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Number of items: 1122.

Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Woolway, Grace, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Cardno, Alastair G., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael J. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2024. Genetic and phenotypic features of Schizophrenia in the UK Biobank. JAMA Psychiatry 81 , pp. 681-690. 10.1001/jamapsychiatry.2024.0200
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Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura, Andlauer, Till, von Scheidt, Moritz, Schizophrenia Working Group of the Psychiatric Genomics Consorti, Budde, Monika, Heilbronner, Urs, Papiol, Sergei, Teumer, Alexander, Homouth, Georg, Falkai, Peter, Volzke, Henry, Dorr, Marcus, Schulze, Thomas, Gagneur, Julien, Iorio, Francesco, Müller-Myhsok, Bertram, Schunkert, Heribert, Ziller, Michael, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Kavanagh, David, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Legge, Sophie, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Richards, Alexander L., Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412 2024. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications 15 , 5534. 10.1038/s41467-024-49338-2
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Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2024. The genetics of cognition in schizophrenia. Brain Medicine
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Hall, Jessica H., Chawner, Samuel J. R. A., Wolstencroft, Jeanne, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2024. Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational Psychiatry 14 (1) , 259. 10.1038/s41398-024-02975-z
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Stevenson-Hoare, Joshua, Legge, Sophie E., Simmonds, Emily, Han, Jun, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2024. Severe psychiatric disorders are associated with increased risk of dementia. BMJ Mental Health 27 (1) , e301097. 10.1136/bmjment-2024-301097
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Haddon, Josephine E. ORCID: https://orcid.org/0000-0001-5975-813X, Titherage, Daniel, Heckenast, Julia R., Carter, Jennifer, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124 and Jones, Matthew W. 2024. Linking haploinsufficiency of the autism- and schizophrenia-associated gene Cyfip1 with striatal-limbic-cortical network dysfunction and cognitive inflexibility. Translational Psychiatry 14 (1) , 256. 10.1038/s41398-024-02969-x
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Cabezas De La Fuente, Daniel, Tamburini, Claudia, Stonelake, Emily, Andrews, Robert, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Li, Meng ORCID: https://orcid.org/0000-0002-4803-4643 2024. Impaired oxysterol-liver X receptor signaling underlies aberrant cortical neurogenesis in a human stem cell model of neurodevelopmental disorder. Cell Reports 43 (3) , 113946. 10.1016/j.celrep.2024.113946
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Kopal, Jakub, Kumar, Kuldeep, Shafighi, Kimia, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Douard, Elise, Jizi, Khadije, Beauchamp-Chatel, Alexis, Kushan, Leila, Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Zatorre, Robert, Jacquemont, Sébastien and Bzdok, Danilo 2024. Using rare genetic mutations to revisit structural brain asymmetry. Nature Communications 15 (1) , 2639. 10.1038/s41467-024-46784-w
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Kappel, Djenifer, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Fenner, Eilidh, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 2024. Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology 80 , pp. 47-54. 10.1016/j.euroneuro.2023.12.007
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Tandon, Rajiv, Nasrallah, Henry, Akbarian, Schahram, Carpenter, William T., DeLisi, Lynn E., Gaebel, Wolfgang, Green, Michael F., Gur, Raquel E., Heckers, Stephan, Kane, John M., Malaspina, Dolores, Meyer-Lindenberg, Andreas, Murray, Robin, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Smoller, Jordan W., Yassin, Walid and Keshavan, Matcheri 2024. The schizophrenia syndrome, circa 2024: What we know and how that informs its nature. Schizophrenia Research 264 , pp. 1-28. 10.1016/j.schres.2023.11.015

Doherty, Joanne L., Cunningham, Adam C., Chawner, Samuel J. R. A., Moss, Hayley M., Dima, Diana C. ORCID: https://orcid.org/0000-0002-9612-5574, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 and Singh, Krish D. ORCID: https://orcid.org/0000-0002-3094-2475 2024. Atypical cortical networks in children at high-genetic risk of psychiatric and eurodevelopmental disorders. Neuropsychopharmacology 49 , pp. 368-376. 10.1038/s41386-023-01628-x
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Boen, Rune, Kaufmann, Tobias, van der Meer, Dennis, Frei, Oleksandr, Agartz, Ingrid, Ames, David, Andersson, Micael, Armstrong, Nicola J., Artiges, Eric, Atkins, Joshua R., Bauer, Jochen, Benedetti, Francesco, Boomsma, Dorret I., Brodaty, Henry, Brosch, Katharina, Buckner, Randy L., Cairns, Murray J., Calhoun, Vince, Caspers, Svenja, Cichon, Sven, Corvin, Aiden P., Facorro, Benedicto Crespo, Dannlowski, Udo, David, Friederike S., de Geus, Eco J.C., de Zubicaray, Greig I., Desrivières, Sylvane, Doherty, Joanne L., Donohoe, Gary, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fisher, Simon E., Forstner, Andreas J., Uyà, Lidia Fortaner, Frouin, Vincent, Fukunaga, Masaki, Ge, Tian, Glahn, David C., Goltermann, Janik, Grabe, Hans J., Green, Melissa J., Groenewold, Nynke A., Grotegerd, Dominik, Hahn, Tim, Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Henskens, Frans A., Holmes, Avram J., Haberg, Asta K., Haavik, Jan, Jacquemont, Sebastien, Jansen, Andreas, Jockwitz, Christiane, Jonsson, Erik G., Kikuchi, Masataka, Kircher, Tilo, Kumar, Kuldeep, Le Hellard, Stephanie, Leu, Costin, Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Liu, Jingyu, Loughnan, Robert, Mather, Karen A., McMahon, Katie L., McRae, Allan F., Medland, Sarah E., Meinert, Susanne, Moreau, Clara A., Morris, Derek W., Mowry, Bryan J., Muhleisen, Thomas W., Nenadi?, Igor, Nöthen, Markus M., Nyberg, Lars, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paolini, Marco, Paus, Tomas, Pausova, Zdenka, Persson, Karin, Quidé, Yann, Marques, Tiago Reis, Sachdev, Perminder S., Sando, Sigrid B., Schall, Ulrich, Scott, Rodney J., Selbæk, Geir, Shumskaya, Elena, Silva, Ana I., Sisodiya, Sanjay M., Stein, Frederike, Stein, Dan J., Straube, Benjamin, Streit, Fabian, Strike, Lachlan T., Teumer, Alexander, Teutenberg, Lea, Thalamuthu, Anbupalam, Tooney, Paul A., Tordesillas-Gutierrez, Diana, Trollor, Julian N., Ent, Dennis van 't, van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254, van Haren, Neeltje E.M., Vazquez-Bourgon, Javier, Volzke, Henry, Wen, Wei, Wittfeld, Katharina, Ching, Christopher R.K., Westlye, Lars T., Thompson, Paul M., Bearden, Carrie E., Selmer, Kaja K., Alnæs, Dag, Andreassen, Ole A. and Sonderby, Ida E. 2024. Beyond the global brain differences: Intra-individual variability differences in 1q21.1 distal and 15q11.2 BP1-BP2 deletion carriers. Biological Psychiatry 95 (2) , pp. 147-160. 10.1016/j.biopsych.2023.08.018
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Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2024. Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes. Nature Reviews Neurology 20 (1) , pp. 7-21. 10.1038/s41582-023-00896-x
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Ge, Ruiyang, Ching, Christopher R. K., Bassett, Anne S., Kushan, Leila, Antshel, Kevin M., van Amelsvoort, Therese, Bakker, Geor, Butcher, Nancy J., Campbell, Linda E., Chow, Eva W. C., Craig, Michael, Crossley, Nicolas A., Cunningham, Adam, Daly, Eileen, Doherty, Joanne L., Durdle, Courtney A., Emanuel, Beverly S., Fiksinski, Ania, Forsyth, Jennifer K., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Gur, Raquel E., Jalbrzikowski, Maria, Kates, Wendy R., Lin, Amy, Linden, David E. J., McCabe, Kathryn L., McDonald‐McGinn, Donna, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Villalon‐Reina, Julio E., Repetto, Gabriela M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Schuite‐Koops, Sanne, Angkustsiri, Kathleen, Sun, Daqiang, Vajdi, Ariana, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Vorstman, Jacob, Thompson, Paul M., Vila‐Rodriguez, Fidel and Bearden, Carrie E. 2024. Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human Brain Mapping 45 (1) , e26553. 10.1002/hbm.26553
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Wang, Sheng, Wang, Belinda, Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Tourette International Collaborative Genetics (TIC Genetics), Bal, Vanessa, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Hoekstra, Pieter, Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary, Tischfield, Jay, Fernandez, Thomas, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, State, Matthew and Willsey, Jeremy 2023. Rare X-linked variants carry predominantly male risk in Autism, Tourette Syndrome, and ADHD. Nature Communications 14 , 8077. 10.1038/s41467-023-43776-0
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Chilvers, Clair and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2023. Mental Health Research, shared goals. Journal of Mental Health 32 , 1017. 10.1080/09638237.2021.1898562
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Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Legge, Sophie, Bracher-Smith, Matthew, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2023. Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance. Biological Psychiatry: Global Open Science 3 (4) , pp. 902-911. 10.1016/j.bpsgos.2022.10.006
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Lock, Siobhan K., Legge, Sophie E., Kappel, Djenifer B., Willcocks, Isabella R. ORCID: https://orcid.org/0000-0002-3568-5236, Helthius, Marinka, Jansen, John, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590 2023. Mediation and longitudinal analysis to interpret the association between clozapine pharmacokinetics, pharmacogenomics, and absolute neutrophil count. Schizophrenia 9 , 74. 10.1038/s41537-023-00404-6
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Doherty, Anna, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Hamshere, Marian ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2023. Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors. The American Journal of Psychiatry 180 (10) , pp. 723-738. 10.1176/appi.ajp.21121266
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Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Legge, Sophie, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2023. Genomic findings in schizophrenia and their implications. Molecular Psychiatry 28 , pp. 3638-3647. 10.1038/s41380-023-02293-8
