andreas, Reininghaus, Eva Z., Ribasés, Marta, Rietschel, Marcella, Schall, Ulrich, Schofield, Peter R., Schulze, Thomas G., Scott, Laura, Scott, Rodney J., Serretti, Alessandro, Smoller, Jordan W., Swiatkowska, Beata, Soler Artigas, Maria, Stein, Dan J., Streit, Fabian, Toma, Claudio, Tooney, Paul, Vawter, Marquis P., Vieta, Eduard, Vincent, John B., Waldman, Irwin D., Weickert, Cynthia Shannon, Weickert, Thomas, Witt, Stephanie H., Hong, Kyung Sue, Ikeda, Masashi, Iwata, Nakao, Won, Hong-Hee, Edenberg, Howard J., Ripke, Stephan, Raj, Towfique, Coleman, Jonathan R. I. and Mullins, Niamh 2025. Fine-mapping genomic loci refines bipolar disorder risk genes. Nature Neuroscience 28 (7) , pp. 1393-1403. 10.1038/s41593-025-01998-z

Byrne, Robert A.J., Nimmo, Jacqui, Torvell, Megan, Carpanini, Sarah M., Daskoulidou, Nikoleta, Hughes, Timothy R. ORCID: https://orcid.org/0000-0003-2348-3490, Noble, Lucy V., Veteleanu, Aurora, Watkins, Lewis M., Zelek, Wioleta M., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Morgan, Bryan Paul ORCID: https://orcid.org/0000-0003-4075-7676 2025. The schizophrenia-associated gene CSMD1 encodes a complement classical pathway inhibitor predominantly expressed by astrocytes and at synapses in mice and humans. Brain, Behavior, and Immunity 127 , pp. 287-302. 10.1016/j.bbi.2025.03.026

Kappel, Djenifer, Smart, Sophie ORCID: https://orcid.org/0000-0002-6709-5425, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Pardiñas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2025. Association between genetic liability to physical health conditions and comorbidities in individuals with severe mental illness: an analysis of two cross-sectional observational studies in the UK. The Lancet Psychiatry 12 (6) , pp. 447-456. 10.1016/S2215-0366(25)00123-3

Lock, Siobhan K., Kappel, Djenifer B., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590 and Legge, Sophie E. 2025. Antipsychotic and pharmacogenomic effects on cross-sectional symptom severity and cognitive ability in schizophrenia. EBioMedicine 116 , 105745. 10.1016/j.ebiom.2025.105745

Koch, Elise, Smart, Sophie ORCID: https://orcid.org/0000-0002-6709-5425, Einarsson, Guðmundur, Kämpe, Anders, Jonsson, Lina, Alver, Maris, Iveson, Matthew, Göteson, Andreas, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Sønderby, Ida E, O'Connell, Kevin S., Li, Qingqin, Lu, Yi, Stefánsson, Hreinn, Stefánsson, Kári, Whalley, Heather, Landén, Mikael, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Smerud, Knut, Dawson, Gerard R., Werge, Thomas, Buil, Alfonso, Reif, Andreas, Milani, Lili, Molden, Espen, Fabbri, Chiara, Serretti, Alessandro, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Lewis, Cathryn M. and Andreassen, Ole A. 2025. Recommendations for defining treatment outcomes in major psychiatric disorders using real-world data. The Lancet Psychiatry 12 (6) , pp. 457-468. 10.1016/S2215-0366(25)00061-6

Andreu-Bernabeu, Álvaro, González-Peñas, Javier, Mora, Alberto, Bernardo, Miguel, Mezquida, Gisela, Amoretti, Silvia, Bobes, Julio, Saiz, Pilar A, García-Portilla, Maria Paz, Sanjuan, Julio, Santos, José Luis, Jiménez-López, Estela, Arrojo, Manuel, Carracedo, Angel, Parellada, Mara, Maric, Nadja P, Atbaşoğlu, Cem, Üçok, Alp, Alptekin, Köksal, Saka, Meram Can, Pries, Lotta-Katrin, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, van Os, Jim, Rutten, Bart P F, Delespaul, Philippe, Guloksuz, Sinan, Arango, Celso and Díaz-Caneja, Covadonga M 2025. Linking prolonged childhood and adolescent loneliness to schizophrenia spectrum disorders: results from EU-GEI study. The British Journal of Psychiatry , pp. 1-9. 10.1192/bjp.2025.100

Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2025. Genomics of schizophrenia, bipolar disorder and major depressive disorder. Nature Reviews Genetics 10.1038/s41576-025-00843-0 Item availability restricted.

