Associated Papers
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 838.321
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.
Rivas MA et al.
Nature Genetics, 2011
21983784 (PubMed )
Supplement: NIHMS335188-supplement-1.pdf
Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
Prescott NJ et al.
Human Molecular Genetics, 2010
Autophagy gene ATG16L1 but not IRGM is associated with Crohn's disease in Canadian children.
Amre DK et al.
Inflammatory Bowel Diseases, 2009
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Parkes M et al.
Nature Genetics, 2007
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