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CREM variant rs17583959 conferred susceptibility to T1D risk in the Tunisian families
Impact of diabetes-related gene polymorphisms on the clinical characteristics of type 2 diabetes Chinese Han population
Altered DNA methylation in neonates born large-for-gestational-age is associated with cardiometabolic risk in children
Common Variant in Glycoprotein Ia Increases Long?Term Adverse Events Risk After Coronary Artery Bypass Graft Surgery
TIMP-2 SNPs rs7342880 and rs4789936 are linked to risk of knee osteoarthritis in the Chinese Han Population
PHACTR1 and SLC22A3 gene polymorphisms are associated with reduced coronary artery disease risk in the male Chinese Han population
Pooled genome wide association detects association upstream of FCRL3 with Graves’ disease
Genome-wide association study of peanut allergy reproduces association with amino acid polymorphisms in HLA-DRB1
Association of multiple genetic variants with breast cancer susceptibility in the Han Chinese population
Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease