Common Variants at VRK2 and TCF4 Conferring Risk of Schizophrenia

Common sequence variants have recently joined rare structural polymorphisms as genetic factors with strong evidence for association with schizophrenia. Here we extend our previous genome-wide association (GWA) study and meta-analysis (totalling 7,946 cases and 19,036 controls) by examining an expand...

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Veröffentlicht in:	Human Molecular Genetics 2011-10, Vol.20 (20), p.4076-4081
Hauptverfasser:	Steinberg, Stacy, de Jong, Simone, Irish Schizophrenia Genomics Consortium, Andreassen, Ole A, Werge, Thomas, Børglum, Anders D, Mors, Ole, Mortensen, Preben B, Gustafsson, Omar, Costas, Javier, Pietiläinen, Olli P.H, Demontis, Ditte, Papiol, Sergi, Huttenlocher, Johanna, Mattheisen, Manuel, Breuer, René, Vassos, Evangelos, Giegling, Ina, Fraser, Gillian, Walker, Nicholas, Tuulio-Henriksson, Annamari, Suvisaari, Jaana, Lönnqvist, Jouko, Paunio, Tiina, Agartz, Ingrid, Melle, Ingrid, Djurovic, Srdjan, Strengman, Eric, GROUP, Jürgens, Gesche, Glenthøj, Birte, Terenius, Lars, Hougaard, David M, Orntoft, Torben, Wiuf, Carsten, Didriksen, Michael, Hollegaard, Mads V, Nordentoft, Merete, van Winkel, Ruud, Kenis, Gunter, Abramova, Lilia, Kaleda, Vasily, Arrojo, Manuel, Sanjuán, Julio, Arango, Celso, Sperling, Swetlana, Rossner, Moritz, Ribolsi, Michele, Magni, Valentina, Siracusano, Alberto, Christiansen, Claus, Kiemeney, Lambertus A, Veldink, Jan, van den Berg, Leonard, Ingason, Andres, Muglia, Pierandrea, Murray, Robin, Nöthen, Markus M, Sigurdsson, Engilbert, Petursson, Hannes, Thorsteinsdottir, Unnur, Kong, Augustine, Rubino, I. Alex, De Hert, Marc, Réthelyi, János M, Bitter, István, Jönsson, Erik G, Golimbet, Vera, Carracedo, Angel, Ehrenreich, Hannelore, Craddock, Nick, Owen, Michael J, O'Donovan, Michael C, Wellcome Trust Case Control Consortium, Ruggeri, Mirella, Tosato, Sarah, Peltonen, Leena, Ophoff, Roel A, Collier, David A, St Clair, David, Rietschel, Marcella, Cichon, Sven, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari
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Sprache:	eng
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