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Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5