Dempster, Emma, Wong, Chloe, Burrage, Joe, Hannon, Eilis, Quattrone, Diego, Trotta, Giulia, Rodriguez, Victoria, Alameda, Luis, Spinazzola, Edouardo, Tripoli, Giada, Austin-Zimmerman, Isabelle, Li, Zhikun, Gayer-Anderson, Charlotte, Freeman, Tom, Johnson, Emma, Jongsma, Hannah, Stilo, Simona, La Cascia, Caterina, Ferraro, Laura, La Barbera, Daniele, Lasalvia, Antonio, Tosato, Sarah, Tarricone, Ilaria, D'Andrea, Giuseppe, Galatolo, Michela, Tortelli, Andrea, Pompili, Maurizio, Selten, Jean-Paul, de Haan, Lieuwe, Rossi Menezes, Paulo, Del Ben, Cristina M., Santos, Jose Luis, Arrojo, Manuel, Bobes, Julio, Sanjuan, Miguel, Arango, Celso, Jones, Peter B., Breen, Gerome, Mondelli, Valeria, Dazzan, Paola, Iyegbe, Conrad, Vassos, Evangelos, Morgan, Craig, Mukherjee, Diptendu, van Os, Jim, Rutten, Bart, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Sham, Pak, Mill, Jonathan, Murray, Robin and Di Forti, Marta 2025. Methylomic signature of current cannabis use in two first-episode psychosis cohorts. Molecular Psychiatry 30 , pp. 1277-1286. 10.1038/s41380-024-02689-0

