Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

- Loh, Po-Ro, Bhatia, Gaurav, Kendler, Kenneth S., O'Donovan, Michael, Neale, Benjamin M., Patterson, Nick, Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Gusev, Alexander, Tooney, Paul A., Wu, Jing Qin, Finucane, Hilary K., Bulik-Sullivan, Brendan K., Pollack, Samuela J., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, de Candia, Teresa R., Lee, Sang Hong, Wray, Naomi R.

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

- Warren, Helen, Evangelou, Evangelos, Kraja, Aldi T., Drenos, Fotios, Loh, Marie, Verweij, Niek, Marten, Jonathan, Karaman, Ibrahim, Segura Lepe, Marcelo P., O'Reilly, Paul F., Knight, Joanne, Scott, Rodney, Cabrera, Claudia P., Attia, John, Gao, He, Ren, Meixia, Mifsud, Borbala, Ntalla, Ioanna, Surendran, Praveen, Liu, Chunyu, Cook, James P.

Five endometrial cancer risk loci identified through genome-wide association analysis

- Cheng, Timothy H. T., Thompson, Deborah J., Gorman, Maggie, Martin, Lynn, National Study of Endometrial Cancer Genetics Group (NSECG),, Hodgson, Shirley, Webb, Penelope M., Australian National Endometrial Cancer Study Group (ANECS),, Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., O'Mara, Tracy A., Dowdy, Sean C., Ashton, Katie, Otton, Geoffrey, Proietto, Tony, Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

- Okbay, Aysu, Baselmans, Bart M. L., Gratten, Jacob, Lee, James J., Liu, Jimmy Z., de Vlaming, Roland, Ahluwalia, Tarunveer S, Buchwald, Jadwiga, Cavadino, Alana, Attia, John, Holliday, Elizabeth, Oldmeadow, Christopher, De Neve, Jan-Emmanuel, Scott , Rodney, Turley, Patrick, Nivard, Michel G., Fontana, Mark Alan, Meddens, S. Fleur W., Linnér, Richard Karlsson, Rietveld, Cornelius A., Derringer, Jamie

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

- Tarpey, Patrick S., Smith, Raffaella, Stephens, Phil, Blow, Matt, Greenman, Chris, Xue, Yali, Tyler-Smith, Chris, Thompson, Deborah, Gray, Kristian, Andrews, Jenny, Barthorpe, Syd, Buck, Gemma, Pleasance, Erin, Hackett, Anna, Whibley, Annabel, Edkins, Sarah, Hardy, Claire, O'Meara, Sarah, Latimer, Calli, Dicks, Ed, Menzies, Andrew

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

- Beecham, Ashley H., Patsopoulos, Nikolaos A., Oturai, Annette, Saarela, Janna, Fontaine, Bertrand, Hemmer, Bernhard, Martin, Claes, Zipp, Frauke, D'Alfonso, Sandra, Martinelli-Boneschi, Filippo, Taylor, Bruce, Harbo, Hanne F., Xifara, Dionysia K., Lechner-Scott, Jeannette, Davis, Mary F., Kemppinen, Anu, Cotsapas, Chris, Shah, Tejas S., Spencer, Chris, Booth, David, Goris, An

