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Number of items: 1091.

Moreau, Clara A., Harvey, Annabelle, Kumar, Kuldeep, Huguet, Guillaume, Urchs, Sebastian G.W., Douard, Elise A., Schultz, Laura M., Sharmarke, Hanad, Jizi, Khadije, Martin, Charles-Olivier, Younis, Nadine, Tamer, Petra, Rolland, Thomas, Martineau, Jean-Louis, Orban, Pierre, Silva, Ana Isabel ORCID: https://orcid.org/0000-0002-1184-4909, Hall, Jeremy, 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, Labbe, Aurelie, Lippé, Sarah, Bearden, Carrie E., Almasy, Laura, Glahn, David C., Thompson, Paul M., Bourgeron, Thomas, Bellec, Pierre and Jacquemont, Sebastien 2023. Genetic heterogeneity shapes brain connectivity in psychiatry. Biological Psychiatry 93 (1) , pp. 45-58. 10.1016/j.biopsych.2022.08.024

Kappel, Djenifer B., Legge, Sophie E., Hubbard, Leon, Willcocks, Isabella R., O'Connell, Kevin S., Smith, Robert L., Molden, Espen, Andreassen, Ole A., King, Adrian, Jansen, John, Helthuis, Marinka, 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 Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590 2023. Genomic stratification of clozapine prescription patterns using schizophrenia polygenic scores. Biological Psychiatry 93 , pp. 149-156. 10.1016/j.biopsych.2022.07.014
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Wolstencroft, Jeanne, Srinivasan, Ramya, 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, IMAGINE Consortium, Raymond, F. Lucy and Skuse, David 2023. Mental health impact of autism on families of children with intellectual and developmental disabilities of genetic origin. JCPP Advances , e12128. 10.1002/jcv2.12128
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Chawner, Samuel J. R. A., Evans, Alexandra ORCID: https://orcid.org/0000-0002-7718-4413, IMAGINE-ID consortium, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, 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 2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13 , 7. 10.1038/s41398-022-02296-z
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Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Kappel, Djenifer, Roberts, Milly, Tipple, Francesca, Shitomi-Jones, Lisa, 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 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2022. Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: A longitudinal analysis and GWAS using clinical monitoring data from the UK. The Lancet Psychiatry
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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 2022. Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance. Biological Psychiatry: Global Open Science
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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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Woolway, Grace, Smart, Sophie ORCID: https://orcid.org/0000-0002-6709-5425, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Lloyd, Jennifer, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 and Legge, Sophie 2022. Schizophrenia polygenic risk and experiences of childhood adversity: a systematic review and meta-analysis. Schizophrenia Bulletin 48 (5) , pp. 967-980. 10.1093/schbul/sbac049
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Liu, Dongjing, Meyer, Dara, Fennessy, Brian, Feng, Claudia, Cheng, Esther, Johnson, Jessica S., Park, You Jeong, Rieder, Marysia-Kolbe, Ascolillo, Steven, de Pins, Agathe, Dobbyn, Amanda, Lebovitch, Dannielle, Moya, Emily, Nguyen, Tan-Hoang, Wilkins, Lillian, Hassan, Arsalan, Burdick, Katherine E., Buxbaum, Joseph D., Domenici, Enrico, Frangou, Sophia, Hartmann, Annette M., Malhotra, Dheeraj, Pato, Carlos N., Pato, Michele T., Ressler, Kerry, Roussos, Panos, Rujescu, Dan, Arango, Celso, Bertolino, Alessandro, Blasi, Giuseppe, Bocchio-Chiavetto, Luisella, Campion, Dominique, Carr, Vaughan, Fullerton, Janice M., Gennarelli, Massimo, Gonzalez-Penas, Javier, Levinson, Douglas F., Mowry, Bryan, Nimgaokar, Vishwajit L., Pergola, Guilio, Rampino, Antonio, Cervilla, Jorge A., Rivera, Margarita, Schwab, Sibylle, Wildenauer, Dieter B., Daly, Mark, Neale, Benjamin, Singh, Tarjinder, 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, Ayub, Muhammad, Malhotra, Anil K., Lencz, Todd, Sullivan, Patrick F., Sklar, Pamela, Stahl, Eli A., Huckins, Laura M. and Charney, Alexander W. 2022. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature Genetics
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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 2022. Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions. Brain 10.1093/brain/awac315
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Chawner, Samuel and Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 2022. Autism: a model of neurodevelopmental diversity informed by genomics. Frontiers in Psychiatry 13 , 981691. 10.3389/fpsyt.2022.981691
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Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Wynn, Sarah, Ford, Tamsin, Baker, Kate, Chawner, Samuel J. R. A., 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, Skuse, David, Raymond, F. Lucy, Wolstencroft, Jeanne, Wicks, Francesca, Srinivasan, Ramya, Erwood, Marie, Lafont, Amy, Timur, Husne, Ye, Zheng, Walker, Susan, Printzlau, Frida, Juj, Manoj, Davies, Sarah, Denyer, Hayley, Watkins, Alice, Kerry, Eleanor, Coscini, Nadia, Fatih, Nasrtullah, Lucock, Anna, Denaxas, Spiros, Mandy, William, Walker, Neil, Wallwork, Sarah, Dewhurst, Eleanor, Cuthbert, Andrew, Challenger, Aimee, Andrews, Sophie, Holmans, Peter, Bowen, Samantha, Bradley, Karen, Birch, Philippa, Tong, Molly, Lewis, Nicola, Ray, Sinead, Sopp, Matthew, Moss, Hayley, Wynn, Sarah, Searle, Beverley, Robertson, Lisa, Berg, Jonathan, Lampe, Anne, Joss, Shelagh, Brennan, Paul, Kraus, Alison, Lahiri, Nayana, Weber, Astrid, Rawson, Myfanwy, Johnson, Diana, Vasudevan, Pradeep, Harrison, Rachel, Williams, Denise, Maher, Eamonn, Kini, Usha, Van Dijk, Fleur, Clowes, Virginia, Gurasashvilli, Jana, Mansour, Sahar, Holder-Espinasse, Muriel, Watford, Amy, Rankin, Julia, Baralle, Diana, Procter, Annie, Ford, Tamsin, Baker, Kate, Chawner, Samuel, Hall, Jeremy, Van den Bree, Marianne B. M., Owen, Michael J., Skuse, David and Raymond, F. Lucy 2022. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study. The Lancet Psychiatry 9 (9) , pp. 715-724. 10.1016/S2215-0366(22)00207-3
