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Kraemer, Dennis; Terumalai, Dillenn; Famiglietti, Maria Livia; Filges, Isabel; Joset, Pascal; Koller, Samuel; Maurer, Fabienne; Meier, Stéphanie; Nouspikel, Thierry; Sanz, Javier; Zweier, Christiane; Abramowicz, Marc; Berger, Wolfgang; Cichon, Sven; Schaller, André; Superti-Furga, Andrea; Barbié, Valérie; Rauch, Anita (2024). SwissGenVar: A Platform for Clinical-Grade Interpretation of Genetic Variants to Foster Personalized Healthcare in Switzerland. Journal of personalized medicine, 14(6) MDPI 10.3390/jpm14060648
Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K; Walters, Raymond K; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; ... (2018). Analysis of shared heritability in common disorders of the brain. Science, 360(6395) American Association for the Advancement of Science 10.1126/science.aap8757
Treutlein, Jens; Frank, Josef; Streit, Fabian; Reinbold, Céline; Juraeva, Dilafruz; Degenhardt, Franziska; Rietschel, Liz; Witt, Stephanie; Forstner, Andreas; Ridinger, Monika; Strohmaier, Jana; Wodarz, Norbert; Dukal, Helene; Foo, Jerome; Hoffmann, Per; Herms, Stefan; Heilmann-Heimbach, Stefanie; Soyka, Michael; Maier, Wolfgang; Gaebel, Wolfgang; ... (2017). Genetic contribution to alcohol dependence: Investigation of a heterogeneous german sample of individuals with alcohol dependence, chronic alcoholic pancreatitis, and alcohol-related cirrhosis. Genes, 8(7), p. 183. MDPI 10.3390/genes8070183
Hibar, Derrek P.; Hieab, H.H. Adams; Chauhan, Ganesh; Stein, Jason L.; Hofer, Edith; Renteria, Miguel E.; Bis, Joshua; Arias-Vasquez, Alejandro; Ikram, Kamran; Desrivières, Sylvane; Vernooij, Meike W.; Abramovic, Lucija; Alhusaini, Saud; Amin, Najaf; Andersson, Micael; Arfanakis, Konstantinos A.; Aribisala, Benjamin S.; Armstrong, Nicola J.; Athanasiu, Lavinia; Axelsson, Tomas; ... (2017). Novel genetic loci associated with hippocampal volume. Nature communications, 8, p. 13624. Nature Publishing Group 10.1038/ncomms13624
Adams, Hieab H H; Hibar, Derrek P; Chouraki, Vincent; Stein, Jason L; Nyquist, Paul A; Rentería, Miguel E; Trompet, Stella; Arias-Vasquez, Alejandro; Seshadri, Sudha; Desrivières, Sylvane; Beecham, Ashley H; Jahanshad, Neda; Wittfeld, Katharina; Van der Lee, Sven J; Abramovic, Lucija; Alhusaini, Saud; Amin, Najaf; Andersson, Micael; Arfanakis, Konstantinos; Aribisala, Benjamin S; ... (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature neuroscience, 19(12), pp. 1569-1582. Nature America 10.1038/nn.4398
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; ... (2015). A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nature genetics, 47(12), pp. 1443-1448. Nature America 10.1038/ng.3417
Marenholz, Ingo; Esparza-Gordillo, Jorge; Rüschendorf, Franz; Bauerfeind, Anja; Strachan, David P; Spycher, Ben D; Baurecht, Hansjörg; Margaritte-Jeannin, Patricia; Sääf, Annika; Kerkhof, Marjan; Ege, Markus; Baltic, Svetlana; Matheson, Melanie C; Li, Jin; Michel, Sven; Ang, Wei Q; McArdle, Wendy; Arnold, Andreas; Homuth, Georg; Demenais, Florence; ... (2015). Meta-analysis identifies seven susceptibility loci involved in the atopic march. Nature communications, 6, p. 8804. Nature Publishing Group 10.1038/ncomms9804
Albayrak, Özgür; Pütter, Carolin; Volckmar, Anna-Lena; Cichon, Sven; Hoffmann, Per; Nöthen, Markus M.; Jöckel, Karl-Heinz; Schreiber, Stefan; Wichmann, H-Erich; Faraone, Stephen V.; Neale, Benjamin M.; Herpertz-Dahlmann, Beate; Lehmkuhl, Gerd; Sinzig, Judith; Renner, Tobias J.; Romanos, Marcel; Warnke, Andreas; Lesch, Klaus-Peter; Reif, Andreas; Schimmelmann, Benno G.; ... (2013). Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. American journal of medical genetics. Part B - Neuropsychiatric genetics, 162B(4), pp. 295-305. Hoboken, N.J.: Wiley-Liss 10.1002/ajmg.b.32144
Håvik, Bjarte; Degenhardt, Franziska A; Johansson, Stefan; Fernandes, Carla P D; Hinney, Anke; Scherag, André; Lybæk, Helle; Djurovic, Srdjan; Christoforou, Andrea; Ersland, Kari M; Giddaluru, Sudheer; O'Donovan, Michael C; Owen, Michael J; Craddock, Nick; Mühleisen, Thomas W; Mattheisen, Manuel; Schimmelmann, Benno G; Renner, Tobias; Warnke, Andreas; Herpertz-Dahlmann, Beate; ... (2012). DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder. PLoS ONE, 7(4), e35424. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0035424
Jostins, Luke; Ripke, Stephan; Weersma, Rinse K; Duerr, Richard H; McGovern, Dermot P; Hui, Ken Y; Lee, James C; Schumm, L Philip; Sharma, Yashoda; Anderson, Carl A; Essers, Jonah; Mitrovic, Mitja; Ning, Kaida; Cleynen, Isabelle; Theatre, Emilie; Spain, Sarah L; Raychaudhuri, Soumya; Goyette, Philippe; Wei, Zhi; Abraham, Clara; ... (2012). Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature, 491(7422), pp. 119-24. London: Macmillan Journals Ltd. 10.1038/nature11582
