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Number of items: 6.

Degenhardt, Frauke; Dirmeier, Andrea; Lopez, Rocio; Lang, Sylvia; Kunst, Claudia; Roggenbuck, Dirk; Reinhold, Dirk; Szymczak, Silke; Rogler, Gerhard; Klebl, Frank; Franke, Andre; Rieder, Florian (2016). Serologic anti-GP2 antibodies are associated with genetic polymorphisms, fibrostenosis, and need for surgical resection in crohn's disease. Inflammatory Bowel Diseases, 22(11):2648-2657.

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.

Forster, Michael; Szymczak, Silke; Ellinghaus, David; Hemmrich, Georg; Rühlemann, Malte; Kraemer, Lars; Mucha, Sören; Wienbrandt, Lars; Stanulla, Martin; Franke, Andre (2015). Vy-PER: eliminating false positive detection of virus integration events in next generation sequencing data. Scientific Reports, 5:11534.

Lemke, Johannes R; Lal, Dennis; Reinthaler, Eva M; Steiner, Isabelle; Nothnagel, Michael; Alber, Michael; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Finsterwalder, Katrin; Franke, Andre; Schilhabel, Markus; Jähn, Johanna A; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; Larsen, Jan; Møller, Rikke S; Hjalgrim, Helle; Addis, Laura; Tang, Shan; Hughes, Elaine; Pal, Deb K; Veri, Kadi; Vaher, Ulvi; Talvik, Tiina; Dimova, Petia; Guerrero López, Rosa; Serratosa, José M; Linnankivi, Tarja; Lehesjoki, Anna-Elina; Ruf, Susanne; Wolff, Markus; Buerki, Sarah; Wohlrab, Gabriele; Kroell, Judith; Datta, Alexandre N; Fiedler, Barbara; Kurlemann, Gerhard; Kluger, Gerhard; Hahn, Andreas; Haberlandt, D Edda; Kutzer, Christina; Sperner, Jürgen; Becker, Felicitas; Weber, Yvonne G; Feucht, Martha; Steinböck, Hannelore; Neophythou, Birgit; Ronen, Gabriel M; Gruber-Sedlmayr, Ursula; Geldner, Julia; Harvey, Robert J; Hoffmann, Per; Herms, Stefan; Altmüller, Janine; Toliat, Mohammad R; Thiele, Holger; Nürnberg, Peter; Wilhelm, Christian; Stephani, Ulrich; Helbig, Ingo; Lerche, Holger; Zimprich, Fritz; Neubauer, Bernd A; Biskup, Saskia; von Spiczak, Sarah (2013). Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nature Genetics, 45(9):1067-1072.

Rebane, Ana; Zimmermann, Maya; Aab, Alar; Baurecht, Hansjörg; Koreck, Andrea; Karelson, Maire; Abram, Kristi; Metsalu, Tauno; Pihlap, Maire; Meyer, Norbert; Fölster-Holst, Regina; Nagy, Nikoletta; Kemeny, Lajos; Kingo, Külli; Vilo, Jaak; Illig, Thomas; Akdis, Mübeccel; Franke, Andre; Novak, Natalija; Weidinger, Stephan; Akdis, Cezmi A (2012). Mechanisms of IFN-γ-induced apoptosis of human skin keratinocytes in patients with atopic dermatitis. Journal of Allergy and Clinical Immunology, 129(5):1297-1306.

Hunt, Karen A; Smyth, Deborah J; Balschun, Tobias; Ban, Maria; Mistry, Vanisha; Ahmad, Tariq; Anand, Vidya; Barrett, Jeffrey C; Bhaw-Rosun, Leena; Bockett, Nicholas A; Brand, Oliver J; Brouwer, Elisabeth; Concannon, Patrick; Cooper, Jason D; Dias, Kerith-Rae M; van Diemen, Cleo C; Dubois, Patrick C; Edkins, Sarah; Fölster-Holst, Regina; Fransen, Karin; Glass, David N; Heap, Graham A R; Hofmann, Sylvia; Huizinga, Tom W J; Hunt, Sarah; Langford, Cordelia; Lee, James; Mansfield, John; Marrosu, Maria Giovanna; Mathew, Christopher G; Mein, Charles A; Müller-Quernheim, Joachim; Nutland, Sarah; Onengut-Gumuscu, Suna; Ouwehand, Willem; Pearce, Kerra; Prescott, Natalie J; Posthumus, Marcel D; Potter, Simon; Rosati, Giulio; Sambrook, Jennifer; Satsangi, Jack; Schreiber, Stefan; Shtir, Corina; Simmonds, Matthew J; Sudman, Marc; Thompson, Susan D; Toes, Rene; Trynka, Gosia; Vyse, Timothy J; Walker, Neil M; Weidinger, Stephan; Zhernakova, Alexandra; Zoledziewska, Magdalena; Weersma, Rinse K; Gough, Stephen C L; Sawcer, Stephen; Wijmenga, Cisca; Parkes, Miles; Cucca, Francesco; Franke, Andre; Deloukas, Panos; Rich, Stephen S; Todd, John A; van Heel, David A (2012). Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nature Genetics, 44(1):3-5.

This list was generated on Sun Nov 19 20:59:45 2017 CET.