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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. |
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Smeland, Olav B., Shadrin, Alexey, Bahrami, Shahram, Broce, Iris, Tesli, Martin, Frei, Oleksandr, Wirgenes, Katrine V., O'Connell, Kevin S., Krull, Florian, Bettella, Francesco, Steen, Nils Eiel, Sugrue, Leo, Wang, Yunpeng, Svenningsson, Per, Sharma, Manu, Pihlstrøm, Lasse, Toft, Mathias, O'Donovan, Michael, Djurovic, Srdjan, Desikan, Rahul, Dale, Anders M. and Andreassen, Ole A. 2021. Genome-wide association analysis of Parkinson's disease and schizophrenia reveals shared genetic architecture and identifies novel risk loci. Biological Psychiatry 89 (3) , pp. 227-235. 10.1016/j.biopsych.2020.01.026 |
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Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Champion, Sinead, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick, 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
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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 |
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Pries, Lotta-Katrin, van Os, Jim, ten Have, Margreet, de Graaf, Ron, van Dorsselaer, Saskia, Bak, Maarten Bak, Lin, Bochao D, van Eijk, Kristel R., Kenis, Gunter, Richards, Alexander, O'Donovan, Michael C., Luykx, Jurjen J., Rutten, Bart P. F. and Guloksuz, Sinan 2020. Association of recent stressful life events with mental and physical health in the context of genomic and exposomic liability for schizophrenia. JAMA Psychiatry 77 (12) , pp. 1296-1304. 10.1001/jamapsychiatry.2020.2304 |
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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. |
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Ward, Joey, Tunbridge, Elizabeth M., Sandor, Cynthia, Lyall, Laura M., Ferguson, Amy, Strawbridge, Rona J., Lyall, Donald M., Cullen, Breda, Graham, Nicholas, Johnston, Keira J. A., Webber, Caleb, Escott-Price, Valentina, O'Donovan, Michael, Pell, Jill P., Bailey, Mark E. S., Harrison, Paul J. and Smith, Daniel J.
2020.
The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function.
Molecular Psychiatry
25
, pp. 3091-3099.
10.1038/s41380-019-0439-8
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Pries, L.-K., Dal Ferro, G. A., van Os, J., Delespaul, P., Kenis, G., Lin, B. D., Luykx, J. J., Richards, A. L., Akdede, B., Binbay, T., Altinyazar, V., Yalinçetin, B., Gümüs-Akay, G., Cihan, B., Soygür, H., Ulas, H., Sahin Cankurtaran, E., Ulusoy Kaymak, S., Mihaljevic, M. M., Andric Petrovic, S., Mirjanic, T., Bernardo, M., Mezquida, G., Amoretti, S., Bobes, J., Saiz, P. A., García-Portilla, M. Paz, Sanjuan, J., Aguilar, E. J., Santos, J. L., Jiménez-López, E., Arrojo, M., Carracedo, A., López, G., González-Peñas, J., Parellada, M., Maric, N. P., Atbasoglu, C., Ucok, A., Alptekin, K., Can Saka, M., Arango, C., O'Donovan, M., Tosato, S., Rutten, B. P. F. and Guloksuz, S.
2020.
Examining the independent and joint effects of genomic and exposomic liabilities for schizophrenia across the psychosis spectrum.
Epidemiology and Psychiatric Sciences
29
, e182.
10.1017/S2045796020000943
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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
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, e139.
10.1192/bjo.2020.42
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van Os, Jim, Pries, Lotta-Katrin, ten Have, Margreet, de Graaf, Ron, van Dorsselaer, Saskia, Delespaul, Philippe, Bak, Maarten, Kenis, Gunter, Lin, Bochao D., Luykx, Jurjen J., Richards, Alexander L., Akdede, Berna, Binbay, Tolga, Altinyazar, Vesile, Yalinçetin, Berna, Gümüs-Akay, Güvem, Cihan, Burçin, Soygür, Haldun, Ulas, Halis, Cankurtaran, Eylem Sahin, Kaymak, Semra Ulusoy, Mihaljevic, Marina M., Petrovic, Sanja Andric, Mirjanic, Tijana, Bernardo, Miguel, Mezquida, Gisela, Amoretti, Silvia, Bobes, Julio, Saiz, Pilar A., García-Portilla, María Paz, Sanjuan, Julio, Aguilar, Eduardo J., Santos, José Luis, Jiménez-López, Estela, Arrojo, Manuel, Carracedo, Angel, López, Gonzalo, González-Peñas, Javier, Parellada, Mara, Maric, Nadja P., Atbasoglu, Cem, Ucok, Alp, Alptekin, Köksal, Saka, Meram Can, Arango, Celso, O'Donovan, Michael, Rutten, Bart P. F. and Guloksuz, Sinan
2020.