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Bracher-Smith, Matthew, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2022. Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK Biobank. Schizophrenia Research 246 , pp. 156-164. 10.1016/j.schres.2022.06.006
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Richards, Alexander, Cardno, Alastair, Harold, Gordon, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, Gordon-Smith, Katherine, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Sellers, Ruth, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2022. Genetic liabilities differentiating bipolar disorder, schizophrenia and major depression and phenotypic heterogeneity in bipolar disorder. JAMA Psychiatry 79 (10) , pp. 1032-1039. 10.1001/jamapsychiatry.2022.2594
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Donnelly, Nicholas A., Bartsch, Ullrich, Moulding, Hayley A. ORCID: https://orcid.org/0000-0002-1277-4404, Eaton, Christopher ORCID: https://orcid.org/0000-0001-6739-1999, Marston, Hugh, Hall, Jessica H., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, 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 Jones, Matt W. 2022. Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms. eLife 11 , e75482. 10.7554/elife.75482
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Creeth, Hugo D. J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Legge, Sophie E., Dennison, Charlotte A., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2022. Ultrarare coding variants and cognitive function in schizophrenia. JAMA Psychiatry 79 (10) , pp. 963-970. 10.1001/jamapsychiatry.2022.2289
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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, Lancaster, T. M. ORCID: https://orcid.org/0000-0003-1322-2449, Tansey, K. E, Singh, K. D ORCID: https://orcid.org/0000-0002-3094-2475, Holmans, P. ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, A. ORCID: https://orcid.org/0000-0002-2137-0452, Davey Smith, G., Zammit, S. ORCID: https://orcid.org/0000-0002-2647-9211, Hall, J. 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, Jones, D. K. ORCID: https://orcid.org/0000-0003-4409-8049 and Linden, D. E ORCID: https://orcid.org/0000-0002-5638-9292 2022. Genetic risk for schizophrenia is associated with increased proportion of indirect connections in brain networks revealed by a semi-metric analysis: evidence from population sample stratified for polygenic risk. Cerebral Cortex 10.1093/cercor/bhac256
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Fiksinski, Ania M., Bearden, Carrie E., Bassett, Anne S., Kahn, René S., Zinkstok, Janneke R., Hooper, Stephen R., Tempelaar, Wanda, McDonald-McGinn, Donna, Swillen, Ann, Emanuel, Beverly, Morrow, Bernice, Gur, Raquel, Chow, Eva, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Vermeesch, Joris, Warren, Stephen, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, van Amelsvoort, Therese, Eliez, Stephan, Gothelf, Doron, Arango, Celso, Kates, Wendy, Simon, Tony, Murphy, Kieran, Repetto, Gabriela, Suner, Damian Heine, Vicari, Stefano, Cubells, Joseph, Armando, Marco, Philip, Nicole, Campbell, Linda, Garcia-Minaur, Sixto, Schneider, Maude, Shashi, Vandana, Vorstman, Jacob and Breetvelt, Elemi J. 2022. A normative chart for cognitive development in a genetically selected population. Neuropsychopharmacology 47 (7) , 1379–1386. 10.1038/s41386-021-00988-6

Palmer, Duncan, Howrigan, Daniel, Chapman, Sinead, Adolfsson, Rolf, Bass, Nick, Blackwood, Douglas, Boks, Marco, Chen, Chia-Yen, Churchhouse, Claire, Corvin, Aiden, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Curtis, David, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Dickerson, Faith, Freimer, Nelson, Goes, Fernando, Jia, Xiaoming, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889, Jonsson, Lina, Kahn, Rene, Landen, Mikael, Locke, Adam, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Ophoff, Roel, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Pedersen, Nancy, Posthuma, Danielle, Reif, Andreas, Risch, Neil, Schaefer, Catherine, Scott, Laura, Singh, Tarjinder, Smoller, Jordan, Solomonson, Matthew, St Clair, David, Stahl, Eli, Vreeker, Annabel, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Wang, Weiqing, Watts, Nicholas, Yolken, Robert, Zandi, Peter and Neale, Benjamin 2022. Exome sequencing in bipolar disorder reveals AKAP11 as a risk gene shared with schizophrenia. Nature Genetics 10.1038/s41588-022-01034-x
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Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Legge, Sophie 2022. The nature of schizophrenia: as broad as it is long. Schizophrenia Research 242 , pp. 109-112. 10.1016/j.schres.2021.10.012