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Kumar, Kuldeep, Modenato, Claudia, Moreau, Clara, Ching, Christopher R.K., Harvey, Annabelle, Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Douard, Elise, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurélie, Kushan, Leila, Isaev, Dmitry, Alpert, Kathryn, Ragothaman, Anjani, Turner, Jessica A., Wang, Lei, Ho, Tiffany C., Schmaal, Lianne, Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E.J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Lippé, Sarah, Dumas, Guillaume, Draganski, Bogdan, Gutman, Boris A., Sønderby, Ida E., Andreassen, Ole A., Schultz, Laura M., Almasy, Laura, Glahn, David C., Bearden, Carrie E., Thompson, Paul M. and Jacquemont, Sébastien 2023. Subcortical brain alterations in carriers of genomic copy number variants. The American Journal of Psychiatry 180 (9) , pp. 685-698. 10.1176/appi.ajp.20220304

Le Guen, Yann, Luo, Guo, Ambati, Aditya, Damotte, Vincent, Jansen, Iris, Yu, Eric, Nicolas, Aude, de Rojas, Itziar, Peixoto Leal, Thiago, Miyashita, Akinori, Bellenguez, Céline, Lian, Michelle Mulan, Parveen, Kayenat, Morizono, Takashi, Park, Hyeonseul, Grenier-Boley, Benjamin, Naito, Tatsuhiko, Küçükali, Fahri, Talyansky, Seth D., Yogeshwar, Selina Maria, Sempere, Vicente, Satake, Wataru, Alvarez, Victoria, Arosio, Beatrice, Belloy, Michael E., Benussi, Luisa, Boland, Anne, Borroni, Barbara, Bullido, María J., Caffarra, Paolo, Clarimon, Jordi, Daniele, Antonio, Darling, Daniel, Debette, Stéphanie, Deleuze, Jean-François, Dichgans, Martin, Dufouil, Carole, During, Emmanuel, Düzel, Emrah, Galimberti, Daniela, Garcia-Ribas, Guillermo, García-Alberca, José María, García-González, Pablo, Giedraitis, Vilmantas, Goldhardt, Oliver, Graff, Caroline, Grünblatt, Edna, Hanon, Olivier, Hausner, Lucrezia, Heilmann-Heimbach, Stefanie, Holstege, Henne, Hort, Jakub, Jung, Yoo Jin, Jürgen, Deckert, Kern, Silke, Kuulasmaa, Teemu, Lee, Kun Ho, Lin, Ling, Masullo, Carlo, Mecocci, Patrizia, Mehrabian, Shima, de Mendonça, Alexandre, Boada, Mercè, Mir, Pablo, Moebus, Susanne, Moreno, Fermin, Nacmias, Benedetta, Nicolas, Gael, Niida, Shumpei, Nordestgaard, Børge G., Papenberg, Goran, Papma, Janne, Parnetti, Lucilla, Pasquier, Florence, Pastor, Pau, Peters, Oliver, Pijnenburg, Yolande A. L., Piñol-Ripoll, Gerard, Popp, Julius, Porcel, Laura Molina, Puerta, Raquel, Pérez-Tur, Jordi, Rainero, Innocenzo, Ramakers, Inez, Real, Luis M., Riedel-Heller, Steffi, Rodriguez-Rodriguez, Eloy, Ross, Owen A., Luís Royo, Jose, Rujescu, Dan, Scarmeas, Nikolaos, Scheltens, Philip, Scherbaum, Norbert, Schneider, Anja, Seripa, Davide, Skoog, Ingmar, Solfrizzi, Vincenzo, Spalletta, Gianfranco, Squassina, Alessio, van Swieten, John, Sánchez-Valle, Raquel, Tan, Eng-King, Tegos, Thomas, Teunissen, Charlotte, Thomassen, Jesper Qvist, Tremolizzo, Lucio, Vyhnalek, Martin, Verhey, Frans, Waern, Margda, Wiltfang, Jens, Zhang, Jing, Zetterberg, Henrik, Blennow, Kaj, He, Zihuai, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Amouyel, Philippe, Jessen, Frank, Kehoe, Patrick G., Andreassen, Ole A., Van Duin, Cornelia, Tsolaki, Magda, Sánchez-Juan, Pascual, Frikke-Schmidt, Ruth, Sleegers, Kristel, Toda, Tatsushi, Zettergren, Anna, Ingelsson, Martin, Okada, Yukinori, Rossi, Giacomina, Hiltunen, Mikko, Gim, Jungsoo, Ozaki, Kouichi, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Foo, Jia Nee, van der Flier, Wiesje, Ikeuchi, Takeshi, Ramirez, Alfredo, Mata, Ignacio, Ruiz, Agustín, Gan-Or, Ziv, Lambert, Jean-Charles, Greicius, Michael D., Mignot, Emmanuel, Bellenguez, Céline, Küçükali, Fahri, Jansen, Iris, Andrade, Victor, Moreno-Grau, Sonia, Amin, Najaf, Grenier-Boley, Benjamin, Campos-Martin, Rafael, Holmans, Peter A., Boland, Anne, Kleineidam, Luca, Damotte, Vincent, van der Lee, Sven J., Kuulasmaa, Teemu, de Rojas, Itziar, Yaqub, Amber, Prokic, Ivana, Costa, Marcos R, Chapuis, Julien, Ahmad, Shahzad, Giedraitis, Vilmantas, Aarsland, Dag, Garcia-Gonzalez, Pablo, Abdelnour, Carla, Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Álvarez, Victoria, Armstrong, Nicola J., Anthoula, Tsolaki, Appollonio, Ildebrando, Arcaro, Marina, Archetti, Silvana, Arias Pastor, Alfonso, Arosio, Beatrice, Athanasiu, Lavinia, Bailly, Henri, Banaj, Nerisa, Baquero, Miquel, Belén Pastor, Ana, Benussi, Luisa, Berr, Claudine, Besse, Céline, Bessi, Valentina, Binetti, Giuliano, Bizarro, Alessandra, Blesa, Rafael, Boada, Mercè, Borroni, Barbara, Boschi, Silvia, Bossù, Paola, Bråthen, Geir, Bresner, Catherine, Brodaty, Henry, Brookes, Keeley J., Ignacio Brusco, Luis, Buiza-Rueda, Dolores, BÛrger, Katharina, Burholt, Vanessa, Calero, Miguel, Chene, Geneviève, Carracedo, Ángel, Cecchetti, Roberta, Cervera-Carles, Laura, Charbonnier, Camille, Chillotti, Caterina, Ciccone, Simona, Claassen, Jurgen A.H.R., Clarimon, Jordi, Clark, Christopher, Conti, Elisa, Corma-Gómez, Anaïs, Costantini, Emanuele, Custodero, Carlo, Daian, Delphine, Dalmasso, Maria Carolina, Daniele, Antonio, Dardiotis, Efthimios, Dartigues, Jean-François, de Deyn, Peter Paul, Debette, Stéphanie, Deckert, Jürgen, del Ser, Teodoro, Denning, Nicola, Dichgans, Martin, Diehl-Schmid, Janine, Diez-Fairen, Mónica, Dionigi Rossi, Paolo, Djurovic, Srdjan, Duron, Emmanuelle, Düzel, Emrah, Dufouil, Carole, Escott-Price, Valentina, Espinosa, Ana, Ewers, Michael, Fernández-Fuertes, Marta, Ferreira, Catarina B, Ferri, Evelyn, Fin, Bertrand, Fischer, Peter, Fladby, Tormod, Fließbach, Klaus, Fortea, Juan, Fostinelli, Silvia, Fox, Nick C., Franco-Macías, Emlio, Bullido, María J., Frank-García, Ana, Froelich, Lutz, Galimberti, Daniela, Maria García-Alberca, Jose, García-González, Pablo, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Ghidoni, Roberta, Giegling, Ina, Giorgio, Giaccone, Goldhardt, Oliver, González-Pérez, Antonio, Graff, Caroline, Grande, Giulia, Green, Emma, Grimmer, Timo, Grünblatt, Edna, Guetta-Baranes, Tamar, Haapasalo, Annakaisa, Hadjigeorgiou, Georgios, Hampel, Harald, Hanon, Olivier, Hardy, John, Hartmann, Annette M., Hausner, Lucrezia, Harwood, Janet, Heilmann-Heimbach, Stefanie, Helisalmi, Seppo, Heneka, Michael T., Hernández, Isabel, Herrmann, Martin J., Hoffmann, Per, Holmes, Clive, Holstege, Henne, Huerto Vilas, Raquel, Hulsman, Marc, Johansson, Charlotte, Kilander, Lena, Kinhult Ståhlbom, Anne, Kivipelto, Miia, Koivisto, Anne, Kornhuber, Johannes, Kosmidis, Mary H., Lage, Carmen, Laukka, Erika J, Lauria, Alessandra, Lehtisalo, Jenni, Lerch, Ondrej, Lleó, Alberto, de Munain, Adolfo Lopez, Löwemark, Malin, Luckcuck, Lauren, Macías, Juan, MacLeod, Catherine A., Maier, Wolfgang, Mangialasche, Francesca, Marco, Spallazzi, Marquié, Marta, Marshall, Rachel, Martín Montes, Angel, Martínez Rodríguez, Carmen, Masullo, Carlo, Mead, Simon, Mecocci, Patrizia, Medina, Miguel, Meggy, Alun, Mehrabian, Shima, Mendoza, Silvia, Menéndez-González, Manuel, Mir, Pablo, Moebus, Susanne, Mol, Merel, Molina-Porcel, Laura, Montrreal, Laura, Morelli, Laura, Moreno, Fermin, Morgan, Kevin, Möthen, Markus M, Muchnik, Carolina, Nacmias, Benedetta, Ngandu, Tiia, Nicolas, Gael, Nordestgaard, Børge G., Olaso, Robert, Orellana, Adelina, Orsini, Michela, Ortega, Gemma, Padovani, Alessandro, Paolo, Caffarra, Papenberg, Goran, Parnetti, Lucilla, 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Ollà, Ivana, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Parras, Alberto, Hernández, Ivó H., Santos-Galindo, María, Picó, Sara, Callado, Luis F., Elorza, Ainara, Rodríguez-López, Claudia, Fernández-Miranda, Gonzalo, Belloc, Eulàlia, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Méndez, Raúl, Toma, Claudio, Meana, J.Javier, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Lucas, José J. 2023. Pathogenic mis-splicing of CPEB4 in schizophrenia. Biological Psychiatry 94 (4) , pp. 341-351. 10.1016/j.biopsych.2023.03.010
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Zhao, Yingjie, Wang, Yujue, Shi, Lijie, McDonald-McGinn, Donna M., Crowley, T. Blaine, McGinn, Daniel E., Tran, Oanh T., Miller, Daniella, Lin, Jhih-Rong, Zackai, Elaine, Johnston, H. Richard, Chow, Eva W. C., Vorstman, Jacob A. S., Vingerhoets, Claudia, van Amelsvoort, Therese, Gothelf, Doron, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Eliez, Stephan, Schneider, Maude, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Kates, Wendy R., Repetto, Gabriela M., Shashi, Vandana, Schoch, Kelly, Bearden, Carrie E., Digilio, M. Cristina, Unolt, Marta, Putotto, Carolina, Marino, Bruno, Pontillo, Maria, Armando, Marco, Vicari, Stefano, Angkustsiri, Kathleen, Campbell, Linda, Busa, Tiffany, Heine-Suñer, Damian, Murphy, Kieran C., Murphy, Declan, García-Miñaúr, Sixto, Fernández, Luis, Zhang, Zhengdong D., Goldmuntz, Elizabeth, Gur, Raquel E., Emanuel, Beverly S., Zheng, Deyou, Marshall, Christian R., Bassett, Anne S., Wang, Tao and Morrow, Bernice E. 2023. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. npj Genomic Medicine 8 (1) , 17. 10.1038/s41525-023-00363-y
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Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Cardno, Alastair G., Gordon-Smith, Katherine, Jones, Lisa, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Craddock, Nicholas J. ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Ian, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2023. Specificity of polygenic signatures across symptom dimensions in bipolar disorder: an analysis of UK Bipolar Disorder Research Network data. The Lancet Psychiatry 10 (8) , pp. 623-631. 10.1016/S2215-0366(23)00186-4
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Kopal, Jakub, Kumar, Kuldeep, Saltoun, Karin, Modenato, Claudia, Moreau, Clara A., Martin-Brevet, Sandra, Huguet, Guillaume, Jean-Louis, Martineau, Martin, Charles-Olivier, Saci, Zohra, Younis, Nadine, Tamer, Petra, Douard, Elise, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, Kushan, Leila, Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Lippé, Sarah, Draganski, Bogdan, Sønderby, Ida E., Andreassen, Ole A., Glahn, David C., Thompson, Paul M., Bearden, Carrie E., Jacquemont, Sébastien and Bzdok, Danilo 2023. Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. Nature Human Behaviour 7 , pp. 1001-1007. 10.1038/s41562-023-01541-9
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Chawner, Samuel J.R.A, Paine, Amy L. ORCID: https://orcid.org/0000-0002-9025-3719, Dunn, Matt J. ORCID: https://orcid.org/0000-0002-0295-2182, Walsh, Alice, Sloane, Poppy, Thomas, Megan, Evans, Alexandra ORCID: https://orcid.org/0000-0002-7718-4413, Hopkin-Jones, Lucinda, Struik, Siske, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Erichsen, Jonathan T. ORCID: https://orcid.org/0000-0003-1545-9853, Leekam, Susan R. ORCID: https://orcid.org/0000-0002-1122-0135, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hay, Dale ORCID: https://orcid.org/0000-0003-2505-0453 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2023. Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions. JCPP Advances 3 (2) , e12162. 10.1002/jcv2.12162
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Niarchou, Maria, Cunningham, Adam, Chawner, Samuel, Moulding, Hayley, Sopp, Matthew, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2023. Psychopathology in mothers of children with pathogenic copy number variants. Journal of Medical Genetics 60 , pp. 706-711. 10.1136/jmg-2022-108752
