Items where Author is "Wellcome Trust Case Control Consortium, "

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Boraska, Vesna and Franklin, Christopher S. and Floyd, James A.B. and Thornton, Laura M. and Huckins, Laura M. and Southam, Lorraine and Rayner, N. William and Tachmazidou, Ioanna and Klumpp, Kelly and Treasure, Janet and Lewis, Cathryn M. and Schmidt, Ulrike and Tozzi, Federica and Kiezebrink, Kirsty and Hebebrand, Johannes and Gorwood, Philip and Adan, Roger A. H. and Kas, Martin J. H. and Favaro, Angela and Santonastaso, Paolo and Fernández-Aranda, Fernando and Gratacòs, Mònica and Rybakowski, Filip and Dmitrzak-Weglarz, Monika and Kaprio, Jaakko and Keski-Rahkonen, Anna and Raevuori, Anu and Van Furth, Eric F. and Slof-Op 't Landt, Margarita and Hudson, James I. and Reichborn-Kjennerud, Ted and Knudsen, Gun Peggy S. and Monteleone, Palmiero and Kaplan, Allan S. and Karwautz, Andreas and Hakonarson, Hakon and Berrettini, Wade H. and Guo, Yiran and Li, Dong and Schork, Nicholas and Komaki, Gen and Ando, Tetsuya and Inoko, Hidetoshi and Esko, Tõnu and Fischer, Krista and Männik, Katrin and Metspalu, Andres and Baker, Jessica H. and Cone, Roger D. and Dackor, Jennifer and DeSocio, Janiece E. and Hilliard, Christopher E. and O'Toole, Julie K. and Pantel, Jacques and Szatkiewicz, Jin P. and Taico, Chrysecolla and Zerwas, Stephanie and Trace, Sara E. and Davis, Oliver S. P. and Helder, Sietske and Buhren, Katherina and Burghardt, Roland and de Zwaan, Martina and Egberts, Karin and Ehrlich, Stefan and Herpertz-Dahlmann, Beate and Herzog, Wolfgang and Imgart, Hartmut and Scherag, André and Scherag, Susann and Zipfel, Stephan and Boni, Claudette and Ramoz, Nicolas and Versini, Audrey and Brandys, Marek K. and Danner, Unna N. and de Kovel, Carolien and Hendriks, Judith and Koeleman, Bobby P. C. and Ophoff, Roel A. and Strengman, Eric and van Elburg, Annemarie A. and Bruson, Alice and Clementi, Maurizio and Degortes, Daniela and Forzan, Monica and Tenconi, Elena and Docampo, Elisa and Escaramis, Georgia and Jiménez-Murcia, Susana and Lissowska, Jolanta and Rajewski, Andrzej and Szeszenia-Dabrowska, Neonila and Slopien, Agnieszka and Hauser, Joanna and Karhunen, Leila and Meulenbelt, Ingrid and Slagboom, P. Eline and Tortorella, Alfonso and Maj, Mario and Dedoussis, George and Dikeos, Dimitris and Gonidakis, Fragiskos and Tziouvas, Konstantinos and Tsitsika, Artemis and Papezova, Hana and Slachtova, Lenka and Martaskova, Debora and Kennedy, James L. and Levitan, Robert D. and Yilmaz, Zeynep and Huemer, Julia and Koubek, Doris and Merler, Elisabeth and Wagner, Gudrun and Lichtenstein, Paul and Breen, Gerome and Cohen-Woods, Sarah and Farmer, Ann and McGuffin, Peter and Cichon, Sven and Giegling, Ina and Herms, Stefan and Rujescu, Dan and Schreiber, Stefan and Wichmann, H-Erich and Dina, Christian and Sladek, Rob and Gambaro, Giovanni and Soranzo, Nicole and Julia, Antonio and Marsal, Sara and Rabionet, Raquel and Gaborieau, Valerie and Dick, Danielle M. and Palotie, Aarno and Ripatti, Samuli and Widen, Elisabeth and Andreassen, Ole A. and Espeseth, Thomas and Lundervold, Astri J. and Reinvang, Ivar and Steen, Vidar M. and Le Hellard, Stephanie and Mattingsdal, Morten and Ntalla, Ioanna and Bencko, Vladimir and Foretova, Lenka and Janout, Vladimir and Navratilova, Marie and Gallinger, Steven and Pinto, Dalila and Scherer, Stephen W. and Aschauer, Harald and Carlberg, Laura and Schosser, Alexandra and Alfredsson, Lars and Ding, Bo and Klareskog, Lars and Padyukov, Leonid and Finan, Chris and Guillaume, Phillippe and Kalsi, Gursharan and Roberts, Marion and Logan, Darren W. and Peltonen, Leena and Ritchie, Graham R. S. and Barrett, Jeffrey C. and Wellcome Trust Case Control Consortium, and Estivill, Xavier and Hinney, Anke and Sullivan, Patrik F. and Collier, David A. and Zeggini, Eleftheria and Bulik, Cynthia M.. (2014) A genome-wide association study of anorexia nervosa. Molecular Psychiatry, 19 (10). pp. 1085-1094.

