Deutsch
TU Dresden

search

Genomic Gastroenterology - Selected Publications

von Kampen, O., Buch, S., Nothnagel, M., Azocar, L., Molina, H., Brosch, M., … , R., Tonjes, A., Wittenburg, H., Stumvoll, M., Kalthoff, H., Lammert, F., Tepel, J., Puschel, K., Becker, T., Schreiber, S., Platzer, M., Volzke, H., Krawczak, M., Miquel, J.F., Schafmayer, C., and Hampe, J. (2013). Genetic and functional identification of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus. Hepatology 57, 2407-2417.

Brosch, M., von Schonfels, W., Ahrens, M., Nothnagel, M., Krawczak, M., Laudes, M., Sipos, B., Becker, T., Schreiber, S., Rocken, C., Schafmayer, C., and Hampe, J. (2012). SFRS10--a splicing factor gene reduced in human obesity? Cell Metab 15, 265-266; author reply 267-269.

Stickel, F., Buch, S., Lau, K., Meyer zu Schwabedissen, H., Berg, T., … , Datz, C., Krawczak, M., Wodarz, N., Volzke, H., and Hampe, J. (2011). Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in caucasians. Hepatology 53, 86-95.

Buch, S., Schafmayer, C., Volzke, H., Seeger, M., Miquel, J.F., Sookoian, S.C., Egberts, J.H., Arlt, A., Pirola, C.J., Lerch, M.M., John, U., Franke, A., von Kampen, O., Brosch, M., Nothnagel, M., Kratzer, W., Boehm, B.O., Broring, D.C., Schreiber, S., Krawczak, M., and Hampe, J. (2010). Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition. Gastroenterology 139, 1942-1951 e1942.

Buch, S., Schafmayer, C., Volzke, H., Becker, C., Franke, A., von Eller-Eberstein, H., … , Fandrich, F., Folsch, U.R., Krawczak, M., Schreiber, S., Nurnberg, P., Tepel, J., and Hampe, J. (2007). A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. Nat Genet 39, 995-999.

Hampe, J., Franke, A., Rosenstiel, P., Till, A., Teuber, M., Huse, K., Albrecht, M., …, Sipos, B., Folsch, U.R., Lengauer, T., Platzer, M., Mathew, C.G., Krawczak, M., and Schreiber, S. (2007). A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat Genet 39, 207-211. 10. Hampe, J., Grebe, J., Nikolaus, S., Solberg, C., Croucher, P.J., Mascheretti, S., Jahnsen, J., Moum, B., Klump, B., Krawczak, M., Mirza, M.M., Foelsch, U.R., Vatn, M., and Schreiber, S. (2002). Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study. Lancet 359, 1661-1665.

Back