Using Genetics to Increase Specificity of Outcome Prediction in Psychiatric Disorders: Prospects for Progression von Holmans, Peter A

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Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders von Holmans, Peter A, Massey, Thomas H, Jones, Lesley

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A Population-Based Cohort Study Examining the Incidence and Impact of Psychotic Experiences From Childhood to Adulthood, and Prediction of Psychotic Disorder von 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, Zammit, Stanley

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The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia von Clifton, Nicholas E., Schulmann, Anton, Holmans, Peter A., O'Donovan, Michael C., Vawter, Marquis P.

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Comparative genetic architectures of schizophrenia in East Asian and European populations von Lam, Max, Chen, Chia-Yen, Li, Zhiqiang, Martin, Alicia R., Bryois, Julien, Ma, Xixian, Gaspar, Helena, Ikeda, Masashi, Benyamin, Beben, Brown, Brielin C., Liu, Ruize, Zhou, Wei, Guan, Lili, Kamatani, Yoichiro, Kim, Sung-Wan, Kubo, Michiaki, Kusumawardhani, Agung A. A. A., Liu, Chih-Min, Ma, Hong, Periyasamy, Sathish, Takahashi, Atsushi, Xu, Zhida, Yu, Hao, Zhu, Feng, Chen, Wei J., Faraone, Stephen, Glatt, Stephen J., He, Lin, Hyman, Steven E., Hwu, Hai-Gwo, McCarroll, Steven A., Neale, Benjamin M., Sklar, Pamela, Wildenauer, Dieter B., Yu, Xin, Zhang, Dai, Mowry, Bryan J., Lee, Jimmy, Holmans, Peter, Xu, Shuhua, Sullivan, Patrick F., Ripke, Stephan, O’Donovan, Michael C., Daly, Mark J., Qin, Shengying, Sham, Pak, Iwata, Nakao, Hong, Kyung S., Schwab, Sibylle G., Yue, Weihua, Tsuang, Ming, Liu, Jianjun, Ma, Xiancang, Kahn, René S., Shi, Yongyong, Huang, Hailiang

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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis von Williams, Nigel M, Dr, Zaharieva, Irina, BSc, Martin, Andrew, BSc, Langley, Kate, PhD, Mantripragada, Kiran, PhD, Fossdal, Ragnheidur, PhD, Stefansson, Hreinn, PhD, Stefansson, Kari, MD, Magnusson, Pall, MD, Gudmundsson, Olafur O, MD, Gustafsson, Omar, PhD, Holmans, Peter, Prof, Owen, Michael J, Prof, O'Donovan, Michael, Prof, Thapar, Anita, Prof

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Complement genes contribute sex-biased vulnerability in diverse disorders von Kamitaki, Nolan, Sekar, Aswin, Handsaker, Robert E., de Rivera, Heather, Tooley, Katherine, Morris, David L., Taylor, Kimberly E., Whelan, Christopher W., Tombleson, Philip, Loohuis, Loes M. Olde, Boehnke, Michael, Kimberly, Robert P., Kaufman, Kenneth M., Harley, John B., Langefeld, Carl D., Seidman, Christine E., Pato, Michele T., Pato, Carlos N., Ophoff, Roel A., Graham, Robert R., Criswell, Lindsey A., Vyse, Timothy J., McCarroll, Steven A.

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De novo mutations in schizophrenia implicate synaptic networks von Fromer, Menachem, Pocklington, Andrew J., Kavanagh, David H., Williams, Hywel J., Dwyer, Sarah, Gormley, Padhraig, Georgieva, Lyudmila, Rees, Elliott, Palta, Priit, Ruderfer, Douglas M., Carrera, Noa, Humphreys, Isla, Johnson, Jessica S., Roussos, Panos, Barker, Douglas D., Banks, Eric, Milanova, Vihra, Grant, Seth G., Hannon, Eilis, Rose, Samuel A., Chambert, Kimberly, Mahajan, Milind, Scolnick, Edward M., Moran, Jennifer L., Kirov, George, Palotie, Aarno, McCarroll, Steven A., Holmans, Peter, Sklar, Pamela, Owen, Michael J., Purcell, Shaun M., O’Donovan, Michael C.

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Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population von Jones, Hannah J, Stergiakouli, Evie, Tansey, Katherine E, Hubbard, Leon, Heron, Jon, Cannon, Mary, Holmans, Peter, Lewis, Glyn, Linden, David E. J, Jones, Peter B, Davey Smith, George, O’Donovan, Michael C, Owen, Michael J, Walters, James T, Zammit, Stanley

