GENETICS & OMICS

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

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  • A frameshift mutation in *NOD2* associated with susceptibility to CD
  • Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease
  • Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
  • Mapping of a susceptibility locus for Crohn’s disease on chromosome 16
  • Familial Occurrence of Inflammatory Bowel Disease