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Bellenguez, Céline, Küçükali, Fahri, Jansen, Iris E., Kleineidam, Luca, Moreno-Grau, Sonia, Amin, Najaf, Naj, Adam C., Campos-Martin, Rafael, Grenier-Boley, Benjamin, Andrade, Victor, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Boland, Anne, Damotte, Vincent, van der Lee, Sven J., Costa, Marcos R., Kuulasmaa, Teemu, Yang, Qiong, de Rojas, Itziar, Bis, Joshua C., Yaqub, Amber, Prokic, Ivana, 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., Tsolaki, Anthoula, Antúnez, Carmen, Appollonio, Ildebrando, Arcaro, Marina, Archetti, Silvana, Pastor, Alfonso Arias, Arosio, Beatrice, Athanasiu, Lavinia, Bailly, Henri, Banaj, Nerisa, Baquero, Miquel, Barral, Sandra, Beiser, Alexa, Pastor, Ana Belén, Below, Jennifer E., Benchek, Penelope, Benussi, Luisa, Berr, Claudine, Besse, Céline, Bessi, Valentina, Binetti, Giuliano, Bizarro, Alessandra, Blesa, Rafael, Boada, Mercè, Boerwinkle, Eric, Borroni, Barbara, Boschi, Silvia, Bossù, Paola, Bråthen, Geir, Bressler, Jan, Bresner, Catherine, Brodaty, Henry, Brookes, Keeley J., Brusco, Luis Ignacio, Buiza-Rueda, Dolores, Bûrger, Katharina, Burholt, Vanessa, Bush, William S., Calero, Miguel, Cantwell, Laura B., Chene, Geneviève, Chung, Jaeyoon, Cuccaro, Michael L., Carracedo, Ángel, Cecchetti, Roberta, Cervera-Carles, Laura, Charbonnier, Camille, Chen, Hung-Hsin, Chillotti, Caterina, Ciccone, Simona, Claassen, Jurgen A. H. R., 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, de Paiva Lopes, Katia, de Witte, Lot D., Debette, Stéphanie, Deckert, Jürgen, del Ser, Teodoro, Denning, Nicola, DeStefano, Anita, Dichgans, Martin, Diehl-Schmid, Janine, Diez-Fairen, Mónica, Rossi, Paolo Dionigi, Djurovic, Srdjan, Duron, Emmanuelle, Düzel, Emrah, Dufouil, Carole, Eiriksdottir, Gudny, Engelborghs, Sebastiaan, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Espinosa, Ana, Ewers, Michael, Faber, Kelley M., Fabrizio, Tagliavini, Nielsen, Sune Fallgaard, Fardo, David W., Farotti, Lucia, Fenoglio, Chiara, Fernández-Fuertes, Marta, Ferrari, Raffaele, Ferreira, Catarina B., Ferri, Evelyn, Fin, Bertrand, Fischer, Peter, Fladby, Tormod, Fließbach, Klaus, Fongang, Bernard, Fornage, Myriam, Fortea, Juan, Foroud, Tatiana M., Fostinelli, Silvia, Fox, Nick C., Franco-Macías, Emlio, Bullido, María J., Frank-García, Ana, Froelich, Lutz, Fulton-Howard, Brian, Galimberti, Daniela, García-Alberca, Jose Maria, García-González, Pablo, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Ghidoni, Roberta, Giegling, Ina, Giorgio, Giaccone, Goate, Alison M., Goldhardt, Oliver, Gomez-Fonseca, Duber, González-Pérez, Antonio, Graff, Caroline, Grande, Giulia, Green, Emma, Grimmer, Timo, Grünblatt, Edna, Grunin, Michelle, Gudnason, Vilmundur, Guetta-Baranes, Tamar, Haapasalo, Annakaisa, Hadjigeorgiou, Georgios, Haines, Jonathan L., Hamilton-Nelson, Kara L., 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, Vilas, Raquel Huerto, Hulsman, Marc, Humphrey, Jack, Biessels, Geert Jan, Jian, Xueqiu, Johansson, Charlotte, Jun, Gyungah R., Kastumata, Yuriko, Kauwe, John, Kehoe, Patrick G., Kilander, Lena, Ståhlbom, Anne Kinhult, Kivipelto, Miia, Koivisto, Anne, Kornhuber, Johannes, Kosmidis, Mary H., Kukull, Walter A., Kuksa, Pavel P., Kunkle, Brian W., Kuzma, Amanda B., Lage, Carmen, Laukka, Erika J., Launer, Lenore, Lauria, Alessandra, Lee, Chien-Yueh, Lehtisalo, Jenni, Lerch, Ondrej, Lleó, Alberto, Longstreth, William, Lopez, Oscar, de Munain, Adolfo Lopez, Love, Seth, Löwemark, Malin, Luckcuck, Lauren, Lunetta, Kathryn L., Ma, Yiyi, Macías, Juan, MacLeod, Catherine A., Maier, Wolfgang, Mangialasche, Francesca, Spallazzi, Marco, Marquié, Marta, Marshall, Rachel, Martin, Eden R., Montes, Angel Martín, Rodríguez, Carmen Martínez, Masullo, Carlo, Mayeux, Richard, 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, Mosley, Thomas, Nöthen, Markus M., Muchnik, Carolina, Mukherjee, Shubhabrata, 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, Pasquier, Florence, Pastor, Pau, Peloso, Gina, Pérez-Cordón, Alba, Pérez-Tur, Jordi, Pericard, Pierre, Peters, Oliver, Pijnenburg, Yolande A. L., Pineda, Juan A., Piñol-Ripoll, Gerard, Pisanu, Claudia, Polak, Thomas, Popp, Julius, Posthuma, Danielle, Priller, Josef, Puerta, Raquel, Quenez, Olivier, Quintela, Inés, Thomassen, Jesper Qvist, Rábano, Alberto, Rainero, Innocenzo, Rajabli, Farid, Ramakers, Inez, Real, Luis M., Reinders, Marcel J. T., Reitz, Christiane, Reyes-Dumeyer, Dolly, Ridge, Perry, Riedel-Heller, Steffi, Riederer, Peter, Roberto, Natalia, Rodriguez-Rodriguez, Eloy, Rongve, Arvid, Allende, Irene Rosas, Rosende-Roca, Maitée, Royo, Jose Luis, Rubino, Elisa, Rujescu, Dan, Sáez, María Eugenia, Sakka, Paraskevi, Saltvedt, Ingvild, Sanabria, Ángela, Sánchez-Arjona, María Bernal, Sanchez-Garcia, Florentino, Juan, Pascual Sánchez, Sánchez-Valle, Raquel, Sando, Sigrid B., Sarnowski, Chloé, Satizabal, Claudia L., Scamosci, Michela, Scarmeas, Nikolaos, Scarpini, Elio, Scheltens, Philip, Scherbaum, Norbert, Scherer, Martin, Schmid, Matthias, Schneider, Anja, Schott, Jonathan M., Selbæk, Geir, Seripa, Davide, Serrano, Manuel, Sha, Jin, Shadrin, Alexey A., Skrobot, Olivia, Slifer, Susan, Snijders, Gijsje J. 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Arfan, de Mendonça, Alexandre, Hort, Jakub, Tsolaki, Magda, Pericak-Vance, Margaret A., Amouyel, Philippe, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Frikke-Schmidt, Ruth, Clarimon, Jordi, Deleuze, Jean-François, Rossi, Giacomina, Seshadri, Sudha, Andreassen, Ole A., Ingelsson, Martin, Hiltunen, Mikko, Sleegers, Kristel, Schellenberg, Gerard D., van Duijn, Cornelia M., Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, van der Flier, Wiesje M., Ruiz, Agustín, Ramirez, Alfredo and Lambert, Jean-Charles 2022. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics 54 (4) , pp. 412-436. 10.1038/s41588-022-01024-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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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 2022. Psychopathology in adults with copy number variants. Psychological Medicine 10.1017/S0033291721005201
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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, 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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Westacott, Laura J., Humby, Trevor ORCID: https://orcid.org/0000-0002-1840-1799, Haan, Niels, Brain, Sophie A., Bush, Emma-Louise, Toneva, Margarita, Baloc, Andreea-Ingrid, Moon, Anna L. ORCID: https://orcid.org/0000-0002-6587-4425, Reddaway, Jack, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Hughes, Timothy R. ORCID: https://orcid.org/0000-0003-2348-3490, Morgan, B. Paul ORCID: https://orcid.org/0000-0003-4075-7676, Gray, William P. ORCID: https://orcid.org/0000-0001-7595-8887 and Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124 2022. Complement C3 and C3aR mediate different aspects of emotional behaviours; relevance to risk for psychiatric disorder. Brain, Behavior, and Immunity 99 , pp. 70-82. 10.1016/j.bbi.2021.09.005