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Rogdaki, Maria, Devroye, Céline, Ciampoli, Mariasole, Veronese, Mattia, Ashok, Abhishekh H., McCutcheon, Robert A., Jauhar, Sameer, Bonoldi, Ilaria, Gudbrandsen, Maria, Daly, Eileen, van Amelsvoort, Therese, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Turkheimer, Federico, Papaleo, Francesco and Howes, Oliver D. 2023. Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study. Molecular Psychiatry 28 , pp. 1995-2006. 10.1038/s41380-021-01108-y
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Adams, Rachael L., Baird, Alister, Smith, Jacqueline, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Linden, Stefanie C. ORCID: https://orcid.org/0000-0003-2120-3811 2023. Psychopathology in adults with copy number variants. Psychological Medicine 53 (7) , pp. 3142-3149. 10.1017/S0033291721005201
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Lin, Jhih-Rong, Zhao, Yingjie, Jabalameli, M Reza, Nguyen, Nha, Mitra, Joydeep, International 22q11.2DS Brain and Behavior Consortium*, Swillen, Ann, Vorstman, Jacob, Chow, Eva, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Emanuel, Beverly, Vermeesch, Joris, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Bassett, Anne, McDonald-McGinn, Donna, Gur, Raquel, Bearden, Carrie, Morrow, Bernice, Lachman, Herbert and Zhang, Zhengdong 2023. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular Psychiatry 28 , pp. 2071-2080. 10.1038/s41380-023-02009-y
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Chen, Zhongbo, Reynolds, Regina H., Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Gagliano Taliun, Sarah A., van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K., Fogh, Isabella, Jones, Ashley R., Robberecht, Wim, Corcia, Philippe, Chiò, Adriano, Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Shaw, Christopher E., Powell, John F., Silani, Vincenzo, Hardy, John A., Houlden, Henry, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Turner, Martin R., Ryten, Mina and Al-Chalabi, Ammar 2023. The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. Neurobiology of Disease 180 , 106082. 10.1016/j.nbd.2023.106082
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Moreau, Clara A., Kumar, Kuldeep, Harvey, Annabelle, Huguet, Guillaume, Urchs, Sebastian, Schultz, Laura M., Sharmarke, Hanad, Jizi, Khadije, Martin, Charles Olivier, Younis, Nadine, Tamer, Petra, Martineau, Jean Louis, Orban, Pierre, Silva, Ana Isabel ORCID: https://orcid.org/0000-0002-1184-4909, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Lippé, Sarah, Bearden, Carrie E., Almasy, Laura, Glahn, David C., Thompson, Paul M., Bourgeron, Thomas, Bellec, Pierre and Jacquemont, Sebastien 2023. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions. Brain 146 (4) , pp. 1686-1696. 10.1093/brain/awac315
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Alsaqati, Mouhamed, Davis, Brittany A., Wood, Jamie, Jones, Megan M., Jones, Lora, Westwood, Aishah, Petter, Olena, Isles, Anthony R. ORCID: https://orcid.org/0000-0002-7587-5712, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Harwood, Adrian J. ORCID: https://orcid.org/0000-0003-3124-5169 2022. NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia. Translational Psychiatry 12 , 438. 10.1038/s41398-022-02199-z
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Singh, Tarjinder, Schizophrenia Exome Meta-Analysis (SCHEMA) Consortium, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2022. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 604 , pp. 509-516. 10.1038/s41586-022-04556-w
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Cunningham, Adam C., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2022. Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs. Psychological Medicine 52 (3) , pp. 574-586. 10.1017/S0033291720002330
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Chapman, Gareth, Alsaqati, Mouhamed, Lunn, Sharna, Singh, Tanya, Linden, Stephanie C. ORCID: https://orcid.org/0000-0003-2120-3811, Linden, David E.J. ORCID: https://orcid.org/0000-0002-5638-9292, van den Bree, Marianne B. V. ORCID: https://orcid.org/0000-0002-4426-3254, Ziller, Mike, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Harwood, Adrian J. ORCID: https://orcid.org/0000-0003-3124-5169 and Syed, Yasir Ahmed ORCID: https://orcid.org/0000-0001-9495-307X 2022. Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome. Molecular Psychiatry 27 , pp. 819-830. 10.1038/s41380-021-01182-2
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Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Wynn, Sarah, Ford, Tamsin, Baker, Kate, Chawner, Samuel, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, IMAGINE Consortium, Skuse, David, Raymond, F. Lucy, Erwood, Marie, Lafont, Amy, Timur, Husniye, Ye, Zheng, Walker, Susan, Printzlau, Frida, Juj, Manoj, Davies, Sarah, Denver, Hayley, Watkins, Alice, Kerry, Eleanor, Lucock, Anna, Fatih, Nasratullay, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Weber, Astrid, Rawson, Myfanwy, Johnson, Diana, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Clowes, Virginia, Gurasashvili, Jana, Mansour, Sahar, Holder-Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana and Procter, Annie 2022. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE - The UK National Cohort Study. [Online]. papers.SSRN.com: Elsevier. Available at: http://dx.doi.org/10.2139/ssrn.4028542
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Mullins, Niamh, Kang, Jooeun, Campos, Adrian I., Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, 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 2022. Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors. Biological Psychiatry 91 (3) , pp. 313-327. 10.1016/j.biopsych.2021.05.029
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Jones, Hannah J., Hammerton, Gemma, McCloud, Tayla, Hines, Lindsey A., Wright, Caroline, Gage, Suzanne H., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Peter B., Smith, George Davey, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, 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. ORCID: https://orcid.org/0000-0002-6980-4053, Munafò, Marcus R., Heron, Jon and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2022. Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence. Psychological Medicine 52 (1) , pp. 132-139. 10.1017/S0033291720001798
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Vassos, Evangelos, Kou, Jiaqi, Tosato, Sarah, Maxwell, Jessye, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Legge, Sophie, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Breen, Gerome, Lewis, Cathryn, Sullivan, Patrick, Hultman, Christina, Ruggeri, Mirella, Walshe, Muriel, Bramon, Elvira, Bergen, Sarah and Murray, Robin 2022. Lack of support for the genes by early environment interaction hypothesis in the pathogenesis of schizophrenia. Schizophrenia Bulletin 48 (1) , pp. 20-26. 10.1093/schbul/sbab052
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Sanders, Bret, D'Andrea, Daniel, Collins, Mark O., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Steward, Tom G. J., Zhu, Ying, Chapman, Gareth, Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Adrian J. ORCID: https://orcid.org/0000-0003-3124-5169, Gray, William P. ORCID: https://orcid.org/0000-0001-7595-8887, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Errington, Adam C. ORCID: https://orcid.org/0000-0002-2171-389X, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Whitcomb, Daniel J., Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 and Shin, Eunju ORCID: https://orcid.org/0000-0002-8865-6834 2022. Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature Communications 13 (1) , 27. 10.1038/s41467-021-27601-0
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Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Smart, Sophie ORCID: https://orcid.org/0000-0002-6709-5425, Willcocks, Isabella ORCID: https://orcid.org/0000-0002-3568-5236, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Legge, Sophie, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2022. Interaction testing and polygenic risk scoring to estimate the contribution of common genetic variants to treatment resistance in schizophrenia. JAMA Psychiatry 79 (3) , pp. 260-269. 10.1001/jamapsychiatry.2021.3799
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Dimitriadis, Stavros I. ORCID: https://orcid.org/0000-0002-0000-5392, Lancaster, Thomas ORCID: https://orcid.org/0000-0003-1322-2449, Perry, Gavin ORCID: https://orcid.org/0000-0003-0468-0421, Tansey, Katherine E., Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049, Singh, Kirsh D. ORCID: https://orcid.org/0000-0002-3094-2475, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Davey Smith, George, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292 2021. Global brain flexibility during working memory is reduced in a high genetic risk group for schizophrenia. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 6 (12) , pp. 1176-1184. 10.1016/j.bpsc.2021.01.007
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Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Yang, Jessica M. K. ORCID: https://orcid.org/0000-0002-3685-4126, Crawford, Karen, Bergink, Veerle, Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Gordon-Smith, Katherine, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889 2021. Post-partum psychosis and its association with bipolar disorder in the UK: a case-control study using polygenic risk scores. The Lancet Psychiatry 8 (12) , pp. 1045-1052. 10.1016/S2215-0366(21)00253-4
