MAGI2 genetic variation and inflammatory bowel disease-Reference-Cited by-同舟云学术

MAGI2 genetic variation and inflammatory bowel disease

Published:2009-01 Issue:1 Volume:15 Page:75-83
ISSN:1078-0998
Container-title:Inflammatory Bowel Diseases
language:en
Short-container-title:Inflammatory Bowel Diseases

Author:

McGovern Dermot P.B.,Taylor Kent D.,Landers Carol,Derkowski Carrie,Dutridge Deb,Dubinsky Marla,Ippoliti Andy,Vasiliauskas Eric,Mei Ling,Mengesha Emebet,King Lily,Pressman Sheila,Targan Stephan R.,Rotter Jerome I.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

Reference43 articles.

1. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

2. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

3. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

4. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

5. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

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