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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, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Dennison, Charlotte, 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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Creeth, Hugo D. J., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Legge, Sophie E., Dennison, Charlotte A., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2022. Ultra-rare coding variants and cognitive function in schizophrenia. JAMA Psychiatry

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 2022. Psychopathology in mothers of children with pathogenic copy number variants. Journal of Medical Genetics
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Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Knott, Sarah, Underwood, Jack ORCID: https://orcid.org/0000-0003-1731-6039, Hubbard, Leon, Agha, Sharifah, Bisson, Jonathan ORCID: https://orcid.org/0000-0001-5170-1243, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Chawner, Samuel, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Roberts, Neil, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2022. DRAGON-Data: A platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts. BJPsych Open
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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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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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Dennison, Charlotte, 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, 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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Mullins, Niamh, Forstner, Andreas J., O'Connell, Kevin S., Coombes, Brandon, Coleman, Jonathan R. 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ORCID: https://orcid.org/0000-0001-6845-7590, Perry, Amy, Pfennig, Andrea, Porichi, Evgenia, Potash, James B., Quested, Digby, Raj, Towfique, Rapaport, Mark H., DePaulo, J. Raymond, Regeer, Eline J., Rice, John P., Rivas, Fabio, Rivera, Margarita, Roth, Julian, Roussos, Panos, Ruderfer, Douglas M., Sánchez-Mora, Cristina, Schulte, Eva C., Senner, Fanny, Sharp, Sally, Shilling, Paul D., Sigurdsson, Engilbert, Sirignano, Lea, Slaney, Claire, Smeland, Olav B., Smith, Daniel J., Sobell, Janet L., Søholm Hansen, Christine, Soler Artigas, Maria, Spijker, Anne T., Stein, Dan J., Strauss, John S., Świątkowska, Beata, Terao, Chikashi, Thorgeirsson, Thorgeir E., Toma, Claudio, Tooney, Paul, Tsermpini, Evangelia-Eirini, Vawter, Marquis P., Vedder, Helmut, Walters, James T. R. 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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

Peterson, Roseann E., Bigdeli, Tim B., Ripke, Stephan, Bacanu, Silviu-Alin, Gejman, Pablo V., Levinson, Douglas F., Li, Qingqin S., Rujescu, Dan, Rietschel, Marcella, Weinberger, Daniel R., Straub, Richard E., 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, Mowry, Bryan J., Ophoff, Roel A., Andreassen, Ole A., Esko, Tõnu, Petryshen, Tracey L., Kendler, Kenneth S. and Fanous, Ayman H. 2021. Genome-wide analyses of smoking behaviors in schizophrenia: findings from the Psychiatric Genomics Consortium. Journal of Psychiatric Research 137 , pp. 215-225. 10.1016/j.jpsychires.2021.02.027
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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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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. 2021. 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 10.1038/s41380-021-01108-y
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Chilvers, Clair and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2021. Mental Health Research, shared goals. Journal of Mental Health 10.1080/09638237.2021.1898562
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Willcocks, Isabella, 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., 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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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, 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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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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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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Blake, Zeggini, Eleftheria, Zerwas, Stephanie, Zipfel, Stephan, Adams, Mark J., Andlauer, Till F.M., Berger, Klaus, Binder, Elisabeth B., Boomsma, Dorret I., Castelao, Enrique, Colodro-Conde, Lucía, Direk, Nese, Docherty, Anna R., Domenici, Enrico, Domschke, Katharina, Dunn, Erin C., Foo, Jerome C., de. Geus, E.J.C., Grabe, Hans J., Hamilton, Steven P., Horn, Carsten, Hottenga, Jouke-Jan, Howard, David, Ising, Marcus, Kloiber, Stefan, Levinson, Douglas F., Lewis, Glyn, Magnusson, Patrik K.E., Mbarek, Hamdi, Middeldorp, Christel M., Mostafavi, Sara, Nyholt, Dale R., Penninx, Brenda WJH., Peterson, Roseann E., Pistis, Giorgio, Porteous, David J., Preisig, Martin, Quiroz, Jorge A., Schaefer, Catherine, Schulte, Eva C., Shi, Jianxin, Smith, Daniel J., Thomson, Pippa A., Tiemeier, Henning, Uher, Rudolf, van der Auwera, Sandra, Weissman, Myrna M., Alexander, Madeline, Begemann, Martin, Bramon, Elvira, Buccola, Nancy G., Cairns, Murray J., Campion, Dominique, Carr, Vaughan J., Cloninger, C. Robert, Cohen, David, Collier, David A., Corvin, Aiden, DeLisi, Lynn E., Donohoe, Gary, Dudbridge, Frank, Duan, Jubao, Freedman, Robert, Gejman, Pablo V., Golimbet, Vera, Godard, Stephanie, Ehrenreich, Hannelore, Hartmann, Annette M., Henskens, Frans A., Ikeda, Masashi, Iwata, Nakao, Jablensky, Assen V., Joa, Inge, Jönsson, Erik G., Kelly, Brian J., Knight, Jo, Konte, Bettina, Laurent-Levinson, Claudine, Lee, Jimmy, Lencz, Todd, Lerer, Bernard, Loughland, Carmel M., Malhotra, Anil K., Mallet, Jacques, McDonald, Colm, Mitjans, Marina, Mowry, Bryan J., Murphy, Kieran C., Murray, Robin M., O'Neill, F. 