A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1-Reference-Cited by-同舟云学术

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

Published:2006-12-31 Issue:2 Volume:39 Page:207-211
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Hampe Jochen,Franke Andre,Rosenstiel Philip,Till Andreas,Teuber Markus,Huse Klaus,Albrecht Mario,Mayr Gabriele,De La Vega Francisco M,Briggs Jason,Günther Simone,Prescott Natalie J,Onnie Clive M,Häsler Robert,Sipos Bence,Fölsch Ulrich R,Lengauer Thomas,Platzer Matthias,Mathew Christopher G,Krawczak Michael,Schreiber Stefan

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1954.pdf

Reference30 articles.

1. Hugot, J.P. et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411, 599–603 (2001).

2. Ogura, Y. et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411, 603–606 (2001).

3. Rioux, J.D. et al. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat. Genet. 29, 223–228 (2001).

4. Peltekova, V.D. et al. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat. Genet. 36, 471–475 (2004).

5. Stoll, M. et al. Genetic variation in DLG5 is associated with inflammatory bowel disease. Nat. Genet. 36, 476–480 (2004).

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