O'Connell, Kevin S., Koromina, Maria, van der Veen, Tracey, Boltz, Toni, David, Friederike S., Yang, Jessica Mei Kay, Lin, Keng-Han, Wang, Xin, Coleman, Jonathan R. I., Mitchell, Brittany L., McGrouther, Caroline C., Rangan, Aaditya V., Lind, Penelope A., Koch, Elise, Harder, Arvid, Parker, Nadine, Bendl, Jaroslav, Adorjan, Kristina, Agerbo, Esben, Albani, Diego, Alemany, Silvia, Alliey-Rodriguez, Ney, Als, Thomas D., Andlauer, Till F. M., Antoniou, Anastasia, Ask, Helga, Bass, Nicholas, Bauer, Michael, Beins, Eva C., Bigdeli, Tim B., Pedersen, Carsten Bøcker, Boks, Marco P., Børte, Sigrid, Bosch, Rosa, Brum, Murielle, Brumpton, Ben M., Brunkhorst-Kanaan, Nathalie, Budde, Monika, Bybjerg-Grauholm, Jonas, Byerley, William, Cabana-Domínguez, Judit, Cairns, Murray J., Carpiniello, Bernardo, Casas, Miquel, Cervantes, Pablo, Chatzinakos, Chris, Chen, Hsi-Chung, Clarence, Tereza, Clarke, Toni-Kim, Claus, Isabelle, Coombes, Brandon, Corfield, Elizabeth C., Cruceanu, Cristiana, Cuellar-Barboza, Alfredo, Czerski, Piotr M., Dafnas, Konstantinos, Dale, Anders M., Dalkner, Nina, Degenhardt, Franziska, DePaulo, J. Raymond, Djurovic, Srdjan, Drange, Ole Kristian, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Fanous, Ayman H., Fellendorf, Frederike T., Ferrier, I. Nicol, Forty, Elizabeth, Frank, Josef, Frei, Oleksandr, Freimer, Nelson B., Fullard, John F., Garnham, Julie, Gizer, Ian R., Gordon, Scott D., Gordon-Smith, Katherine, Greenwood, Tiffany A., Grove, Jakob, Guzman-Parra, José, Ha, Tae Hyon, Hahn, Tim, Haraldsson, Magnus, Hautzinger, Martin, Havdahl, Alexandra, Heilbronner, Urs, Hellgren, Dennis, Herms, Stefan, Hickie, Ian B., Hoffmann, Per, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Huang, Ming-Chyi, Ikeda, Masashi, Jamain, Stéphane, Johnson, Jessica S., Jonsson, Lina, Kalman, Janos L., Kamatani, Yoichiro, Kennedy, James L., Kim, Euitae, Kim, Jaeyoung, Kittel-Schneider, Sarah, Knowles, James A., Kogevinas, Manolis, Kranz, Thorsten M., Krebs, Kristi, Kushner, Steven A., Lavebratt, Catharina, Lawrence, Jacob, Leber, Markus, Lee, Heon-Jeong, Liao, Calwing, Lucae, Susanne, Lundberg, Martin, MacIntyre, Donald J., Maier, Wolfgang, Maihofer, Adam X., Malaspina, Dolores, Manchia, Mirko, Maratou, Eirini, Martinsson, Lina, Mattheisen, Manuel, McGregor, Nathaniel W., McInnis, Melvin G., McKay, James D., Medeiros, Helena, Meyer-Lindenberg, Andreas, Millischer, Vincent, Morris, Derek W., Moutsatsou, Paraskevi, Mühleisen, Thomas W., O'Donovan, Claire, Olsen, Catherine M., Panagiotaropoulou, Georgia, Papiol, Sergi, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Park, Hye Youn, Perry, Amy, Pfennig, Andrea, Pisanu, Claudia, Potash, James B., Quested, Digby, Rapaport, Mark H., Regeer, Eline J., Rice, John P., Rivera, Margarita, Schulte, Eva C., Senner, Fanny, Shadrin, Alexey, Shilling, Paul D., Sigurdsson, Engilbert, Sindermann, Lisa, Sirignano, Lea, Siskind, Dan, Slaney, Claire, Sloofman, Laura G., Smeland, Olav B., Smith, Daniel J., Sobell, Janet L., Soler Artigas, Maria, Stein, Dan J., Stein, Frederike, Su, Mei-Hsin, Sung, Heejong, Swiatkowska, Beata, Terao, Chikashi, Tesfaye, Markos, Tesli, Martin, Thorgeirsson, Thorgeir E., Thorp, Jackson G., Toma, Claudio, Tondo, Leonardo, Tooney, Paul A., Tsai, Shih-Jen, Tsermpini, Evangelia Eirini, Vawter, Marquis P., Vedder, Helmut, Vreeker, Annabel, Walters, James T. R., Winsvold, Bendik S., Witt, Stephanie H., Won, Hong-Hee, Ye, Robert, Young, Allan H., Zandi, Peter P., Zillich, Lea, Lee, Byung-Chul, Kim, Ji-Woong, Lee, Young Kee, Kang, Joon Ho, Cheon, Myeong Jae, Kim, Dong Jun, Aslan, Mihaela, Harvey, Philip D., Huang, Grant D., Adolfsson, Rolf, Alda, Martin, Alfredsson, Lars, Backlund, Lena, Baune, Bernhard T., Bellivier, Frank, Bengesser, Susanne, Berrettini, Wade H., Biernacka, Joanna M., Boehnke, Michael, Børglum, Anders D., Breen, Gerome, Carr, Vaughan J., Catts, Stanley, Cichon, Sven, Corvin, Aiden, Craddock, Nicholas, Dannlowski, Udo, Dikeos, Dimitris, Etain, Bruno, Ferentinos, Panagiotis, Frye, Mark, Fullerton, Janice M., Gawlik, Micha, Gershon, Elliot S., Goes, Fernando S., Green, Melissa J., Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Henskens, Frans A., Hjerling-Leffler, Jens, Hougaard, David M., Hveem, Kristian, Iwata, Nakao, Jones, Ian, Jones, Lisa A., Kahn, René S., Kelsoe, John R., Kircher, Tilo, Kirov, George, Kuo, Po-Hsiu, Landén, Mikael, Leboyer, Marion, Li, Qingqin S., Lissowska, Jolanta, Lochner, Christine, Loughland, Carmel, Luykx, Jurjen J., Martin, Nicholas G., Mathews, Carol A., Mayoral, Fermin, McElroy, Susan L., McIntosh, Andrew M., McMahon, Francis J., Medland, Sarah E., Melle, Ingrid, Milani, Lili, Mitchell, Philip B., Morken, Gunnar, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Myers, Richard M., Myung, Woojae, Neale, Benjamin M., Nievergelt, Caroline M., Nordentoft, Merete, Nöthen, Markus M., Nurnberger, John I., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Oedegaard, Ketil J., Olsson, Tomas, Owen, Michael J., Paciga, Sara A., Pantelis, Christos, Pato, Carlos N., Pato, Michele T., Patrinos, George P., Pawlak, Joanna M., Ramos-Quiroga, Josep Antoni, Reif, Andreas, Reininghaus, Eva Z., Ribasés, Marta, Rietschel, Marcella, Ripke, Stephan, Rouleau, Guy A., Roussos, Panos, Saito, Takeo, Schall, Ulrich, Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Scott, Laura J., Scott, Rodney J., Serretti, Alessandro, Smoller, Jordan W., Squassina, Alessio, Stahl, Eli A., Stefansson, Hreinn, Stefansson, Kari, Stordal, Eystein, Streit, Fabian, Sullivan, Patrick F., Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Waldman, Irwin D., Weickert, Cynthia S., Weickert, Thomas W., Werge, Thomas, Whiteman, David C., Zwart, John-Anker, Edenberg, Howard J., McQuillin, Andrew, Forstner, Andreas J., Mullins, Niamh, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Ophoff, Roel A., Andreassen, Ole A., van der Veen, Tracey and Siskind, Dan 2025. Genomics yields biological and phenotypic insights into bipolar disorder. Nature 639 , pp. 968-975. 10.1038/s41586-024-08468-9 Item availability restricted.

