Browse by Current Cardiff authors

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., Owen, Michael J., O'Donovan, Michael C., 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

Dennison, Charlotte A., Legge, Sophie E., Bracher-Smith, Matthew, Menzies, Georgina, Escott-Price, Valentina, Smith, Daniel J., Doherty, Aiden R., Owen, Michael J., O'Donovan, Michael C. and Walters, James T. R. 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

Clifton, Nicholas E., Collado-Torres, Leonardo, Burke, Emily E., Pardinas, Antonio F., Harwood, Janet C., Di Florio, Arianna, Walters, James T. R., Owen, Michael J., O'Donovan, Michael C., Weinberger, Daniel R., Holmans, Peter A., Jaffe, Andrew E. and Hall, Jeremy 2021. Developmental profile of psychiatric risk associated with voltage-gated cation channel activity. Biological Psychiatry 10.1016/j.biopsych.2021.03.009

Tigaret, Cezar M., Tzu-Ching, E. Lin, Morrell, Edward R., Sykes, Lucy, Moon, Anna L., O'Donovan, Michael, Owen, Michael J., Wilkinson, Lawrence S., Jones, Matthew W., Thomas, Kerrie L. and Hall, Jeremy 2021. Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c. Molecular Psychiatry 10.1038/s41380-020-01001-0 Item availability restricted.

Cunningham, Adam, Hall, Jeremy, Owen, Michael and Van den Bree, Marianne 2021. Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants. Psychological Medicine 51 (2) , pp. 290-299. 10.1017/S0033291719003210

Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Champion, Sinead, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, Di Florio, Arianna, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O'Donovan, Michael, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P. and Scott, Laura J. 2021. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry 10.1038/s41380-020-01006-9

Owen, Michael J. and O'Donovan, Michael C. 2021. Large-scale genomics: a paradigm shift in psychiatry? Biological Psychiatry 89 , pp. 5-7. 10.1016/j.biopsych.2020.01.017

Chawner, Samuel, Doherty, Joanne L., Anney, Richard, 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, Owen, Michael J. and van den Bree, Marianne B.M. 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 Item availability restricted.

Willcocks, Isabella, Legge, Sophie, Nalmpanti, Mariana, Mazzeo, Lucy, King, Adrian, Jansen, John, Helthius, Marinka, Owen, Michael, O'Donovan, Michael, Walters, James and Pardinas, Antonio 2021. Clozapine metabolism is associated with absolute neutrophil count in individuals with treatment-resistant schizophrenia. Frontiers in Pharmacology Item availability restricted.

Dennison, Charlotte, Legge, Sophie, Hubbard, Leon, Lynham, Amy, Zammit, Stanley, Holmans, Peter, Cardno, Alastair, Owen, Michael, O'Donovan, Michael and Walters, James 2021. Risk factors, clinical features, and polygenic risk scores in schizophrenia and schizoaffective disorder depressive-type. Schizophrenia Bulletin Item availability restricted.

Sønderby, Ida E., Hall, Jeremy, Owen, Michael, Van Den Bree, Marianne, Linden, David, Silva, Ana 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

Davies, Robert, International 22q11.2, Brain and Behavior Consortium, Fiksinski, Ania M., Breetvelt, Elemi J., Williams, Nigel M., Hooper, Stephen R., Monfueuga, Thomas, Bassett, Anne S., Owen, Michal J., Gur, Raquel E., Morrow, Bernice E., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne, 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 Item availability restricted.

Hubbard, Leon, Rees, Elliott, Morris, Derek W., Lynham, Amy J., Richards, Alex L., Pardinas, Antonio F., Legge, Sophie E., Harold, Denise, Zammit, Stanley, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Donohoe, Gary, Kirov, George, Pocklington, Andrew and Walters, James T.R. 2020. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 10.1016/j.biopsych.2020.11.025 Item availability restricted.

