Binding an Event to Its Source at Encoding Improves Children's Source Monitoring von Roberts, Kim P., Evans, Angela D., Duncanson, Sara

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Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins von Postmus, Iris, Trompet, Stella, Deshmukh, Harshal A., Barnes, Michael R., Li, Xiaohui, Warren, Helen R., Chasman, Daniel I., Zhou, Kaixin, Arsenault, Benoit J., Donnelly, Louise A., Wiggins, Kerri L., Avery, Christy L., Griffin, Paula, Feng, QiPing, Taylor, Kent D., Li, Guo, Evans, Daniel S., Smith, Albert V., de Keyser, Catherine E., Johnson, Andrew D., de Craen, Anton J. M., Buckley, Brendan M., Ford, Ian, Westendorp, Rudi G. J., Eline Slagboom, P., Sattar, Naveed, Munroe, Patricia B., Sever, Peter, Poulter, Neil, Stanton, Alice, Shields, Denis C., O’Brien, Eoin, Shaw-Hawkins, Sue, Ida Chen, Y.-D., Nickerson, Deborah A., Smith, Joshua D., Pierre Dubé, Marie, Matthijs Boekholdt, S., Kees Hovingh, G., Kastelein, John J. P., McKeigue, Paul M., Betteridge, John, Neil, Andrew, Durrington, Paul N., Doney, Alex, Carr, Fiona, Morris, Andrew, McCarthy, Mark I., Groop, Leif, Ahlqvist, Emma, Bis, Joshua C., Rice, Kenneth, Smith, Nicholas L., Lumley, Thomas, Whitsel, Eric A., Stürmer, Til, Boerwinkle, Eric, Ngwa, Julius S., O’Donnell, Christopher J., Wei, Wei-Qi, Wilke, Russell A., Liu, Ching-Ti, Sun, Fangui, Guo, Xiuqing, Heckbert, Susan R, Post, Wendy, Sotoodehnia, Nona, Arnold, Alice M., Stafford, Jeanette M., Ding, Jingzhong, Herrington, David M., Kritchevsky, Stephen B., Eiriksdottir, Gudny, Launer, Leonore J., Harris, Tamara B., Chu, Audrey Y., Giulianini, Franco, MacFadyen, Jean G., Barratt, Bryan J., Nyberg, Fredrik, Stricker, Bruno H., Uitterlinden, André G., Hofman, Albert, Rivadeneira, Fernando, Emilsson, Valur, Franco, Oscar H., Ridker, Paul M., Gudnason, Vilmundur, Liu, Yongmei, Denny, Joshua C., Ballantyne, Christie M., Adrienne Cupples, L., Psaty, Bruce M., Palmer, Colin N. A., Tardif, Jean-Claude, Colhoun, Helen M., Hitman, Graham, Krauss, Ronald M., Wouter Jukema, J, Caulfield, Mark J.

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Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility von Evans, David M, Spencer, Chris C A, Pointon, Jennifer J, Su, Zhan, Harvey, David, Kochan, Grazyna, Oppermann, Udo, Dilthey, Alexander, Pirinen, Matti, Stone, Millicent A, Appleton, Louise, Moutsianas, Loukas, Leslie, Stephen, Wordsworth, Tom, Kenna, Tony J, Karaderi, Tugce, Thomas, Gethin P, Ward, Michael M, Weisman, Michael H, Farrar, Claire, Bradbury, Linda A, Danoy, Patrick, Inman, Robert D, Maksymowych, Walter, Gladman, Dafna, Rahman, Proton, Morgan, Ann, Marzo-Ortega, Helena, Bowness, Paul, Gaffney, Karl, Gaston, J S Hill, Smith, Malcolm, Bruges-Armas, Jacome, Couto, Ana-Rita, Sorrentino, Rosa, Paladini, Fabiana, Ferreira, Manuel A, Xu, Huji, Liu, Yu, Jiang, Lei, Lopez-Larrea, Carlos, Díaz-Peña, Roberto, López-Vázquez, Antonio, Zayats, Tetyana, Band, Gavin, Bellenguez, Céline, Blackburn, Hannah, Blackwell, Jenefer M, Bramon, Elvira, Bumpstead, Suzannah J, Casas, Juan P, Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Duncanson, Audrey, Edkins, Sarah, Freeman, Colin, Gillman, Matthew, Gray, Emma, Gwilliam, Rhian, Hammond, Naomi, Hunt, Sarah E, Jankowski, Janusz, Jayakumar, Alagurevathi, Langford, Cordelia, Liddle, Jennifer, Markus, Hugh S, Mathew, Christopher G, McCann, Owen T, McCarthy, Mark I, Palmer, Colin N A, Peltonen, Leena, Plomin, Robert, Potter, Simon C, Rautanen, Anna, Ravindrarajah, Radhi, Ricketts, Michelle, Samani, Nilesh, Sawcer, Stephen J, Strange, Amy, Trembath, Richard C, Viswanathan, Ananth C, Waller, Matthew, Weston, Paul, Whittaker, Pamela, Widaa, Sara, Wood, Nicholas W, McVean, Gilean, Reveille, John D, Wordsworth, B Paul, Brown, Matthew A, Donnelly, Peter