Evidence, and replication thereof, that molecular-genetic and environmental risks for psychosis impact through an affective pathway.
Psychological Medicine
10.1017/S0033291720003748
Item availability restricted. |
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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
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Henquet, Cécile, van Os, Jim, Pries, Lotta K., Rauschenberg, Christian, Delespaul, Philippe, Kenis, Gunter, Luykx, Jurjen J., Lin, Bochao D., Richards, Alexander L., Akdede, Berna, Binbay, Tolga, Altinyazar, Vesile, Yalinçetin, Berna, Gümüs-Akay, Güvem, Cihan, Burçin, Soygür, Haldun, Ulas, Halis, Cankurtaran, Eylem S., Kaymak, Semra U., Mihaljevic, Marina M., Petrovic, Sanja S., Mirjanic, Tijana, Bernardo, Miguel, Mezquida, Gisela, Amoretti, Silvia, Bobes, Julio, Saiz, Pilar A., García-Portilla, Maria P., Sanjuan, Julio, Aguilar, Eduardo J., Santos, Jose L., Jiménez-López, Estela, Arrojo, Manuel, Carracedo, Angel, López, Gonzalo, González-Peñas, Javier, Parellada, Mara, Maric, Nadja P., Atbasoglu, Cem, Ucok, Alp, Alptekin, Köksal, Saka, Meram C., Arango, Celso, O'Donovan, Michael, Rutten, Bart P.F. and Gülöksüz, Sinan
2020.
A replication study of JTC bias, genetic liability for psychosis and delusional ideation.
Psychological Medicine
10.1017/S0033291720003578
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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
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Wong, Hilary, Wadon, Megan, Evans, Alexandra, Kirov, George, Modi, Neena, O'Donovan, Michael and Thapar, Anita 2020. Contribution of de novo and inherited rare copy number variants to very preterm birth. Journal of Medical Genetics 57 (8) , pp. 552-557. 10.1136/jmedgenet-2019-106619 |
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van Os, Jim, Pries, Lotta-Katrin, Delespaul, Philippe, Kenis, Gunter, Luykx, Jurjen J., Lin, Bochao D., Richards, Alexander L., Akdede, Berna, Binbay, Tolga, Altınyazar, Vesile, Yalınçetin, Berna, Gümüş-Akay, Güvem, Cihan, Burçin, Soygür, Haldun, Ulaş, Halis, Cankurtaran, Şahin, Kaymak, Semra Ulusoy, Mihaljevic, Marina M., Petrovic, Sanja Andric, Mirjanic, Tijana, Bernardo, Miguel, Cabrera, Bibiana, Bobes, Julio, Saiz, Pilar A., García-Portilla, María Paz, Sanjuan, Julio, Aguilar, Eduardo J., Santos, José Luis, Jiménez-López, Estela, Arrojo, Manuel, Carracedo, Angel, López, Gonzalo, González-Peñas, Javier, Parellada, Mara, Maric, Nadja P., Atbaşoğlu, Cem, Ucok, Alp, Alptekin, Köksal, Saka, Meram Can, Arango, Celso, O'Donovan, Michael, Rutten, Bart P. F. and Guloksuz, Sinan 2020. Replicated evidence that endophenotypic expression of schizophrenia polygenic risk is greater in healthy siblings of patients compared to controls, suggesting gene-environment interaction. The EUGEI study. Psychological Medicine 50 (11) , pp. 1884-1897. 10.1017/S003329171900196X |
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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, 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 |
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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, 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 and Tansey, Katherine E.