Dennison, Charlotte A. ORCID: https://orcid.org/0000-0002-7493-2041, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Shakeshaft, Amy ORCID: https://orcid.org/0000-0003-1412-5413, Riglin, Lucy, Powell, Victoria ORCID: https://orcid.org/0000-0003-1599-1209, 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 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2025. Early manifestations of neurodevelopmental copy number variants in children: A population-based investigation. Biological Psychiatry 10.1016/j.biopsych.2025.03.004

Schipper, Marijn, Leeuw, Christiaan, Maciel, Bernardo, Wightman, Hubers, Boomsma, Dorret, O’Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Posthuma, Danielle 2025. Prioritizing effector genes at trait-associated loci using multimodal evidence. Nature Genetics 57 , pp. 323-333. 10.1038/s41588-025-02084-7

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 226 , pp. 79-90. 10.1192/bjp.2024.125

Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2025. The genetics of cognition in schizophrenia. Genomic Psychiatry 1 (1) , pp. 28-35. 10.61373/gp024i.0040

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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, 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Hannon, Eilis, Dempster, Emma L., Mansell, Georgina, Burrage, Joe, Bass, Nick, Bohlken, Marc M., Corvin, Aiden, Curtis, Charles J., Dempster, David, Di Forti, Marta, Dinan, Timothy G., Donohoe, Gary, Gaughran, Fiona, Gill, Michael, Gillespie, Amy, Gunasinghe, Cerisse, Hulshoff, Hilleke E., Hultman, Christina M., Johansson, Viktoria, Kahn, René S., Kaprio, Jaakko, Kenis, Gunter, Kowalec, Kaarina, MacCabe, James, McDonald, Colm, McQuillin, Andrew, Morris, Derek W., Murphy, Kieran C., Mustard, Colette J., Nenadic, Igor, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Quattrone, Diego, Richards, Alexander L., Rutten, Bart P.F., St. Clair, David, Therman, Sebastian, Toulopoulou, Timothea, Van Os, Jim, Waddington, John L., Sullivan, Patrick, Vassos, Evangelos, Breen, Gerome, Collier, David A., Murray, Robin M., Schalwyk, Leo and Mill, Jonathan 2021. DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia. eLife 10 , e58430. 10.7554/eLife.58430

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Hasmi, Laila, Pries, Lotta-Katrin, ten Have, Margreet, de Graaf, Ron, van Dorsselaer, Saskia, Bak, Maarten, Kenis, Gunter, Richards, Alexander, Lin, Bochao D., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Luykx, Jurjen J., Rutten, Bart P.F., Guloksuz, Sinan and van Os, Jim 2021. What makes the psychosis 'clinical high risk' state risky: psychosis itself or the co-presence of a non-psychotic disorder? Epidemiology and Psychiatric Sciences 30 , e53. 10.1017/S204579602100041X

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Jones, Hannah J., Martin, David, Lewis, Sarah J., Davey Smith, George, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2020. A Mendelian randomization study of the causal association between anxiety phenotypes and schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 183 (6) , pp. 360-369. 10.1002/ajmg.b.32808

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Lee, Sze Chim, DelPozo-Banos, Marcos, Lloyd, Keith, Jones, Ian, 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 ORCID: https://orcid.org/0000-0001-7073-2379 and John, Ann 2020. Area deprivation, urbanicity, severe mental illness and social drift — a population-based linkage study using routinely collected primary and secondary care data. Schizophrenia Research 220 , pp. 130-140. 10.1016/j.schres.2020.03.044

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Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Hosking, Grace, Wadon, Megan, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Owen, Michael 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 Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2020. A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Translational Psychiatry 10 , 135. 10.1038/s41398-020-0821-y