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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease von Sims, Rebecca, Gerrish, Amy, Abraham, Richard, Hamshere, Marian L, Moskvina, Valentina, Jones, Nicola, Thomas, Charlene, Widdowson, Caroline, Chapman, Jade, Powell, John, Proitsi, Petroula, Lupton, Michelle K, Gill, Michael, Lawlor, Brian, Passmore, Peter A, Craig, David, McGuinness, Bernadette, Todd, Stephen, Mann, David, Smith, A David, Warden, Donald, Kehoe, Patrick G, Hardy, John, Mead, Simon, Collinge, John, Maier, Wolfgang, Schürmann, Britta, Heun, Reiner, Kölsch, Heike, van den Bussche, Hendrik, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Gallacher, John, Hüll, Michael, Rujescu, Dan, Giegling, Ina, Goate, Alison M, Kauwe, John S K, Nowotny, Petra, Morris, John C, Bettens, Karolien, Engelborghs, Sebastiaan, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E, Tsolaki, Magda, Guerreiro, Rita, Klopp, Norman, Wichmann, H-Erich, Barcikowska, Maria, Wszolek, Zbigniew K, Dickson, Dennis W, van Duijn, Cornelia M, Breteler, Monique M B, Ikram, M Arfan, Fitzpatrick, Annette L, Seshadri, Sudha, Berr, Claudine, Epelbaum, Jacques, Dartigues, Jean-François, Tzourio, Christophe, Feulner, Thomas M, Riehle, Caterina, Krawczak, Michael, Mayhaus, Manuel, Nicolhaus, S, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Snædal, Jon, Björnsson, Sigurbjörn, Chouraki, Vincent, Zelenika, Diana, Delepine, Marc, Pasquier, Florence, Porcellini, Elisa, Hanon, Olivier, Alvarez, Victoria, Bosco, Paolo, Siciliano, Gabriele, Solfrizzi, Vincenzo, Bossù, Paola, Piccardi, Paola, Seripa, Davide, Pilotto, Alberto, Scarpini, Elio, Brice, Alexis, Hannequin, Didier, Jones, Lesley, Holmans, Peter A, Jonsson, Thorlakur, Morgan, Kevin, Younkin, Steven G, Owen, Michael J, O'Donovan, Michael, Amouyel, Philippe, Williams, Julie

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications von Levinson, Douglas F., Duan, Jubao, Oh, Sang, Wang, Kai, Sanders, Alan R., Shi, Jianxin, Zhang, Nancy, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Kendler, Kenneth S., Freedman, Robert, Dudbridge, Frank, Pe'er, Itsik, Hakonarson, Hakon, Bergen, Sarah E., Fanous, Ayman H., Holmans, Peter A., Gejman, Pablo V.

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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease von Deloukas, Panagiotis, Hamshere, Marian L, Lovestone, Simon, Mead, Simon, Nöthen, Markus M, Gerrish, Amy, O'Donovan, Michael, Hüll, Michael, Hardy, John, Hampel, Harald, Passmore, Peter A, Engelborghs, Sebastiaan, Abraham, Richard, Thomas, Charlene, Moskvina, Valentina, Brayne, Carol, Lawlor, Brian, Bass, Nicholas J, McQuillin, Andrew, Holmans, Peter A, Jones, Nicola, Pahwa, Jaspreet Singh, Morgan, Kevin, Klopp, Norman, Schürmann, Britta, Carrasquillo, Minerva M, Jessen, Frank, Tsolaki, Magda, McGuinness, Bernadette, Van Broeckhoven, Christine, De Deyn, Peter P, Cruchaga, Carlos, Mayo, Kevin, Wichmann, H-Erich, Brown, Kristelle S, Fox, Nick, Proitsi, Petroula, Mühleisen, Thomas W, Lupton, Michelle K, Lynch, Aoibhinn, Williams, Julie, Singleton, Andrew B, Moebus, Susanne, Dowzell, Kimberley, Livingston, Gill, Powell, John, Todd, Stephen, Wiltfang, Jens, Kornhuber, Johannes, Shaw, Christopher E, Pankratz, V Shane, Owen, Michael J, Holmes, Clive, Kehoe, Patrick G, Al-Chalabi, Ammar, Morgan, Angharad R, Heuser, Isabella, Williams, Amy, Mann, David, Gurling, Hugh, Kauwe, John S K, Goate, Alison M, Frölich, Lutz, Rubinsztein, David C, Love, Seth, Rossor, Martin, Rujescu, Dan, Hollingworth, Paul, Bettens, Karolien, Younkin, Steven G, Nowotny, Petra, Dichgans, Martin, Smith, A David, Collinge, John, van den Bussche, Hendrik, Gwilliam, Rhian, Guerreiro, Rita, Jöckel, Karl-Heinz, Sims, Rebecca, Morris, John C, Gill, Michael, Craig, David, Sleegers, Kristel, Harold, Denise, Stretton, Alexandra, Maier, Wolfgang

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A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes von Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah A., Hensman Moss, Davina J., Alshammari, Asma M., Flower, Michael D., Durr, Alexandra, Leavitt, Blair R., Roos, Raymund A.C., Holmans, Peter, Jones, Lesley, Langbehn, Douglas R., Kwak, Seung, Tabrizi, Sarah J., Monckton, Darren G.

