Genetic Research Centers
Data Coordinating Center
Rinse K. Weersma
Trans-ethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals shared but also ethnicity-specific disease associations
Genetic effects on the commensal microbiota in inflammatory bowel disease patients
IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Fine-mapping inflammatory bowel disease loci to single-variant resolution
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Genome-wide association identifies multiple ulcerative colitis susceptibility loci