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Lewis, Katie J.S., Richards, Alexander, Karlsson, Robert, Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Jones, Samuel E. ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Hannah J. ORCID: https://orcid.org/0000-0001-5821-5889, Gordon-Smith, Katherine, Forty, Liz, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Weedon, Michael N., Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Landén, Mikael, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748 2020. Comparison of genetic liability for sleep traits among individuals with Bipolar Disorder I or II and control participants. JAMA Psychiatry 77 (3) , pp. 303-310. 10.1001/jamapsychiatry.2019.4079

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. 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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. 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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. 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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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Green, Elaine Karen, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Forty, Elizabeth, Gordon-Smith, K., Fraser, Christine, Russell, Elen Elizabeth, Grozeva, Detelina Valentinova ORCID: https://orcid.org/0000-0003-3239-8415, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, 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, Jones, L. ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2013. Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. Molecular Psychiatry 18 (12) , pp. 1302-1307. 10.1038/mp.2012.142

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de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R. and Keller, Matthew C. 2013. Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. American Journal of Human Genetics 93 (3) , pp. 463-470. 10.1016/j.ajhg.2013.07.007

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Hudson, G., Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Chapman, Jade Alice, Hollingworth, Paul, Gerrish, Amy, Russo, Giancarlo, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, 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, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Chinnery, P. F. 2012. No consistent evidence for association between mtDNA variants and Alzheimer disease. Neurology 78 (14) , pp. 1038-1042. 10.1212/WNL.0b013e31824e8f1d

Keller, Matthew C., Simonson, Matthew A., Ripke, Stephan, Neale, Ben M., Gejman, Pablo V., Howrigan, Daniel P., Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F., Sullivan, Patrick F., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Georgieva, Lyudmila, Nikolov, Ivan, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, 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 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2012. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Plos Genetics 8 (4) , e1002656. 10.1371/journal.pgen.1002656

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

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. 2012. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Molecular Psychiatry 18 , pp. 461-470. 10.1038/mp.2012.14

Collins, A. L., Kim, Y., Sklar, P., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Sullivan, P. F. 2012. Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results. Psychological Medicine 42 (3) , pp. 607-616. 10.1017/S0033291711001607

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Ikeda, M., Ruderfer, D., Moran, J., Chambert, K., Toncheva, D., Georgieva, Lyudmila, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Fjodorova, Marija, Wollerton, Rebecca Louise, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Nikolov, Ivan, van de Lagemaat, L. N., Bayés, À., Fernandez, E., Olason, P. I., Böttcher, Y., Komiyama, N. H., Collins, M. O., Choudhary, J., Stefansson, K., Stefansson, H., Grant, S. G. N., Purcell, S., Sklar, P., 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. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry 17 (2) , pp. 142-153. 10.1038/mp.2011.154

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

Gerrish, Amy, Russo, Giancarlo, Richards, Alexander, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Abraham, Richard Alun, Hollingworth, Paul, Chapman, Jade Alice, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Pahwa, Jaspreet Singh, Dowzell, Kimberley Frances, Williams, Amy, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad Rhys, 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, McGuinness, 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, Maier, Wolfgang, Jessen, Frank, Kölsch, Heike, Heun, Reinhard, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Davies, Gail, Harris, Sarah E., Starr, John M., Deary, Ian J., Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Carrasquillo, Minerva M, Pankratz, V. Shane, Younkin, Steven G., 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 2012. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's Disease. Journal of Alzheimer's Disease 28 (2) , pp. 377-387. 10.3233/JAD-2011-110824

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

Chapman, Ria M., Tinsley, Caroline L., Doyle, A. Michelle, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Blake, Derek John ORCID: https://orcid.org/0000-0002-5005-4731 2012. Inducible over-expression and siRNA mediated knock-down of the schizophrenia susceptibility gene ZNF804A: Detection of altered gene expression and splicing using whole genome exon arrays. International Journal of Developmental Neuroscience 30 (8) , p. 673. 10.1016/j.ijdevneu.2012.10.011

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

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

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

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

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

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, O'Dushlaine, Colm, Purcell, Shaun, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2011. Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study. Genetic Epidemiology 35 (8) , pp. 861-866. 10.1002/gepi.20636

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

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

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

Wiles, Nicola J., Mulligan, Jean, Peters, Tim J., Cowen, Philip J., Mason, Victoria, Nutt, David, Sharp, Deborah, Tallon, Debbie, Thomas, Laura, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Lewis, Glyn 2011. Severity of depression and response to antidepressants: GENPOD randomised controlled trial. British Journal of Psychiatry 200 (2) , pp. 130-136. 10.1192/bjp.bp.110.091223

Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Purcell, S. M., Smit, A. B., Verhage, M, Sullivan, P. F., Visscher, P. M. and Posthuma, D 2011. Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry , pp. 1-11. 10.1038/mp.2011.117

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.