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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Riglin, Lucy, Thapar, Ajay, Leppert, Beate, Martin, Joanna, Richards, Alexander, Anney, Richard, Davey Smith, George, Tilling, Kate, Stegiakouli, Evie, Lahey, Benjamin, O'Donovan, Michael, Collishaw, Stephan and Thapar, Anita
2020.
Using genetics to examine a general liability to childhood psychopathology.
Behavior Genetics
50
, pp. 213-220.
10.1007/s10519-019-09985-4
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Wong, Hilary S., Hopkins, Lucinda, O'Donovan, Michael C., Thapar, Anita and Modi, Neena
2020.
Pilot study to establish a prospective neonatal cohort: Study of Preterm Infants and Neurodevelopmental Genes (SPRING).
Molecular Psychiatry
4
(1)
, e000648.
10.1136/bmjpo-2020-000648
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Riglin, Lucy, Leppert, Beate, Langley, Kate, Thapar, Ajay K., O’Donovan, Michael, Davey Smith, George, Stergiakouli, Evie, Tilling, Kate and Thapar, Anita
2020.
Investigating attention‐deficit hyperactivity disorder and autism spectrum disorder traits in the general population: What happens in adult life?
Journal of Child Psychology and Psychiatry
10.1111/jcpp.13297
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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 |
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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
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Wadon, Megan, Modi, Neena, Wong, Hilary, Thapar, Anita and O'Donovan, Michael
2020.
Recent advances in the genetics of preterm birth.
Annals of Human Genetics
84
(3)
, pp. 205-213.
10.1111/ahg.12373
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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 |
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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
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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 |
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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
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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 |
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Tripoli, Giada, Quattrone, Diego, Ferraro, Laura, Gayer-Anderson, Charlotte, Rodriguez, Victoria, La Cascia, Caterina, La Barbera, Daniele, Sartorio, Crocettarachele, Seminerio, Fabio, Tarricone, Ilaria, Berardi, Domenico, Szöke, Andrei, Arango, Celso, Tortelli, Andrea, Llorca, Pierre-Michel, de Haan, Lieuwe, Velthorst, Eva, Bobes, Julio, Bernardo, Miguel, Sanjuán, Julio, Santos, Jose Luis, Arrojo, Manuel, Del-Ben, Cristina Marta, Menezes, Paulo Rossi, Selten, Jean-Paul, Jones, Peter B., Jongsma, Hannah E, Kirkbride, James B, Lasalvia, Antonio, Tosato, Sarah, Richards, Alex, O'Donovan, Michael, Rutten, Bart PF, Os, Jim van, Morgan, Craig, Sham, Pak C, Murray, Robin M., Murray, Graham K. and Di Forti, Marta 2020. Jumping to conclusions, general intelligence, and psychosis liability: findings from the multi-centre EU-GEI case-control study. Psychological Medicine 10.1017/S003329171900357X |
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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 |
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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
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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
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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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Ripke, Stephan, Wray, Naomi R, Lewis, Cathryn M, Hamilton, Steven P, Weissman, Myrna M, Breen, Gerome, Byrne, Enda M, Blackwood, Douglas H R, Boomsma, Dorret I, Cichon, Sven, Heath, Andrew C, Holsboer, Florian, Lucae, Susanne, Madden, Pamela A F, Martin, Nicholas G, McGuffin, Peter, Muglia, Pierandrea, Noethen, Markus M, Penninx, Brenda P, Pergadia, Michele L, Potash, James B, Rietschel, Marcella, Lin, Danyu, Müller-Myhsok, Bertram, Shi, Jianxin, Steinberg, Stacy, Grabe, Hans