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Emebet Mengesha
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Prevalence and Effect of Genetic Risk of Thromboembolic Disease in Inflammatory Bowel Disease
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease
The TNF family member TL1A induces IL-22 secretion in committed human Th17 cells via IL-9 induction
Variants in ZNF365 isoform D are associated with Crohn's disease
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease
IL23R haplotypes provide a large population attributable risk for Crohn's disease
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