Dwyer, Sarah Lynne, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, 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 2011. Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder [letter]. Molecular Psychiatry 16 (8) , pp. 790-791. 10.1038/mp.2011.2

Ruderfer, D. M., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Chambert, K., Moran, J. L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Sklar, P. and Purcell, S. M. 2011. A family-based study of common polygenic variation and risk of schizophrenia [Letter]. Molecular Psychiatry 16 (9) , pp. 887-888. 10.1038/mp.2011.34

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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

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O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melvillle ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2007. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia [Conference Abstract]. Schizophrenia bulletin 33 (2) , pp. 311-312. 10.1093/schbul/sbm004

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Gunnell, D., Lewis, S., Wilkinson, J., Georgieva, Lyudmila, Davey, G. Smith, Day, I.N.M., Holly, J.M.P., 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 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2007. IGF1, growth pathway polymorphisms and schizophrenia: A pooling study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (1) , pp. 117-120. 10.1002/ajmg.b.30396

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Morgan, A.R., Hamilton, G., Turic, Dragana, Jehu, L., Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Abraham, Richard Alun, Hollingworth, Paul, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Brayne, C., Rubinsztein, D.C., Lynch, A., Lawlor, B., Gill, M., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Powell, J., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2007. Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (6) , pp. 727-731. 10.1002/ajmg.b.30670

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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 2007. Phenotypic and genetic complexity of psychosis Invited commentary on ... Schizophrenia: a common disease caused by multiple rare alleles. British Journal of Psychiatry 190 (3) , pp. 200-203. 10.1192/bjp.bp.106.033761

Harold, D, Paracchini, S, Scerri, T, Dennis, M, Cope, N, Hill, G, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Walter, J, Richardson, A J, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Stein, J F, Green, E D, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, J and Monaco, A P 2006. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry 11 (12) , pp. 1085-91. 10.1038/sj.mp.4001904

O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Scambler, P. J, Paylora, R, Glaser, B, Mupod, A, Ataliotis, P, Spencer, C, Sobotka, A, Sparks, 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 2006. Genetic dissection of behavioural abnormalities in mouse models of DiGeorge/velocardiofacial syndrome. Journal of intellectual disability research 50 (11) , 781 -781.

Glaser, Beate, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Murphy, Kieran C., Williams, Hywel, Williams Melville, Nigel 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 2006. Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophrenia Research 87 (1-3) , p. 21. 10.1016/j.schres.2006.05.024

Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Lewis, G., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Owen, R., Jones, G., Jones, S., Sanders, R., Milham, C., Mahdi, A., 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. Phenotypic variation between parent-offspring trios and non-trios in genetic studies of schizophrenia. Journal of Psychiatric Research 40 (7) , pp. 622-626. 10.1016/j.jpsychires.2005.05.006

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, van Den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, 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. Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , pp. 723-724.

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

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. Investigating cis-acting regulatory variation using assays of relative allelic expression. Psychiatric Genetics 16 (4) , pp. 173-177. 10.1097/01.ypg.0000218612.35139.84

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

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

Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2006. The genetics of developmental dyslexia. European Journal of Human Genetics 14 (6) , pp. 681-89. 10.1038/sj.ejhg.5201575

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

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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

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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.

Khan, Imtiaz Ali, Mort, Matthew, Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Cooper, D. N. and Chuzhanova, N. A. 2006. In silico discrimination of single nucleotide polymorphisms and pathological mutations in human gene promoter regions by means of local DNA sequence context and regularity. In silico Biology 6 (1-2) , pp. 23-34.

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

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

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

Gough, S. C. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Clustering of metabolic comorbidity in schizophrenia: a genetic contribution? Journal of Psychopharmacology 19 (6) , pp. 47-55. 10.1177/0269881105058380

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

Buckland, Paul Robert, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Coleman, Sharon Louise, Guy, Carol, Smith, Susan Kaye and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Strong bias in the location of functional promoter polymorphisms. Human Mutation 26 (3) , pp. 214-223. 10.1002/humu.20207

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

Redfern, A., Hughes, G., McGuffin, P., Aitchison, K., Vollmayr, B., Gass, P., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2005. Global gene expression profiling in the hippocampus and frontal cortex of Escitalopram-treated Learned Helplessness rats. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 138B (1) , p. 107.