J, Lichtenstein, Paul, Magnusson, Patrik, Perlis, Roy H, Preisig, Martin, Smoller, Jordan W, Stefansson, Kari, Uher, Rudolf, Kutalik, Zoltan, Tansey, Katherine E., Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Binder, Elisabeth B, Breuer, René, Castro, Victor M, Churchill, Susanne E, Coryell, William H, Craddock, Nicholas John, Craig, Ian W, Czamara, Darina, De Geus, Eco J, Degenhardt, Franziska, Farmer, Anne E, Fava, Maurizio, Frank, Josef, Gainer, Vivian S, Gallagher, Patience J, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Guipponi, Michel, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Hottenga, Jouke Jan, Iosifescu, Dan V, Ising, Marcus, Jones, Ian Richard, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohane, Isaac S, Kohli, Martin A, Korszun, Ania, Landen, Mikael, Lawson, William B, Lewis, Glyn, MacIntyre, Donald, Maier, Wolfgang, Mattheisen, Manuel, McGrath, Patrick J, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, Nyholt, Dale R, O'Donovan, Michael Conlon, Oskarsson, Högni, Pedersen, Nancy, Scheftner, William A, Schulz, Andrea, Schulze, Thomas G, Shyn, Stanley I, Sigurdsson, Engilbert, Slager, Susan L, Smit, Johannes H, Stefansson, Hreinn, Steffens, Michael, Thorgeirsson, Thorgeir, Tozzi, Federica, Treutlein, Jens, Uhr, Manfred, van den Oord, Edwin J C G, Van Grootheest, Gerard, Völzke, Henry, Weilburg, Jeffrey B, Willemsen, Gonneke, Zitman, Frans G, Neale, Benjamin, Daly, Mark, Levinson, Douglas F and Sullivan, Patrick F 2013. A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry 18 (4) , pp. 497-511. 10.1038/mp.2012.21 |
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Gibson, Greg, Schork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael Conlon, Furberg, Helena, Schork, Nicholas J., Andreassen, Ole A. and Dale, Anders M. 2013. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genetics 9 (4) , e1003449. 10.1371/journal.pgen.1003449 |
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Terwisscha van Scheltinga, Afke F., Bakker, Steven C., van Haren, Neeltje E.M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B.M., Cahn, Wiepke, Hulshoff Pol, Hilleke E., Ripke, Stephan, Ophoff, Roel A., Kahn, René S., Craddock, Nicholas John, Dwyer, Sarah, Escott-Price, Valentina, Georgieva, Lyudmila, Hamshere, Marian Lindsay, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, Doug, Williams, Nigel Melville and Zammit, Stanley 2013. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological Psychiatry 73 (6) , pp. 525-531. 10.1016/j.biopsych.2012.08.017 |
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Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K., Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M., Moran, Jennifer L., Chambert, Kimberly D., Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill,, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M., Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael John, O'Donovan, Michael Conlon, Lencz, Todd and Kirov, George 2013. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 70 (3) , pp. 253-260. 10.1001/2013.jamapsychiatry.71 |
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Donohoe, G., Walters, James Tynan Rhys, Hargreaves, A., Rose, E. J., Morris, D. W., Fahey, C., Bellini, S., Cummins, E., Giegling, I., Hartmann, A. M., Möller, H.-J., Muglia, P., Owen, Michael John, Gill, M., O'Donovan, Michael Conlon, Tropea, D., Rujescu, D. and Corvin, A. 2013. Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. Genes, Brain and Behavior 12 (2) , pp. 203-209. 10.1111/gbb.12016 |
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Williams, Hywel John, Monks, Stephen, Murphy, Kieran C., Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2013. Schizophrenia two-hit hypothesis in velo-cardio facial syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 (2) , pp. 177-182. 10.1002/ajmg.b.32129 |
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Chapman, J., Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, P, Stretton, A., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon, Williams, Julie and Kirov, George 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476 |
