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

J Hampe, A Franke, P Rosenstiel, A Till, M Teuber, K Huse, M Albrecht, G Mayr, F M De La Vega, J Briggs, S Gunther, N J Prescott, C M Onnie, R Hasler, B Sipos, U R Folsch, T Lengauer, M Platzer, C G Mathew, M KrawczakS Schreiber

Research output: Contribution to journalArticlepeer-review

1620 Citations (Scopus)

Abstract

We performed a genome-wide association study of 19,779 nonsynonymous SNPs in 735 individuals with Crohn disease and 368 controls. A total of 7,159 of these SNPs were informative. We followed up on all 72 SNPs with P 0.4), these data suggest that the underlying biological process may be specific to Crohn disease
Original languageEnglish
Pages (from-to)207 - 211
Number of pages5
JournalNature Genetics
Volume39
Issue number2
DOIs
Publication statusPublished - Feb 2007

Fingerprint

Dive into the research topics of 'A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1'. Together they form a unique fingerprint.

Cite this