GENETICS & OMICS

Dr Laura Fachal (Wellcome Sanger Institute, UK) has played a pivotal role in supporting this section

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  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
  • Sequence variants in the autophagy gene *IRGM* and multiple other replicating loci contribute to Crohn’s disease susceptibility
  • Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
  • GWAS Identifies *IL23R* as an IBD Gene
  • SNPs identifies a susceptibility variant for CD in *ATG16L1*
  • Single nucleotide polymorphisms in *TNFSF15* confer susceptibility to Crohn’s disease
  • Disease Concordance, Zygosity, and NOD2/CARD15 Status. Follow-Up of a Population-Based Cohort of Danish Twins with Inflammatory Bowel Disease
  • Genetic variation in DLG5 is associated with inflammatory bowel disease
  • NOD2/CARD15 gene polymorphisms and CD in the Chinese population
  • Association between insertion mutation in NOD2 gene and Crohn’s disease in German and British populations