Browse by Current Cardiff authors

Leonenko, Ganna, Di Florio, Arianna, Allardyce, Judith, Forty, Liz, Knott, Sarah, Jones, Lisa, Gordon-Smith, Katherine, Owen, Michael J., Jones, Ian, Walters, James, Craddock, Nick, O'Donovan, Michael C. and Escott-Price, Valentina 2018. A data-driven investigation of relationships between bipolar psychotic symptoms and schizophrenia genome-wide significant genetic loci. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (4) , pp. 468-475. 10.1002/ajmg.b.32635

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, Owen, Michael, Pardinas, Antonio, Ryge, Jesper, Walters, James T R, 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 Item availability restricted.

Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. F., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bryois, Julien, Buttenschøn, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. R., Colodro-Conde, Lucía, Couvy-Duchesne, Baptiste, Craddock, Nick, Crawford, Gregory E., Crowley, Cheynna A., Dashti, Hassan S., Davies, Gail, Deary, Ian J., Degenhardt, Franziska, Derks, Eske M., Direk, Nese, Dolan, Conor V., Dunn, Erin C., Eley, Thalia C., Eriksson, Nicholas, Escott-Price, Valentina, Kiadeh, Farnush Hassan Farhadi, Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Gaspar, Héléna A., Gill, Michael, Giusti-Rodríguez, Paola, Goes, Fernando S., Gordon, Scott D., Grove, Jakob, Hall, Lynsey S., Hannon, Eilis, Hansen, Christine Søholm, Hansen, Thomas F., Herms, Stefan, Hickie, Ian B., Hoffmann, Per, Homuth, Georg, Horn, Carsten, Hottenga, Jouke-Jan, Hougaard, David M., Hu, Ming, Hyde, Craig L., Ising, Marcus, Jansen, Rick, Jin, Fulai, Jorgenson, Eric, Knowles, James A., Kohane, Isaac S., Kraft, Julia, Kretzschmar, Warren W., Krogh, Jesper, Kutalik, Zoltán, Lane, Jacqueline M., Li, Yihan, Li, Yun, Lind, Penelope A., Liu, Xiaoxiao, Lu, Leina, MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Maier, Wolfgang, Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, McGuffin, Peter, Medland, Sarah E., Mehta, Divya, Middeldorp, Christel M., Mihailov, Evelin, Milaneschi, Yuri, Milani, Lili, Mill, Jonathan, Mondimore, Francis M., Montgomery, Grant W., Mostafavi, Sara, Mullins, Niamh, Nauck, Matthias, Ng, Bernard, Nivard, Michel G., Nyholt, Dale R., O'Reilly, Paul F., Oskarsson, Hogni, Owen, Michael J., Painter, Jodie N., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Peterson, Roseann E., Pettersson, Erik, Peyrot, Wouter J., Pistis, Giorgio, Posthuma, Danielle, Purcell, Shaun M., Quiroz, Jorge A., Qvist, Per, Rice, John P., Riley, Brien P., Rivera, Margarita, Saeed Mirza, Saira, Saxena, Richa, Schoevers, Robert, Schulte, Eva C., Shen, Ling, Shi, Jianxin, Shyn, Stanley I., Sigurdsson, Engilbert, Sinnamon, Grant B. C., Smit, Johannes H., Smith, Daniel J., Stefansson, Hreinn, Steinberg, Stacy, Stockmeier, Craig A., Streit, Fabian, Strohmaier, Jana, Tansey, Katherine E., Teismann, Henning, Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Tian, Chao, Traylor, Matthew, Treutlein, Jens, Trubetskoy, Vassily, Uitterlinden, André G., Umbricht, Daniel, Van der Auwera, Sandra, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Webb, Bradley T., Weinsheimer, Shantel Marie, Wellmann, Jürgen, Willemsen, Gonneke, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Arolt, Volker, Baune, Bernhard T., Berger, Klaus, Boomsma, Dorret I., Cichon, Sven, Dannlowski, Udo, de Geus, E. C. J., DePaulo, J. Raymond, Domenici, Enrico, Domschke, Katharina, Esko, Tõnu, Grabe, Hans J., Hamilton, Steven P., Hayward, Caroline, Heath, Andrew C., Hinds, David A., Kendler, Kenneth S., Kloiber, Stefan, Lewis, Glyn, Li, Qingqin S., Lucae, Susanne, Madden, Pamela F. A., 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 C., 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, Winslow, Ashley R., Lewis, Cathryn M., Levinson, Douglas F., Breen, Gerome, Børglum, Anders D. and Sullivan, Patrick F. 2018. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics 50 (5) , pp. 668-681. 10.1038/s41588-018-0090-3 Item availability restricted.

Guyatt, Anna L., Stergialouli, Evie, Martin, Joanna, Walters, James, O'Donovan, Michael Conlon, Owen, Michael J., Thapar, Anita, Kirov, George, Rodriguez, Santiago, Rai, Dheeraj and Zammit, Stanley 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 10.1002/ajmg.b.32637

Cooper, Miriam, Hammerton, Gemma, Collishaw, Stephan, Langley, Kate, Thapar, Anita, Dalsgaard, Soren, Stergiakouli, Evie, Tilling, Kate, George, Davey Smith, Maughan, Barbara, O'Donovan, Michael, Thapar, Ajay and Riglin, Lucy 2018. Investigating late-onset ADHD: a population cohort investigation. Journal of Child Psychology and Psychiatry 10.1111/jcpp.12911

Gusev, Alexander, Mancuso, Nicholas, Won, Hyejung, Kousi, Maria, Finucane, Hilary K., Reshef, Yakir, Song, Lingyun, Safi, Alexias, McCarroll, Steven, Neale, Benjamin M., Ophoff, Roel A., O'Donovan, Michael C., Crawford, Gregory E., Geschwind, Daniel H., Katsanis, Nicholas, Sullivan, Patrick F., Pasaniuc, Bogdan and Price, Alkes L. 2018. Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights. Nature Genetics 50 (4) , pp. 538-548. 10.1038/s41588-018-0092-1

Cosgrove, Donna, Mothersill, David O., Whitton, Laura, Harold, Denise, Kelly, Sinead, Holleran, Laurena, Holland, Jessica, Anney, Richard, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, Michael, Corvin, Aiden, Morris, Derek W. and Donohoe, Gary 2018. Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (3) , pp. 369-376. 10.1002/ajmg.b.32620 Item availability restricted.

