Browse by Current Cardiff authors

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 2019. Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits. JAMA Psychiatry 76 (12) , pp. 1256-1265. 10.1001/jamapsychiatry.2019.2508

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

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 10.1001/jamapsychiatry.2019.4079

Cunningham, Adam, Hall, Jeremy, Owen, Michael and Van den Bree, Marianne 2019. Coordination difficulties, IQ and psychopathology in children with high-risk Copy Number Variants. Psychological Medicine 10.1017/S0033291719003210

Hall, Lynsey S, Medway, Christopher W, Pain, Oliver, Pardinas, Antonio F, Rees, Elliott G, Escott-Price, Valentina, Pocklington, Andrew, Bray, Nicholas J, Holmans, Peter A, Walters, James T R, Owen, Michael and O'Donovan, Michael 2019. A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics 10.1093/hmg/ddz253 Item availability restricted.

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 2019. Convergent evidence that ZNF804A is a regulator of pre-messenger RNA processing and gene expression. Schizophrenia Bulletin 45 (6) , pp. 1267-1278. 10.1093/schbul/sby183

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. 2019. Characterization of single gene copy number variants in schizophrenia. Biological Psychiatry 10.1016/j.biopsych.2019.09.023 Item availability restricted.

Sykes, Lucy, Haddon, Josephine, Lancaster, Thomas, Sykes, Arabella, Azzouni, Karima, Niklas, Ihssen, Moon, Anna, Lin, Tzu-Ching, Linden, David, Owen, Michael, O'Donovan, Michael, Humby, Trevor, Wilkinson, Lawrence, Thomas, Kerrie and Hall, Jeremy 2019. Genetic variation in the psychiatric risk gene CACNA1C modulates reversal learning across species. Schizophrenia Bulletin 45 (5) , pp. 1024-1032. 10.1093/schbul/sby146

Pain, Oliver, Pocklington, Andrew, Holmans, Peter, Bray, Nichloas, O'Brian, Heath, Hall, Lynsey, Pardinas, Antonio, O'Donovan, Michael, Owen, Michael and Anney, Richard 2019. Novel insight into the aetiology of autism spectrum disorder gained by integrating expression data with genome-wide association statistics. Biological Psychiatry 86 (4) , pp. 265-273. 10.1016/j.biopsych.2019.04.034

Mulllins, Niamh, Bigdeli, Tim, Børglum, Anders, Coleman, Jonathan, Demontis, Ditte, Mehta, Divya, Power, Roberts, Ripke, Stephan, Stahl, Eli, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan, Forstner, Andreas, Reif, Andreas, Koller, Anna, Świątkowska, Beata, Baune, Bernhard, Müller-Myhsok, Bertram, Konte, Bettina, Penninx, Brenda, Pato, Carlos, Zai, Clement, Rujescu, Dan, Hougaard, David, Quested, Digby, Levinson, Douglas, Binder, Elisabeth, Byrne, Enda, Agerbo, Esben, Streit, Fabin, Mayoral, Fermin, Bellivier, Frank, Dehenhardt, Franziska, Breen, Gerome, Morken, Gunnar, Turecki, Gustavo, Rouleau, Guy, Grabe, Hans, Völzke, Henry, Jones, Ian, Giegling, Ina, Agartz, Ingrid, Melle, Ingrid, Lawrence, Jacob, Potash, James, Walters, James, Strohmaier, Jana, Shi, Jianxin, Hauser, Joanna, Biernacka, Joanna, Vincent, John, Kelsoe, John, Strauss, John, Lissowska, Jolanta, Pimm, Jonathan, Smoller, Jordan, Parra, José, Berger, Klaus, Scott, Laura, Jones, Lisa, Azevedo, M. Helena, Trzaskowski, Maciej, Kogevinas, Manolis, Rietsche, Marcella, Boks, Marco, Ising, Marcus, Grigoroiu-Serbanescu, Maria, Hamshere, Marian, Leboyer, Marion, Frye, Mark, Nöthen, Markus, Alda, Martin, Preisig, Martin, Nordentoft, Merete, Boehnke, Michael, O'Donovan, Michael, Owen, Michael, Pato, Michele, Renteria, Miguel, Budda, Monika, Weissman, Myrna, Wray, Naomi, Bass, Nicholas, Craddock, Nicholas, Smeland, Olav, Andreassen, Ole, Mors, Ole, Gejman, Pablo, Sklar, Pamela, McGrath, Patrick, Hoffman, Per, McGuffin, Peter, Lee, Phil, Mortensen, Preben, Kahn, René, Ophoff, Roel, Adolfsson, Rolf, Van der Auwera, Sandra, Djurovic, Srdjan, Shyn, Stanley, Kloiber, Stefan, Heilmann-Heimbach, Stefanie, Jamain, Stéphane, Hamilton, Steven, McElroy, Susan, Lucae, Susanne, Cichon, Sven, Schulze, Thomas, Hansen, Thomas, Werge, Thomas, Air, Tracy, Nimgaonkar, Vishwajit, Appadurai, Vivek, Cahn, Wiepke, Milaneschi, Yuri, Kendler, Kenneth, Fanous, Ayman, McQuillin, Andrew and Lewis, Cathryn 2019. GWAS of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores. American Journal of Psychiatry 176 (8) , pp. 651-660. 10.1176/appi.ajp.2019.18080957 Item availability restricted.