Nowotny, P., Hinrichs, A. L., Smemo, S., Kauwe, J. S., Maxwell, T., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Turic, D., Jehu, L., Hollingworth, P., Moore, P., Bryden, L., Myers, A., Doil, L. M., Tacey, K. M., Gibson, A. M., McKeith, I. G., Perry, R. H., Morris, C. M., Thal, L., Morris, J. C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lovestone, S. and Grupe, A. 2005. Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 136B (1) , pp. 62-68. 10.1002/ajmg.b.30186

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

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. An evaluation of chromatin condensation and DNA integrity in the spermatozoa of men with cancer before and after therapy. Andrologia -Berlin- 37 (2-3) , pp. 83-90. 10.1111/j.1439-0272.2005.00658.x

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

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

Buckland, Paul Robert, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Guy, Carol, Smith, Susan Kaye, Coleman, Sharon Louise and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Low gene expression conferred by association of an allele of the 5-HT2C receptor gene with antipsychotic-induced weight gain. American Journal of Psychiatry 162 (3) , pp. 613-615. 10.1176/appi.ajp.162.3.613

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

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

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

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

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

Buckland, Paul Robert, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Guy, C. A., Coleman, S. L., Smith, S. K., Buxbaum, J. D., Hartoutunian, V. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. A high proportion of polymorphisms in the promoters of brain expressed genes influences transcriptional activity. Acta Biochimica et Biophysica 1690 (3) , pp. 238-249.

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

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, 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.

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

Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Coleman, Sharon Louise, Guy, Carol, Smith, Susan Kaye, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Buckland, Paul Robert 2004. Functional analysis of polymorphisms in the promoter regions of genes on 22q11. Human Mutation 24 (1) , pp. 35-42. 10.1002/humu.20061

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

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

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

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

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

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

Huezo-Diaz, P., Arranz, M.J., Munro, J., Osborne, S., Makoff, A., Kerwin, R.W., Austin, J. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. An association study of the neurotensin receptor gene with schizophrenia and clozapine response. Schizophrenia Research 66 (2-3) , pp. 193-195. 10.1016/S0920-9964(03)00128-2

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

Guy, Carol, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Smith, Susan Kay, Coleman, Sharon Louise, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Buckland, Paul Robert 2004. Promoter polymorphisms in glutathione-S-transferase genes affect transcription. Pharmacogenetics 14 (1) , pp. 45-51. 10.1097/00008571-200401000-00005

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

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

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

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

Smith, Susan Kay, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Guy, Carol, Coleman, Sharon Louise, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Buckland, Paul Robert 2003. Lack of functional promoter polymorphisms in genes involved in glutamate neurotransmission. Psychiatric Genetics 13 (4) , pp. 193-199. 10.1097/00041444-200312000-00001

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

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

Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Coleman, Sharon Louise, Guy, Carol, Smith, Susan Kaye, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Buckland, Paul Robert and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. Functional analysis of human promoter polymorphisms. Human Molecular Genetics 12 (18) , pp. 2249-2254. 10.1093/hmg/ddg246

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

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 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

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

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

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

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

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2003. Anticipation and repeat expansion in bipolar disorder. American Journal of Medical Genetics 123C (1) , pp. 10-17. 10.1002/ajmg.c.20009

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)

Buckland, Paul Robert, Coleman, Sharon Louise, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Guy, Carol, Smith, Susan Kaye and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. A high proportion of chromosome 21 promoter polymorphisms influence transcriptional activity. Gene Expression 11 (5) , pp. 233-239. 10.3727/000000003783992225

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

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

Coleman, Sharon Louise, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Guy, Carol, Smith, Susan Kaye, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Buckland, Paul Robert 2002. Streamlined approach to functional analysis of promoter-region polymorphisms. Biotechniques 33 (2) , pp. 412-418.

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

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

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

Coleman, Sharon Louise, Buckland, Paul Robert, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Guy, Carol, Smith, Susan Kaye and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2002. Experimental analysis of the annotation of promoters in the public database. Human Molecular Genetics 11 (16) , pp. 1817-1821. 10.1093/hmg/11.16.1817

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

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

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.

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

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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)

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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

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

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.

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

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

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

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.

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

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

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

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.

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.

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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

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

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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

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-#

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O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Oefner, P. J., Roberts, S. C., Austin, J., Hoogendoorn, B., Guy, C., Speight, G., Upadhyaya, M., Sommer, S. S. and McGuffin, P. 1998. Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection. Genomics 52 (1) , pp. 44-49. 10.1006/geno.1998.5411

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

Oretti, R. G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, McGuffin, Peter and Buckland, Paul Robert 1998. Tryptophan pyrrolase gene expression in an alcohol preferring and non-preferring mouse strain. Addiction Biology 3 (1) , pp. 71-77. 10.1080/13556219872362

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

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

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

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

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.