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. Joseph, Black, Donald W., Brown, Lawrence W., Budman, Cathy, Cath, Danielle, Cheon, Keun-Ah, Ciullo, Valentina, Coffey, Barbara J., Cusi, Daniele, Davis, Lea K., Denys, Damiaan, Depienne, Christel, Dietrich, Andrea, Eapen, Valsamma, Falkai, Peter, Fernandez, Thomas V., Garcia-Delgar, Blanca, Geller, Daniel A., Gilbert, Donald L., Grados, Marco A., Greenberg, Erica, Grünblatt, Edna, Hagstrøm, Julie, Hanna, Gregory L., Hartmann, Andreas, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hong, Hyun Ju, Huang, Alden, Huyser, Chaim, Ibanez-Gomez, Laura, Khramtsova, Ekaterina A., Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Konstantinidis, Anastasios, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett L., Lochner, Christine, Ludolph, Andrea G., Madruga-Garrido, Marcos, Malaty, Irene, Maras, Athanasios, McCracken, James T., Meijer, Inge A., Mir, Pablo, Morer, Astrid, Müller-Vahl, Kirsten R., Münchau, Alexander, Murphy, Tara L., Naarden, Allan, Nagy, Peter, Nestadt, Gerald, Nestadt, Paul S., Nicolini, Humberto, Nurmi, Erika L., Okun, Michael S., Paschou, Peristera, Piras, Fabrizio, Piras, Federica, Pittenger, Christopher, Plessen, Kerstin J., Richter, Margaret A., Rizzo, Renata, Robertson, Mary, Roessner, Veit, Ruhrmann, Stephan, Samuels, Jack F., Sandor, Paul, Schlögelhofer, Monika, Shin, Eun-Young, Singer, Harvey, Song, Dong-Ho, Song, Jungeun, Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Stuhrmann, Manfred, Tarnok, Zsanett, Tischfield, Jay A., Tübing, Jennifer, Visscher, Frank, Vulink, Nienke, Wagner, Michael, Walitza, Susanne, Wanderer, Sina, Woods, Martin, Worbe, Yulia, Zai, Gwyneth, Zinner, Samuel H., Sullivan, Patrick F., Franke, Barbara, Daly, Mark J., Bulik, Cynthia M., Lewis, Cathryn M., McIntosh, Andrew M., O'Donovan, Michael C. 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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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Reghan, Franklin, Christopher S., Futema, Marta, Gallagher, Louise, Geihs, Matthias, Geschwind, Daniel, Griffin, Heather, Guo, Xueqin, Guo, Xiaosen, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Howie, Bryan, Huang, Liren, Hubbard, Tim, Humphries, Steve E., Hurles, Matthew E., Hysi, Pirro, Jackson, David K., Jamshidi, Yalda, Jing, Tian, Joyce, Chris, Kaye, Jane, Keane, Thomas, Keogh, Julia, Kemp, John, Kennedy, Karen, Kolb-Kokocinski, Anja, Lachance, Genevieve, Langford, Cordelia, Lawson, Daniel, Lee, Irene, Lek, Monkol, Liang, Jieqin, Lin, Hong, Li, Rui, Li, Yingrui, Liu, Ryan, Lönnqvist, Jouko, Lopes, Margarida, Iotchkova, Valentina, MacArthur, Daniel, Marchini, Jonathan, Maslen, John, Massimo, Mangino, Mathieson, Iain, Marenne, Gaëlle, McGuffin, Peter, McIntosh, Andrew, McKechanie, Andrew G., McQuillin, Andrew, Metrustry, Sarah, Mitchison, Hannah, Moayyeri, Alireza, Morris, James, Muntoni, Francesco, Northstone, Kate, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Onoufriadis, Alexandros, O'Rahilly, Stephen, Oualkacha, Karim, Owen, Michael J. 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Lucy, Rehnstrom, Karola, Reid, Evan, Rhodes, Christopher J., Richards, Michael, Richardson, Sylvia, Richter, Alex, Roberts, Irene, Rondina, Matthew, Rosser, Elisabeth, Roughley, Catherine, Rue-Albrecht, Kevin, Samarghitean, Crina, Sanchis-Juan, Alba, Sandford, Richard, Santra, Saikat, Sargur, Ravishankar, Savic, Sinisa, Schulman, Sol, Schulze, Harald, Scott, Richard, Scully, Marie, Seneviratne, Suranjith, Sewell, Carrock, Shamardina, Olga, Shipley, Debbie, Simeoni, Ilenia, Sivapalaratnam, Suthesh, Smith, Kenneth, Sohal, Aman, Southgate, Laura, Staines, Simon, Staples, Emily, Stauss, Hans, Stein, Penelope, Stephens, Jonathan, Stirrups, Kathleen, Stock, Sophie, Suntharalingam, Jay, Tait, R. Campbell, Talks, Kate, Tan, Yvonne, Thachil, Jecko, Thaventhiran, James, Thomas, Ellen, Thomas, Moira, Thompson, Dorothy, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Toh, Cheng-Hock, Toshner, Mark, Treacy, Carmen, Trembath, Richard, Tuna, Salih, Turek, Wojciech, Turro, Ernest, Van Geet, Chris, Veltman, Marijke, Vogt, Julie, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Warner, Timothy Q., Wassmer, Evangeline, Watkins, Hugh, Webster, Andrew, Welch, Steve, Westbury, Sarah, Wharton, John, Whitehorn, Deborah, Wilkins, Martin, Willcocks, Lisa, Williamson, Catherine, Woods, Geoffrey, Wort, John, Yeatman, Nigel, Yong, Patrick, Young, Tim and Yu, Ping 2019. Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia. American Journal of Human Genetics 104 (5) , pp. 948-956. 10.1016/j.ajhg.2019.03.005
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Silva, Ana I. ORCID: https://orcid.org/0000-0002-1184-4909, Ulfarsson, Magnus O., Stefansson, Hreinn, Gustafsson, Omar, Walters, G. Bragi, Linden, David E.J. ORCID: https://orcid.org/0000-0002-5638-9292, Wilkinson, Lawrence S. ORCID: https://orcid.org/0000-0002-9337-6124, Drakesmith, Mark ORCID: https://orcid.org/0000-0001-8574-9560, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 and Stefansson, Kari 2019. Reciprocal white matter changes associated with copy number variation at 15q11.2 BP1-BP2: A diffusion tensor imaging study. Biological Psychiatry 85 (7) , pp. 563-572. 10.1016/j.biopsych.2018.11.004
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Harold, Denise, Connolly, Siobhan, Riley, Brien P., Kendler, Kenneth S., McCarthy, Shane E., McCombie, William R., Richards, Alex, 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 ORCID: https://orcid.org/0000-0002-6980-4053, Donohoe, Gary, Gill, Michael, Corvin, Aiden, Morris, Derek W. and Hopkins, Lucinda 2019. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 (3) , pp. 223-231. 10.1002/ajmg.b.32716