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Kalman, Janos L., Olde Loohuis, Loes M., Vreeker, Annabel, McQuillin, Andrew, Stahl, Eli A., Ruderfer, Douglas, Grigoroiu-Serbanescu, Maria, Panagiotaropoulou, Georgia, Ripke, Stephan, Bigdeli, Tim B., Stein, Frederike, Meller, Tina, Meinert, Susanne, Pelin, Helena, Streit, Fabian, Papiol, Sergi, Adams, Mark J., Adolfsson, Rolf, Adorjan, Kristina, Agartz, Ingrid, Aminoff, Sofie R., Anderson-Schmidt, Heike, Andreassen, Ole A., Ardau, Raffaella, Aubry, Jean-Michel, Balaban, Ceylan, Bass, Nicholas, Baune, Bernhard T., Bellivier, Frank, Benabarre, Antoni, Bengesser, Susanne, Berrettini, Wade H, Boks, Marco P., Bromet, Evelyn J., Brosch, Katharina, Budde, Monika, Byerley, William, Cervantes, Pablo, Chillotti, Catina, Cichon, Sven, Clark, Scott R., Comes, Ashley L., Corvin, Aiden, Coryell, William, Craddock, Nick, Craig, David W., Croarkin, Paul E., Cruceanu, Cristiana, Czerski, Piotr M., Dalkner, Nina, Dannlowski, Udo, Degenhardt, Franziska, Del Zompo, Maria, DePaulo, J. Raymond, Djurovic, Srdjan, Edenberg, Howard J., Eissa, Mariam Al, Elvsåshagen, Torbjørn, Etain, Bruno, Fanous, Ayman H., Fellendorf, Frederike, Fiorentino, Alessia, Forstner, Andreas J., Frye, Mark A., Fullerton, Janice M., Gade, Katrin, Garnham, Julie, Gershon, Elliot, Gill, Michael, Goes, Fernando S., Gordon-Smith, Katherine, Grof, Paul, Guzman-Parra, Jose, Hahn, Tim, Hasler, Roland, Heilbronner, Maria, Heilbronner, Urs, Jamain, Stephane, Jimenez, Esther, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa, Jonsson, Lina, Kahn, Rene S., Kelsoe, John R., Kennedy, James L., Kircher, Tilo, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kittel-Schneider, Sarah, Klöhn-Saghatolislam, Farah, Knowles, James A., Kranz, Thorsten M., Lagerberg, Trine Vik, Landen, Mikael, Lawson, William B., Leboyer, Marion, Li, Qingqin S., Maj, Mario, Malaspina, Dolores, Manchia, Mirko, Mayoral, Fermin, McElroy, Susan L., McInnis, Melvin G., McIntosh, Andrew M., Medeiros, Helena, Melle, Ingrid, Milanova, Vihra, Mitchell, Philip B., Monteleone, Palmiero, Monteleone, Alessio Maria, Nöthen, Markus M., Novak, Tomas, Nurnberger, John I., O'Brien, Niamh, O'Connell, Kevin S., O'Donovan, Claire, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Opel, Nils, Ortiz, Abigail, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pålsson, Erik, Pato, Carlos, Pato, Michele T., Pawlak, Joanna, Pfarr, Julia-Katharina, Pisanu, Claudia, Potash, James B., Rapaport, Mark H, Reich-Erkelenz, Daniela, Reif, Andreas, Reininghaus, Eva, Repple, Jonathan, Richard-Lepouriel, Hélène, Rietschel, Marcella, Ringwald, Kai, Roberts, Gloria, Rouleau, Guy, Schaupp, Sabrina, Scheftner, William A, Schmitt, Simon, Schofield, Peter R., Schubert, K. Oliver, Schulte, Eva C., Schweizer, Barbara, Senner, Fanny, Severino, Giovanni, Sharp, Sally, Slaney, Claire, Smeland, Olav B., Sobell, Janet L., Squassina, Alessio, Stopkova, Pavla, Strauss, John, Tortorella, Alfonso, Turecki, Gustavo, Twarowska-Hauser, Joanna, Veldic, Marin, Vieta, Eduard, Vincent, John B., Xu, Wei, Zai, Clement C., Zandi, Peter P., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Smoller, Jordan W., Biernacka, Joanna M., McMahon, Francis J., Alda, Martin, Müller-Myhsok, Bertram, Koutsouleris, Nikolaos, Falkai, Peter, Freimer, Nelson B., Andlauer, Till F.M., Schulze, Thomas G. and Ophoff, Roel A. 2021. Characterisation of age and polarity at onset in bipolar disorder. The British Journal of Psychiatry 219 (6) , pp. 659-669. 10.1192/bjp.2021.102
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Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Pharmacogenomics: A road ahead for precision medicine in psychiatry. Neuron 109 (24) , pp. 3914-3929. 10.1016/j.neuron.2021.09.011
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Dimitriadis, S. I ORCID: https://orcid.org/0000-0002-0000-5392, Perry, G. ORCID: https://orcid.org/0000-0003-0468-0421, Foley, S. F ORCID: https://orcid.org/0000-0002-8390-2709, Tansey, K. E, Jones, D. K ORCID: https://orcid.org/0000-0003-4409-8049, Holmans, P. ORCID: https://orcid.org/0000-0003-0870-9412, Zammit, S. ORCID: https://orcid.org/0000-0002-2647-9211, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, O’Donovan, M. C ORCID: https://orcid.org/0000-0001-7073-2379, Owen, M. J ORCID: https://orcid.org/0000-0003-4798-0862, Singh, K. D ORCID: https://orcid.org/0000-0002-3094-2475 and Linden, D. E ORCID: https://orcid.org/0000-0002-5638-9292 2021. Genetic risk for schizophrenia is associated with altered visually-induced gamma band activity: evidence from a population sample stratified polygenic risk. Translational Psychiatry 11 , 592. 10.1038/s41398-021-01678-z
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Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Champion, Sinead, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P. and Scott, Laura J. 2021. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry 26 , pp. 5239-5250. 10.1038/s41380-020-01006-9
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Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Legge, Sophie, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Cardno, Alastair, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2021. Risk factors, clinical features, and polygenic risk scores in schizophrenia and schizoaffective disorder depressive-type. Schizophrenia Bulletin 47 (5) , pp. 1375-1384. 10.1093/schbul/sbab036
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Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Collado-Torres, Leonardo, Burke, Emily E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Janet C., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Weinberger, Daniel R., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Jaffe, Andrew E. and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2021. Developmental profile of psychiatric risk associated with voltage-gated cation channel activity. Biological Psychiatry 90 (6) 10.1016/j.biopsych.2021.03.009
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Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Creeth, Hugo, Hwo, Hai-Gwo, Chen, Wei J., Tsuang, Ming, Glatt, Stephen J., Rey, Romain, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2021. Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications 12 , 5353. 10.1038/s41467-021-25532-4
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Cleynen, Isabelle, International q.DS Brain and Behavior Consortium, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A.S., Bearden, Carrie E., Chow, Eva W. C., Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Emanuel, Beverley S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Chopra, Pankaj, Cutler, David J., Duncan, Richard, Kotlar, Alex V., Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Golden, Aaron, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Merico, Daniele, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Demaeral, Wolfman, Boot, Erik, Butcher, Nancy J., Costain, Gregory A., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A. M. J., van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koren, Vergaelen, Elfi, Vogels, Annick, Crowley, Blaine, McGinn, Daniel E., Moss, Edward M., Sharkus, Robert J., Unolt, Marta, Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Moss, Hayley, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan C., Buzzanca, Antonio, Fabio, Fabio Di, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Gothelf, Doron, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Kushan, Leila, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stephan, Sandini, Corrado, Schneider, Maude, Bena, Frederique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Busa, Tiffany, McCabe, Kathryn L., Philip, Nicole, Campbell, Linda E., Shashi, Vandana, Hooper, Stephen R., Schoch, Kelly, Simon, Tony J., Tassone, Flora, Arango, Celso, Fraguas, David, Garcia-Miñaur, Sixto, Morey-Canyelles, Jaume, Rosell, Jordi, Suner, Damia H., Raventos-Simic, Jasna, Epstein, Michael, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Bassett, Anne S. 2021. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry , pp. 4496-4510. 10.1038/s41380-020-0654-3
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Legge, Sophie, Cardno, Alastair, Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Hubbard, Leon, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Associations between schizophrenia polygenic liability, symptom dimensions, and cognitive ability in schizophrenia. JAMA Psychiatry 78 (10) , pp. 1143-1151. 10.1001/jamapsychiatry.2021.1961
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Clifton, Nicholas E. ORCID: https://orcid.org/0000-0003-2597-5253, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Pardinas, Antonio. F. ORCID: https://orcid.org/0000-0001-6845-7590, Harwood, Janet, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452 2021. Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry 26 , pp. 2977-2990. 10.1038/s41380-020-00912-2
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Forsyth, Jennifer K., Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R. K., Villalon-Reina, Julio E., Thompson, Paul M., Bearden, Carrie E., Cunningham, Adam, Doherty, Joanne L., Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 31 (7) , pp. 3285-3298. 10.1093/cercor/bhab008
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Modenato, Claudia, Kumar, Kuldeep, Moreau, Clara, Martin-Brevet, Sandra, Huguet, Guillaume, Schramm, Catherine, Jean-Louis, Martineau, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Douard, Elise, Thébault-Dagher, Fanny, Côté, Valérie, Charlebois, Audrey-Rose, Deguire, Florence, Maillard, Anne M., Rodriguez-Herreros, Borja, Pain, Aurèlie, Richetin, Sonia, Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujat, Geneviève, Sloan-Béna, Frédérique, Belfiore, Marco, Bonneau, Dominique, Bouquillon, Sonia, Boute, Odile, Brusco, Alfredo, Busa, Tiffany, Caberg, Jean- Hubert, Campion, Dominique, Colombert, Vanessa, Cordier, Marie-Pierre, David, Albert, Debray, François-Guillaume, Delrue, Marie-Ange, Doco-Fenzy, Martine, Dunkhase-Heinl, Ulrike, Edery, Patrick, Fagerberg, Christina, Faivre, Laurence, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Héron, Delphine, Isidor, Bertrand, Jacquette, Aurélia, Jaillard, Sylvie, Journel, Hubert, Keren, Boris, Lacombe, Didier, Lebon, Sébastien, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Mathieu-Dramart, Michèle, Mercier, Sandra, Mignot, Cyril, Missirian, Chantal, Petit, Florence, Pilekær Sørensen, Kristina, Pinson, Lucile, Plessis, Ghislaine, Prieur, Fabienne, Raymond, Alexandre, Rooryck-Thambo, Caroline, Rossi, Massimiliano, Sanlaville, Damien, Schlott Kristiansen, Britta, Schluth-Bolard, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Alupay, Hanalore, Aaronson, Benjamin, Ackerman, Sean, Ankenman, Katy, Anwar, Ayesha, Atwell, Constance, Bowe, Alexandra, Beaudet, Arthur L., Benedetti, Marta, Berg, Jessica, Berman, Jeffrey, Berry, Leandra N., Bibb, Audrey L., Blaskey, Lisa, Brennan, Jonathan, Brewton, Christie M., Buckner, Randy, Bukshpun, Polina, Burko, Jordan, Cali, Phil, Cerban, Bettina, Chang, Yishin, Cheong, Maxwell, Chow, Vivian, Chu, Zili, Chudnovskaya, Darina, Cornew, Lauren, Dale, Corby, Dell, John, Dempsey, Allison G., Deschamps, Trent, Earl, Rachel, Edgar, James, Elgin, Jenna, Olson, Jennifer Endre, Evans, Yolanda L., Findlay, Anne, Fischbach, Gerald D., Fisk, Charlie, Fregeau, Brieana, Gaetz, Bill, Gaetz, Leah, Garza, Silvia, Gerdts, Jennifer, Glenn, Orit, Gobuty, Sarah E., Golembski, Rachel, Greenup, Marion, Heiken, Kory, Hines, Katherine, Hinkley, Leighton, Jackson, Frank I., Jenkins, Julian, Jeremy, Rita J., Johnson, Kelly, Kanne, Stephen M., Kessler, Sudha, Khan, Sarah Y., Ku, Matthew, Kuschner, Emily, Laakman, Anna L., Lam, Peter, Lasala, Morgan W., Lee, Hana, LaGuerre, Kevin, Levy, Susan, Cavanagh, Alyss Lian, Llorens, Ashlie V., Campe, Katherine Loftus, Luks, Tracy L., Marco, Elysa J., Martin, Stephen, Martin, Alastair J., Marzano, Gabriela, Masson, Christina, McGovern, Kathleen E., Keehn, Rebecca McNally, Miller, David T., Miller, Fiona K., Moss, Timothy J., Murray, Rebecca, Nagarajan, Srikantan S., Nowell, Kerri P., Owen, Julia, Paal, Andrea M., Packer, Alan, Page, Patricia Z., Paul, Brianna M., Peters, Alana, Peterson, Danica, Poduri, Annapurna, Pojman, Nicholas J., Porche, Ken, Proud, Monica B., Qasmieh, Saba, Ramocki, Melissa B., Reilly, Beau, Roberts, Timothy P. L., Shaw, Dennis, Sinha, Tuhin, Smith-Packard, Bethanny, Gallagher, Anne Snow, Swarnakar, Vivek, Thieu, Tony, Triantafallou, Christina, Vaughan, Roger, Wakahiro, Mari, Wallace, Arianne, Ward, Tracey, Wenegrat, Julia, Wolken, Anne, Melie-Garcia, Lester, Kushan, Leila, Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, Van Den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Lippé, Sarah, Chakravarty, Mallar, Bzdok, Danilo, Bearden, Carrie E., Draganski, Bogdan and Jacquemont, Sébastien 2021. Effects of eight neuropsychiatric copy number variants on human brain structure. Translational Psychiatry 11 (1) , 399. 10.1038/s41398-021-01490-9
