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7
The NLR gene family: a standard nomenclature
On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Development and validation of the Nancy histological index for UC.
Systematic association mapping identifies NELL1 as a novel IBD disease gene
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5
