Studies

A frameshift mutation in *NOD2* associated with susceptibility to CD

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease

Association between insertion mutation in NOD2 gene and Crohn’s disease in German and British populations

NOD2/CARD15 gene polymorphisms and CD in the Chinese population

Genetic variation in DLG5 is associated with inflammatory bowel disease

Disease Concordance, Zygosity, and NOD2/CARD15 Status. Follow-Up of a Population-Based Cohort of Danish Twins with Inflammatory Bowel Disease

Single nucleotide polymorphisms in *TNFSF15* confer susceptibility to Crohn’s disease

GWAS Identifies *IL23R* as an IBD Gene

SNPs identifies a susceptibility variant for CD in *ATG16L1*

Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn’s disease in Japanese patients