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 2019. Cyfip1 haploinsufficient rats show white matter changes, myelin thinning, abnormal oligodendrocytes and behavioural inflexibility. Nature Communications 10 , 3455. 10.1038/s41467-019-11119-7

Smeeth, Demelza M., Dima, Danai, Jones, Lisa, Jones, Ian, Craddock, Nicholas, Owen, Michael J., Rietschel, Marcella, Maier, Wolfgang, Korszun, Ania, Rice, John P., Mors, Ole, Preisig, Martin, Uher, Rudolf, Lewis, Cathryn M., Thuret, Sandrine and Powell, Timothy R. 2019. Polygenic risk for circulating reproductive hormone levels and their influence on hippocampal volume and depression susceptibility. Psychoneuroendocrinology 106 , pp. 284-292. 10.1016/j.psyneuen.2019.04.011

Villalon-Reina, Julio, Martinez, Kenia, Qu, Xiaoping, Ching, Christopher, Nir, Talia, Kothapalli, Deydeep, Corbin, Conor, Dagiang, Sun, Lin, Amy, Forsyth, Jennifer, Kushan, Lelia, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel, van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy, Antshel, Kevin, Fremont, Wanda, Campbell, Linda, McCable, Kathryn, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh, Murphy, Declan, Craig, Michael, Emanual, Beverly, McDonna-McGinn, Donna, Vorstman, Jacob, Fiksinski, Ania, Koops, Sanne, Ruparel, Kosha, Roalf, David, Raquel, Gur, Eric, Schmitt, Simon, Tony, Goodrich-Hunsaker, Naomi, Durdle, Courtney, Doherty, Joanne, Cunningham, Adam, Van Den Bree, Marianne, Linden, David, Owen, Michael, Moss, Hayley, Kelly, Sinead, Donohoe, Gary, Murphy, Kieran, Arango, Celso, Jahanshad, Neda, Thompson, Paul and Bearden, Carrie 2019. Altered white matter microstructure in 22q11.2 deletion syndrome: a multi-site diffusion tensor imaging study. Molecular Psychiatry 10.1038/s41380-019-0450-0

Romagnoni, Alberto, Jégou, Simon, Van Steen, Kristel, Wainrib, Gilles, Hugot, Jean-Pierre, Forty, Liz, Gordon-Smith, Katherine, Green, Elaine, Grozeva, Detelina, Jones, Ian R, Kirov, George, O'Donovan, Michael C, Owen, Michael J, Russell, Ellie and Craddock, Nick 2019. Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data. Scientific Reports 9 (1) , -. 10.1038/s41598-019-46649-z