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, Linden, David, Owen, Michael, 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

Kendall, Kimberley M., John, Ann, Lee, Sze Chim, Rees, Elliott, Pardiñas, Antonio F., Del Pozo Banos, Marcos, Owen, Michael J., O’Donovan, Michael C., Kirov, George, Lloyd, Keith, Jones, Ian, Legge, Sophie E. and Walters, James T. R. 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

Clifton, Nicholas, Rees, Elliott, Holmans, Peter, Pardiñas, Antonio, Harwood, Janet, Di Florio, Arianna, Kirov, George, Walters, James, O’Donovan, Michael, Owen, Michael, Hall, Jeremy and Pocklington, Andrew 2020. Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry 10.1038/s41380-020-00912-2

Legge, Sophie E., Christensen, Rune H., Petersen, Liselotte, Pardinas, Antonio F., Bracher-Smith, Matthew, Knapper, Steven, Bybjerg-Grauholm, Jonas, Baekvad-Hansen, Marie, Hougaard, David M., Werge, Thomas, Nordentoft, Merete, Mortensen, Preben Bo, Owen, Michael J., O'Donovan, Michael C., Benros, Michael E. and Walters, James T. R. 2020. The Duffy-null genotype and risk of infection. Human Molecular Genetics 29 (20) , pp. 3341-3349. 10.1093/hmg/ddaa208

Jones, Hannah J., Martin, David, Lewis, Sarah J., Davey Smith, George, O'Donovan, Michael C., Owen, Michael J., Walters, James T. R. and Zammit, Stanley 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

Dima, Diana C., Adams, Rachael, Linden, Stefanie C., Baird, Alister, Smith, Jacqueline, Foley, Sonya, Perry, Gavin, Routley, Bethany C., Magazzini, Lorenzo, Drakesmith, Mark, Williams, Nigel, Doherty, Joanne, van den Bree, Marianne B. M., Owen, Michael J., Hall, Jeremy, Linden, David E. J. and Singh, Krish D. 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

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., Linden, David E. J., Moss, Hayley, Owen, Michael J., 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

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, 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., Richards, Alexander L., Escott-Price, Valentina, Forty, Liz, Fraser, Christine, Hamshere, Marian L., Craddock, Nicholas, Jones, Ian, Kirov, George, O'Donovan, Michael C., Owen, Michael J., Di Florio, Arianna, 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

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, Escott-Price, Valentina, Jones, Ian, Owen, Michael J., O'Donovan, Michael C. 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

Cunningham, Adam, Fung, Wilson, Massey, Thomas, Hall, Jeremy, Owen, Michael, Van Den Bree, Marianne and Peall, Kathryn 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7) , pp. 1272-1274. 10.1002/mds.28078

Cunningham, Adam C., Hall, Jeremy, Owen, Michael and van den Bree, Marianne B. M. 2020. Assessment of emotions and behaviour by the Developmental Behaviour Checklist in young people with neurodevelopmental CNVs. Psychological Medicine 10.1017/S0033291720002330

Jones, Hannah J, Hammerton, Gemma, McCloud, Tayla, Hines, Lindsey A., Wright, Caroline, Gage, Suzanne H., Holmans, Peter, Jones, Peter B., Smith, George Davey, Linden, David E. J., O'Donovan, Michael C., Owen, Michael J., Walters, James T., Munafò, Marcus R., Heron, Jon and Zammit, Stanley 2020. Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence. Psychological Medicine 10.1017/S0033291720001798

Ching, Christopher R.K., Gutman, Boris A., Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K., Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K., Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Campbell, Linda E., McCabe, Kathryn L., Craig, Michael C., Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M., Murphy, Declan G., Murphy, Kieran C., Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T. Blaine, Emanuel, Beverly S., Gur, Raquel E., McDonald-McGinn, Donna M., Roalf, David R., Ruparel, Kosha, Schmitt, J. Eric, Zackai, Elaine H., Durdle, Courtney A., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Bassett, Anne S., Butcher, Nancy J., Chow, Eva W.C., Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne, Linden, David E., Moss, Hayley, Owen, Michael J., van den Bree, Marianne, Crossley, Nicolas A., Repetto, Gabriela M., Thompson, Paul M. and Bearden, Carrie E. 2020. Mapping subcortical brain alterations in 22q11.2 deletion syndrome: effects of seletion size and convergence with idiopathic neuropsychiatric illness. American Journal of Psychiatry 177 (7) , pp. 589-600. 10.1176/appi.ajp.2019.19060583

Lee, Sze Chim, DelPozo-Banos, Marcos, Lloyd, Keith, Jones, Ian, Walters, James T.R., Owen, Michael J., O'Donovan, Michael 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

Legge, Sophie, Dennison, Charlotte, Pardinas, Antonio, Rees, Elliott, Lynham, Amy, Hopkins, Lucinda, Bates, Lesley, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2020. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 216 (5) , pp. 259-266. 10.1192/bjp.2019.120