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

- Barban, Nicola, Jansen, Rick, de Vlaming, Ronald, Vaez, Ahmad, Mandemakers, Jornt J., Tropf, Felix C., Shen, Xia, Wilson, James F., Chasman, Daniel I., Nolte, Ilja M., Tragante, Vinicius, van der Laan, Sander W., Perry, John R. B., Kong, Augustine, BIOS Consortium, Ahluwalia, Tarunveer S., Albrecht, Eva, Yerges-Armstrong, Laura, Atzmon, Gil, Auro, Kirsi, Ayers, Kristin, Bakshi, Andrew, Ben-Avraham, Danny, Berger, Klaus, Bergman, Aviv, Bertram, Lars, Bielak, Lawrence F., Bjornsdottir, Gyda, Bonder, Marc Jan, Broer, Linda, Bui, Minh, Barbieri, Caterina, Cavadino, Alana, Chavarro, Jorge E., Turman, Constance, Concas, Maria Pina, Cordell, Heather J., Davies, Gail, Eibich, Peter, Eriksson, Nicholas, Esko, Tõnu, Eriksson, Joel, Falahi, Fahimeh, Felix, Janine F., Fontana, Mark Alan, Franke, Lude, Gandin, Ilaria, Gaskins, Audrey J., Gieger, Christian, Gunderson, Erica P., Guo, Xiuqing, Hayward, Caroline, He, Chunyan, Hofer, Edith, Huang, Hongyang, Joshi, Peter K., Kanoni, Stavroula, Karlsson, Robert, Kiechl, Stefan, Kifley, Annette, Kluttig, Alexander, Kraft, Peter, Lagou, Vasiliki, Lecoeur, Cecile, Lahti, Jari, Li-Gao, Ruifang, Lind, Penelope A., Liu, Tian, Makalic, Enes, Mamasoula, Crysovalanto, Matteson, Lindsay, Mbarek, Hamdi, McArdle, Patrick F., Holliday, Elizabeth G.

A recently evolved hexose transporter variant confers resistance to multiple pathogens in wheat

- Moore, John W., Herrera-Foessel, Sybil, Kong, Xiuying, Spielmeyer, Wolfgang, Talbot, Mark, Bariana, Harbans, Patrick, John W., Dodds, Peter, Singh, Ravi, Lagudah, Evans, Lan, Caixia, Schnippenkoetter, Wendelin, Ayliffe, Michael, Huerta-Espino, Julio, Lillemo, Morten, Viccars, Libby, Milne, Ricky, Periyannan, Sambasivam

Genome-wide association study identifies a common variant associated with risk of endometrial cancer

- Spurdle, Amanda B., Thompson, Deborah J., Fahey, Paul, Montgomery, Grant W., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Lambrechts, Diether, Coenegrachts, Lieve, Vergote, Ignace, Ahmed, Shahana, Amant, Frederic, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Helland, Harald, Scott, Rodney J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, National Study of Endometrial Cancer Genetics Group,, Ferguson, Kaltin, Tomlinson, Ian, Gorman, Maggie, Howarth, Kimberley, Hodgson, Shirley, Garcia-Closas, Montserrat, Wentzensen, Nicolas, Yang, Hannah, Chanock, Stephen, Hall, Per, Czene, Kamila, Healey, Catherine S., Liu, Jianjun, Li, Jingmei, Shu, Xiao-Ou, Zheng, Wei, Long, Jirong, Xiang, Yong-Bing, Shah, Mitul, Morrison, Jonathan, Michailidou, Kyriaki, Pharoah, Paul D., O'Mara, Tracy, Dunning, Alison M., Easton, Douglas F., Walker, Logan C,, Montgomery, Stephen B., Dermitzakis, Emmanouil T., Australian National Endometrial Cancer Study Group,

Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations

- Okada, Yukinori, Sim, Xueling, Lim, Su-Chi, Wong, Tien-Yin, Liu, Jianjun, Young, Terri L., Aung, Tin, Seielstad, Mark, Teo, Yik-Ying, Kim, Young Jin, Lee, Jong-Young, Han, Bok-Ghee, Go, Min Jin, Kang, Daehee, Chen, Chien-Hsiun, Tsai, Fuu-Jen, Chang, Li-Ching, Fann, S-J. Cathy, Mei, Hao, Rao, Dabeeru C., Hixson, James E., Chen, Shufeng, Katsuya, Tomohiro, Wu, Jer-Yuarn, Isono, Masato, Ogihara, Toshio, Chambers, John C., Zhang, Weihua, Kooner, Jaspal S., Albrecht, Eva, Yamamoto, Kazuhiko, Kubo, Michiaki, Nakamura, Yusuke, Kamatani, Naoyuki, Gu, Dongfeng, Kato, Norihiro, He, Jiang, Chen, Yuan-Tsong, Cho, Yoon Shin, Tai, E-Shyong, Tanaka, Toshihiro, Oldmeadow, C. J., Scott, R., Holliday, E. G., Attia, J. R., Takeuchi, Fumihiko, Takahashi, Atsushi, Maeda, Shiro, Tsunoda, Tatsuhiko, Chen, Peng