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Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases von Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart

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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome von Aung, Tin, Ozaki, Mineo, Li, Zheng, Uebe, Steffen, Harder, Jeffrey M, Chan, Anita S Y, Lee, Mei Chin, Burdon, Kathryn P, Pakravan, Mohammad, Wang, Ya Xing, Williams, Susan, Huang, Lulin, Foo, Jia Nee, Kumar, Rajesh S, Ueno, Morio, Manabe, Shin-ichi, Hayashi, Ken, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Yoshida, Akitoshi, Yanagi, Masahide, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Yamashiro, Kenji, Gotoh, Norimoto, Osman, Essam A, Al-Obeidan, Saleh A, Al-Jasim, Leyla, Shahwan, Sami Al, Leo, Paul, Yetkin, Yaz, Oğuz, Çilingir, Kanavi, Mozhgan Rezaei, Yazdani, Shahin, Akopov, Evgeny L, Howell, Gareth R, Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N, Wong, Tien Yin, Liu, Yutao, Challa, Pratap, Hewitt, Alex W, Mitchell, Paul, Ziskind, Ari, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Guadarrama-Vallejo, Dalia, Perera, Shamira A, Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Schloetzer-Schrehardt, Ursula, Herms, Stefan, Nöthen, Markus M, Weisschuh, Nicole, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A, Lischinsky, Ignacio, Crowston, Jonathan G, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Founti, Panayiota, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Rhee, Douglas J, May-Bolchakova, Inna, Heegaard, Steffen, Alward, Wallace L M, Jonas, Jost B, Xu, Liang, Chowbay, Balram, Schaeffeler, Elke, Lerner, Fabian, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Inatani, Masaru, Tashiro, Kei, Reis, André, Edward, Deepak P, Pasquale, Louis R, Wiggs, Janey L, Yoshimura, Nagahisa, Ritch, Robert, Khor, Chiea-Chuen

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Common genetic determinants of intraocular pressure and primary open-angle glaucoma von van Koolwijk, Leonieke M E, Ramdas, Wishal D, Ikram, M Kamran, Jansonius, Nomdo M, Pasutto, Francesca, Hysi, Pirro G, Macgregor, Stuart, Janssen, Sarah F, Hewitt, Alex W, Viswanathan, Ananth C, ten Brink, Jacoline B, Hosseini, S Mohsen, Amin, Najaf, Despriet, Dominiek D G, Willemse-Assink, Jacqueline J M, Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S, Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y, Gramer, Eugen, Welge-Lüssen, Ulrich, Montgomery, Grant W, Carbonaro, Francis, Young, Terri L, Bellenguez, Céline, McGuffin, Peter, Foster, Paul J, Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y, Czudowska, Monika A, Hofman, Albert, Uitterlinden, Andre G, Wolfs, Roger C W, de Jong, Paulus T V M, Oostra, Ben A, Paterson, Andrew D, Mackey, David A, Bergen, Arthur A B, Reis, André, Hammond, Christopher J, Vingerling, Johannes R, Lemij, Hans G, Klaver, Caroline C W, van Duijn, Cornelia M