Lancaster, Thomas, Dimitriadis, Stavros, Tansey, Katherine E., Perry, Gavin, Ihssen, Niklas, Jones, Derek K., Singh, Krish Devi, Holmans, Peter Alan, Pocklington, Andrew, Davey Smith, George, Zammit, Stanley, Hall, Jeremy, O'Donovan, Michael Conlon, Owen, Michael J. and Linden, David Edmund Johannes 2018. Structural and functional neuroimaging of polygenic risk for schizophrenia: a recall-by-genotype based approach. Schizophrenia Bulletin , sby037. 10.1093/schbul/sby037

Escott-Price, Valentina, Smith, Daniel J., Kendall, Kimberley, Ward, Joey, Kirov, George, Owen, Michael J., Walters, James and O'Donovan, Michael C. 2018. Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort. Psychological Medicine 10.1017/S0033291718000454 Item availability restricted.

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 10.1017/S0033291717002987

Allardyce, Judith, Leonenko, Ganna, Hamshere, Marian, Pardinas, Antonio, Forty, Liz, Knott, Sarah, Gordon-Smith, Katherine, Porteous, David, Hayward, Caroline, Di Florio, Arianna, Jones, Lisa, McIntosh, Andrew, Owen, Michael J., Holmans, Peter, Walters, James, Craddock, Nicholas, Jones, Ian, O'Donovan, Michael C. and Escott-Price, Valentina 2018. Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia. JAMA - The Journal of the American Medical Association 10.1101/160119 Item availability restricted.

Baker, Emily, Schmidt, Karl Michael, Sims, Rebecca, O'Donovan, Michael C., Williams, Julie, Holmans, Peter and Escott-Price, Valentina 2018. POLARIS: polygenic LD-adjusted risk score approach for set-based analysis of GWAS data. Genetic Epidemiology 10.1002/gepi.22117

John, Ann, McGregor, Joanna, Jones, Ian, Lee, Sze Chim, Walters, James T. R., Owen, Michael J., O'Donovan, Michael C., Del Pozo Banos, Marcos, Berridge, Damon and Lloyd, Keith 2018. Premature mortality among people with severe mental illness – new evidence from linked primary care data. Royal Society Open Science 10.1098/rsos.180333

Fabbri, Chiara, Tansey, Katherine, Perlis, Roy H., Hauser, Joanna, Maier, Wolfgang, Mors, Ole, Placentino, Anna, Rietschel, Marcella, Souery, Daniel, Breen, Gerome, Lee, Charles Curtis, Newhouse, Stephen, Patel, Hamel, O'Donovan, Michael C., Lewis, Glyn, Jenkins, Gregory, Weinshilboum, Richard M., Farmer, Anne, Aitchison, Katherine J., Craig, Ian, McGuffin, Peter, Schruers, Koen, Biernacka, Joanna M., Uher, Rudolf and Lewis, Cathryn M. 2018. Effect of cytochrome CYP2C19 metabolizing activity on antidepressant response and side effects: meta-analysis of data from genome-wide association studies. European Neuropsychopharmacology Item availability restricted.

Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas, Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F., Rajagopal, Veera M., Als, Thomas D., Tan Hoang, Hoang, Girdhar, Kiran, Boocock, James, Roussos, Panagiotis, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric, Purcell, Shaun, Demontis, Ditte, Borglum, Anders, Walters, James, O'Donovan, Michael C., Sullivan, Patrick F., Owen, Michael J., Devlin, Bernie, Sieberts, Solveig, Cox, Nancy, Kyung Im, Hae, Sklar, Pamela and Ayumi Stahl, Eli 2018. Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development. Nature Genetics

Escott-Price, Valentina, Bracher-Smith, Matthew, Menzies, Georgina, Walters, James, Kirov, George, Owen, Michael J. and O'Donovan, Michael C. 2018. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank. Journal of Molecular Psychiatry

Kopczynska, Maja, Zelek, Wioleta, Touchard, Samuel, Gaughran, Fiona, Di Forti, Marta, Mondelli, Valeria, Murray, Robin, O'Donovan, Michael and Morgan, B. Paul 2017. Complement system biomarkers in first episode psychosis. Schizophrenia Research 10.1016/j.schres.2017.12.012

Riglin, Lucy, Collishaw, Stephan, Richards, Alexander, Thapar, Ajay, Rice, Frances, Maughan, B., O'Donovan, Michael Conlon and Thapar, Anita 2017. The impact of schizophrenia and mood disorder risk alleles on emotional problems: investigating change from childhood to middle age. Psychological Medicine 10.1017/S0033291717003634

Martin, Joanna, Walters, Raymond K., Demontis, Ditte, Mattheisen, Manuel, Lee, S. Hong, Robinson, Elise, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Eriksson, Nicholas, 23andMe Research Team, , Psychiatric Genomics Consortium: ADHD Subgroup, , iPSYCH–Broad ADHD Workgroup, , Werge, Thomas, Mortensen, Preben Bo, Giortz Pedersen, Marianne, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Wray, Naomi R., Franke, Barbara, Faraone, Stephen V., O'Donovan, Michael Conlon, Thapar, Anita, Borglum, Anders D. and Neale, Benjamin M. 2017. A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder. Biological Psychiatry 83 (12) , pp. 1044-1053. 10.1016/j.biopsych.2017.11.026 Item availability restricted.

Green, Elaine K., Di Florio, Arianna, Forty, Elizabeth, Gordon-Smith, Katherine, Grozeva, Detelina, Fraser, Christine, Richards, Alexander, Moran, Jennifer L., Purcell, Shaun, Sklar, Pamela, Kirov, George, Owen, Michael, O'Donovan, Michael, Craddock, Nicholas, Jones, Lisa and Jones, Ian 2017. Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 (8) , pp. 767-771. 10.1002/ajmg.b.32572 Item availability restricted.