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Hubbard, Leon, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Morris, Derek W., Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Richards, Alex L., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Legge, Sophie E., Harold, Denise, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, 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, Donohoe, Gary, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 90 (1) , pp. 28-34. 10.1016/j.biopsych.2020.11.025
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Byrne, Enda, Zhu, Zhihong, Qi, Ting, Skene, Nathan, Bryois, Julien, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Stahl, Eli, Smoller, Jordon, Rietschel, Marcella, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, McGarth, John, Hjerling-Leffler, Jens, Sullivan, Patrick, Goddard, Michael, Visscher, Peter, Yang, Jian and Wray, Naomi 2021. Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. Molecular Psychiatry 26 , pp. 2070-2081. 10.1038/s41380-020-0705-9
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Hall, Lynsey S., Pain, Oliver, O’Brien, Heath E., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X 2021. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Molecular Psychiatry 26 , pp. 2082-2088. 10.1038/s41380-020-0743-3
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Amare, Azmeraw T., Schubert, Klaus Oliver, Hou, Liping, Clark, Scott R., Papiol, Sergi, Cearns, Micah, Heilbronner, Urs, Degenhardt, Franziska, Tekola-Ayele, Fasil, Hsu, Yi-Hsiang, Shekhtman, Tatyana, Adli, Mazda, Akula, Nirmala, Akiyama, Kazufumi, Ardau, Raffaella, Arias, Bárbara, Aubry, Jean-Michel, Backlund, Lena, Bhattacharjee, Abesh Kumar, Bellivier, Frank, Benabarre, Antonio, Bengesser, Susanne, Biernacka, Joanna M., Birner, Armin, Brichant-Petitjean, Clara, Cervantes, Pablo, Chen, Hsi-Chung, Chillotti, Caterina, Cichon, Sven, Cruceanu, Cristiana, Czerski, Piotr M., Dalkner, Nina, Dayer, Alexandre, Del Zompo, Maria, DePaulo, J. Raymond, Étain, Bruno, Jamain, Stephane, Falkai, Peter, Forstner, Andreas J., Frisen, Louise, Frye, Mark A., Fullerton, Janice M., Gard, Sébastien, Garnham, Julie S., Goes, Fernando S., Grigoroiu-Serbanescu, Maria, Grof, Paul, Hashimoto, Ryota, Hauser, Joanna, Herms, Stefan, Hoffmann, Per, Hofmann, Andrea, Jiménez, Esther, Kahn, Jean-Pierre, Kassem, Layla, Kuo, Po-Hsiu, Kato, Tadafumi, Kelsoe, John R., Kittel-Schneider, Sarah, Kliwicki, Sebastian, König, Barbara, Kusumi, Ichiro, Laje, Gonzalo, Landén, Mikael, Lavebratt, Catharina, Leboyer, Marion, Leckband, Susan G., Tortorella, Alfonso, Manchia, Mirko, Martinsson, Lina, McCarthy, Michael J., McElroy, Susan L., Colom, Francesc, Mitjans, Marina, Mondimore, Francis M., Monteleone, Palmiero, Nievergelt, Caroline M., Nöthen, Markus M., Novák, Tomas, O'Donovan, Claire, Ozaki, Norio, Ösby, Urban, Pfennig, Andrea, Potash, James B., Reif, Andreas, Reininghaus, Eva, Rouleau, Guy A., Rybakowski, Janusz K., Schalling, Martin, Schofield, Peter R., Schweizer, Barbara W., Severino, Giovanni, Shilling, Paul D., Shimoda, Katzutaka, Simhandl, Christian, Slaney, Claire M., Squassina, Alessio, Stamm, Thomas, Stopkova, Pavla, Maj, Mario, Turecki, Gustavo, Vieta, Eduard, Veeh, Julia, Witt, Stephanie H., Wright, Adam, Zandi, Peter P., Mitchell, Philip B., Bauer, Michael, Alda, Martin, Rietschel, Marcella, McMahon, Francis J., Schulze, Thomas G., Baune, Bernhard T., Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Tansey, Katherine 2021. Association of polygenic score for major depression with response to lithium in patients with bipolar disorder. Molecular Psychiatry 26 , pp. 2457-2470. 10.1038/s41380-020-0689-5
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Tigaret, Cezar M. ORCID: https://orcid.org/0000-0001-5848-6697, Tzu-Ching, E. Lin, Morrell, Edward R., Sykes, Lucy, Moon, Anna L. ORCID: https://orcid.org/0000-0002-6587-4425, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124, Jones, Matthew W., Thomas, Kerrie L. ORCID: https://orcid.org/0000-0003-3355-9583 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2021. Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c. Molecular Psychiatry 26 , pp. 1748-1760. 10.1038/s41380-020-01001-0
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Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 2021. Explaining the missing heritability of psychiatric disorders. World Psychiatry 20 (2) , pp. 294-295. 10.1002/wps.20870

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Haan, Niels, Westacott, Laura J., Carter, Jenny, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Gray, William P. ORCID: https://orcid.org/0000-0001-7595-8887, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124 2021. Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms. Translational Psychiatry 11 (1) , 313. 10.1038/s41398-021-01415-6
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Willcocks, Isabella ORCID: https://orcid.org/0000-0002-3568-5236, Legge, Sophie, Nalmpanti, Mariana, Mazzeo, Lucy, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 2021. Clozapine metabolism is associated with absolute neutrophil count in individuals with treatment-resistant schizophrenia. Frontiers in Pharmacology 12 , 658734. 10.3389/fphar.2021.658734
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Dennison, Charlotte A. ORCID: https://orcid.org/0000-0002-7493-2041, Legge, Sophie E., Bracher-Smith, Matthew, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Smith, Daniel J., Doherty, Aiden R., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank. PLoS ONE 16 (3) , e0249189. 10.1371/journal.pone.0249189
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Linden, Stefanie C. ORCID: https://orcid.org/0000-0002-5638-9292, Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M. ORCID: https://orcid.org/0000-0003-1322-2449, Evans, Ffion, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Skuse, David, Raymond, F. Lucy, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2021. The psychiatric phenotypes of 1q21 distal deletion and duplication. Translational Psychiatry 11 , 105. 10.1038/s41398-021-01226-9
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Cunningham, Adam, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants. Psychological Medicine 51 (2) , pp. 290-299. 10.1017/S0033291719003210
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Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2021. Large-scale genomics: a paradigm shift in psychiatry? Biological Psychiatry 89 , pp. 5-7. 10.1016/j.biopsych.2020.01.017
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Chawner, Samuel, Doherty, Joanne L., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Antshel, Kevin M., Bearden, Carrie E., Bernier, Raphael, Chung, Wendy K., Clements, Caitlin C., Curran, Sarah R., Cuturilo, Goran, Fiksinski, Ania M., Gallagher, Louise, Goin-Koche, Robin P., Kushan, Leila, Gur, Raquel E., Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R., Maillard, Anne M., McDonald-McGinn, Donna M., MihaljevicMihaljevic, Marina Mihaljevic, Miller, Judith S., Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T., Green-Snyder, LeeAnne, Vorstman, Jacob A., Wenger, Tara L., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254 2021. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. American Journal of Psychiatry 178 (1) , pp. 77-86. 10.1176/appi.ajp.2020.20010015
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Sønderby, Ida E., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David ORCID: https://orcid.org/0000-0002-5638-9292, Silva, Ana ORCID: https://orcid.org/0000-0002-1184-4909 and Doherty, Joanne 2021. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational Psychiatry 11 , 182. 10.1038/s41398-021-01213-0
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Davies, Robert, International 22q11.2, Brain and Behavior Consortium, Fiksinski, Ania M., Breetvelt, Elemi J., Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Hooper, Stephen R., Monfueuga, Thomas, Bassett, Anne S., Owen, Michal J. ORCID: https://orcid.org/0000-0003-4798-0862, Gur, Raquel E., Morrow, Bernice E., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Emanuel, Beverly S., Vermeesch, Joris R., van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E., Cubells, Joseph F., Eliez, Stephan, Garia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan G., Philip, Nicole, Repetto, Gabriela M., Shashi, Vandana, Simon, Tony J., Suñer, Damiàn Heine., Vicari, Stefano, Scherer, Stephen W., Bearden, Carrie E., Vorstman, Jacob A. S. and Chawner, Samuel 2020. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 Deletion Syndrome. Nature Medicine 26 , pp. 1912-1918. 10.1038/s41591-020-1103-1
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Villalon-Reina, Julio, Martinez, Kenia, Qu, Xiaoping, Ching, Christopher, Nir, Talia, Kothapalli, Deydeep, Corbin, Conor, Dagiang, Sun, Lin, Amy, Forsyth, Jennifer, Kushan, Lelia, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel, van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy, Antshel, Kevin, Fremont, Wanda, Campbell, Linda, McCable, Kathryn, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh, Murphy, Declan, Craig, Michael, Emanual, Beverly, McDonna-McGinn, Donna, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David, Raquel, Gur, Eric, Schmitt, Simon, Tony, Goodrich-Hunsaker, Naomi, Durdle, Courtney, Doherty, Joanne, Cunningham, Adam, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Moss, Hayley, Kelly, Sinead, Donohoe, Gary, Murphy, Kieran, Arango, Celso, Jahanshad, Neda, Thompson, Paul and Bearden, Carrie 2020. Altered white matter microstructure in 22q11.2 deletion syndrome: a multi-site diffusion tensor imaging study. Molecular Psychiatry 25 , pp. 2818-2831. 10.1038/s41380-019-0450-0
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Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, John, Ann, Lee, Sze Chim, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Del Pozo Banos, Marcos, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lloyd, Keith, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Legge, Sophie E. and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2020. Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: a data linkage study. BJPsych Open 6 (6) , e139. 10.1192/bjo.2020.42