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Ischemic stroke is associated with the ABO locus: The EuroCLOT study von Williams, Frances M. K., Carter, Angela M., Hysi, Pirro G., Surdulescu, Gabriela, Hodgkiss, Dylan, Soranzo, Nicole, Traylor, Matthew, Bevan, Steve, Dichgans, Martin, Rothwell, Peter M. W., Sudlow, Cathie, Farrall, Martin, Silander, Kaisa, Kaunisto, Mari, Wagner, Peter, Saarela, Olli, Kuulasmaa, Kari, Virtamo, Jarmo, Salomaa, Veikko, Amouyel, Philippe, Arveiler, Dominique, Ferrieres, Jean, Wiklund, Per-Gunnar, Arfan Ikram, M., Hofman, Albert, Boncoraglio, Giorgio B., Parati, Eugenio A., Helgadottir, Anna, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Thorleifsson, Gudmar, Stefansson, Kari, Seshadri, Sudha, DeStefano, Anita, Gschwendtner, Andreas, Psaty, Bruce, Longstreth, Will, Mitchell, Braxton D., Cheng, Yu-Ching, Clarke, Robert, Ferrario, Marco, Bis, Joshua C., Levi, Christopher, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Fornage, Myriam, Sharma, Pankaj, Furie, Karen L., Rosand, Jonathan, Nalls, Mike, Meschia, James, Mosely, Thomas H., Evans, Alun, Palotie, Aarno, Markus, Hugh S., Grant, Peter J., Spector, Tim D.

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Multi-scale lidar measurements suggest miombo woodlands contain substantially more carbon than thought von Demol, Miro, Aguilar-Amuchastegui, Naikoa, Bernotaite, Gabija, Disney, Mathias, Duncanson, Laura, Elmendorp, Elise, Espejo, Andres, Furey, Allister, Hancock, Steven, Hansen, Johannes, Horsley, Harold, Langa, Sara, Liang, Mengyu, Locke, Annabel, Manjate, Virgílio, Mapanga, Francisco, Omidvar, Hamidreza, Parsons, Ashleigh, Peneva-Reed, Elitsa, Perry, Thomas, Puma Vilca, Beisit L, Rodríguez-Veiga, Pedro, Sutcliffe, Chloe, Upham, Robin, de Walque, Benoît, Burt, Andrew

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GWAS meta-analysis of 16 790 patients with Barrett’s oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology be... von Speller, Jan, Borisov, Oleg, Hess, Timo, Kreuser, Nicole, Alakus, Hakan, May, Andrea, Schmidt, Thomas, Thieme, Rene, Hillmer, Axel M, Lyros, Orestis, Dietrich, Arne, Lordick, Florian, Stocker, Gertraud, Hohaus, Michael, Reim, Daniel, Kandler, Jennis, Fuchs, Claudia, Lang, Hauke, Grimminger, Peter P, Dakkak, Dani, Görg, Siegfried, Franke, Andre, Galavotti, Sara, Dommermuth, Jens, Rösch, Thomas, Messmann, Helmut, Nöthen, Markus M, Vaughan, Thomas L, Tomlinson, Ian, Jankowski, Janusz, Vieth, Michael, MacGregor, Stuart, Gockel, Ines, Palles, Claire, Schumacher, Johannes, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin NA, Plomin, Robert, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Pearson, Richard, Strange, Amy, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Gwilliam, Rhian, Bumpstead, Suzannah J, Dronov, Serge, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Beckett, Conrad, Cullen, Sue, Dhar, Ameet, Kejariwal, Deepak, Sargeant, Ian, Winter, Helen, Dixon, Andrew, McMurty, Hugh, Johnson, Matthew, MacDonald, Chris, Haig, Chris, Senapati, Siba, Bhandari, Pradeep, Ang, Yeng, Smith, Mark, Ramadas, Arvind, Panter, Simon, Lovat, Laurence, Patel, Praful, Falk, Stephen, Nwokolo, Chuka, deCaestecker, John, Ramakrishnan, Subramaniam, Kelly, Sean, Prenen, Hans, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Whiteman, David C

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Genome-Wide Association Study Implicates HLA-C01:02 as a Risk Factor at the Major Histocompatibility Complex Locus in Schizophrenia

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Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis von Holliday, Elizabeth G, Smith, Albert V, Cornes, Belinda K, Buitendijk, Gabriëlle H S, Jensen, Richard A, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N, Boerwinkle, Eric, Cheng, Ching Yu, van Duijn, Cornelia M, Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W, Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E K, Launer, Lenore, Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M, Rochtchina, Elena, Rotter, Jerome I, Scott, Rodney J, Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, André G, Viswanathan, Ananth, Xie, Sophia, Vingerling, Johannes R, Klaver, Caroline C W, Tai, E Shyong, Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y, Attia, John, Wang, Jie Jin