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Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Helthuis, Marinka, Jansen, John A., Jollie, Karel, Knapper, Steven ORCID: https://orcid.org/0000-0002-6405-4441, MacCabe, James H., Rujescu, Dan, Collier, David A., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2019. A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia. Molecular Psychiatry 24 , pp. 328-337. 10.1038/s41380-018-0335-7
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ORCID: https://orcid.org/0000-0002-6600-6507, Jin, Lee-Way, Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Real, Luis M., Jun, Gyungah R., Baldwin, Clinton T., Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Karydas, Anna, Russo, Giancarlo, Kaye, Jeffrey A., Kim, Ronald, Jessen, Frank, Kowall, Neil W., Vellas, Bruno, Kramer, Joel H., Vardy, Emma, LaFerla, Frank M., Jöckel, Karl-Heinz, Lah, James J., Dichgans, Martin, Leverenz, James B., Mann, David, Levey, Allan I., Pickering-Brown, Stuart, Lieberman, Andrew P., Klopp, Norman, Lunetta, Kathryn L., Wichmann, H-Erich, Lyketsos, Constantine G., Morgan, Kevin, Marson, Daniel C., Brown, Kristelle, Martiniuk, Frank, Medway, Christopher, Mash, Deborah C., Nöthen, Markus M., Masliah, Eliezer, Hooper, Nigel M., McCormick, Wayne C., Daniele, Antonio, McCurry, Susan M., Bayer, Antony ORCID: https://orcid.org/0000-0002-7514-248X, McDavid, Andrew N., Gallacher, John ORCID: https://orcid.org/0000-0002-2394-5299, McKee, Ann C., van den Bussche, Hendrik, Mesulam, Marsel, Brayne, Carol, Miller, Bruce L., Riedel-Heller, Steffi, Miller, Carol A., Miller, Joshua W., Al-Chalabi, Ammar, Morris, John C., Shaw, Christopher E., Myers, Amanda J., Wiltfang, Jens, O'Bryant, Sid, Olichney, John M., Alvarez, Victoria, Parisi, Joseph E., Singleton, Andrew B., Paulson, Henry L., Collinge, John, Perry, William R., Mead, Simon, Peskind, Elaine, Cribbs, David H., Rossor, Martin, Pierce, Aimee, Ryan, Natalie S., Poon, Wayne W., Nacmias, Benedetta, Potter, Huntington, Sorbi, Sandro, Quinn, Joseph F., Sacchinelli, Eleonora, Raj, Ashok, Spalletta, Gianfranco, Raskind, Murray, Caltagirone, Carlo, Bossù, Paola, Orfei, Maria Donata, Reisberg, Barry, Clarke, Robert, Reitz, Christiane, Smith, A David, Ringman, John M., Warden, Donald, Roberson, Erik D., Wilcock, Gordon, Rogaeva, Ekaterina, Bruni, Amalia Cecilia, Rosen, Howard J., Gallo, Maura, Rosenberg, Roger N., Ben-Shlomo, Yoav, Sager, Mark A., Mecocci, Patrizia, Saykin, Andrew J., Pastor, Pau, Cuccaro, Michael L., Vance, Jeffery M., Schneider, Julie A., Schneider, Lori S., Slifer, Susan, Seeley, William W., Smith, Amanda G., Sonnen, Joshua A., Spina, Salvatore, Stern, Robert A., Swerdlow, Russell H., Tang, Mitchell, Tanzi, Rudolph E., Trojanowski, John Q., Troncoso, Juan C., Van Deerlin, Vivianna M., Van Eldik, Linda J., Vinters, Harry V., Vonsattel, Jean Paul, Weintraub, Sandra, Welsh-Bohmer, Kathleen A., Wilhelmsen, Kirk C., Williamson, Jennifer, Wingo, Thomas S., Woltjer, Randall L., Wright, Clinton B., Yu, Chang-En, Yu, Lei, Saba, Yasaman, Pilotto, Alberto, Bullido, Maria J., Peters, Oliver, Crane, Paul K., Bennett, David, Bosco, Paola, Coto, Eliecer, Boccardi, Virginia, De Jager, Phil L., Lleo, Alberto, Warner, Nick, Lopez, Oscar L., Ingelsson, Martin, Deloukas, Panagiotis, Cruchaga, Carlos, Graff, Caroline, Gwilliam, Rhian, Fornage, Myriam, Goate, Alison M., Sanchez-Juan, Pascual, Kehoe, Patrick G., Amin, Najaf, Ertekin-Taner, Nilifur, Berr, Claudine, Debette, Stéphanie, Love, Seth, Launer, Lenore J., Younkin, Steven G., Dartigues, Jean-Francois, Corcoran, Chris, Ikram, M. Arfan, Dickson, Dennis W., Nicolas, Gael, Campion, Dominique, Tschanz, JoAnn, Schmidt, Helena, Hakonarson, Hakon, Clarimon, Jordi, Munger, Ron, Schmidt, Reinhold, Farrer, Lindsay A., Van Broeckhoven, Christine, O'Donovan, Michael C ORCID: https://orcid.org/0000-0001-7073-2379, DeStefano, Anita L., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Haines, Jonathan L., Deleuze, Jean-Francois, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, Gudnason, Vilmundur, Mayeux, Richard, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Psaty, Bruce M., Ramirez, Alfredo, Wang, Li-San, Ruiz, Agustin, van Duijn, Cornelia M., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Seshadri, Sudha, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Amouyel, Phillippe, Schellenberg, Gerard D., Lambert, Jean-Charles, Pericak-Vance, Margaret A., Alzheimer Disease Genetics Consortium (ADGC), The European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Con and Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consort 2019. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics 51 (3) , pp. 414-430. 10.1038/s41588-019-0358-2
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Drakesmith, Mark ORCID: https://orcid.org/0000-0001-8574-9560, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Jones, Derek K. ORCID: https://orcid.org/0000-0003-4409-8049 and Linden, David E. J. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) , 102. 10.1038/s41398-019-0440-7
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Chawner, Samuel J.R.A., Doherty, Joanne L., Maillard, Anne M., Jacquemont, Sbastien, Chung, Wendy K., Green-Snyder, LeeAnne, Bernier, Raphael A., Goin-Kochel, Robin P., Hanson, Ellen, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Linden, Stefanie C. ORCID: https://orcid.org/0000-0002-5638-9292, Raymond, F. Lucy, Skuse, David, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2019. Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry 10.1038/s41398-018-0339-8
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Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Bracher-Smith, Matthew, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2019. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank. Journal of Molecular Psychiatry , -. 10.1038/s41380-018-0328-6
Item availability restricted.