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

- Khor, Chiea Chuen, Davila, Sonia, Wong, Tien Yin, Pang, Junxiong, Mitchell, Paul, Cimaz, Rolando, Dahdah, Nagib, Cheung, Yiu-Fai, Huang, Guo-Ying, Yang, Wanling, Park, In-Sook, Lee, Jong-Keuk, Breunis, Willemijn B., Wu, Jer-Yuarn, Levin, Michael, Burns, Jane C., Burgner, David, Kuijpers, Taco W., Hibberd, Martin L., Attia, John, Scott, Rodney, Holliday, Elizabeth, Lee, Yi-Ching, Shimizu, Chisato, Wright, Victoria J., Yeung, Rae S. M, Tan, Dennis E. K., Sim, Kar Seng, Wang, Jie Jin

Partitioning heritability by functional annotation using genome-wide association summary statistics

- Finucane, Hilary K., Bulik-Sullivan, Brendan, Ripke, Stephan, Day, Felix R., ReproGen Consortium,, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, The RACI Consortium,, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R. B., Okada, Yukinori, Gusev, Alexander, Raychaudhuri, Soumya, Daly, Mark J., Patterson, Nick, Neale, Benjamin M., Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Trynka, Gosia, Tooney, Paul A., Wu, Jing Qin, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle

Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

- Jenkinson, Emma M., Rodero, Mathieu P., Bhaskar, Sanjeev S., O'Sullivan, James, Baerlocher, Gabriela M., Haubitz, Monika, Aubert, Geraldine, Barañano, Kristin W., Barnicoat, Angela J., Battini, Roberta, Berger, Andrea, Blair, Edward M., Kasher, Paul R., Brunstrom-Hernandez, Janice E., Buckard, Johannes A., Cassiman, David M., Caumes, Rosaline, Cordelli, Duccio M., De Waele, Liesbeth M., Fay, Alexander J., Ferreira, Patrick, Fletcher, Nicholas A., Fryer, Alan E., Uggenti, Carolina, Goel, Himanshu, Hemingway, Cheryl A., Henneke, Marco, Hughes, Imelda, Jefferson, Rosalind J., Kumar, Ram, Lagae, Lieven, Landrieu, Pierre G., Lourenço, Charles M., Malpas, Timothy J., Oojageer, Anthony, Mehta, Sarju G., Metz, Imke, Naidu, Sakkubai, Õunap, Katrin, Panzer, Axel, Prabhakar, Prab, Quaghebeur, Geraldine, Schiffmann, Raphael, Sherr, Elliott H., Sinnathuray, Kanaga R., Goosey, Laurence C., Soh, Calvin, Stewart, Helen S., Stone, John, Van Esch, Hilde, Van Mol, Christine E. G., Vanderver, Adeline, Wakeling, Emma L., Whitney, Andrea, Pavitt, Graham D., Griffiths-Jones, Sam, Rose, Yoann, Rice, Gillian I., Revy, Patrick, van der Knaap, Margo S., Livingston, John H., O'Keefe, Raymond T., Crow, Yanick J., Kershaw, Christopher J., Urquhart, Jill E., Williams, Simon G.

Genome-wide association study identifies five new schizophrenia loci

- The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J.

Genome-wide association meta-analysis identifies new endometriosis risk loci

- Nyholt, Dale R., Low, Siew-Kee, Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Knichi, Nakamura, Yusuke, Anderson, Carl A., Zondervan, Krina T., Zembutsu, Hitoshi, Montgomery, Grant W., Painter Jodie N., Yun-Chul, Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G.