Allardyce, Judith, Leonenko, Ganna, Hamshere, Marian, Pardiñas, Antonio F., Forty, Elizabeth, Knott, Sarah, Gordon-Smith, Katherine, Porteous, David J., Haywood, Caroline, Di Florio, Arianna, Jones, Lisa, McIntosh, Andrew M., Owen, Michael John, Holmans, Peter Alan, Walters, James T. R., Craddock, Nicholas, Jones, Ian R., O'Donovan, Michael Conlon and Escott-Price, Valentina 2017. Association between schizophrenia-related polygenic liability and the occurrence and level of mood incongruent psychotic symptoms in bipolar disorder. JAMA Psychiatry 10.1001/jamapsychiatry.2017.3485

Li, Zhiqiang, Chen, Jianhua, Yu, Hao, He, Lin, Xu, Yifeng, Zhang, Dai, Yi, Qizhong, Li, Changgui, Li, Xingwang, Shen, Jiawei, Song, Zhijian, Ji, Weidong, Wang, Meng, Zhou, Juan, Chen, Boyu, Liu, Yahui, Wang, Jiqiang, Wang, Peng, Yang, Ping, Wang, Qingzhong, Feng, Guoyin, Liu, Benxiu, Sun, Wensheng, Li, Baojie, He, Guang, Li, Weidong, Wan, Chunling, Xu, Qi, Li, Wenjin, Wen, Zujia, Liu, Ke, Huang, Fang, Ji, Jue, Ripke, Stephan, Yue, Weihua, Sullivan, Patrick F, O'Donovan, Michael Conlon and Shi, Yongyong 2017. Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. Nature Genetics 49 (11) , pp. 1576-1583. 10.1038/ng.3973

Riglin, Lucy, Eyre, Olga, Cooper, Miriam, Collishaw, Stephan, Martin, Joanna, Langley, Kate, Leibenluft, E, Stringaris, A, Thapar, A, Maughan, B, O'Donovan, Michael and Thapar, Anita 2017. Investigating the genetic underpinnings of early-life irritability. Translational Psychiatry 7 , e1241. doi:10.1038/tp.2017.212

Direk, Nese, Williams, Stephanie, Smith, Jennifer A., Ripke, Stephan, Air, Tracy, Amare, Azmeraw T., Amin, Najaf, Baune, Bernhard T., Bennett, David A., Blackwood, Douglas H.R., Boomsma, Dorret, Breen, Gerome, Buttenschøn, Henriette N., Byrne, Enda M., Børglum, Anders D., Castelao, Enrique, Cichon, Sven, Clarke, Toni-Kim, Cornelis, Marilyn C., Dannlowski, Udo, De Jager, Philip L., Demirkan, Ayse, Domenici, Enrico, van Duijn, Cornelia M., Dunn, Erin C., Eriksson, Johan G., Esko, Tonu, Faul, Jessica D., Ferrucci, Luigi, Fornage, Myriam, de Geus, Eco, Gill, Michael, Gordon, Scott D., Grabe, Hans Jörgen, van Grootheest, Gerard, Hamilton, Steven P., Hartman, Catharina A., Heath, Andrew C., Hek, Karin, Hofman, Albert, Homuth, Georg, Horn, Carsten, Jan Hottenga, Jouke, Kardia, Sharon L.R., Kloiber, Stefan, Koenen, Karestan, Kutalik, Zoltán, Ladwig, Karl-Heinz, Lahti, Jari, Levinson, Douglas F., Lewis, Cathryn M., Lewis, Glyn, Li, Qingqin S., Llewellyn, David J., Lucae, Susanne, Lunetta, Kathryn L., MacIntyre, Donald J., Madden, Pamela, Martin, Nicholas G., McIntosh, Andrew M., Metspalu, Andres, Milaneschi, Yuri, Montgomery, Grant W., Mors, Ole, Mosley, Thomas H., Murabito, Joanne M., Müller-Myhsok, Bertram, Nöthen, Markus M., Nyholt, Dale R., O'Donovan, Michael Conlon, Penninx, Brenda W., Pergadia, Michele L., Perlis, Roy, Potash, James B., Preisig, Martin, Purcell, Shaun M., Quiroz, Jorge A., Räikkönen, Katri, Rice, John P., Rietschel, Marcella, Rivera, Margarita, Schulze, Thomas G., Shi, Jianxin, Shyn, Stanley, Sinnamon, Grant C., Smit, Johannes H., Smoller, Jordan W., Snieder, Harold, Tanaka, Toshiko, Tansey, Katherine E., Teumer, Alexander, Uher, Rudolf, Umbricht, Daniel, Van der Auwera, Sandra, Ware, Erin B., Weir, David R., Weissman, Myrna M., Willemsen, Gonneke, Yang, Jingyun, Zhao, Wei, Tiemeier, Henning and Sullivan, Patrick F. 2017. An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry 82 (5) , pp. 322-329. 10.1016/j.biopsych.2016.11.013

Sims, Rebecca, van der Lee, Sven J, Naj, Adam C, Badarinarayan, Nandini, Morgan, Taniesha, Denning, Nicola, Majounie, Elisa, O'Donovan, Michael, Owen, Michael, Jones, Lesley, Escott-Price, Valentina, Holmans, Peter and Williams, Julie 2017. Rare coding variants in PLCG2, ABI3 and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics 49 , pp. 1373-1384. 10.1038/ng.3916

Leonenko, Ganna, Allardyce, Judith, Forty, Liz, Knott, Sarah, Craddock, Nicholas, Owen, Michael J., O'Donovan, Michael Conlon, Jones, Ian and Escott-Price, Valentina 2017. Investigation of relationships between bipolar disorder phenotypes and genome-wide significant loci from PGC2 schizophrenia. European Neuropsychopharmacology 27 (S3) , S383-S384. 10.1016/j.euroneuro.2016.09.416 Item availability restricted.