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Vivian-Griffiths, Timothy, Baker, Emily, Schmidt, Karl M. ORCID: https://orcid.org/0000-0002-0227-3024, Bracher-Smith, Matthew, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Artemiou, Andreas ORCID: https://orcid.org/0000-0002-7501-4090, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2019. Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 (1) , pp. 80-85. 10.1002/ajmg.b.32705
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Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Byrne, Enda, Trzaskowski, Maciej, Sidorenko, Julia, Kemper, Kathryn, McGrath, John J., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Wray, Naomi R. 2019. Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Translational Psychiatry 10 , 51. 10.1038/s41398-020-0688-y
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Brieva, Jorge, Lepore, Natasha, Romero, Eduardo, Cunningham, Adam C., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Schmitt, Eric, Gur, Raquel E., Roalf, David, Ruparel, Kosha, McDonald-McGinn, Donna, Emanuel, Beverly, Craig, Michael, Murphy, Declan, Murphy, Clodaph, Gudbrandsen, Maria, Daly, Eileen, Kates, Wendy R., Bakker, Geor, van Amelsvoort, Therese, Jonas, Rachel, Hansen, Laura, Lin, Amy, Nir, Talia, Sun, Daqiang V., Kothapalli, Deydeep, Ching, Christopher R., Thompson, Paul M., Bearden, Carrie E., Jahanshad, Neda, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Linden, David E., Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Doherty, Joanne, Durdle, Courtney A., McCabe, Kathryn L., Campbell, Linda E., Fremont, Wanda, Antshel, Kevin M., Jalbrzikowski, Maria, Vajdi, Ariana V., Kushan, Leila V., Forsyth, Jennifer K. and Villalón-Reina, Julio 2018. Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome. Presented at: 14th International Symposium on Medical Information Processing and Analysis,, Mazatlán, Mexico, 24-26 October 2018. Published in: Romero, Eduardo, Lepore, Natasha and Brieva, Jorge eds. 14th International Symposium on Medical Information Processing and Analysis. Proceedings of SPIE , vol.10975 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788

Arnau-Soler, Aleix, Adams, Mark J., Hayward, Caroline, Thomson, Pippa A., Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, M J ORCID: https://orcid.org/0000-0003-4798-0862, Tansey, Katherine and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2018. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PLoS ONE 13 (12) , e0209160. 10.1371/journal.pone.0209160
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Li, Mingfeng, Santpere, Gabriel, Imamura Kawasawa, Yuka, Evgrafov, Oleg V., Gulden, Forrest O., Pochareddy, Sirisha, Sunkin, Susan M., Li, Zhen, Shin, Yurae, Zhu, Ying, Sousa, André M. M., Werling, Donna M., Kitchen, Robert R., Kang, Hyo Jung, Pletikos, Mihovil, Choi, Jinmyung, Muchnik, Sydney, Xu, Xuming, Wang, Daifeng, Lorente-Galdos, Belen, Liu, Shuang, Giusti-Rodríguez, Paola, Won, Hyejung, de Leeuw, Christiaan A., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Hu, Ming, Jin, Fulai, Li, Yun, 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, Posthuma, Danielle, Reimers, Mark A., Levitt, Pat, Weinberger, Daniel R., Hyde, Thomas M., Kleinman, Joel E., Geschwind, Daniel H., Hawrylycz, Michael J., State, Matthew W., Sanders, Stephan J., Sullivan, Patrick F., Gerstein, Mark B., Lein, Ed S., Knowles, James A. and Sestan, Nenad 2018. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science 362 (6420) , eaat7615. 10.1126/science.aat7615
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Owen, David ORCID: https://orcid.org/0000-0003-4798-0862, Bracher Smith, Mathew, Kendall, Kimberley M. ORCID: https://orcid.org/0000-0002-6755-6121, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Einon, Mark ORCID: https://orcid.org/0000-0003-3797-7352, 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 Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2018. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics 19 (1) , 867. 10.1186/s12864-018-5292-7
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O'Brien, Heath E. ORCID: https://orcid.org/0000-0003-2309-8736, Hannon, Eilis, Hill, Matthew J. ORCID: https://orcid.org/0000-0001-6776-8709, Toste, Carolina C., Robertson, Matthew J., Morgan, Joanne E., McLaughlin, Gemma, Lewis, Cathryn M., Schalkwyk, Leonard C., Hall, Lynsey S., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Mill, Jonathan and Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X 2018. Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders. Genome Biology 19 , 194. 10.1186/s13059-018-1567-1
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Chawner, Samuel J.R.A., Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Doherty, Joanne L., Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2018. The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome. Journal of Psychiatric Research 109 , pp. 10-17. 10.1016/j.jpsychires.2018.11.002
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Zhao, Yingjie, Guo, Tingwei, Fiksinski, Ania, Breetvelt, Elemi, McDonald-McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, van Amelsvoort, Thérèse A., Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Bearden, Carrie E., Ornstein, Claudia, Pontillo, Maria, Buzzanca, Antonino, Vicari, Stefano, Armando, Marco, Murphy, Kieran C., Murphy, Clodagh, Garcia-Minaur, Sixto, Philip, Nicole, Campbell, Linda, Morey-Cañellas, Jaume, Raventos, Jasna, Rosell, Jordi, Heine-Suner, Damian, Shprintzen, Robert J., Gur, Raquel E., Zackai, Elaine, Emanuel, Beverly S., Wang, Tao, Kates, Wendy R., Bassett, Anne S., Vorstman, Jacob A. S., Morrow, Bernice E., International 22q11.2, Brain and Behavior Consortium and Chawner, Samuel 2018. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics Part A 176 (10) , pp. 2172-2181. 10.1002/ajmg.a.40359
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John, Ann, McGregor, Joanna, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Lee, Sze Chim, 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, Banos, Marcos Del Pozo, Berridge, Damon and Lloyd, Keith 2018. Premature mortality among people with severe mental illness - new evidence from linked primary care data. Schizophrenia Research 199 , pp. 154-162. 10.1016/j.schres.2018.04.009