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

- Milne, Roger L., Kuchenbaecker, Karoline B., Jiang, Xia, Rostamianfar, Asha, Finucane, Hilary, Bolla, Manjeet K., McGuffog, Lesley, Wang, Qin, Aalfs, Cora M., ABCTB Investigators,, Braye, Stephen, Forbes, John, Michailidou, Kyriaki, Scott, Rodney J., Beesley, Jonathan, Kar, Siddhartha, Lindström, Sara, Hui, Shirley, Lemaçon, Audrey, Soucy, Penny, Dennis, Joe

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

- Bellenguez, Céline, Bevan, Steve, Band, Gavin, Syme, Paul D., Malik, Rainer, Pera, Joanna, Norrving, Bo, Lemmens, Robin, Freeman, Colin, Schanz, Renata, James, Tom, Poole, Deborah, Gschwendtner, Andreas, Murphy, Lee, Segal, Helen, Cortellini, Lynelle, Cheng, Yu-Ching, Woo, Daniel, Nalls, Michael A., Müller-Myhsok, Bertram, Meisinger, Christa, Seedorf, Udo, Ross-Adams, Helen, Spencer, Chris C. A., Boonen, Steven, Wloch-Kopec, Dorota, Valant, Valerie, Slark, Julia, Furie, Karen, Delavaran, Hossein, Langford, Cordelia, Deloukas, Panos, Edkins, Sarah, Hunt, Sarah, Burgess, Annette I., Gray, Emma, Dronov, Serge, Peltonen, Leena, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boncoraglio, Giorgio B., Parati, Eugenio A., Attia, John, Pirinen, Matti, Holliday, Elizabeth, Levi, Chris, Franzosi, Maria-Grazia, Goel, Anuj, Helgadottir, Anna, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Jackson, Caroline A., Duncanson, Audrey, Jankowski, Janusz, Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Traylor, Matthew, Worrall, Bradford B., Kittner, Steven J., Mitchell, Braxton D., Kissela, Brett, Meschia, James F., Thijs, Vincent, Lindgren, Arne, Macleod, Mary Joan, Slowik, Agnieszka, Walters, Matthew, Strange, Amy, Rosand, Jonathan, Sharma, Pankaj, Farrall, Martin, Sudlow, Cathie L. M., Rothwell, Peter M., Dichgans, Martin, Donnelly, Peter, Markus, Hugh S., Su, Zhan

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

- Thompson, Bryony A., Spurdle, Amanda B., du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P., Farrington, Susan M., Frayling, Ian M., Frebourg, Thierry, Goldgar, David E., Heinen, Christopher D., Holinski-Feder, Elke, Kohonen-Corish, Maija, Plazzer, John-Paul, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pat, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Greenblatt, Marc S., Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J., Sijmons, Rolf, Tavtigian, Sean V., Tops, Carli M., Weber, Thomas, Wijnen, Juul, Woods, Michael O., Macrae, Finlay, Akagi, Kiwamu, Genuardi, Maurizio, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, John T.

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20

- Bahlo, Melanie, Booth, David R., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Broadley, Simon A., Brown, Matthew A., Foote, Simon J., Griffiths, Lyn R., Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Moscato, Pablo, Perreau, Victoria M.

LD score regression distinguishes confounding from polygenicity in genome-wide association studies

- Bulik-Sullivan, Brendan K., Albus, M, Alexander, M, Amin, F, Bacanu, SA, Begemann, M, Belliveau, RA, Bene, J, Bergen, SE, Bruggeman, R, Bevilacqua, E, Bigdeli, TB, Black, DW, Buccola, NG, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Cairns, MJ, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Chan, RCK, Chen, RYL, Cohen, D, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, N, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Loh, Po-Ru, Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Patterson, Nick, Daly, Mark J., Price, Alkes L., Neale, Benjamin M., Finucane, Hilary K., Ripke, Stephan, Yang, Jian, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M.