Leonenko, Ganna, Richards, Alexander L., Walters, James T., Pocklington, Andrew, Chambert, Kimberly, Al Eissa, Mariam M., Sharp, Sally I., O'Brien, Niamh L., Curtis, David, Bass, Nicholas J., McQuillin, Andrew, Hultman, Christina, Moran, Jennifer L., McCarroll, Steven A., Sklar, Pamela, Neale, Benjamin M., Holmans, Peter A., Owen, Michael J., Sullivan, Patrick F. and O'Donovan, Michael C. 2017. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 10.1002/ajmg.b.32560

Kendall, Kimberley, Rees, Elliott, Escott-Price, Valentina, Einon, Mark, Thomas, Rhys, Hewitt, Jonathan, O'Donovan, Michael Conlon, Owen, Michael John, Walters, James Tynan Rhys and Kirov, George 2017. Cognitive performance among carriers of pathogenic copy number variants: analysis of 152,000 UK Biobank subjects. Biological Psychiatry 82 (2) , pp. 103-110. 10.1016/j.biopsych.2016.08.014

Hendricks, Audrey E., Bochukova, Elena G., Marenne, Gaëlle, Keogh, Julia M., Atanassova, Neli, Bounds, Rebecca, Wheeler, Eleanor, Mistry, Vanisha, Henning, Elana, Körner, Antje, Muddyman, Dawn, McCarthy, Shane, Hinney, Anke, Hebebrand, Johannes, Scott, Robert A., Langenberg, Claudia, Wareham, Nick J., Surendran, Praveen, Howson, Joanna M., Butterworth, Adam S., Danesh, John, Nordestgaard, Børge G, Nielsen, Sune F., Afzal, Shoaib, Papadia, Sofia, Ashford, Sofie, Garg, Sumedha, Millhauser, Glenn L., Palomino, Rafael I., Kwasniewska, Alexandra, Tachmazidou, Ioanna, O'Rahilly, Stephen, Zeggini, Eleftheria, Barroso, Ines, Farooqi, I. Sadaf, UK10K, Consortium, Craddock, Nicholas, Holmans, Peter, O'Donovan, Michael C., Owen, Michael J., Walters, James T. R. and Williams, Hywel J. 2017. Rare variant analysis of human and rodent obesity genes in individuals with severe childhood obesity. Scientific Reports 7 , 4394. 10.1038/s41598-017-03054-8

Singh, Tarjinder, Walters, James, Johnstone, Mandy, Curtis, David, Suvisaari, Jaana, Torniainen, Minna, Rees, Elliott, Iyegbe, Conrad, Blackwood, Douglas, McIntosh, Andrew M., Kirov, George, Geschwind, Daniel, Murray, Robin M, Di Forti, Marta, Bramon, Elvira, Gandal, Michael, Hultman, Christina M., Sklar, Pamela, Palotie, Aarno, Patrick F., Sullivan, O'Donovan, Michael C., Owen, Michael and Barrett, Jeffrey C. 2017. The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nature Genetics 49 , pp. 1167-1173. 10.1038/ng.3903

Witt, Stephanie H, Streit, Fabian, Jungkunz, Martin, Frank, Josef, Awasthi, Swapnil, Reinbold, Céline S, Treutlein, Jens, Degenhardt, Franziska, Forstner, Andreas J, Heilmann-Heimbach, Stefanie, Dietl, Lydie, Schwarze, Cornelia E, Schende, Darja l, Strohmaier, Jana, Bethell, Andrew, Craddock, Nicholas, Di Florio, Arianna, Forty, Elizabeth, Fraser, Christine, Hamshere, Marian, Holmans, Peter, Jones, Ian, Kirov, George, O'Donovan, Michael C and Owen, Michael J 2017. Genome-wide association study of borderline personality disorder reveals genetic overlap with the bipolar disorder, schizophrenia and major depression. Translational Psychiatry

Ward, Joey, Strawbridge, Rona J., Bailey, Mark E. S., Graham, Nicholas, Ferguson, Amy, Lyall, Donald M., Cullen, Brenda, Pidgeon, Laura M., Cavanagh, Jonathan, Mackay, Daniel F., Pell, Jill P., O'Donovan, Michael, Escott-Price, Valentina and Smith, Daniel J. 2017. Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with MDD, anxiety disorder and schizophrenia. Translational Psychiatry 10.1101/117796

Hannon, Eilis, Weedon, Mike, Bray, Nicholas, O'Donovan, Michael and Mill, Jonathan 2017. Pleiotropic effects of trait-associated genetic variation on DNA methylation: utility for refining GWAS loci. American Journal of Human Genetics 100 (6) , pp. 954-959. 10.1016/j.ajhg.2017.04.013

García-González, Judit, Tansey, Katherine E., Hauser, Joanna, Henigsberg, Neven, Maier, Wolfgang, Mors, Ole, Placentino, Anna, Rietschel, Marcella, Souery, Daniel, Zagar, Tina, Czerski, Piotr M., Jerman, Borut, Buttenschøn, Henriette N., Schulze, Thomas G., Zobel, Astrid, Farmer, Anne, Aitchison, Katherine J., Craig, Ian, McGuffin, Peter, Giupponi, Michel, Perroud, Nader, Bondolfi, Guido, Evans, David, O'Donovan, Michael Conlon, Peters, Tim J., Wendland, Jens R., Lewis, Glyn, Kapur, Shitij, Perlis, Roy, Arolt, Volker, Domschke, Katharina, Breen, Gerome, Curtis, Charles, Sang-Hyuk, Lee, Kan, Carol, Newhouse, Stephen, Patel, Hamel, Baune, Bernhard T., Uher, Rudolf, Lewis, Cathryn M. and Fabbri, Chiara 2017. Pharmacogenetics of antidepressant response: a polygenic approach. Progress in Neuro-Psychopharmacology and Biological Psychiatry 75 , pp. 128-134. 10.1016/j.pnpbp.2017.01.011