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 WP2 Group, 2019. The relationship between polygenic risk scores and cognition in schizophrenia. Schizophrenia Bulletin 10.1093/schbul/sbz061

Zhang, Xianglong, Abdellaoui, Abdel, Rucker, James, de Jong, Simone, Potash, James B., Weissman, Myrna M., Shi, Jianxin, Knowles, James A., Pato, Carlos, Pato, Michele, Sobell, Janet, Smit, Johannes H., Hottenga, Jouke-Jan, de Geus, Eco J.C., Lewis, Cathryn M., Buttenschøn, Henriette N., Craddock, Nick, Jones, Ian, Jones, Lisa, McGuffin, Peter, Mors, Ole, Owen, Michael J., Preisig, Martin, Rietschel, Marcella, Rice, John P., Rivera, Margarita, Uher, Rudolf, Gejman, Pablo V., Sanders, Alan R., Boomsma, Dorret, Penninx, Brenda W.J.H., Breen, Gerome and Levinson, Douglas F. 2019. Genome-wide burden of rare short deletions is enriched in major depressive disorder in four cohorts. Biological Psychiatry 85 (12) , pp. 1065-1073. 10.1016/j.biopsych.2019.02.022

Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O'Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S., Theis, Fabian J., Räikkönen, Katri, Binder, Elisabeth B., Craddock, Nick, Escott-Price, Valentina, Owen, Michael J. and O'Donovan, Michael C. 2019. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications 10 , 2548. 10.1038/s41467-019-10461-0

Cunningham, Adam, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn, Linden, David, Hall, Jeremy, Owen, Michael and van den Bree, Marianne 2019. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion Syndrome. Journal of Neurodevelopmental Disorders 11 , 8. 10.1186/s11689-019-9271-3

Legge, Sophie, Dennison, Charlotte, Pardinas, Antonio, Rees, Elliott, Lynham, Amy, Hopkins, Lucinda, Bates, Lesley, Kirov, George, Owen, Michael, O'Donovan, Michael and Walters, James 2019. Clinical indicators of treatment-resistant psychosis. British Journal of Psychiatry 10.1192/bjp.2019.120

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 2019. Pharmacogenomic variants and drug interactions identified through the genetic analysis of clozapine metabolism. American Journal of Psychiatry 176 (6) , pp. 477-486. 10.1176/appi.ajp.2019.18050589 Item availability restricted.

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 2019. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. British Journal of Psychiatry 214 (05) , pp. 297-304. 10.1192/bjp.2018.301