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Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O'Donovan, Michael Conlon, Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S. and Dale, Anders M. 2013. Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. American Journal of Human Genetics 92 (2) , pp. 197-209. 10.1016/j.ajhg.2013.01.001 |
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Kim, Y., Ripke, Stephan, Kirov, George, Sklar, Pamela, Purcell, Shaun M., Owen, Michael John, O'Donovan, Michael Conlon and Sullivan, Patrick F. 2013. Non-random mating, parent-of-origin, and maternal-fetal incompatibility effects in schizophrenia. Schizophrenia Research 143 (1) , pp. 11-17. 10.1016/j.schres.2012.11.002 |
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Visscher, Peter M., Andreassen, Ole A., Thompson, Wesley K., Schork, Andrew J., Ripke, Stephan, Mattingsdal, Morten, Kelsoe, John R., Kendler, Kenneth S., O'Donovan, Michael Conlon, Rujescu, Dan, Werge, Thomas, Sklar, Pamela, Roddey, J. Cooper, Chen, Chi-Hua, McEvoy, Linda, Desikan, Rahul S., Djurovic, Srdjan and Dale, Anders M. 2013. Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate. PLoS Genetics 9 (4) , e1003455. 10.1371/journal.pgen.1003455 |
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Chapuis, J, Hansmannel, F, Gistelinck, M, Mounier, A, Van Cauwenberghe, C, Kolen, K V, Geller, F, Sottejeau, Y, Harold, D, Dourlen, P, Grenier-Boley, B, Kamatani, Y, Delepine, B, Demiautte, F, Zelenika, D, Zommer, N, Hamdane, M, Bellenguez, C, Dartigues, J-F, Hauw, J-J, Letronne, F, Ayral, A-M, Sleegers, K, Schellens, A, Broeck, L V, Engelborghs, S, De Deyn, P P, Vandenberghe, R, O'Donovan, Michael Conlon, Owen, Michael John, Epelbaum, J, Mercken, M, Karran, E, Bantscheff, M, Drewes, G, Joberty, G, Campion, D, Octave, J-N, Berr, C, Lathrop, M, Callaerts, P, Mann, D, Williams, Julie, Buée, L, Dewachter, I, Van Broeckhoven, C, Amouyel, P, Moechars, D, Dermaut, B and Lambert, J-C 2013. Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology [Article]. Molecular Psychiatry 18 (11) , pp. 1225-1234. 10.1038/mp.2013.1 |
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Green, Elaine Karen, Grozeva, Detelina Valentinova, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, Farmer, A., Hamshere, Marian Lindsay, Jones, Ian Richard, Jones, L., McGuffin, P., Moran, J. L., Purcell, S., Sklar, P., Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2013. Association at SYNE1 in both bipolar disorder and recurrent major depression. Molecular Psychiatry 18 , pp. 614-617. 10.1038/mp.2012.48 |
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Prata, Diana P., Kanaan, Richard A., Barker, Gareth J., Shergill, Sukhwinder, Woolley, James, Georgieva, Lyudmila, Picchioni, Marco M., Kravariti, Eugenia, Walshe, Muriel, Allin, Matt, Toulopoulou, Timothea, Bramon, Elvira, McDonald, Colm, Giampietro, Vincent, Murray, Robin M., Brammer, Michael, O'Donovan, Michael Conlon and McGuire, Philip 2013. Risk variant of oligodendrocyte lineage transcription factor 2 is associated with reduced white matter integrity. Human Brain Mapping 34 (9) , pp. 2025-2031. 10.1002/hbm.22045 |
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Kirov, George, Rees, Elliott, Walters, James Tynan Rhys, Escott-Price, Valentina, Georgieva, Lyudmila, Richards, Alexander, Chambert, Kimberly D., Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O'Donovan, Michael Conlon and Owen, Michael John 2013. The penetrance of copy number variations for schizophrenia and developmental delay. Biological Psychiatry 75 (5) , pp. 378-385. 10.1016/j.biopsych.2013.07.022 |
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Aberg, Karolina A., Liu, Youfang, Bukszár, Jozsef, McClay, Joseph L., Khachane, Amit N., Andreassen, Ole A., Blackwood, Douglas, Corvin, Aiden, Djurovic, Srdjan, Gurling, Hugh, Ophoff, Roel, Pato, Carlos N., Pato, Michele T., Riley, Brien, Webb, Todd, Kendler, Kenneth, O'Donovan, Michael Conlon, Craddock, Nicholas John, Kirov, George, Owen, Michael John, Rujescu, Dan, St Clair, David, Werge, Thomas, Hultman, Christina M., Delisi, Lynn E., Sullivan, Patrick and van den Oord, Edwin J. 2013. |