McLaughlin, Russell L., Schijven, Dick, van Rheenen, Wouter, van Eijk, Kristel R., O'Brien, Margaret, Kahn, René S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, van den Berg, Leonard H., Luykx, Jurjen J., Hardiman, Orla, Veldink, Jan H., Shatunov, Aleksey, Dekker, Annelot M., Diekstra, Frank P., Pulit, Sara L., van der Spek, Rick A. A., van Doormaal, Perry T. C., Sproviero, William, Jones, Ashley R., Nicholson, Garth A., Rowe, Dominic B., Pamphlett, Roger, Kiernan, Matthew C., Bauer, Denis, Kahlke, Tim, Williams, Kelly, Eftimov, Filip, Fogh, Isabella, Ticozzi, Nicola, Lin, Kuang, Millecamps, Stéphanie, Salachas, François, Meininger, Vincent, de Carvalho, Mamede, Pinto, Susana, Mora, Jesus S., Rojas-García, Ricardo, Polak, Meraida, Chandran, Siddharthan, Colville, Shuna, Swingler, Robert, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Orrell, Richard W., Pittman, Alan, Sidle, Katie, Fratta, Pietro, Malaspina, Andrea, Petri, Susanne, Abdulla, Susanna, Drepper, Carsten, Sendtner, Michael, Meyer, Thomas, Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Basak, Nazli, Meitinger, Thomas, Lichtner, Peter, Blagojevic-Radivojkov, Milena, Andres, Christian R., Maurel, Cindy, Bensimon, Gilbert, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A. M., Saker-Delye, Safa, Dürr, Alexandra, Wood, Nicholas, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Rietschel, Marcella, Cichon, Sven, Nöuthen, Markus M., Amouyel, Philippe, Tzourio, Christophe, Dartigues, Jean- François, Uitterlinden, Andre G., Rivadeneira, Fernando, Estrada, Karol, Hofman, Albert, Curtis, Charles, van der Kooi, Anneke J., de Visser, Marianne, Weber, Markus, Shaw, Christopher E., Smith, Bradley N., Pansarasa, Orietta, Cereda, Cristina, Del Bo, Roberto, Comi, Giacomo P., D'Alfonso, Sandra, Bertolin, Cinzia, Sorarù, Gianni, Mazzini, Letizia, Pensato, Viviana, Gellera, Cinzia, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Arcuti, Simon, Capozzo, Rosa, Zecca, Chiara, Lunetta, Christian, Penco, Silvana, Riva, Nilo, Padovani, Alessandro, Filosto, Massimiliano, Blair, Ian, Leigh, P Nigel, Casale, Federico, Chio, Adriano, Beghi, Ettore, Pupillo, Elisabetta, Tortelli, Rosanna, Logroscino, Giancarlo, Powell, John, Ludolph, Albert C., Weishaupt, Jochen H., Robberecht, Wim, Van Damme, Philip, Brown, Robert H., Glass, Jonathan, Landers, John E., Andersen, Peter M., Corcia, Philippe, Vourc'h, Patrick, Silani, Vincenzo, van Es, Michael A., Pasterkamp, R Jeroen, Lewis, Cathryn M., Breen, Gerome, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. 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Stergiakouli, Evangelia, Langley, Kate, Williams, Hywel, Walters, James Tynan Rhys, Williams, Nigel Melville, Suren, S., Giegling, I., Wilkinson, Lawrence, Owen, Michael John, O'Donovan, Michael Conlon, Rujescu, D., Thapar, Anita and Davies, William 2011. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes Brain and Behavior 10 (3) , pp. 334-344. 10.1111/j.1601-183x.2010.00672.x

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Ikeda, Masashi, Aleksic, Branko, Kinoshita, Yoko, Okochi, Tomo, Kawashima, Kunihiro, Kushima, Itaru, Ito, Yoshihito, Nakamura, Yukako, Kishi, Taro, Okumura, Takenori, Fukuo, Yasuhisa, Williams, Hywel John, Hamshere, Marian Lindsay, Ivanov, Dobril, Inada, Toshiya, Suzuki, Michio, Hashimoto, Ryota, Ujike, Hiroshi, Takeda, Masatoshi, Craddock, Nicholas John, Kaibuchi, Kozo, Owen, Michael John, Ozaki, Norio, O'Donovan, Michael Conlon and Iwata, Nakao 2011. Genome-Wide Association Study of Schizophrenia in a Japanese Population. Biological Psychiatry 69 (5) , pp. 472-478. 10.1016/j.biopsych.2010.07.010

Zuliani, Riccardo, Moorhead, T. William J., Bastin, Mark E., Johnstone, Eve C., Lawrie, Stephen M., Brambilla, Paolo, O'Donovan, Michael Conlon, Owen, Michael John, Hall, Jeremy and McIntosh, Andrew M. 2011. Genetic variants in the ErbB4 gene are associated with white matter integrity. Psychiatry Research: Neuroimaging 191 (2) , pp. 133-137. 10.1016/j.pscychresns.2010.11.001

Reilly, Muredach P, Li, Mingyao, He, Jing, Ferguson, Jane F, Stylianou, Ioannis M, Mehta, Nehal N, Burnett, Mary Susan, Devaney, Joseph M, Knouff, Christopher W, Thompson, John R, Horne, Benjamin D, Stewart, Alexandre FR, Assimes, Themistocles L, Wild, Philipp S, Allayee, Hooman, Nitschke, Patrick Linsel, Patel, Riyaz S, Martinelli, Nicola, Girelli, Domenico, Quyyumi, Arshed A, Anderson, Jeffrey L, Erdmann, Jeanette, Hall, Alistair S, Schunkert, Heribert, Quertermous, Thomas, Blankenberg, Stefan, Hazen, Stanley L, Roberts, Robert, Kathiresan, Sekar, Samani, Nilesh J, Epstein, Stephen E, Rader, Daniel J, Craddock, Nicholas John, Escott-Price, Valentina, Fraser, Christine, Green, Elaine, Grozeva, Detelina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2011. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. The Lancet 377 (9763) , pp. 383-392. 10.1016/S0140-6736(10)61996-4

Williams, Hywel John, Craddock, Nicholas John, Russo, Giancarlo, Hamshere, Marian Lindsay, Escott-Price, Valentina, Dwyer, Sarah Lynne, Smith, Rhodri L., Green, Elaine Karen, Grozeva, Detelina Valentinova, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2011. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Human Molecular Genetics 20 (2) , pp. 387-391. 10.1093/hmg/ddq471

