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Number of items: 2.

Buch, Stephan; Stickel, Felix; Trépo, Eric; Way, Michael; Herrmann, Alexander; Nischalke, Hans Dieter; Brosch, Mario; Rosendahl, Jonas; Berg, Thomas; Ridinger, Monika; Rietschel, Marcella; McQuillin, Andrew; Frank, Josef; Kiefer, Falk; Schreiber, Stefan; Lieb, Wolfgang; Soyka, Michael; Semmo, Nasser; Aigner, Elmar; Datz, Christian; Schmelz, Renate; Brückner, Stefan; Zeissig, Sebastian; Stephan, Anna-Magdalena; Wodarz, Norbert; Devière, Jacques; Clumeck, Nicolas; Sarrazin, Christoph; Lammert, Frank; Gustot, Thierry; Deltenre, Pierre; Völzke, Henry; Lerch, Markus M; Mayerle, Julia; Eyer, Florian; Schafmayer, Clemens; Cichon, Sven; Nöthen, Markus M; Nothnagel, Michael; Ellinghaus, David; Huse, Klaus; Franke, Andre; Zopf, Steffen; Hellerbrand, Claus; Moreno, Christophe; Franchimont, Denis; Morgan, Marsha Y; Hampe, Jochen (2015). A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nature Genetics, 47(12):1443-1448.

Jarick, Ivonne; Volckmar, Anna-Lena; Pütter, Carolin; Pechlivanis, Sonali; Nguyen, Trang T; Dauvermann, Maria R; Beck, Sebastian; Albayrak, Özgür; Scherag, Susann; Gilsbach, Susanne; Cichon, Sven; Hoffmann, Per; Degenhardt, Franziska A; Nöthen, Markus M; Schreiber, Stefan; Wichmann, H-Erich; Jöckel, Karl-Heinz; Heinrich, Joachim; Tiesler, Carla M T; Faraone, Stephen V; Walitza, Susanne; Sinzig, Judith; Freitag, Christine; Meyer, Jobst; Herpertz-Dahlmann, Beate; Lehmkuhl, Gerd; Renner, Tobias J; Warnke, Andreas; Romanos, Marcel; Lesch, Klaus-Peter; Reif, Andreas; Schimmelmann, Benno G; Hebebrand, Johannes; Scherag, André; Hinney, Anke (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular Psychiatry, 19(1):115-121.

This list was generated on Thu May 23 00:39:18 2019 CEST.