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

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Guy, C 1997. Bias in the genomic distribution of CAG and CTG trinucleotide repeats. American Journal of Medical Genetics 74 (1) , pp. 62-64. 10.1002/(SICI)1096-8628(19970221)74:1<62::AID-AJMG14>3.0.CO;2-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 1996. Introducing Selfcite 2.0--career enhancing software. BMJ 313 (7072) , pp. 1659-1660. 10.1136/bmj.313.7072.1659

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

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

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.

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1996. Genetics of Mental disorders .1. Theoretical aspects - Mendlewicz,J, Papadimitriou,GN. British Journal of Psychiatry 168 (2) , p. 256.

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

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

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

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.

Spurlock, G., Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, P. 1994. Lack of effect of antidepressant drugs on the levels of mRNAs encoding serotonergic receptors, synthetic enzymes and 5HT transporter. Neuropharmacology 33 (3-4) , pp. 433-440. 10.1016/0028-3908(94)90073-6

Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, Peter 1993. Clozapine and sulpiride up-regulate dopamine D3 receptor mRNA levels. Neuropharmacology 32 (9) , pp. 901-907. 10.1016/0028-3908(93)90146-T

McGuffin, P. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1993. Taking a balanced view on triazolam. British Medical Journal (BMJ) 306 (6893) , pp. 1690-1691. 10.1136/bmj.306.6893.1690-c

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, P 1993. Correction: Short acting benzodiazepines. British Medical Journal (BMJ) 306 (6886) , p. 1146. 10.1136/bmj.306.6886.1146

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, P 1993. Short acting benzodiazepines. British Medical Journal (BMJ) 306 (6883) , pp. 945-946. 10.1136/bmj.306.6883.945

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1993. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72 (6) , pp. 971-983. 10.1016/0092-8674(93)90585-E

Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, Peter 1993. Both splicing variants of the dopamine D2 receptor mRNA are up-regulated by antipsychotic drugs. Neuroscience Letters 150 (1) , pp. 25-28. 10.1016/0304-3940(93)90099-7

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Buckland, Paul Robert, Spurlock, Gillian and McGuffin, Peter 1992. Bi-directional changes in the levels of messenger RNAs encoding γ-aminobutyric acidA receptor α subunits after flurazepam treatment. European Journal of Pharmacology: Molecular Pharmacology 226 (4) , pp. 335-341. 10.1016/0922-4106(92)90051-V

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

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Buckland, Paul Robert and McGuffin, Peter 1992. Levels of GABAa receptor subunit mRNA in rat brain following flurazepam treatment. Journal of Psychopharmacology 6 (3) , pp. 364-369. 10.1177/026988119200600304

Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, Peter 1992. Changes in dopamine D1, D2 and D3 receptor mRNA levels in rat brain following antipsychotic treatment. Psychopharmacology 106 (4) , pp. 479-483. 10.1007/BF02244818

Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, Peter 1992. Changes in dopa decarboxylase mRNA but not tyrosine hydroxylase mRNA levels in rat brain following antipsychotic treatment. Psychopharmacology 108 (1-2) , pp. 98-102. 10.1007/BF02245292

Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, Peter 1992. Lack of effect of chronic antipsychotic treatment on dopamine D5 receptor mRNA level. European Neuropsychopharmacology 2 (4) , pp. 405-409. 10.1016/0924-977X(92)90002-P

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Buckland, Paul Robert and McGuffin, P. 1992. The expression of neuroreceptor genes and benzodiazepine tolerance. Clinical Neuropharmacology 15 (Supp1) , 218A-219A. 10.1097/00002826-199201001-00114

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, P 1991. Growing points in psychiatric genetics. British Journal of Hospital Medicine 46 (6) , pp. 359-360.

Havard, H. L., Buckland, Paul Robert, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, Peter 1991. The effects of antidepressant drugs on kainate receptor mRNA levels. Neuropharmacology 30 (6) , pp. 675-677. 10.1016/0028-3908(91)90090-X

O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Buckland, Paul Robert 1991. Simultaneous quantification of several mRNA species by solution hybridisation with oligonucleotides. Nucleic Acids Research 19 (12) , p. 3466. 10.1093/nar/19.12.3466

Espie, C.A., Pashley, A.S., Bonham, K.G., Sourindhrin, I. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1989. The mentally handicapped person with epilepsy: a comparative study investigating psychosocial functioning. Journal of Mental Health Defiency Research 33 (2) , pp. 123-135.