Bridges, Michael, Heron, Elizabeth A., O'Dushlaine, Colm, Segurado, Ricardo, Morris, Derek, Corvin, Aiden, Gill, Michael, Pinto, Carlos, O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra and Owen, Michael John 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802

Hamshere, Marian Lindsay, O'Donovan, Michael Conlon, Jones, Ian Richard, Jones, L., Kirov, George, Green, Elaine Karen, Escott-Price, Valentina, Grozeva, Detelina Valentinova, Bass, N., McQuillin, A., Gurling, H., St Clair, D., Young, A. H., Ferrier, I. N., Farmer, Anne, McGuffin, Peter, Sklar, P., Purcell, S., Holmans, Peter Alan, Owen, Michael John and Craddock, Nicholas John 2011. Polygenic dissection of the bipolar phenotype. British Journal of Psychiatry 198 (4) , pp. 284-288. 10.1192/bjp.bp.110.087866

Williams, Nigel Melville, O'Donovan, Michael Conlon, Owen, Michael John and Thapar, Anita 2011. Structural variations in attention-deficit hyperactivity disorder - Authors' reply [Letter]. The Lancet 377 (9763) , p. 378. 10.1016/S0140-6736(11)60121-9

Carroll, Liam Stuart, Williams, Hywel John, Walters, James Tynan Rhys, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2011. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 844-849. 10.1002/ajmg.b.31231

Green, Elaine Karen, Grozeva, Detelina Valentinova, Sims, Rebecca, Raybould, Rachel, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, St. Clair, D., Young, A.H., Ferrier, I.N., Kirov, George, Jones, Ian Richard, Jones, L., Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2011. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (4) , pp. 490-492. 10.1002/ajmg.b.31187

Smith, Rhodri L., Knight, Deborah, Williams, Hywel John, Dwyer, Sarah Lynne, Richards, Alexander, Kirov, George, O'Donovan, Michael Conlon and Owen, Michael John 2011. Analysis of neurogranin (NRGN) in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (5) , pp. 532-535. 10.1002/ajmg.b.31191

Sims, Rebecca, Dwyer, Sarah Lynne, Harold, Denise, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade Alice, Denning, Nicola, Abraham, Richard Alun, Ivanov, Dobril, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 764-771. 10.1002/ajmg.b.31216

Williams, Hywel John, Escott-Price, Valentina, Smith, Rhodri L., Dwyer, Sarah Lynne, Russo, Giancarlo, Owen, Michael John and O'Donovan, Michael Conlon 2011. Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 781-784. 10.1002/ajmg.b.31219

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Escott-Price, Valentina, O'Dushlaine, Colm, Purcell, Shaun, Craddock, Nicholas John, Holmans, Peter Alan and O'Donovan, Michael Conlon 2011. Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study. Genetic Epidemiology 35 (8) , pp. 861-866. 10.1002/gepi.20636

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Hansen, Thomas, Ingason, Andrés, Djurovic, Srdjan, Melle, Ingrid, Fenger, Mogens, Gustafsson, Omar, Jakobsen, Klaus D., Rasmussen, Henrik B., Tosato, Sarah, Rietschel, Marcella, Frank, Josef, Owen, Michael John, Bonetto, Chiara, Suvisaari, Jaana, Thygesen, Johan Hilge, Pétursson, Hannes, Lönnqvist, Jouko, Sigurdsson, Engilbert, Giegling, Ina, Craddock, Nicholas John, O'Donovan, Michael Conlon, Ruggeri, Mirella, Cichon, Sven, Ophoff, Roel A., Pietiläinen, Olli, Peltonen, Leena, Nöthen, Markus M., Rujescu, Dan, St. Clair, David, Collier, David A., Andreassen, Ole A. and Werge, Thomas 2011. At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biological Psychiatry 70 (1) , pp. 59-63. 10.1016/j.biopsych.2011.01.031

Donohoe, Gary, Walters, James Tynan Rhys, Morris, Derek W., Da Costa, Andreia, Rose, Emma, Hargreaves, April, Maher, Katie, Hayes, Eimear, Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Muglia, Pierandrea, Moskvina, Valentina, Owen, Michael John, O'Donovan, Michael Conlon, Gill, Michael, Corvin, Aiden and Rujescu, Dan 2011. A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809 [Letter]. Schizophrenia Research 125 (2-3) , pp. 304-306. 10.1016/j.schres.2010.10.019

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Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Kamatani, Y., Kamatani, N., Stoianov, D., Vazharova, R., Karachanak, S., Zaharieva, I., Dimova, I., Hadjidekova, S., Milanova, V., Madjirova, N., Gerdjikov, I., Tolev, T., Poryazova, N., O'Donovan, Michael Conlon, Owen, Michael John, Kirov, George, Toncheva, D. and Nakamura, Y. 2011. Genome-wide association study on bipolar disorder in the Bulgarian population. Genes, Brain and Behavior 10 (7) , pp. 789-797. 10.1111/j.1601-183X.2011.00721.x

Lewis, Glyn, Mulligan, Jean, Wiles, Nicola, Cowen, Philip, Craddock, Nicholas John, Ikeda, Masashi, Grozeva, Detelina Valentinova, Mason, Victoria, Nutter, David, Sharp, Deborah, Tallon, Debbie, Thomas, Laura, O'Donovan, Michael Conlon and Peters, Tim J. 2011. Polymorphism of the 5-HT transporter and response to antidepressants: randomised controlled trial. British Journal of Psychiatry 198 (6) , pp. 464-471. 10.1192/bjp.bp.110.082727

Owen, Michael John, O'Donovan, Michael Conlon, Thapar, Anita and Craddock, Nicholas John 2011. Neurodevelopmental hypothesis of schizophrenia. British Journal of Psychiatry 198 (3) , pp. 173-175. 10.1192/bjp.bp.110.084384

Wiles, Nicola J., Mulligan, Jean, Peters, Tim J., Cowen, Philip J., Mason, Victoria, Nutt, David, Sharp, Deborah, Tallon, Debbie, Thomas, Laura, O'Donovan, Michael Conlon and Lewis, Glyn 2011. Severity of depression and response to antidepressants: GENPOD randomised controlled trial. British Journal of Psychiatry 200 (2) , pp. 130-136. 10.1192/bjp.bp.110.091223

Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., Holmans, Peter Alan, O'Donovan, Michael Conlon, Purcell, S. M., Smit, A. B., Verhage, M, Sullivan, P. F., Visscher, P. M. and Posthuma, D 2011. Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry , pp. 1-11. 10.1038/mp.2011.117

Langley, Kate, Martin, Joanna, Agha, Sharifah Shameem, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5) , pp. 398-403.

