Associated Papers
Deep Resequencing of Ulcerative Colitis-Associated Genes Identifies Novel Variants in Candidate Genes in the Korean Population.
Moon CM et al.
Inflammatory Bowel Diseases, 2018
29733354 (PubMed )
Supplement: izy122_suppl_supporting_data.pdf
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2.
Visschedijk MC et al.
Plos One, 2016
27490946 (PubMed )
Supplement: pone.0159609.s002.xlsx › Results_Discovery_phase_I
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
25671699 (PubMed )
Supplement: pgen.1004955.s006.xlsx › SNVs
Role of genetic variants of autophagy genes in susceptibility for non-medullary thyroid cancer and patients outcome.
Plantinga TS et al.
Plos One, 2014
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 variant IRGM -261T contributes to protection from tuberculosis caused by Mycobacterium tuberculosis but not by M. africanum strains.
Intemann CD et al.
Plos Pathogens, 2009
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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