Stahl, Eli A., Breen, Gerome, Forstner, Andreas J., McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan R. I., Gaspar, Héléna A., de Leeuw, Christiaan A., Steinberg, Stacy, Pavlides, Jennifer M. Whitehead, Trzaskowski, Maciej, Byrne, Enda M., Pers, Tune H., Holmans, Peter A., Richards, Alexander L., Abbott, Liam, Agerbo, Esben, Akil, Huda, Albani, Diego, Alliey-Rodriguez, Ney, Als, Thomas D., Anjorin, Adebayo, Antilla, Verneri, Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie, Barchas, Jack D., Bass, Nicholas, Bauer, Michael, Belliveau, Richard, Bergen, Sarah E., Pedersen, Carsten Bøcker, Bøen, Erlend, Boks, Marco P., Boocock, James, Budde, Monika, Bunney, William, Burmeister, Margit, Bybjerg-Grauholm, Jonas, Byerley, William, Casas, Miquel, Cerrato, Felecia, Cervantes, Pablo, Chambert, Kimberly, Charney, Alexander W., Chen, Danfeng, Churchhouse, Claire, Clarke, Toni-Kim, Coryell, William, Craig, David W., Cruceanu, Cristiana, Curtis, David, Czerski, Piotr M., Dale, Anders M., de Jong, Simone, Degenhardt, Franziska, Del-Favero, Jurgen, DePaulo, J. Raymond, Djurovic, Srdjan, Dobbyn, Amanda L., Dumont, Ashley, Elvsåshagen, Torbjørn, Escott-Price, Valentina, Fan, Chun Chieh, Fischer, Sascha B., Flickinger, Matthew, Foroud, Tatiana M., Forty, Elizabeth, Frank, Josef, Fraser, Christine, Freimer, Nelson B., Frisén, Louise, Gade, Katrin, Gage, Diane, Garnham, Julie, Giambartolomei, Claudia, Pedersen, Marianne Giørtz, Goldstein, Jaqueline, Gordon, Scott D., Gordon-Smith, Katherine, Green, Elaine K., Green, Melissa J., Greenwood, Tiffany A., Grove, Jakob, Guan, Weihua, Guzman-Parra, José, Hamshere, Marian, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hipolito, Maria, Hoffmann, Per, Holland, Dominic, Huckins, Laura, Jamain, Stéphane, Johnson, Jessica S., Juréus, Anders, Kandaswamy, Radhika, Karlsson, Robert, Kennedy, James L., Kittel-Schneider, Sarah, Knowles, James A., Kogevinas, Manolis, Koller, Anna C., Kupka, Ralph, Lavebratt, Catharina, Lawrence, Jacob, Lawson, William B., Leber, Markus, Lee, Phil H., Levy, Shawn E., Li, Jun Z., Liu, Chunyu, Lucae, Susanne, Maaser, Anna, MacIntyre, Donald J., Mahon, Pamela B., Maier, Wolfgang, Martinsson, Lina, McCarroll, Steve, McGuffin, Peter, McInnis, Melvin G., McKay, James, Medeiros, Helena, Medland, Sarah E., Meng, Fan, Milani, Lili, Montgomery, Grant W., Morris, Derek W., Mühleisen, Thomas W., Mullins, Niamh, Nguyen, Hoang, Nievergelt, Caroline M., Adolfsson, Annelie Nordin, Nwulia, Evaristus A., O'Donovan, Claire, Loohuis, Loes M. Olde, Ori, Anil