Dwyer, Sarah Lynne, Williams, Hywel John, Jones, Ian Richard, Jones, L, Walters, James Tynan Rhys, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2011. Investigation of rare non-synonymous variants at ABCA13 in schizophrenia and bipolar disorder [letter]. Molecular Psychiatry 16 (8) , pp. 790-791. 10.1038/mp.2011.2

Ruderfer, D. M., Kirov, George, Chambert, K., Moran, J. L., Owen, Michael John, O'Donovan, Michael Conlon, Sklar, P. and Purcell, S. M. 2011. A family-based study of common polygenic variation and risk of schizophrenia [Letter]. Molecular Psychiatry 16 (9) , pp. 887-888. 10.1038/mp.2011.34

Rietschel, M., Mattheisen, M., Degenhardt, F., Kahn, René S, Linszen, Don H., Os, Jim van, Wiersma, Durk, Bruggeman, Richard, Cahn, Wiepke, de Haan, Lieuwe, Krabbendam, Lydia, Myin-Germeys, Inez, Mühleisen, T. W., Kirsch, P., Esslinger, C., Herms, S., Demontis, D., Steffens, M., Strohmaier, J., Haenisch, B., Breuer, R., Czerski, P. M., Giegling, I., Strengman, E., Schmael, C., Mors, O., Mortensen, P. B., Hougaard, D. M., Ørntoft, T., Kapelski, P., Priebe, L., Basmanav, F. B., Forstner, A. J., Hoffmann, P., Meier, S., Nikitopoulos, J., Moebus, S., Alexander, M., Mössner, R., Wichmann, H.-E., Schreiber, S., Rivandeneira, F., Hofman, A., Uitterlinden, A. G., Wienker, T. F., Schumacher, J., Hauser, J., Maier, W., Cantor, R. M., Erk, S.., Schulze, T. G., Stefansson, Hreinn, Steinberg, Stacy, Gustafsson, Omar, Sigurdsson, Engilbert, Petursson, Hannes, Kong, Augustine, Stefansson, Kari, Pietiläinen, Olli P. H., Tuulio-Henriksson, Annamari, Paunio, Tiina, Lonnqvist, Jouko, Suvisaari, Jaana, Peltonen, Leena, Ruggeri, Mirella, Tosato, Sarah, Walshe, Muriel, Murray, Robin, Collier, David A., St. Clair, David, Hansen, Thomas, Ingason, Andres, Jakobsen, Klaus D., Duong, Linh, Werge, Thomas, Melle, Ingrid, Andreassen, Ole A., Djurovic, Srdjan, Bitter, István, Réthelyi, János M., Abramova, Lilia, Kaleda, Vasily, Golimbet, Vera, Jönsson, Erik G., Terenius, Lars, Agartz, Ingrid, Winkel, Ruud van, Kenis, Gunter, Hert, Marc De, Veldink, Jan, Wiuf, Carsten, Didriksen, Michael, Craddock, Nicholas John, Owen, Michael John, O'Donovan, Michael Conlon, Børglum, A. D., Rujescu, D., Walter, H., Meyer-Lindenberg, A., Nöthen, M. M., Ophoff, R. A. and Cichon, S. 2011. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Molecular Psychiatry , pp. 1-12. 10.1038/mp.2011.80

Langley, Kate, Heron, Jon, O'Donovan, Michael Conlon, Owen, Michael John and Thapar, Anita 2010. Genotype link with extreme antisocial behavior: The contribution of cognitive pathways. Archives of General Psychiatry 67 (12) , pp. 1317-1323. 10.1001/archgenpsychiatry.2010.163

Carroll, Liam Stuart, Williams, Nigel Melville, Escott-Price, Valentina, Russell, Elen, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Grozeva, Detelina Valentinova, Greene, E., Farmer, A., McGuffin, P., Morris, D. W., Corvin, A., Gill, M., Rujescu, D., Sham, P., Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Craddock, Nicholas John, O'Donovan, Michael Conlon and Owen, Michael John 2010. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry 15 (11) , pp. 1101-1111. 10.1038/mp.2009.96

Craddock, Nicholas John, Jones, Lesley, Jones, Ian Richard, Kirov, George, Green, Elaine Karen, Grozeva, Detelina Valentinova, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Vukcevic, D., Caesar, S., Gordon-Smith, Katherine, Fraser, Christine, Russell, E., Norton, Nadine, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A, McGuffin, P., Holmans, Peter Alan, Donnelly, Peter, Owen, Michael John and O'Donovan, Michael Conlon 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype [Corrigendum]. Molecular Psychiatry 15 (11) , p. 1121. 10.1038/mp.2010.62

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Williams, Nigel Melville, Zaharieva, Irina, Martin, Andrew Kenneth, Langley, Kate, Mantripragada, Kiran Kumar, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O., Gustafsson, Omar, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2010. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. The Lancet 376 (9750) , pp. 1401-1408. 10.1016/S0140-6736(10)61109-9

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Allison, David B., Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J., O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila and Owen, Michael John 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) , e1001097. 10.1371/journal.pgen.1001097

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Escott-Price, Valentina, Smith, Michael, Ivanov, Dobril, Blackwood, Douglas, StClair, David, Hultman, Christina, Toncheva, Draga, Gill, Michael, Corvin, Aiden, O'Dushlaine, Colm, Morris, Derek W., Wray, Naomi R., Sullivan, Patrick, Pato, Carlos, Pato, Michele T., Sklar, Pamela, Purcell, Shaun, Holmans, Peter Alan, O'Donovan, Michael Conolon, Owen, Michael John and Kirov, George 2010. Genetic differences between five European populations. Human Heredity 70 (2) , pp. 141-149. 10.1159/000313854

