Jochen Hampe
Jochen Hampe
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A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
J Hampe, A Franke, P Rosenstiel, A Till, M Teuber, K Huse, M Albrecht, ...
Nature genetics 39 (2), 207-211, 2007
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
J Hampe, A Cuthbert, PJP Croucher, MM Mirza, S Mascheretti, S Fisher, ...
The Lancet 357 (9272), 1925-1928, 2001
Reduction in diversity of the colonic mucosa associated bacterial microflora in patients with active inflammatory bowel disease
SJ Ott, M Musfeldt, DF Wenderoth, J Hampe, O Brant, UR Fölsch, ...
Gut 53 (5), 685-693, 2004
Activation of nuclear factor κB in inflammatory bowel disease
S Schreiber, S Nikolaus, J Hampe
Gut 42 (4), 477-484, 1998
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease
AP Cuthbert, SA Fisher, MM Mirza, K King, J Hampe, PJP Croucher, ...
Gastroenterology 122 (4), 867-874, 2002
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity
S Wahl, A Drong, B Lehne, M Loh, WR Scott, S Kunze, PC Tsai, JS Ried, ...
Nature 541 (7635), 81-86, 2017
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
A Tenesa, SM Farrington, JGD Prendergast, ME Porteous, M Walker, ...
Nature genetics 40 (5), 631-637, 2008
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23. 3
IPM Tomlinson, E Webb, L Carvajal-Carmona, P Broderick, K Howarth, ...
Nature genetics 40 (5), 623-630, 2008
Obesity accelerates epigenetic aging of human liver
S Horvath, W Erhart, M Brosch, O Ammerpohl, W von Schönfels, M Ahrens, ...
Proceedings of the National Academy of Sciences 111 (43), 15538-15543, 2014
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
L Carvajal-Carmona, K Howarth, E Jaeger, SL Spain, A Walther, ...
Nature genetics 40 (12), 1426-1435, 2008
Genetic variation in DLG5 is associated with inflammatory bowel disease
M Stoll, B Corneliussen, CM Costello, GH Waetzig, B Mellgard, WA Koch, ...
Nature genetics 36 (5), 476-480, 2004
Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study
J Hampe, J Grebe, S Nikolaus, C Solberg, PJP Croucher, S Mascheretti, ...
The Lancet 359 (9318), 1661-1665, 2002
Sarcoidosis is associated with a truncating splice site mutation in BTNL2
R Valentonyte, J Hampe, K Huse, P Rosenstiel, M Albrecht, A Stenzel, ...
Nature genetics 37 (4), 357-364, 2005
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
J Hampe, S Schreiber, SH Shaw, KF Lau, S Bridger, AJS Macpherson, ...
The American journal of human genetics 64 (3), 808-816, 1999
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
S Buch, F Stickel, E Trepo, M Way, A Herrmann, HD Nischalke, M Brosch, ...
Nature genetics 47 (12), 1443-1448, 2015
DNA methylation analysis in nonalcoholic fatty liver disease suggests distinct disease-specific and remodeling signatures after bariatric surgery
M Ahrens, O Ammerpohl, W von Schönfels, J Kolarova, S Bens, T Itzel, ...
Cell metabolism 18 (2), 296-302, 2013
Detection of diverse bacterial signatures in atherosclerotic lesions of patients with coronary heart disease
SJ Ott, NE El Mokhtari, M Musfeldt, S Hellmig, S Freitag, A Rehman, ...
Circulation 113 (7), 929-937, 2006
Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study
JC Chambers, M Loh, B Lehne, A Drong, J Kriebel, V Motta, S Wahl, ...
The lancet Diabetes & endocrinology 3 (7), 526-534, 2015
Single base‐pair substitutions in exon–intron junctions of human genes: nature, distribution, and consequences for mRNA splicing
M Krawczak, NST Thomas, B Hundrieser, M Mort, M Wittig, J Hampe, ...
Human mutation 28 (2), 150-158, 2007
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease
S Buch, C Schafmayer, H Völzke, C Becker, A Franke, ...
Nature genetics 39 (8), 995-999, 2007
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