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Common variant at 16p11.2 conferring risk of psychosis von Steinberg, S, de Jong, S, Pietiläinen, O P H, Lin, K, Papiol, S, Huttenlocher, J, Sigurdsson, E, Giegling, I, Breuer, R, Fraser, G, Walker, N, Melle, I, Djurovic, S, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Olsen, L, Ingason, A, Pirinen, M, Strengman, E, Hougaard, D M, Ørntoft, T, Didriksen, M, Abramova, L, Kaleda, V, Arrojo, M, Arango, C, Etain, B, Bellivier, F, Méary, A, Schürhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rossner, M, Christiansen, C, Kiemeney, L A, Franke, B, Veldink, J, Curran, S, Bolton, P, Poot, M, Rehnstrom, K, Freitag, C M, Magnusson, P, Saemundsen, E, Martsenkovsky, I, Bikshaieva, I, Martsenkovska, I, Vashchenko, O, Raleva, M, Paketchieva, K, Pejovic Milovancevic, M, Naneishvili, N, Mikeladze, N, Vincent, J B, Farmer, A, Mitchell, P B, Wright, A, Schofield, P R, Fullerton, J M, Montgomery, G W, Rubino, I A, Kenis, G, Bitter, I, Terenius, L, Jönsson, E G, Bakker, S, van Os, J, Jablensky, A, Powell, J, Murray, R, Corvin, A, Gill, M, Morris, D, O'Neill, F A, Kendler, K, Riley, B, Craddock, N, O'Donovan, M C, Thorsteinsdottir, U, Ehrenreich, H, Carracedo, A, Golimbet, V, Børglum, A D, Mortensen, P B, Werge, T, Ophoff, R A, Rietschel, M, Cichon, S, Ruggeri, M, Tosato, S, Palotie, A, St Clair, D, Rujescu, D, Collier, D A, Stefansson, K

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Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process von Springelkamp, Henriët., Höhn, René, Mishra, Aniket, Hysi, Pirro G., Khor, Chiea-Chuen, Loomis, Stephanie J., Bailey, Jessica N. Cooke, Gibson, Jane, Thorleifsson, Gudmar, Janssen, Sarah F., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Nongpiur, Monisha E., Montgomery, Grant W., Xu, Liang, Mountain, Jenny E., Gharahkhani, Puya, Lu, Yi, Amin, Najaf, Karssen, Lennart C., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Iglesias, Adriana I., Verhoeven, Virginie J. M., Hauser, Michael A., Loon, Seng-Chee, Despriet, Dominiek D. G., Nag, Abhishek, Venturini, Cristina, Sanfilippo, Paul G., Schillert, Arne, Kang, Jae H., Landers, John, Jonasson, Fridbert, Cree, Angela J., van Koolwijk, Leonieke M. E., Rivadeneira, Fernando, Souzeau, Emmanuelle, Jonsson, Vesteinn, Menon, Geeta, Weinreb, Robert N., de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Ennis, Sarah, Thorsteinsdottir, Unnur, Burdon, Kathryn P., Spector, Timothy D., Mirshahi, Alireza, Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Haines, Jonathan L., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jansonius, Nomdo M., Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Viswanathan, Ananth C., Klaver, Caroline C. W., Craig, Jamie E., Macgregor, Stuart, Mackey, David A., Lotery, Andrew J., Stefansson, Kari, Bergen, Arthur A. B., Young, Terri L., Wiggs, Janey L., Pfeiffer, Norbert, Wong, Tien-Yin, Pasquale, Louis R., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.

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The correlation between reading and mathematics ability at age twelve has a substantial genetic component von Davis, Oliver S. P., Band, Gavin, Pirinen, Matti, Haworth, Claire M. A., Meaburn, Emma L., Kovas, Yulia, Harlaar, Nicole, Docherty, Sophia J., Hanscombe, Ken B., Trzaskowski, Maciej, Curtis, Charles J. C., Strange, Amy, Freeman, Colin, Bellenguez, Céline, Su, Zhan, Pearson, Richard, Vukcevic, Damjan, Langford, Cordelia, Deloukas, Panos, Hunt, Sarah, Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Edkins, Sarah, Bumpstead, Suzannah J., Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz A. Z., Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Barroso, Ines, Peltonen, Leena, Dale, Philip S., Petrill, Stephen A., Schalkwyk, Leonard S., Craig, Ian W., Lewis, Cathryn M., Price, Thomas S., Donnelly, Peter, Plomin, Robert, Spencer, Chris C. A.