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Legge, Sophie E., Christensen, Rune H., Petersen, Liselotte, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Bracher-Smith, Matthew, Knapper, Steven, Bybjerg-Grauholm, Jonas, Baekvad-Hansen, Marie, Hougaard, David M., Werge, Thomas, Nordentoft, Merete, Mortensen, Preben Bo, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Benros, Michael E. and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2020. The Duffy-null genotype and risk of infection. Human Molecular Genetics 29 (20) , pp. 3341-3349. 10.1093/hmg/ddaa208
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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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Dima, Diana C. ORCID: https://orcid.org/0000-0002-9612-5574, Adams, Rachael, Linden, Stefanie C. ORCID: https://orcid.org/0000-0002-5638-9292, Baird, Alister, Smith, Jacqueline, Foley, Sonya ORCID: https://orcid.org/0000-0002-8390-2709, Perry, Gavin ORCID: https://orcid.org/0000-0003-0468-0421, Routley, Bethany C., Magazzini, Lorenzo ORCID: https://orcid.org/0000-0002-8934-8374, Drakesmith, Mark ORCID: https://orcid.org/0000-0001-8574-9560, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Doherty, Joanne, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292 and Singh, Krish D. ORCID: https://orcid.org/0000-0002-3094-2475 2020. Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk. Translational Psychiatry 10 , 324. 10.1038/s41398-020-00998-w
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Sun, Daqiang, Ching, Christopher R. K., Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Villalon-Reina, Julio E., Qu, Xiaoping, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan, Craig, Michael, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David R., Gur, Raquel E., Schmitt, J. Eric, Simon, Tony J., Goodrich-Hunsaker, Naomi J., Durdle, Courtney A., Bassett, Anne S., Chow, Eva W. C., Butcher, Nancy J., Vila-Rodriguez, Fidel, Doherty, Joanne, Cunningham, Adam, Van Den Bree, Marianne B M. ORCID: https://orcid.org/0000-0002-4426-3254, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., McDonald-McGinn, Donna M., Emanuel, Beverly, van Erp, Theo G. M., Turner, Jessica A., Thompson, Paul M. and Bearden, Carrie E. 2020. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size. Molecular Psychiatry 25 , pp. 1822-1834. 10.1038/s41380-018-0078-5
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Coleman, Jonathan R. I., Peyrot, Wouter J., Purves, Kirstin L., Davis, Katrina A. S., Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A., Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M., Choi, Karmel W., Dunn, Erin C., Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J., Lewis, Cathryn M., O'Reilly, Paul F., McIntosh, Andrew M., Smith, Daniel J., Wray, Naomi R., Hotopf, Matthew, Eley, Thalia C., Breen, Gerome, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Tansey, Katherine E. 2020. Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Molecular Psychiatry 25 , pp. 1430-1446. 10.1038/s41380-019-0546-6
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Cunningham, Adam, Fung, Wilson, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7) , pp. 1272-1274. 10.1002/mds.28078
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Akingbuwa, Wonuola A., Hammerschlag, Anke R., Jami, Eshim S., Allegrini, Andrea G., Karhunen, Ville, Sallis, Hannah, Ask, Helga, Askeland, Ragna B., Baselmans, Bart, Diemer, Elizabeth, Hagenbeek, Fiona A., Havdahl, Alexandra, Hottenga, Jouke-Jan, Mbarek, Hamdi, Rivadeneira, Fernando, Tesli, Martin, van Beijsterveldt, Catharina, Breen, Gerome, Lewis, Cathryn M., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Boomsma, Dorret I., Kuja-Halkola, Ralf, Reichborn-Kjennerud, Ted, Magnus, Per, Rimfeld, Kaili, Ystrom, Eivind, Jarvelin, Marjo-Riitta, Lichtenstein, Paul, Lundstrom, Sebastian, Munafò, Marcus R., Plomin, Robert, Tiemeier, Henning, Nivard, Michel G., Bartels, Meike, Middeldorp, Christel M., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Richards, Alexander L., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Forty, Liz, Fraser, Christine, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Ian, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Tansey, Katherine E. and The Bipolar Disorder and Major Depressive Disorder Working Group 2020. Genetic associations between childhood psychopathology and adult depression and associated traits in 42 998 individuals. JAMA Psychiatry 77 (7) , pp. 715-728. 10.1001/jamapsychiatry.2020.0527
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Ching, Christopher R.K., Gutman, Boris A., Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K., Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K., Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Campbell, Linda E., McCabe, Kathryn L., Craig, Michael C., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan G., Murphy, Kieran C., Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T. Blaine, Emanuel, Beverly S., Gur, Raquel E., McDonald-McGinn, Donna M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Zackai, Elaine H., Durdle, Courtney A., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Bassett, Anne S., Butcher, Nancy J., Chow, Eva W.C., Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne, Linden, David E., Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Crossley, Nicolas A., Repetto, Gabriela M., Thompson, Paul M. and Bearden, Carrie E. 2020. Mapping subcortical brain alterations in 22q11.2 deletion syndrome: effects of seletion size and convergence with idiopathic neuropsychiatric illness. American Journal of Psychiatry 177 (7) , pp. 589-600. 10.1176/appi.ajp.2019.19060583

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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Legge, Sophie, Dennison, Charlotte ORCID: https://orcid.org/0000-0002-7493-2041, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Hopkins, Lucinda, Bates, Lesley, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2020. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 216 (5) , pp. 259-266. 10.1192/bjp.2019.120
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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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Moulding, Hayley ORCID: https://orcid.org/0000-0002-1277-4404, Bartsch, Ullrich, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Jones, M., Linden, David, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2020. Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS). Psychological Medicine 50 , pp. 1191-1202. 10.1017/S0033291719001119
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Foley, Claire, Heron, Elizabeth A., Harold, Denise, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Sebat, Jonathan, Kelleher, Eric, Mooney, Christina, Durand, Amy, Pinto, Carlos, Cormican, Paul, Morris, Derek, Donohoe, Gary, Gill, Michael, Gallagher, Louise and Corvin, Aiden 2020. Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study. British Journal of Psychiatry 216 (5) , pp. 275-279. 10.1192/bjp.2019.262
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van der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, de Geus, Eco J. C., de Zubicaray, Greig I., de Zwarte, Sonja M. C., Delanty, Norman, den Braber, Anouk, Desrivieres, Sylvane, Di Forti, Marta, Doherty, Joanne L., Donohoe, Gary, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fisher, Simon E., Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Glahn, David C., Grabe, Hans J., Groenewold, Nynke A., Gústafsson, Ómar, Haavik, Jan, Haberg, Asta K., Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Hibar, Derrek P., Hillegers, Manon H. J., Hoffmann, Per, Holleran, Laurena, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E., Ikeda, Masashi, Jacquemont, Sébastien, Jahanshad, Neda, Jockwitz, Christiane, Johansson, Stefan, Jönsson, Erik G., Kikuchi, Masataka, Knowles, Emma E. M., Kwok, John B., Le Hellard, Stephanie, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri J., Martin, Nicholas G., Mather, Karen A., Mathias, Samuel R., McMahon, Katie L., McRae, Allan F., Medland, Sarah E., Moberget, Torgeir, Moreau, Clara, Morris, Derek W., Mühleisen, Thomas W., Murray, Robin M., Nordvik, Jan E., Nyberg, Lars, Olde Loohuis, Loes M., Ophoff, Roel A., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paus, Tomas, Pausova, Zdenka, Peralta, Juan M., Pike, Bruce, Prieto, Carlos, Quinlan, Erin Burke, Reinbold, Céline S., Reis Marques, Tiago, Rucker, James J. H., Sachdev, Perminder S., Sando, Sigrid B., Schofield, Peter R., Schork, Andrew J., Schumann, Gunter, Shin, Jean, Shumskaya, Elena, Silva, Ana I., Sisodiya, Sanjay M., Steen, Vidar M., Stein, Dan J., Strike, Lachlan T., Tamnes, Christian K., Teumer, Alexander, Thalamuthu, Anbupalam, Tordesillas-Gutiérrez, Diana, Uhlmann, Anne, Úlfarsson, Magnús Ö., van 't Ent, Dennis, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Vassos, Evangelos, Wen, Wei, Wittfeld, Katharina, Wright, Margaret J., Zayats, Tetyana, Dale, Anders M., Djurovic, Srdjan, Agartz, Ingrid, Westlye, Lars T., Stefánsson, Hreinn, Stefánsson, Kári, Thompson, Paul M. and Andreassen, Ole A. 2020. Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry 77 (4) , pp. 420-430. 10.1001/jamapsychiatry.2019.3779

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. Translating insights from neuropsychiatric genetics and genomics for precision psychiatry. Genome Medicine 12 (1) , 43. 10.1186/s13073-020-00734-5
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Eaton, Christopher B. ORCID: https://orcid.org/0000-0001-6739-1999, Thomas, Rhys H., Hamandi, Khalid, Payne, Gareth C., Kerr, Michael P., Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Cunningham, Adam C., Bartsch, Ullrich, Struik, Siske S. and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2020. Response to letter to editor: 'Knowing when and how to use epilepsy screening questionnaires'. Epilepsia 61 (4) , pp. 826-827. 10.1111/epi.16463

Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Bergen, Sarah, Hultman, Christina, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J. and Ruderfer, Douglas M. 2020. Characterization of single gene copy number variants in schizophrenia. Biological Psychiatry 87 (8) , pp. 736-744. 10.1016/j.biopsych.2019.09.023
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Sullivan, Sarah A., Kounali, Daphne, Cannon, Mary, David, Anthony S., Fletcher, Paul C., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Hannah, Jones, Peter B., Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Lewis, Glyn, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Rammos, Alexandros, Thompson, Andrew, Wolke, Dieter, Heron, Jon and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2020. A population-based cohort study examining the incidence and impact of psychotic experiences from childhood to adulthood, and prediction of psychotic disorder. American Journal of Psychiatry 177 (4) , pp. 308-317. 10.1176/appi.ajp.2019.19060654