P. S., Oruc, Lilijana, Ösby, Urban, Perlis, Roy H., Perry, Amy, Pfennig, Andrea, Potash, James B., Purcell, Shaun M., Regeer, Eline J., Reif, Andreas, Reinbold, Céline S., Rice, John P., Rivas, Fabio, Rivera, Margarita, Roussos, Panos, Ruderfer, Douglas M., Ryu, Euijung, Sánchez-Mora, Cristina, Schatzberg, Alan F., Scheftner, William A., Schork, Nicholas J., Shannon Weickert, Cynthia, Shehktman, Tatyana, Shilling, Paul D., Sigurdsson, Engilbert, Slaney, Claire, Smeland, Olav B., Sobell, Janet L., Søholm Hansen, Christine, Spijker, Anne T., St Clair, David, Steffens, Michael, Strauss, John S., Streit, Fabian, Strohmaier, Jana, Szelinger, Szabolcs, Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Weiqing, Watson, Stanley J., Weickert, Thomas W., Witt, Stephanie H., Xi, Simon, Xu, Wei, Young, Allan H., Zandi, Peter, Zhang, Peng, Zöllner, Sebastian, Adolfsson, Rolf, Agartz, Ingrid, Alda, Martin, Backlund, Lena, Baune, Bernhard T., Bellivier, Frank, Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H. R., Boehnke, Michael, Børglum, Anders D., Corvin, Aiden, Craddock, Nicholas, Daly, Mark J., Dannlowski, Udo, Esko, Tõnu, Etain, Bruno, Frye, Mark, Fullerton, Janice M., Gershon, Elliot S., Gill, Michael, Goes, Fernando, Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Hougaard, David M., Hultman, Christina M., Jones, Ian, Jones, Lisa A., Kahn, René S., Kirov, George, Landén, Mikael, Leboyer, Marion, Lewis, Cathryn M., Li, Qingqin S., Lissowska, Jolanta, Martin, Nicholas G., Mayoral, Fermin, McElroy, Susan L., McIntosh, Andrew M., McMahon, Francis J., Melle, Ingrid, Metspalu, Andres, Mitchell, Philip B., Morken, Gunnar, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Myers, Richard M., Neale, Benjamin M., Nimgaonkar, Vishwajit, Nordentoft, Merete, Nöthen, Markus M., O'Donovan, Michael C., Oedegaard, Ketil J., Owen, Michael J., Paciga, Sara A., Pato, Carlos, Pato, Michele T., Posthuma, Danielle, Ramos-Quiroga, Josep Antoni, Ribasés, Marta, Rietschel, Marcella, Rouleau, Guy A., Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Serretti, Alessandro, Smoller, Jordan W., Stefansson, Hreinn, Stefansson, Kari, Stordal, Eystein, Sullivan, Patrick F., Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Werge, Thomas, Nurnberger, John I., Wray, Naomi R., Di Florio, Arianna, Edenberg, Howard J., Cichon, Sven, Ophoff, Roel A., Scott, Laura J., Andreassen, Ole A., Kelsoe, John and Sklar, Pamela 2019. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics 51 (5) , pp. 793-803. 10.1038/s41588-019-0397-8