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 von Rees, Elliott, Walters, James T R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis von Robinson, P C, Leo, P J, Pointon, J J, Harris, J, Cremin, K, Bradbury, L A, Stebbings, S, Harrison, A A, Evans, D M, Duncan, E L, Wordsworth, B P, Brown, M A

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A genome-wide association study of anorexia nervosa von Boraska, V, Franklin, C S, Floyd, J A B, Rayner, N W, Tachmazidou, I, Klump, K L, Treasure, J, Kiezebrink, K, Gorwood, P, Adan, R A H, Favaro, A, Gratacos, M, Dmitrzak-Weglarz, M, Kaprio, J, Keski-Rahkonen, A, Raevuori, A, Van Furth, E F, Slof-Op 't Landt, M C T, Hudson, J I, Reichborn-Kjennerud, T, Knudsen, G P S, Kaplan, A S, Hakonarson, H, Berrettini, W H, Guo, Y, Li, D, Schork, N J, Komaki, G, Ando, T, Männik, K, Baker, J H, Cone, R D, Dackor, J, O'Toole, J K, Taico, C, Zerwas, S, Trace, S E, Davis, O S P, Helder, S, Burghardt, R, Egberts, K, Herzog, W, Imgart, H, Ramoz, N, Hendriks, J, Ophoff, R A, van Elburg, A A, Bruson, A, Clementi, M, Degortes, D, Forzan, M, Tenconi, E, Docampo, E, Escaramís, G, Jiménez-Murcia, S, Lissowska, J, Szeszenia-Dabrowska, N, Hauser, J, Karhunen, L, Meulenbelt, I, Slagboom, P E, Maj, M, Dedoussis, G, Slachtova, L, Martaskova, D, Kennedy, J L, Levitan, R D, Koubek, D, Wagner, G, Lichtenstein, P, Breen, G, Farmer, A, McGuffin, P, Herms, S, Wichmann, H-E, Dina, C, Sladek, R, Gambaro, G, Julia, A, Marsal, S, Palotie, A, Ripatti, S, Widén, E, Espeseth, T, Lundervold, A, Reinvang, I, Steen, V M, Le Hellard, S, Janout, V, Pinto, D, Scherer, S W, Aschauer, H, Padyukov, L, Courtet, P, Kalsi, G, Peltonen, L, Estivill, X, Hinney, A, Sullivan, P F, Bulik, C M

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A robust clustering algorithm for identifying problematic samples in genome-wide association studies von Bellenguez, Céline, Strange, Amy, Freeman, Colin, Donnelly, Peter, Spencer, Chris C.A.

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A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation von BRAMON, Elvira, PIRINEN, Matti, LANGFORD, Cordelia, DELOUKAS, Panos, HUNT, Sarah, GRAY, Emma, DRONOV, Serge, POTTER, Simon C, TASHAKKORI-GHANBARIA, Avazeh, EDKINS, Sarah, BUMPSTEAD, Suzannah J, ARRANZ, Maria J, STRANGE, Amy, BAKKER, Steven, BENDER, Stephan, BRUGGEMAN, Richard, CAHN, Wiepke, CHANDLER, David, COLLIER, David A, CRESPO-FACORRO, Benedicto, DAZZAN, Paola, DE HAAN, Lieuwe, DI FORTI, Marta, KUANG LIN, DRAGOVIC, Milan, GIEGLING, Ina, HALL, Jeremy, LYEGBE, Conrad, JOBLENSKY, Assen, KAHN, René S, KALAYDJIEVA, Luba, KRAVARITI, Eugenia, LAWRIE, Stephen, LINSZEN, Don H, FREEMAN, Colin, MATA, Ignacio, MCDONALD, Colm, MCINTOSH, Andrew, MYIN-GERMEYS, Inez, OPHOFF, Roel A, PARIANTE, Carmine M, PAUNIO, Tiina, PICCHIONI, Marco, RIPKE, Stephan, RUJESCU, Dan, BELLENGUEZ, Celine, SAUER, Heinrich, SHAIKH, Madiha, SUSSMANN, Jessika, SUVISAARI, Jaana, TOSATO, Sarah, TOULOPOULOU, Timothea, VAN OS, Jim, WALSHE, Muriel, WEISBROD, Matthias, WHALLEY, Heather, ZHAN SU, BAND, Gavin, PEARSON, Richard, VUKCEVIC, Damjan

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Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis von KNIGHT, Jo, SPAIN, Sarah L, CAPON, Francesca, HAYDAY, Adrian, NESTLE, Frank O, CLOP, Alex, BARKER, Jonathan N, WEALE, Michael E, TREMBATH, Richard C

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