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Escott-Price, Valentina, Smith, Daniel J., Kendall, Kimberley, Ward, Joey, Kirov, George, Owen, Michael J., Walters, James and O'Donovan, Michael C. 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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Human Molecular Genetics
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Chapman, Ria M, Tinsley, Caroline L, Hill, Matthew J, Forrest, Marc P, Tansey, Katherine E, Pardiñas, Antonio F, Rees, Elliott, Doyle, A Michelle, Wilkinson, Lawrence S, Owen, Michael J, O?Donovan, Michael C and Blake, Derek J
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Legge, Sophie, Jones, Hannah, Kendall, Kimberley, Pardinas, Antonio, Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina, Hotopf, Matthew, Savage, Jeanne, Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael, O'Donovan, Michael, Zammit, Stanley and Walters, James
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Pain, Oliver, Pocklington, Andrew, Holmans, Peter, Bray, Nichloas, O'Brian, Heath, Hall, Lynsey, Pardinas, Antonio, O'Donovan, Michael, Owen, Michael and Anney, Richard
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Dos Santos Silva, Ana, Haddon, Josephine, Syed, Yasir Ahmed, Trent, Simon, Tzu-Ching, E.Lin, Patel, Yateen, Carter, Jenny, Haan, Niels, Honey, Robert, Humby, Trevor, Assaf, Yaniv, Owen, Michael, Linden, David, Hall, Jeremy and Wilkinson, Lawrence
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Pardinas, Antonio, Nalmpanti, Mariana, Pocklington, Andrew, Legge, Sophie, Medway, Christopher, King, Adrian, Jansen, John, Helthuis, Marinka, Zammit, Stanley, MacCabe, James, Owen, Michael, O'Donovan, Michael and Walters, James
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Kendall, Kimberley M., Bracher-Smith, Matthew, Fitzpatrick, Harry, Lynham, Amy, Rees, Elliott, Escott-Price, Valentina, Owen, Michael J., O'Donovan, Michael C., Walters, James T.R. and Kirov, George
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Niarchou, Maria, Chawner, Samuel, Fiksinski, Ania, Vorstman, Jacob A.S., Maeder, Johanna, Schneider, Maude, Eliez, Stephan, Armando, Marco, Pontillo, Maria, Vicari, Stefano, McDonald-McGinn, Donna M., Emanuel, Beverly, Zackai, Elaine, Bearden, Carrie E., Shashi, Vandana, Hooper, Stephen R., Owen, Michael J., Gur, Raquel A., Wray, Naomi R., van den Bree, Marianne and Thapar, Anita
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Richards, Alexander, Horwood, John, Boden, Joseph, Kennedy, Martin, Sellers, Ruth, Riglin, Lucy, Mistry, Sumit, Jones, Hannah, Smith, Daniel, Zammit, Stanley, Owen, Michael, O'Donovan, Michael and Harold, Gordon
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Niarchou, Maria, 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., Linden, Stefanie, Raymond, Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J. and Van Den Bree, Marianne 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, Bracher-Smith, Matthew, Menzies, Georgina, Walters, James, Kirov, George, Owen, Michael J. and O'Donovan, Michael C.
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Vivian-Griffiths, Timothy, Baker, Emily, Schmidt, Karl M., Bracher-Smith, Matthew, Walters, James, Artemiou, Andreas, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Pocklington, Andrew and Escott-Price, Valentina
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Sullivan, Sarah, Kounali, Daphne, Cannon, Mary, David, Anthony, Fletcher, Paul, Holmans, Peter, Jones, Hannah, Jones, Peter, Linden, David, Lewis, Glyn, Owen, Michael, O'Donovan, Michael, Rammos, Alexandros, Thompson, Andrew, Wolke, Dieter, Heron, Jon and Zammit, Stanley
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A population-based cohort study examining the incidence and impact of psychotic experiences from childhood to adulthood, and prediction of psychotic disorder.