Byrne, Enda, Zhu, Zhihong, Qi, Ting, Skene, Nathan, Bryois, Julien, Pardinas, Antonio, Stahl, Eli, Smoller, Jordon, Rietschel, Marcella, Owen, Michael, Walters, James, O'Donovan, Michael, McGarth, John, Hjerling-Leffler, Jens, Sullivan, Patrick, Goddard, Michael, Visscher, Peter, Yang, Jian and Wray, Naomi 2020. Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders. Molecular Psychiatry 10.1038/s41380-020-0705-9

Martin, Joanna, Hosking, Grace, Wadon, Megan, Agha, Sharifah Shameem, Langley, Kate, Rees, Elliott, Owen, Michael, O'Donovan, Michael, Kirov, George and Thapar, Anita 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

Moulding, Hayley, Bartsch, Ullrich, Hall, Jeremy, Jones, M., Linden, David, Owen, Michael and Van Den Bree, Marianne 2020. Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS). Psychological Medicine 50 , pp. 1191-1202. 10.1017/S0033291719001119

Hall, Lynsey S., Pain, Oliver, O’Brien, Heath E., Anney, Richard, Walters, James T. R., Owen, Michael J., O'Donovan, Michael C. and Bray, Nicholas J. 2020. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Molecular Psychiatry 10.1038/s41380-020-0743-3

Foley, Claire, Heron, Elizabeth A., Harold, Denise, Walters, James, Owen, Michael, O'Donovan, Michael, 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

van der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, de Geus, Eco J. C., de Zubicaray, Greig I., de Zwarte, Sonja M. C., Delanty, Norman, den Braber, Anouk, Desrivieres, Sylvane, Di Forti, Marta, Doherty, Joanne L., Donohoe, Gary, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fisher, Simon E., Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Glahn, David C., Grabe, Hans J., Groenewold, Nynke A., Gústafsson, Ómar, Haavik, Jan, Haberg, Asta K., Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Hibar, Derrek P., Hillegers, Manon H. J., Hoffmann, Per, Holleran, Laurena, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E., Ikeda, Masashi, Jacquemont, Sébastien, Jahanshad, Neda, Jockwitz, Christiane, Johansson, Stefan, Jönsson, Erik G., Kikuchi, Masataka, Knowles, Emma E. M., Kwok, John B., Le Hellard, Stephanie, Linden, David E. J., Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri J., Martin, Nicholas G., Mather, Karen A., Mathias, Samuel R., McMahon, Katie L., McRae, Allan F., Medland, Sarah E., Moberget, Torgeir, Moreau, Clara, Morris, Derek W., Mühleisen, Thomas W., Murray, Robin M., Nordvik, Jan E., Nyberg, Lars, Olde Loohuis, Loes M., Ophoff, Roel A., Owen, Michael J., Paus, Tomas, Pausova, Zdenka, Peralta, Juan M., Pike, Bruce, Prieto, Carlos, Quinlan, Erin Burke, Reinbold, Céline S., Reis Marques, Tiago, Rucker, James J. H., Sachdev, Perminder S., Sando, Sigrid B., Schofield, Peter R., Schork, Andrew J., Schumann, Gunter, Shin, Jean, Shumskaya, Elena, Silva, Ana I., Sisodiya, Sanjay M., Steen, Vidar M., Stein, Dan J., Strike, Lachlan T., Tamnes, Christian K., Teumer, Alexander, Thalamuthu, Anbupalam, Tordesillas-Gutiérrez, Diana, Uhlmann, Anne, Úlfarsson, Magnús Ö., van 't Ent, Dennis, van den Bree, Marianne B. M., Vassos, Evangelos, Wen, Wei, Wittfeld, Katharina, Wright, Margaret J., Zayats, Tetyana, Dale, Anders M., Djurovic, Srdjan, Agartz, Ingrid, Westlye, Lars T., Stefánsson, Hreinn, Stefánsson, Kári, Thompson, Paul M. and Andreassen, Ole A. 2020. Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry 77 (4) , pp. 420-430. 10.1001/jamapsychiatry.2019.3779

Rees, Elliott and Owen, Michael J. 2020. Translating insights from neuropsychiatric genetics and genomics for precision psychiatry. Genome Medicine 12 (1) , 43. 10.1186/s13073-020-00734-5