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Richards, Alexander, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Frizzati, Aura ORCID: https://orcid.org/0000-0002-7002-6180, Tansey, Katherine, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Legge, Sophie, Savage, Jeanna, Agartz, Ingrid, Andreassen, Ole, Blokland, Gabriella, Corvin, Aiden, Cosgrove, Donna, Degenhardt, Franzoska, Djurovic, Srdjan, Espeseth, Thomas, Ferraro, Laura, Gayer-Anderson, Charlotte, Giegking, Ina, van Haren, Neeltje, Hartmann, Annette, Hubert, John, Jonsson, Erik, Konte, Bettina, Lennertz, Leonhard, Olde Loohuis, Loes, Melle, Ingrid, Morgan, Craig, Morris, Derek, Murray, Robin, Nyman, Håkan, Ophoff, Roel, van Os, Jim, Petryshen, Tracey, Quattrone, Diego, Rietschel, Marcella, Rujescu, Dan, Ruttan, Bart, Streit, Fabin, Strohmaier, Janna, Sullivan, Patrick, Sundet, Kjetil, Wagner, MIchael, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Donohoe, Gary, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Schizophrenia Working Group of the Psychiatric Genomics Consorti and EUGEI WP Group 2020. The relationship between polygenic risk scores and cognition in schizophrenia. Schizophrenia Bulletin 46 (2) , -. 10.1093/schbul/sbz061
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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
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Sullivan, Patrick F. and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. Increasing the clinical psychiatric knowledge base about pathogenic copy number variation. American Journal of Psychiatry 177 (3) , pp. 204-209. 10.1176/appi.ajp.2019.19040335
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Raymond, Domenici, Enrico, Domschke, Katharina, Esko, Tõnu, Grabe, Hans J., Hamilton, Steven P., Hayward, Caroline, Heath, Andrew C., Kendler, Kenneth S., Kloiber, Stefan, Lewis, Glyn, Li, Qingqin S., Lucae, Susanne, Madden, Pamela AF., Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Nordentoft, Merete, Nöthen, Markus M., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Paciga, Sara A., Pedersen, Nancy L., Penninx, Brenda W.J.H., Perlis, Roy H., Porteous, David J., Potash, James B., Preisig, Martin, Rietschel, Marcella, Schaefer, Catherine, Schulze, Thomas G., Smoller, Jordan W., Stefansson, Kari, Tiemeier, Henning, Uher, Rudolf, Völzke, Henry, Weissman, Myrna M., Werge, Thomas, Lewis, Cathryn, Levinson, Douglas F., Breen, Gerome, Børglum, Anders D., Sullivan, Patrick F. and Wray, Naomi 2020. Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated with depression. Biological Psychiatry 87 (5) , pp. 419-430. 10.1016/j.biopsych.2019.06.031
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Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, GROUP Investigators, Han, Jun, Morgan, Joanne, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2
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Morrison, Sinead, Chawner, Samuel J. R. A., van Amelsvoort, Therese A. M. J., Swillen, Ann, Vingerhoets, Claudia, Vergaelen, Elfi, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Linden, Stefanie ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2020. Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology. Translational Psychiatry 10 , 53. 10.1038/s41398-020-0736-7
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Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. A developmental perspective on the convergence of genetic risk factors for neuropsychiatric disorders. Biological Psychiatry 87 (2) , pp. 98-99. 10.1016/j.biopsych.2019.09.010
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Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E., Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong and Zwick, Michael 2020. Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects. American Journal of Human Genetics 106 (1) , pp. 26-40. 10.1016/j.ajhg.2019.11.010
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Hall, Lynsey S, Medway, Christopher W ORCID: https://orcid.org/0000-0002-1764-0587, Pain, Oliver, Pardinas, Antonio F ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott G ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Bray, Nicholas J ORCID: https://orcid.org/0000-0002-4357-574X, Holmans, Peter A ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T R ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2020. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 29 (1) , pp. 159-167. 10.1093/hmg/ddz253
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Legge, Sophie E., Jones, Hannah J., Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Bracher-Smith, Matthew, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Davis, Katrina A., Hotopf, Matthew, Savage, Jeanne E., Posthuma, Danielle, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of genetic liability to psychotic experiences with neuropsychotic disorders and traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508
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Anthony, Oh, Sang-Yun, Palotie, Aarno, Pantelis, Christos, Pulver, Ann E., Petryshen, Tracey L., Quested, Digby J., Riley, Brien, Sanders, Alan R., Schall, Ulrich, Schwab, Sibylle G., Scott, Rodney J., Sham, Pak C., Silverman, Jeremy M., Sim, Kang, Steixner, Agnes A., Tooney, Paul A., van Os, Jim, Vawter, Marquis P., Walsh, Dermot, Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Wormley, Brandon K., Zhang, Fuquan, Androutsos, Christos, Arnold, Paul D., Barr, Cathy L., Barta, Csaba, Bey, Katharina, Bienvenu, O. 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Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Smith, Daniel J., Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Ward, Joey, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2019. Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort. Psychological Medicine 49 (15) , pp. 2499-2504. 10.1017/S0033291718000454
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Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J ORCID: https://orcid.org/0000-0001-6776-8709, Forrest, Marc P, Tansey, Katherine E, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Doyle, A. Michelle, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731 2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183
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Sykes, Lucy, Haddon, Josephine, Lancaster, Thomas M. ORCID: https://orcid.org/0000-0003-1322-2449, Sykes, Arabella, Azzouni, Karima, Niklas, Ihssen, Moon, Anna L. ORCID: https://orcid.org/0000-0002-6587-4425, Lin, Tzu-Ching E., Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Humby, Trevor ORCID: https://orcid.org/0000-0002-1840-1799, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124, Thomas, Kerrie L. ORCID: https://orcid.org/0000-0003-3355-9583 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2019. Genetic variation in the psychiatric risk gene CACNA1C modulates reversal learning across species. Schizophrenia Bulletin 45 (5) , pp. 1024-1032. 10.1093/schbul/sby146
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Eaton, C. B. ORCID: https://orcid.org/0000-0001-6739-1999, Thomas, R. H. ORCID: https://orcid.org/0000-0003-2062-8623, Hamandi, K. H., Payne, G. C., Kerr, M. P., Linden, D. E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Cunningham, A. C., Bartsch, U. B., Struik, S. S. and van den Bree, M. B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2019. Prevalence and aetiology of epileptic seizures in young people with 22Q11.2 Deletion syndrome and relationships with other neurodevelopmental disorders. Presented at: SSBP 22nd Educational Day and Research Symposium 2019, Birmingham, England, 4-6 September 2019. Journal of Intellectual Disability Research. , vol.63 (9) Wiley, p. 1080. 10.1111/jir.12676

Pain, Oliver, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Bray, Nichloas J. ORCID: https://orcid.org/0000-0002-4357-574X, O'Brian, Heath E., Hall, Lynsey S., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2019. Novel insight into the etiology of autism spectrum disorder gained by integrating expression data with genome-wide association statistics. Biological Psychiatry 86 (4) , pp. 265-273. 10.1016/j.biopsych.2019.04.034
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Mulllins, Niamh, Bigdeli, Tim, Børglum, Anders, Coleman, Jonathan, Demontis, Ditte, Mehta, Divya, Power, Roberts, Ripke, Stephan, Stahl, Eli, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan, Forstner, Andreas, Reif, Andreas, Koller, Anna, Świątkowska, Beata, Baune, Bernhard, Müller-Myhsok, Bertram, Konte, Bettina, Penninx, Brenda, Pato, Carlos, Zai, Clement, Rujescu, Dan, Hougaard, David, Quested, Digby, Levinson, Douglas, Binder, Elisabeth, Byrne, Enda, Agerbo, Esben, Streit, Fabin, Mayoral, Fermin, Bellivier, Frank, Dehenhardt, Franziska, Breen, Gerome, Morken, Gunnar, Turecki, Gustavo, Rouleau, Guy, Grabe, Hans, Völzke, Henry, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Giegling, Ina, Agartz, Ingrid, Melle, Ingrid, Lawrence, Jacob, Potash, James, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Strohmaier, Jana, Shi, Jianxin, Hauser, Joanna, Biernacka, Joanna, Vincent, John, Kelsoe, John, Strauss, John, Lissowska, Jolanta, Pimm, Jonathan, Smoller, Jordan, Parra, José, Berger, Klaus, Scott, Laura, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, Azevedo, M. Helena, Trzaskowski, Maciej, Kogevinas, Manolis, Rietsche, Marcella, Boks, Marco, Ising, Marcus, Grigoroiu-Serbanescu, Maria, Hamshere, Marian ORCID: https://orcid.org/0000-0002-8990-0958, Leboyer, Marion, Frye, Mark, Nöthen, Markus, Alda, Martin, Preisig, Martin, Nordentoft, Merete, Boehnke, Michael, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Pato, Michele, Renteria, Miguel, Budda, Monika, Weissman, Myrna, Wray, Naomi, Bass, Nicholas, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Smeland, Olav, Andreassen, Ole, Mors, Ole, Gejman, Pablo, Sklar, Pamela, McGrath, Patrick, Hoffman, Per, McGuffin, Peter, Lee, Phil, Mortensen, Preben, Kahn, René, Ophoff, Roel, Adolfsson, Rolf, Van der Auwera, Sandra, Djurovic, Srdjan, Shyn, Stanley, Kloiber, Stefan, Heilmann-Heimbach, Stefanie, Jamain, Stéphane, Hamilton, Steven, McElroy, Susan, Lucae, Susanne, Cichon, Sven, Schulze, Thomas, Hansen, Thomas, Werge, Thomas, Air, Tracy, Nimgaonkar, Vishwajit, Appadurai, Vivek, Cahn, Wiepke, Milaneschi, Yuri, Kendler, Kenneth, Fanous, Ayman, McQuillin, Andrew and Lewis, Cathryn 2019. GWAS of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores. American Journal of Psychiatry 176 (8) , pp. 651-660. 10.1176/appi.ajp.2019.18080957
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Smeeth, Demelza M., Dima, Danai, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Rietschel, Marcella, Maier, Wolfgang, Korszun, Ania, Rice, John P., Mors, Ole, Preisig, Martin, Uher, Rudolf, Lewis, Cathryn M., Thuret, Sandrine and Powell, Timothy R. 2019. Polygenic risk for circulating reproductive hormone levels and their influence on hippocampal volume and depression susceptibility. Psychoneuroendocrinology 106 , pp. 284-292. 10.1016/j.psyneuen.2019.04.011