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Cunningham, Adam, Hall, Jeremy, Owen, Michael and Van den Bree, Marianne
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Psychological Medicine
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Swaden Lewis, Katie, Richards, Alexander, Karlsson, Robert, Leonenko, Ganna, Jones, Samuel, Jones, Hannah, Gordon-Smith, K., Forty, Liz, Escott-Price, V, Owen, Michael J, Weedon, M., Jones, Lisa, Craddock, Nick, Jones, Ian, Landén, Mikael, O'Donovan, Michael and Di Florio, Arianna 2019. Comparison of genetic liability for sleep traits among individuals with Bipolar Disorder I or II and control participants. JAMA Psychiatry |
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Rees, Elliott, Han, Jun, Morgan, Joanne, Carrera, Noa, Escott-Price, Valentina, Pocklington, Andrew, Duffield, Madeleine, Hall, Lynsey, Legge, Sophie, Pardinas, Antonio, Richards, Alexander, Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George, Walters, James, Holmans, Peter, O'Donovan, Michael and Owen, Michael
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Analyses of de novo and common alleles implicate rare missense variants in SLC6A1 in schizophrenia.
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Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, 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, Niarchou, Maria, Williams, Nigel, Emanuel, B, Vermeesch, J, Warren, S, Owen, Michael, Chopra, P, Cutler, D, Duncan, R, Mulle, J, Kotlar, A, Voss, A, Zwick, M, Diacou, A, Golden, A, Guo, T, Lin, J, Wang, T, Zhang, Z, Zhao, Y, Marshall, C, Merico, D, Jin, A, Lilley, B, Salmons, H, Tran, O, Holmans, Peter, Pardinas, Antonio, Walters, James, Demaeral, W, Boot, E, Butcher, N, Costain, G, Lowther, C, Evers, R, van Amelsvoort, T, van Duin, E, Vingerhoets, C, Breckpot, J, Devriendt, K, Vergaelen, E, Vogels, A, Crowley, B, McGinn, D, Moss, E, Sharkus, R, Unolt, M, Zackai, E, Calkins, M, Gallagher, R, Gur, R, Tang, S, Fritsch, R, Ornstein, C, Repetto, G, Breetvelt, E, Duijff, S, Fiksinski, A and Moss, Hayley
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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, Linden, David E., Van Den Bree, Marianne, 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 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788 |
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Arnau-Soler, Aleix, Adams, Mark J., Hayward, Caroline, Thomson, Pippa A., Craddock, Nick, Escott-Price, Valentina, Owen, M J, Tansey, Katherine and O'Donovan, Michael
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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., Hu, Ming, Jin, Fulai, Li, Yun, Owen, Michael J., O'Donovan, Michael C., Walters, James T. R., 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
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Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
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Owen, David, Bracher Smith, Mathew, Kendall, Kimberley M., Rees, Elliott, Einon, Mark, Escott-Price, Valentina, Owen, Michael J., O'Donovan, Michael C. and Kirov, George
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Effects of pathogenic CNVs on physical traits in participants of the UK Biobank.
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O'Brien, Heath E., Hannon, Eilis, Hill, Matthew J., Toste, Carolina C., Robertson, Matthew J., Morgan, Joanne E., McLaughlin, Gemma, Lewis, Cathryn M., Schalkwyk, Leonard C., Hall, Lynsey S., Pardinas, Antonio F., Owen, Michael J., O'Donovan, Michael C., Mill, Jonathan and Bray, Nicholas J. 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, Doherty, Joanne L., Moss, Hayley, Owen, Michael J. and Van Den Bree, Marianne 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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Crawford, Karen, Bracher-Smith, Matthew, Owen, David, Kendall, Kimberley M, Rees, Elliott, Pardinas, Antonio F, Einon, Mark, Escott-Price, Valentina, Walters, James TR, O'Donovan, Michael C, Owen, Michael J and Kirov, George 2018. Medical consequences of pathogenic CNVs in adults: Analysis of the UK Biobank. Journal of Medical Genetics 10.1136/jmedgenet-2018-105477 |
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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, Owen, Michael, Niarchou, Maria, 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, Lee, Sze Chim, Walters, James T.R., Owen, Michael J., O'Donovan, Michael, 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, Lewis, Glyn, Linden, David E. J., O'Donovan, Michael C., Owen, Michael J., Walters, James and Zammit, Stanley 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, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, 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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Williams, Hywel John, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2012. Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample [Letter]. Schizophrenia Research 141 (2-3) , pp. 274-276. 10.1016/j.schres.2012.08.024 |
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