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Jones, Hannah J., Heron, Jon, Hammerton, Gemma, Stochl, Jan, Jones, Peter B., Cannon, Mary, Smith, George Davey, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Lewis, Glyn, 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 ORCID: https://orcid.org/0000-0002-6980-4053 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2018. Investigating the genetic architecture of general and specific psychopathology in adolescence. Translational Psychiatry 8 (1) , 145. 10.1038/s41398-018-0204-9
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Donohoe, G., Holland, J., Mothersill, D., McCarthy-Jones, S., Cosgrove, D., Harold, D., Richards, A., Mantripragada, K. ORCID: https://orcid.org/0000-0003-2070-8105, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379, Gill, M., Corvin, A. and Morris, D. W. 2018. Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation. Psychological Medicine 48 (10) , pp. 1608-1615. 10.1017/S0033291717002987
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Guyatt, Anna L., Stergialouli, Evie, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Walters, James, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rodriguez, Santiago, Rai, Dheeraj and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2018. Association of copy number variation across the genome with neuropsychiatric traits in the general population. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (5) , pp. 489-502. 10.1002/ajmg.b.32637
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Skene, Nathan G., Bryois, Julien, Bakken, Trygve E., Breen, Gerome, Crowley, James J., Gaspar, Héléna A., Giusti-Rodriguez, Paola, Hodge, Rebecca D., Jeremy A., Miller, Muñoz-Manchado, Ana, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Ryge, Jesper, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Linnarsson, Sten, Lein, Ed S., Sullivan, Patrick F. and Hjerling-Leffler, Jens 2018. Genetic identification of brain cell types underlying schizophrenia. Nature Genetics 50 , pp. 825-833. 10.1038/s41588-018-0129-5
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Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K., Walters, Raymond K., Bras, Jose, Duncan, Laramie, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Falcone, Guido J., Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A., Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H., Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N., Reitz, Christiane, Goate, Alison M., Huentelman, Matthew J., Kamboh, M. Ilyas, Larson, Eric B., Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A., Farrer, Lindsay A., Barnes, Lisa L., Beach, Thomas G., Demirci, F. Yesim, Head, Elizabeth, Hulette, Christine M., Jicha, Gregory A., Kauwe, John S.K., Kaye, Jeffrey A., Leverenz, James B., Levey, Allan I., Lieberman, Andrew P., Pankratz, Vernon S., Poon, Wayne W., Quinn, Joseph F., Saykin, Andrew J., Schneider, Lon S., Smith, Amanda G., Sonnen, Joshua A., Stern, Robert A., Van Deerlin, Vivianna M., Van Eldik, Linda J., Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Russo, Giancarlo, Rubinsztein, David C., Bayer, Antony ORCID: https://orcid.org/0000-0002-7514-248X, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C., Hampel, Harald, Owen, Michael J. 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P., Helder, Sietske G., Ehrlich, Stefan, Herpertz-Dahlmann, Beate, Danner, Unna N., van Elburg, Annemarie A., Clementi, Maurizio, Forzan, Monica, Docampo, Elisa, Lissowska, Jolanta, Hauser, Joanna, Tortorella, Alfonso, Maj, Mario, Gonidakis, Fragiskos, Tziouvas, Konstantinos, Papezova, Hana, Yilmaz, Zeynep, Wagner, Gudrun, Cohen-Woods, Sarah, Herms, Stefan, Julià, Antonio, Rabionet, Raquel, Dick, Danielle M., Ripatti, Samuli, Andreassen, Ole A., Espeseth, Thomas, Lundervold, Astri J., Steen, Vidar M., Pinto, Dalila, Scherer, Stephen W., Aschauer, Harald, Schosser, Alexandra, Alfredsson, Lars, Padyukov, Leonid, Halmi, Katherine A., Mitchell, James, Strober, Michael, Bergen, Andrew W., Kaye, Walter, Szatkiewicz, Jin Peng, Cormand, Bru, Ramos-Quiroga, Josep Antoni, Sánchez-Mora, Cristina, Ribasés, Marta, Casas, Miguel, Hervas, Amaia, Arranz, Maria Jesús, Haavik, Jan, Zayats, Tetyana, Johansson, Stefan, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Dempfle, Astrid, Rothenberger, Aribert, Kuntsi, Jonna, Oades, Robert D., Banaschewski, Tobias, Franke, Barbara, Buitelaar, Jan K., Arias Vasquez, Alejandro, Doyle, Alysa E., Reif, Andreas, Lesch, Klaus-Peter, Freitag, Christine, Rivero, Olga, Palmason, Haukur, Romanos, Marcel, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Rietschel, Marcella, Witt, Stephanie H., Dalsgaard, Soeren, Børglum, Anders D., Waldman, Irwin, Wilmot, Beth, Molly, Nikolas, Bau, Claiton H.D., Crosbie, Jennifer, Schachar, Russell, Loo, Sandra K., McGough, James J., Grevet, Eugenio H., Medland, Sarah E., Robinson, Elise, Weiss, Lauren A., Bacchelli, Elena, Bailey, Anthony, Bal, Vanessa, Battaglia, Agatino, Betancur, Catalina, Bolton, Patrick, Cantor, Rita, Celestino-Soper, Patrícia, Dawson, Geraldine, De Rubeis, Silvia, Duque, Frederico, Green, Andrew, Klauck, Sabine M., Leboyer, Marion, Levitt, Pat, Maestrini, Elena, Mane, Shrikant, De-Luca, Daniel Moreno-, Parr, Jeremy, Regan, Regina, Reichenberg, Abraham, Sandin, Sven, Vorstman, Jacob, Wassink, Thomas, Wijsman, Ellen, Cook, Edwin, Santangelo, Susan, Delorme, Richard, Rogé, Bernadette, Magalhaes, Tiago, Arking, Dan, Schulze, Thomas G., Thompson, Robert C., Strohmaier, Jana, Matthews, Keith, Melle, Ingrid, Morris, Derek, Blackwood, Douglas, McIntosh, Andrew, Bergen, Sarah E, Schalling, Martin, Jamain, Stéphane, Maaser, Anna, Fischer, Sascha B., Reinbold, Céline S., Fullerton, Janice M., Guzman-Parra, José, Mayoral, Fermin, Schofield, Peter R., Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska, Schumacher, Johannes, Bauer, Michael, Mitchell, Philip B., Gershon, Elliot S., Rice, John, Potash, James B., Zandi, Peter P., Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Ferrier, I. 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