Eaton, Christopher B., Thomas, Rhys H., Hamandi, Khalid, Payne, Gareth C., Kerr, Michael P., Linden, David E. J., Owen, Michael J., Cunningham, Adam C., Bartsch, Ullrich, Struik, Siske S. and van den Bree, Marianne B. M. 2020. Response to letter to editor: 'Knowing when and how to use epilepsy screening questionnaires'. Epilepsia 61 (4) , pp. 826-827. 10.1111/epi.16463

Szatkiewicz, Jin P., Fromer, Menachem, Nonneman, Randal J., Ancalade, NaEshia, Johnson, Jessica S., Stahl, Eli A., Rees, Elliott, Bergen, Sarah, Hultman, Christina, Kirov, George, O'Donovan, Michael, Owen, Michael, Holmans, Peter, Sklar, Pamela, Sullivan, Patrick F., Purcell, Shaun M., Crowley, James J. and Ruderfer, Douglas M. 2020. Characterization of single gene copy number variants in schizophrenia. Biological Psychiatry 87 (8) , pp. 736-744. 10.1016/j.biopsych.2019.09.023

Sullivan, Sarah A., Kounali, Daphne, Cannon, Mary, David, Anthony S., Fletcher, Paul C., Holmans, Peter, Jones, Hannah, Jones, Peter B., Linden, David E. J., Lewis, Glyn, Owen, Michael J., O'Donovan, Michael, Rammos, Alexandros, Thompson, Andrew, Wolke, Dieter, Heron, Jon and Zammit, Stanley 2020. A population-based cohort study examining the incidence and impact of psychotic experiences from childhood to adulthood, and prediction of psychotic disorder. American Journal of Psychiatry 177 (4) , pp. 308-317. 10.1176/appi.ajp.2019.19060654

Sullivan, Patrick F. and Owen, Michael J. 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

Swaden Lewis, Katie J., Richards, Alexander, Karlsson, Robert, Leonenko, Ganna, Jones, Samuel E., Jones, Hannah J., Gordon-Smith, Katherine, Forty, Liz, Escott-Price, Valentina, Owen, Michael J., Weedon, Michael N., Jones, Lisa, Craddock, Nick, Jones, Ian, Landén, Mikael, O'Donovan, Michael C. and Di Florio, Arianna 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

Richards, Alexander, Pardinas, Antonio, Frizzati, Aura, Tansey, Katherine, Lynham, Amy, Holmans, Peter, 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, Owen, Michael, Donohoe, Gary, O'Donovan, Michael, Walters, James, 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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L., Psaty, B. M., Van Broeckhoven, C., Holmans, P., Launer, L. J., Mayeux, R., Lathrop, M., Goate, A. M., Escott-Price, V., Seshadri, S., Pericak-Vance, M. A., Amouyel, P., Williams, J., van Duijn, C. M., Schellenberg, G. D. and Farrer, L. A. 2016. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry 21 , pp. 108-117. 10.1038/mp.2015.23

Hubbard, Leon, Tansey, Katherine E., Rai, Dheeraj, Jones, Peter, Ripke, Stephan, Chambert, Kimberly D., Moran, Jennifer L., McCarroll, Steven A., Linden, David Edmund Johannes, Owen, Michael John, O'Donovan, Michael Conlon, Walters, James Tynan Rhys and Zammit, Stanley 2016. Evidence of common genetic overlap between schizophrenia and cognition. Schizophrenia Bulletin 42 (3) , pp. 832-842. 10.1093/schbul/sbv168

Peall, Kathryn J., Dijk, Joke M., Saunders-Pullman, Rachel, Dreissen, Yasmine E. M., van Loon, Ilke, Cath, Danielle, Kurian, Manju A., Owen, Michael John, Foncke, Elisabeth M. J., Morris, Huw R., Gasser, Thomas, Bressman, Susan, Asmus, Friedrich and Tijssen, Marina A. J. 2016. Psychiatric disorders, myoclonus dystonia and SGCE: an international study. Annals of Clinical and Translational Neurology 3 (1) , pp. 4-11. 10.1002/acn3.263

Harrison, Judith and Owen, Michael John 2016. Alzheimer's disease: the amyloid hypothesis on trial. British Journal of Psychiatry 208 (1) , pp. 1-3. 10.1192/bjp.bp.115.167569