Steinberg, S. and de Jong, S. and Mattheisen, M. and Costas, J. and Demontis, D. and Jamain, S. and Pietiläinen, O. P. H. and Lin, K. and Papiol, S. and Huttenlocher, J. and Sigurdsson, E. and Vassos, E. and Giegling, I. and Breuer, R. and Fraser, G. and Walker, N. and Melle, I. and Djurovic, S. and Agartz, I. and Tuulio-Henriksson, A. and Suvisaari, J. and Lönnqvist, J. and Paunio, T. and Olsen, L. and Hansen, T. and Ingason, A. and Pirinen, M. and Strengman, E. and Group, and Hougaard, D. M. and Ørntoft, T. and Didriksen, M. and Hollegaard, M. V. and Nordentoft, M. and Abramova, L. and Kaleda, V. and Arrojo, M. and Sanjuán, J. and Arango, C. and Etain, B. and Bellivier, F. and Méary, A. and Schürhoff, F. and Szoke, A. and Ribolsi, M. and Magni, V. and Siracusano, A. and Sperling, S. and Rossner, M. and Christiansen, C. and Kiemeney, L. A. and Franke, B. and van den Berg, L. H. and Veldink, J. and Curran, S. and Bolton, P. and Poot, M. and Staal, W. and Rehnstrom, K. and Kilpinen, H. and Freitag, C. M. and Meyer, J. and Magnusson, P. and Saemundsen, E. and Martsenkovsky, I. and Bikshaieva, I. and Martsenkovska, I. and Vashchenko, O. and Raleva, M. and Paketchieva, K. and Stefanovski, B. and Durmishi, N. and Pejovic Milovancevic, M. and Lecic Tosevski, D. and Silagadze, T. and Naneishvili, N. and Mikeladze, N. and Surguladze, S. and Vincent, J. B. and Farmer, A. and Mitchell, P. B. and Wright, A. and Schofield, P. R. and Fullerton, J. M. and Montgomery, G. W. and Martin, N. G. and Rubino, I. A. and van Winkel, R. and Kenis, G. and De Hert, M. and Réthelyi, J. M. and Bitter, I. and Terenius, L. and Jönsson, E. G. and Bakker, S. and van Os, J. and Jablensky, A. and Leboyer, M. and Bramon, E. and Powell, J. and Murray, R. and Corvin, A. and Gill, M. and Morris, D. and O'Neill, F. A. and Kendler, K. and Riley, B. and Wellcome Trust Case Control Consortium, and Craddock, N. and Owen, M. J. and O'Donovan, M. C. and Thorsteinsdottir, U. and Kong, A. and Ehrenreich, H. and Carracedo, A. and Golimbet, V. and Andreassen, O. A. and Børglum, A. D. and Mors, O. and Mortensen, P. B. and Werge, T. and Ophoff, R. A. and Nöthen, M. M. and Rietschel, M. and Cichon, S. and Ruggeri, M. and Tosato, S. and Palotie, A. and St Clair, D. and Rujescu, D. and Collier, D. A. and Stefansson, H. and Stefansson, K.. (2014) Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1). pp. 108-114.

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