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A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder von Walters, Raymond K., Lee, S. Hong, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Bell, Robert K., Bryc, Katarzyna, Fontanillas, Pierre, Hromatka, Bethann S., Huber, Karen E., Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Vacic, Vladimir, Anney, Richard J.L., Vasquez, Alejandro Arias, Arranz, Maria Jesús, Banaschewski, Tobias, Banaschewski, Tobias J., Mortensen, Preben Bo, Børglum, Anders, Charach, Alice, Crosbie, Jennifer, Dalsgaard, Soeren, Demontis, Ditte, Dempfle, Astrid, Elia, Josephine, Faraone, Stephen V., Franke, Barbara, Freitag, Christine, Gelernter, Joel, Grevet, Eugenio, Haavik, Jan, Hakonarson, Hakon, Hawi, Ziarih, Hinney, Anke, Holmans, Peter, Ickowitz, Abel, Kent, Lindsey, Kittel-Schneider, Sarah, Langley, Kate, Lesch, Klaus-Peter, Loo, Sandra K., Martin, Joanna, Medland, Sarah E., Mulas, Fernando, Mulligan, Aisling, O’Donovan, Michael C., Oades, Robert D., Palmason, Haukur, Rhode, Luis, Roeyers, Herbert, Romanos, Marcel, Romanos, Jasmin, Rothenberger, Aribert, Schäfer, Helmut, Scherag, André, Schimmelmann, Benno G., Sergeant, Joseph, Smalley, Susan L., Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Sullivan, Patrick F., Todorov, Alexandre, Waldman, Irwin, Wang, Yufeng, Warnke, Andreas, Williams, Nigel, Witt, Stephanie H., Yang, Li, Agerbo, Esben, Belliveau, Rich, Børglum, Anders D., Chambert, Kimberly, Dalsgaard, Søren, Dumont, Ashley, Goldstein, Jacqueline, Grove, Jakob, Howrigan, Daniel P., Huang, Hailiang, Martin, Alicia R., Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Pallesen, Jonatan, Poterba, Timothy, Poulsen, Jesper Buchhave, Robinson, Elise B., Satterstrom, F. Kyle, Stevens, Christine, Turley, Patrick, Pedersen, Marianne Giørtz, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Franke, Barbara, Neale, Benjamin M.

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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel von Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan, Soranzo, Nicole

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Novel Insight Into the Etiology of Autism Spectrum Disorder Gained by Integrating Expression Data With Genome-wide Association Statistics von Pain, Oliver, Pocklington, Andrew J., Holmans, Peter A., Bray, Nicholas J., O’Brien, Heath E., Hall, Lynsey S., Pardiñas, Antonio F., O’Donovan, Michael C., Owen, Michael J., Anney, Richard

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder von Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia von Pardiñas, Antonio F, Smart, Sophie E, Willcocks, Isabella R, Holmans, Peter A, Dennison, Charlotte A, Lynham, Amy J, Legge, Sophie E, Baune, Bernhard T, Bigdeli, Tim B, Cairns, Murray J, Corvin, Aiden, Fanous, Ayman H, Frank, Josef, Kelly, Brian, McQuillin, Andrew, Melle, Ingrid, Mortensen, Preben B, Mowry, Bryan J, Pato, Carlos N, Periyasamy, Sathish, Rietschel, Marcella, Rujescu, Dan, Simonsen, Carmen, St Clair, David, Tooney, Paul, Wu, Jing Qin, Andreassen, Ole A, Kowalec, Kaarina, Sullivan, Patrick F, Murray, Robin M, Owen, Michael J, MacCabe, James H, O’Donovan, Michael C, Walters, James T. R, Ajnakina, Olesya, Alameda, Luis, Barnes, Thomas R. E, Berardi, Domenico, Bonora, Elena, Camporesi, Sara, Cleusix, Martine, Conus, Philippe, Crespo-Facorro, Benedicto, D’Andrea, Giuseppe, Demjaha, Arsime, Do, Kim Q, Doody, Gillian A, Eap, Chin B, Ferchiou, Aziz, Di Forti, Marta, Guidi, Lorenzo, Homman, Lina, Jenni, Raoul, Joyce, Eileen M, Kassoumeri, Laura, Khadimallah, Inès, Lastrina, Ornella, Muratori, Roberto, Noyan, Handan, O’Neill, Francis A, Pignon, Baptiste, Restellini, Romeo, Richard, Jean-Romain, Schürhoff, Franck, Španiel, Filip, Szöke, Andrei, Tarricone, Ilaria, Tortelli, Andrea, Üçok, Alp, Vázquez-Bourgon, Javier

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Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants von Martin, Joanna, BSc, Cooper, Miriam, MRCPsych, MSc, Hamshere, Marian L., PhD, Pocklington, Andrew, PhD, Scherer, Stephen W., PhD, FRSC, Kent, Lindsey, MD, PhD, Gill, Michael, MD, MRCPsych, Owen, Michael J., FRCPsych, PhD, Williams, Nigel, PhD, O'Donovan, Michael C., FRCPsych, PhD, Thapar, Anita, FRCPsych, PhD, Holmans, Peter, PhD

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Pathway analyses implicate glial cells in schizophrenia von Duncan, Laramie E, Holmans, Peter A, Lee, Phil H, O'Dushlaine, Colm T, Kirby, Andrew W, Smoller, Jordan W, Öngür, Dost, Cohen, Bruce M

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