Stephan, Klaas E, Binder, Elisabeth B, Breakspear, Michael, Dayan, Peter, Johnstone, Eve C, Meyer-Lindenberg, Andreas, Schnyder, Ulrich, Wang, Xiao-Jing, Bach, Dominik R, Fletcher, Paul C, Flint, Jonathan, Frank, Michael J, Heinz, Andreas, Huys, Quentin J M, Montague, P Read, Owen, Michael John and Friston, Karl J 2016. Charting the landscape of priority problems in psychiatry, part 2: pathogenesis and aetiology. The Lancet Psychiatry 3 (1) , pp. 84-90. 10.1016/S2215-0366(15)00360-0

Stephan, Klaas E, Bach, Dominik R, Fletcher, Paul C, Flint, Jonathan, Frank, Michael J, Friston, Karl J, Heinz, Andreas, Huys, Quentin J M, Owen, Michael John, Binder, Elisabeth B, Dayan, Peter, Johnstone, Eve C, Meyer-Lindenberg, Andreas, Montague, P Read, Schnyder, Ulrich, Wang, Xiao-Jing and Breakspear, Michael 2016. Charting the landscape of priority problems in psychiatry, part 1: classification and diagnosis. The Lancet Psychiatry 3 (1) , pp. 77-83. 10.1016/S2215-0366(15)00361-2

D'Angelo, Debra, Lebon, Sébastien, Chen, Qixuan, Martin-Brevet, Sandra, Snyder, LeeAnne Green, Hippolyte, Loyse, Hanson, Ellen, Maillard, Anne M., Faucett, W. Andrew, Macé, Aurélien, Pain, Aurélie, Bernier, Raphael, Chawner, Samuel, David, Albert, Andrieux, Joris, Aylward, Elizabeth, Baujat, Genevieve, Caldeira, Ines, Conus, Philippe, Ferrari, Carrina, Forzano, Francesca, Gérard, Marion, Goin-Kochel, Robin P., Grant, Ellen, Hunter, Jill V., Isidor, Bertrand, Jacquette, Aurélia, Jønch, Aia E., Keren, Boris, Lacombe, Didier, Le Caignec, Cédric, Martin, Christa Lese, Männik, Katrin, Metspalu, Andres, Mignot, Cyril, Mukherjee, Pratik, Owen, Michael John, Passeggeri, Marzia, Rooryck-Thambo, Caroline, Rosenfeld, Jill A., Spence, Sarah J., Steinman, Kyle J., Tjernagel, Jennifer, Van Haelst, Mieke, Shen, Yiping, Draganski, Bogdan, Sherr, Elliott H., Ledbetter, David H., Van Den Bree, Marianne Bernadette, Beckmann, Jacques S., Spiro, John E., Reymond, Alexandre, Jacquemont, Sébastien and Chung, Wendy K. 2016. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. JAMA Psychiatry 73 (1) , pp. 20-30. 10.1001/jamapsychiatry.2015.2123

O'Donovan, Michael Conlon and Owen, Michael John 2016. The implications of the shared genetics of psychiatric disorders. Nature Medicine 22 , pp. 1214-1219. 10.1038/nm.4196

Tansey, Katherine E., Rees, Elliott, Linden, David Edmun Johannes, Ripke, S, Chambert, K D, Moran, J L, McCarroll, S A, Holmans, Peter Alan, Kirov, George, Walters, James Tynan Rhys, Owen, Michael John and O'Donovan, Michael Conlon 2015. Common alleles contribute to schizophrenia in CNV carriers [Erratum]. Molecular Psychiatry 21 , 1153. 10.1038/mp.2015.170

Escott-Price, Valentina, Kirov, George, Rees, Elliott, Isles, Anthony Roger, Owen, Michael John and O'Donovan, Michael Conlon 2015. No evidence for enrichment in schizophrenia for common allelic associations at imprinted loci. PLoS ONE 10 (12) , -. 10.1371/journal.pone.0144172

Niarchou, Maria, Martin, Joanna, Thapar, Anita, Owen, Michael John and van den Bree, Marianne Bernadette 2015. The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 (8) , pp. 730-738. 10.1002/ajmg.b.32378

Heyes, Samuel, Pratt, Wendy S., Rees, Elliott, Dahimene, Shehrazade, Ferron, Laurent, Owen, Michael John and Dolphin, Annette C. 2015. Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders. Progress in Neurobiology 134 , pp. 36-54. 10.1016/j.pneurobio.2015.09.002