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Silva, Ana I., Haddon, Josephine E., Syed, Yasir Ahmed ORCID: https://orcid.org/0000-0001-9495-307X, Trent, Simon ORCID: https://orcid.org/0000-0001-9563-4281, Tzu-Ching, E. Lin, Patel, Yateen, Carter, Jenny, Haan, Niels, Honey, Robert C. ORCID: https://orcid.org/0000-0001-6870-1880, Humby, Trevor ORCID: https://orcid.org/0000-0002-1840-1799, Assaf, Yaniv, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124 2019. Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility. Nature Communications 10 , 3455. 10.1038/s41467-019-11119-7
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Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Santiago, Enrique, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2019. The relationship between common variant schizophrenia liability and number of offspring in the UK Biobank. American Journal of Psychiatry 176 (8) , pp. 661-666. 10.1176/appi.ajp.2018.18020140
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Romagnoni, Alberto, Jégou, Simon, Van Steen, Kristel, Wainrib, Gilles, Hugot, Jean-Pierre, Forty, Liz, Gordon-Smith, Katherine, Green, Elaine, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Jones, Ian R ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael C ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, Russell, Ellie and Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610 2019. Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data. Scientific Reports 9 (1) , -. 10.1038/s41598-019-46649-z
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Zhang, Xianglong, Abdellaoui, Abdel, Rucker, James, de Jong, Simone, Potash, James B., Weissman, Myrna M., Shi, Jianxin, Knowles, James A., Pato, Carlos, Pato, Michele, Sobell, Janet, Smit, Johannes H., Hottenga, Jouke-Jan, de Geus, Eco J.C., Lewis, Cathryn M., Buttenschøn, Henriette N., Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, McGuffin, Peter, Mors, Ole, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Preisig, Martin, Rietschel, Marcella, Rice, John P., Rivera, Margarita, Uher, Rudolf, Gejman, Pablo V., Sanders, Alan R., Boomsma, Dorret, Penninx, Brenda W.J.H., Breen, Gerome and Levinson, Douglas F. 2019. Genome-wide burden of rare short deletions is enriched in major depressive disorder in four cohorts. Biological Psychiatry 85 (12) , pp. 1065-1073. 10.1016/j.biopsych.2019.02.022
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Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O'Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S., Theis, Fabian J., Räikkönen, Katri, Binder, Elisabeth B., Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2019. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications 10 , 2548. 10.1038/s41467-019-10461-0
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Cunningham, Adam, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944, Linden, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2019. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion Syndrome. Journal of Neurodevelopmental Disorders 11 , 8. 10.1186/s11689-019-9271-3
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Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Nalmpanti, Mariana, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Legge, Sophie E., Medway, Christopher ORCID: https://orcid.org/0000-0002-1764-0587, King, Adrian, Jansen, John, Helthuis, Marinka, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, MacCabe, James, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R ORCID: https://orcid.org/0000-0002-6980-4053 2019. Pharmacogenomic variants and drug interactions identified through the genetic analysis of clozapine metabolism. American Journal of Psychiatry 176 (6) , pp. 477-486. 10.1176/appi.ajp.2019.18050589
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Chawner, Samuel J. R. A., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Raymond, F. Lucy, Skuse, David, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2019. Genotype–phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study. Lancet Psychiatry 6 (6) , 493 - 505. 10.1016/S2215-0366(19)30123-3
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Stahl, Eli A., Breen, Gerome, Forstner, Andreas J., McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan R. I., Gaspar, Héléna A., de Leeuw, Christiaan A., Steinberg, Stacy, Pavlides, Jennifer M. Whitehead, Trzaskowski, Maciej, Byrne, Enda M., Pers, Tune H., Holmans, Peter A. 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Raymond, Djurovic, Srdjan, Dobbyn, Amanda L., Dumont, Ashley, Elvsåshagen, Torbjørn, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Fan, Chun Chieh, Fischer, Sascha B., Flickinger, Matthew, Foroud, Tatiana M., Forty, Elizabeth, Frank, Josef, Fraser, Christine, Freimer, Nelson B., Frisén, Louise, Gade, Katrin, Gage, Diane, Garnham, Julie, Giambartolomei, Claudia, Pedersen, Marianne Giørtz, Goldstein, Jaqueline, Gordon, Scott D., Gordon-Smith, Katherine, Green, Elaine K., Green, Melissa J., Greenwood, Tiffany A., Grove, Jakob, Guan, Weihua, Guzman-Parra, José, Hamshere, Marian ORCID: https://orcid.org/0000-0002-8990-0958, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hipolito, Maria, Hoffmann, Per, Holland, Dominic, Huckins, Laura, Jamain, Stéphane, Johnson, Jessica S., Juréus, Anders, Kandaswamy, Radhika, Karlsson, Robert, Kennedy, James L., Kittel-Schneider, Sarah, Knowles, James A., Kogevinas, Manolis, Koller, Anna C., Kupka, Ralph, Lavebratt, Catharina, Lawrence, Jacob, Lawson, William B., Leber, Markus, Lee, Phil H., Levy, Shawn E., Li, Jun Z., Liu, Chunyu, Lucae, Susanne, Maaser, Anna, MacIntyre, Donald J., Mahon, Pamela B., Maier, Wolfgang, Martinsson, Lina, McCarroll, Steve, McGuffin, Peter, McInnis, Melvin G., McKay, James, Medeiros, Helena, Medland, Sarah E., Meng, Fan, Milani, Lili, Montgomery, Grant W., Morris, Derek W., Mühleisen, Thomas W., Mullins, Niamh, Nguyen, Hoang, Nievergelt, Caroline M., Adolfsson, Annelie Nordin, Nwulia, Evaristus A., O'Donovan, Claire ORCID: https://orcid.org/0000-0001-7073-2379, Loohuis, Loes M. Olde, Ori, Anil P. S., Oruc, Lilijana, Ösby, Urban, Perlis, Roy H., Perry, Amy, Pfennig, Andrea, Potash, James B., Purcell, Shaun M., Regeer, Eline J., Reif, Andreas, Reinbold, Céline S., Rice, John P., Rivas, Fabio, Rivera, Margarita, Roussos, Panos, Ruderfer, Douglas M., Ryu, Euijung, Sánchez-Mora, Cristina, Schatzberg, Alan F., Scheftner, William A., Schork, Nicholas J., Shannon Weickert, Cynthia, Shehktman, Tatyana, Shilling, Paul D., Sigurdsson, Engilbert, Slaney, Claire, Smeland, Olav B., Sobell, Janet L., Søholm Hansen, Christine, Spijker, Anne T., St Clair, David, Steffens, Michael, Strauss, John S., Streit, Fabian, Strohmaier, Jana, Szelinger, Szabolcs, Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Weiqing, Watson, Stanley J., Weickert, Thomas W., Witt, Stephanie H., Xi, Simon, Xu, Wei, Young, Allan H., Zandi, Peter, Zhang, Peng, Zöllner, Sebastian, Adolfsson, Rolf, Agartz, Ingrid, Alda, Martin, Backlund, Lena, Baune, Bernhard T., Bellivier, Frank, Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H. R., Boehnke, Michael, Børglum, Anders D., Corvin, Aiden, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Daly, Mark J., Dannlowski, Udo, Esko, Tõnu, Etain, Bruno, Frye, Mark, Fullerton, Janice M., Gershon, Elliot S., Gill, Michael, Goes, Fernando, Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Hougaard, David M., Hultman, Christina M., Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A. ORCID: https://orcid.org/0000-0001-5821-5889, Kahn, René S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Landén, Mikael, Leboyer, Marion, Lewis, Cathryn M., Li, Qingqin S., Lissowska, Jolanta, Martin, Nicholas G., Mayoral, Fermin, McElroy, Susan L., McIntosh, Andrew M., McMahon, Francis J., Melle, Ingrid, Metspalu, Andres, Mitchell, Philip B., Morken, Gunnar, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Myers, Richard M., Neale, Benjamin M., Nimgaonkar, Vishwajit, Nordentoft, Merete, Nöthen, Markus M., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Oedegaard, Ketil J., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paciga, Sara A., Pato, Carlos, Pato, Michele T., Posthuma, Danielle, Ramos-Quiroga, Josep Antoni, Ribasés, Marta, Rietschel, Marcella, Rouleau, Guy A., Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Serretti, Alessandro, Smoller, Jordan W., Stefansson, Hreinn, Stefansson, Kari, Stordal, Eystein, Sullivan, Patrick F., Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Werge, Thomas, Nurnberger, John I., Wray, Naomi R., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Edenberg, Howard J., Cichon, Sven, Ophoff, Roel A., Scott, Laura J., Andreassen, Ole A., Kelsoe, John and Sklar, Pamela 2019. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics 51 , pp. 793-803. 10.1038/s41588-019-0397-8
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Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Bracher-Smith, Matthew, Fitzpatrick, Harry, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, 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 Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05) , pp. 297-304. 10.1192/bjp.2018.301
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Eaton, Christopher ORCID: https://orcid.org/0000-0001-6739-1999, Thomas, Rhys ORCID: https://orcid.org/0000-0003-2062-8623, Hamandi, Khalid, Payne, Gareth, Kerr, Michael, Linden, David, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Cunningham, Adam, Bartsch, Ullrich, Struik, Siske and van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2019. Epilepsy and seizures in young people with 22q11.2 deletion syndrome: prevalence and links with other neurodevelopmental disorders. Epilepsia 60 (5) , pp. 818-829. 10.1111/epi.14722
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Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas M., Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Rajagopal, Veera M., Als, Thomas D., Tan Hoang, Hoang T., Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Demontis, Ditte, Borglum, Anders, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Sullivan, Patrick, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Devlin, Bernie, Sieberts, Solveig K., Cox, Nancy J., Kyung Im, Hae, Sklar, Pamela, Ayumi Stahl, Eli A., The Schizophrenia Working Group of the Psychiatric Genomics Cons and iPSYCH-GEMS Schizophrenia Working Group 2019. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics 51 , pp. 659-674. 10.1038/s41588-019-0364-4
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Kendall, Kimberley M ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Bracher-Smith, Matthew, Legge, Sophie, Riglin, Lucy, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, 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 ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 2019. Association of rare copy number variants with risk of depression. JAMA Psychiatry 76 (8) , pp. 818-825. 10.1001/jamapsychiatry.2019.0566
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