Publication Details

Differential effects of NOD2 variants on Crohn's disease risk and phenotype in diverse populations: a metaanalysis.

Economou M, Trikalinos TA, Loizou KT, Tsianos EV, Ioannidis JP. Am J Gastroenterol. 2004; 99 (12): 2393-404

Three variants of the CARD15/NOD2 gene (SNP8, SNP12, and SNP13) have been associated with Crohn's disease (CD). We assessed the impact of NOD2 variants on the CD risk across diverse populations and examined possible associations with disease phenotype.

PubMedID: 15571588