PuSH - Publication Server of Helmholtz Zentrum München

11 Records found.
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1.
Momozawa, Y.* et al.: IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes. Nat. Commun. 9:2427 (2018)
2.
Rivas, M.A.* et al.: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 14:e1007329 (2018)
3.
Prins, B.P.* et al.: Investigating the causal relationship of c-reactive protein with 32 complex somatic and psychiatric outcomes: A large-scale cross-consortium mendelian randomization study. PLoS Med. 13:e1001976 (2016)
4.
Westra, H.J.* et al.: Cell specific eQTL analysis without sorting cells. PLoS Genet. 11:e1005223 (2015)
5.
Ellinghaus, D.* et al.: Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4. Hepatology 58, 1074-1083 (2013)
6.
Ellinghaus, D.* et al.: Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies. Gastroenterology 145, 339-347 (2013)
7.
Liu, J.Z.* et al.: Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat. Genet. 45, 670-675 (2013)
8.
Folseraas, T.* et al.: Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci. J. Hepatol. 57, 366-375 (2012)
9.
Jostins, L.* et al.: Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491, 119-124 (2012)
10.
Melum, E.* et al.: Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. Nat. Genet. 43, 17-19 (2011)
11.
Sotoodehnia, N.* et al.: Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat. Genet. 42, 1068-1076 (2010)