Lancaster, Thomas M., Brindley, Lisa M., Tansey, Katherine E., Sims, Rebecca C., Mantripragada, Kiran, Owen, Michael J., Williams, Julie and Linden, David E. J. 2015. Alzheimer's disease risk variant in CLU is associated with neural inefficiency in healthy individuals. Alzheimer's and Dementia 11 (10) , pp. 1144-1152. 10.1016/j.jalz.2014.10.012

Lee, S Hong, Byrne, Enda M, Hultman, Christina M, Kähler, Anna, Vinkhuyzen, Anna AE, Ripke, Stephan, Andreassen, Ole A, Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X, McGrath, John J, Mehta, Divya, Stahl, Eli A, Zhao, Qiongyi, Kendler, Kenneth S, Sullivan, Patrick F, Price, Alkes L, O'Donovan, Michael Conlon, Okada, Yukinori, Mowry, Bryan J, Raychaudhuri, Soumya, Wray, Naomi R, Byerley, William, Cahn, Wiepke, Cantor, Rita M, Cichon, Sven, Cormican, Paul, Curtis, David, Djurovic, Srdjan, Escott-Price, Valentina, Gejman, Pablo V, Georgieva, Lyudmila, Giegling, Ina, Hansen, Thomas F, Ingason, Andrés, Kim, Yunjung, Konte, Bettina, Lee, Phil H, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek W, Nöthen, Markus M, O'Dushlaine, Colm, Olincy, Ann, Olsen, Line, Pato, Carlos N, Pato, Michele T, Pickard, Benjamin S, Posthuma, Danielle, Rasmussen, Henrik B, Rietschel, Marcella, Rujescu, Dan, Schulze, Thomas G, Silverman, Jeremy M, Thirumalai, Srinivasa, Werge, Thomas, Agartz, Ingrid, Amin, Farooq, Azevedo, Maria H, Bass, Nicholas, Black, Donald W, Blackwood, Douglas H R, Bruggeman, Richard, Buccola, Nancy G, Choudhury, Khalid, Cloninger, Robert C, Corvin, Aiden, Craddock, Nicholas John, Daly, Mark J, Datta, Susmita, Donohoe, Gary J, Duan, Jubao, Dudbridge, Frank, Fanous, Ayman, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Gill, Michael, Gurling, Hugh, De Haan, Lieuwe, Hamshere, Marian L., Hartmann, Annette M, Holmans, Peter Alan, Kahn, René S, Keller, Matthew C, Kenny, Elaine, Kirov, George, Krabbendam, Lydia, Krasucki, Robert, Lawrence, Jacob, Lencz, Todd, Levinson, Douglas F, Lieberman, Jeffrey A, Lin, Dan-Yu, Linszen, Don H, Magnusson, Patrik KE, Maier, Wolfgang, Malhotra, Anil K, Mattheisen, Manuel, Mattingsdal, Morten, McCarroll, Steven A, Medeiros, Helena, Melle, Ingrid, Milanova, Vihra, Myin-Germeys, Inez, Neale, Benjamin M, Ophoff, Roel A, Owen, Michael John, Pimm, Jonathan, Purcell, Shaun M, Puri, Vinay, Quested, Digby J, Rossin, Lizzy, Ruderfer, Douglas, Sanders, Alan R, Shi, Jianxin, Sklar, Pamela, St. Clair, David, Scott Stroup, T, Van Os, Jim, Visscher, Peter M, Wiersma, Durk, Zammit, Stanley, Louis Bridges, S, Choi, Hyon K, Coenen, Marieke JH, de Vries, Niek, Dieud, Philippe, Greenberg, Jeffrey D, Huizinga, Tom WJ, Padyukov, Leonid, Siminovitch, Katherine A, Tak, Paul P, Worthington, Jane, De Jager, Philip L, Denny, Joshua C, Gregersen, Peter K, Klareskog, Lars, Mariette, Xavier, Plenge, Robert M, van Laar, Mart and van Riel, Piet 2015. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology 44 (5) , pp. 1706-1721. 10.1093/ije/dyv136

Hall, Jeremy and Owen, Michael John 2015. Psychiatric classification - a developmental perspective. British Journal of Psychiatry 207 (4) , pp. 281-282. 10.1192/bjp.bp.114.159996

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