Eaton, Christopher, Thomas, Rhys, Hamandi, Khalid, Payne, Gareth, Kerr, Michael, Linden, David, Owen, Michael, Cunningham, Adam, Bartsch, Ullrich, Struik, Siske and van den Bree, Marianne 2019. Epilepsy and seizures in young people with 22q11.2 deletion syndrome: prevalence and links with other neurodevelopmental disorders. Epilepsia 60 (5) , pp. 818-829. 10.1111/epi.14722

Gorman, Kathleen M., Meyer, Esther, Grozeva, Detelina, Spinelli, Egidio, McTague, Amy, Sanchis-Juan, Alba, Carss, Keren J., Bryant, Emily, Reich, Adi, Schneider, Amy L., Pressler, Ronit M., Simpson, Michael A., Debelle, Geoff D., Wassmer, Evangeline, Morton, Jenny, Sieciechowicz, Diana, Jan-Kamsteeg, Eric, Paciorkowski, Alex R., King, Mary D., Cross, J. Helen, Poduri, Annapurna, Mefford, Heather C., Scheffer, Ingrid E., Haack, Tobias B., McCullagh, Gary, Millichap, John J., Carvill, Gemma L., Clayton-Smith, Jill, Maher, Eamonn R., Raymond, F. Lucy, Kurian, Manju A., McRae, Jeremy F., Clayton, Stephen, Fitzgerald, Tomas W., Kaplanis, Joanna, Prigmore, Elena, Rajan, Diana, Sifrim, Alejandro, Aitken, Stuart, Akawi, Nadia, Alvi, Mohsan, Ambridge, Kirsty, Barrett, Daniel M., Bayzetinova, Tanya, Jones, Philip, Jones, Wendy D., King, Daniel, Krishnappa, Netravathi, Mason, Laura E., Singh, Tarjinder, Tivey, Adrian R., Ahmed, Munaza, Anjum, Uruj, Archer, Hayley, Armstrong, Ruth, Awada, Jana, Balasubramanian, Meena, Banka, Siddharth, Baralle, Diana, Barnicoat, Angela, Batstone, Paul, Baty, David, Bennett, Chris, Berg, Jonathan, Bernhard, Birgitta, Bevan, A. Paul, Bitner-Glindzicz, Maria, Blair, Edward, Blyth, Moira, Bohanna, David, Bourdon, Louise, Bourn, David, Bradley, Lisa, Brady, Angela, Brent, Simon, Brewer, Carole, Brunstrom, Kate, Bunyan, David J., Burn, John, Canham, Natalie, Castle, Bruce, Chandler, Kate, Chatzimichali, Elena, Cilliers, Deirdre, Clarke, Angus, Clasper, Susan, Clayton-Smith, Jill, Clowes, Virginia, Coates, Andrea, Cole, Trevor, Colgiu, Irina, Collins, Amanda, Collinson, Morag N., Connell, Fiona, Cooper, Nicola, Cox, Helen, Cresswell, Lara, Cross, Gareth, Crow, Yanick, D?Alessandro, Mariella, Dabir, Tabib, Davidson, Rosemarie, Davies, Sally, de Vries, Dylan, Dean, John, Deshpande, Charu, Devlin, Gemma, Dixit, Abhijit, Dobbie, Angus, Donaldson, Alan, Donnai, Dian, Donnelly, Deirdre, Donnelly, Carina, Douglas, Angela, Douzgou, Sofia, Duncan, Alexis, Eason, Jacqueline, Ellard, Sian, Ellis, Ian, Elmslie, Frances, Evans, Karenza, Everest, Sarah, Fendick, Tina, Fisher, Richard, Flinter, Frances, Foulds, Nicola, Fry, Andrew, Fryer, Alan, Gardiner, Carol, Gaunt, Lorraine, Ghali, Neeti, Gibbons, Richard, Gill, Harinder, Goodship, Judith, Goudie, David, Gray, Emma, Green, Andrew, Greene, Philip, Greenhalgh, Lynn, Gribble, Susan, Harrison, Rachel, Harrison, Lucy, Harrison, Victoria, Hawkins, Rose, He, Liu, Hellens, Stephen, Henderson, Alex, Hewitt, Sarah, Hildyard, Lucy, Hobson, Emma, Holden, Simon, Holder, Muriel, Holder, Susan, Hollingsworth, Georgina, Homfray, Tessa, Humphreys, Mervyn, Hurst, Jane, Hutton, Ben, Ingram, Stuart, Irving, Melita, Islam, Lily, Jackson, Andrew, Jarvis, Joanna, Jenkins, Lucy, Johnson, Diana, Jones, Elizabeth, Josifova, Dragana, Joss, Shelagh, Kaemba, Beckie, Kazembe, Sandra, Kelsell, Rosemary, Kerr, Bronwyn, Kingston, Helen, Kini, Usha, Kinning, Esther, Kirby, Gail, Kirk, Claire, Kivuva, Emma, Kraus, Alison, Kumar, Dhavendra, Kumar, V. 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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 2019. Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome. Schizophrenia Research 204 , pp. 320-325. 10.1016/j.schres.2018.07.044

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 2019. Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a New Zealand longitudinal population cohort study. British Journal of Psychiatry 214 (2) , pp. 96-102. 10.1192/bjp.2018.227

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

Escott-Price, Valentina, Bracher-Smith, Matthew, Menzies, Georgina, Walters, James, Kirov, George, Owen, Michael J. and O'Donovan, Michael C. 2019. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank. Journal of Molecular Psychiatry , -. 10.1038/s41380-018-0328-6 Item availability restricted.

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 2019. Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 180 (1) , pp. 80-85. 10.1002/ajmg.b.32705

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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 2019. 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 Item availability restricted.

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 2019. Analyses of de novo and common alleles implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience Item availability restricted.

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Niarchou, Maria, Byrne, Enda, Trzaskowski, Maciej, Sidorenko, Julia, Kemper, Kathryn, McGrath, John J., O'Donovan, Michael C., Owen, Michael J. and Wray, Naomi R. 2019. Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Translational Psychiatry Item availability restricted.

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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 2018. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science 362 (6420) , -. 10.1126/science.aat7615

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 2018. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics 19 (1) , 867. 10.1186/s12864-018-5292-7

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

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

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

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

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

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

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

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 177 (5) , pp. 489-502. 10.1002/ajmg.b.32637

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