Walters, James Tynan Rhys, Corvin, A., Owen, Michael John, Williams, Hywel John, Dragovic, M., Quinn, E. M., Judge, R., Smith, Daniel J., Norton, Nadine, Giegling, I., Hartmann, A. M., Moller, H.-J., Muglia, P., Escott-Price, Valentina, Dwyer, Sarah Lynne, O'Donoghue, T., Morar, B., Cooper, M., Chandler, D., Jablensky, A., Gill, M., Kaladjieva, L., Morris, D. W., O'Donovan, Michael Conlon, Rujescu, D. and Donohoe, G. 2010. Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia. Archives of General Psychiatry 67 (7) , pp. 692-700. 10.1001/archgenpsychiatry.2010.81

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Langley, Kate, Fowler, Tom Alan, Ford, Tamsin, Thapar, Ajay Kumar, van den Bree, Marianne Bernadette, Harold, Gordon Thomas, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2010. Adolescent clinical outcomes for young people with attention-deficit hyperactivity disorder. British Journal of Psychiatry 196 (3) , pp. 235-240. 10.1192/bjp.bp.109.066274

Craddock, Nicholas John, Jones, L, Jones, Ian Richard, Kirov, George, Green, Elaine Karen, Grozeva, Detelina Valentinova, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Vukcevic, D., Caesar, S., Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen Elizabeth, Norton, Nadine, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, Peter Alan, Donnelly, P., Owen, Michael John and O'Donovan, Michael Conlon 2010. Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype. Molecular Psychiatry 15 (2) , pp. 146-153. 10.1038/mp.2008.66

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Mechelli, A., Viding, E., Kumar, A., Pettersson-Yeo, W., Fusar-Poli, P., Tognin, S., O'Donovan, Michael Conlon and McGuire, P. 2010. Dysbindin modulates brain function during visual processing in children. NeuroImage 49 (1) , pp. 817-822. 10.1016/j.neuroimage.2009.07.030

Owen, Michael John, Craddock, Nicholas John and O'Donovan, Michael Conlon 2010. Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia. Archives of General Psychiatry 67 (7) , pp. 667-673. 10.1001/archgenpsychiatry.2010.69

Ikeda, Masashi, Williams, Nigel Melville, Williams, Hywel John, Smith, Rhodri, Monks, Stephen, Owen, Michael John, Murphy, Kieran C. and O'Donovan, Michael Conlon 2010. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 980-982. 10.1002/ajmg.b.31060

Green, Elaine Karen, Grozeva, Detelina Valentinova, Escott-Price, Valentina, Hamshere, Marian Lindsay, Jones, Ian Richard, Jones, Lisa, Forty, Elizabeth, Caesar, Sian, Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen, St Clair, David, Young, Allan H., Ferrier, Nicol, Farmer, Anne, McGuffin, Peter, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2010. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7) , pp. 1347-1349. 10.1002/ajmg.b.31108

Dwyer, Sarah Lynne, Williams, Hywel, Holmans, Peter Alan, Escott-Price, Valentina, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2010. No evidence that rare coding variants in ZNF804A confer risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (8) , pp. 1411-1416. 10.1002/ajmg.b.31117

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Blake, Derek J., Forrest, Marc, Chapman, Ria M., Tinsley, Caroline L., O'Donovan, Michael Conlon and Owen, Michael John 2010. TCF4, Schizophrenia, and Pitt-Hopkins Syndrome. Schizophrenia Bulletin 36 (3) , pp. 443-447. 10.1093/schbul/sbq035

Liu, Y., Blackwood, D. H., Caesar, S., de Geus, E. J. C., Farmer, A., Ferreira, M. A. R., Ferrier, I. N., Fraser, Christine, Gordon-Smith, K., Green, Elaine Karen, Grozeva, Detelina Valentinova, Gurling, H. M., Hamshere, Marian Lindsay, Heutink, P., Holmans, Peter Alan, Hoogendijk, W. J., Hottenga, J. J., Jones, L., Jones, Ian Richard, Kirov, George, Lin, D., McGuffin, P., Escott-Price, Valentina, Nolen, W. A., Perlis, R. H., Posthuma, D., Scolnick, E. M., Smit, A. B., Smit, J. H., Smoller, J. W., St Clair, D., van Dyck, R., Verhage, M., Willemsen, G., Young, A. H., Zandbelt, T., Boomsma, D. I., Craddock, Nicholas John, O'Donovan, Michael Conlon, Owen, Michael John, Penninx, B. W. J. H., Purcell, S., Sklar, P. and Sullivan, P. F. 2010. Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder [Letter]. Molecular Psychiatry 16 (1) , pp. 2-4. 10.1038/mp.2009.107

Breuer, R., Hamshere, Marian Lindsay, Strohmaier, J., Mattheisen, M., Degenhardt, F., Meier, S., Paul, T., O'Donovan, Michael Conlon, Mühleisen, T. W., Schulze, T. G., Nöthen, M. M., Cichon, S., Craddock, Nicholas John and Rietschel, M. 2010. Independent evidence for the selective influence of GABAA receptors on one component of the bipolar disorder phenotype [letter]. Molecular Psychiatry 16 (6) , pp. 587-589. 10.1038/mp.2010.67

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Fowler, Tom Alan, Langley, Kate, Rice, Frances, van den Bree, Marianne Bernadette, Ross, Kenny, Wilkinson, Lawrence Stephen, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2009. Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatric Genetics 19 (6) , pp. 312-319. 10.1097/YPG.0b013e3283328df4

Hayesmoore, Jesse B. G., Bray, Nicholas John, Cross, William C., Owen, Michael John, O'Donovan, Michael Conlon and Morris, Huw Rees 2009. The effect of age and the H1c MAPT haplotype on MAPT expression in human brain. Neurobiology of Aging 30 (10) , pp. 1652-1656. 10.1016/j.neurobiolaging.2007.12.017

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