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A prospective study of the impact of AGTR1 A1166C on the effects of candesartan in patients with heart failure
A new locus regulating MICALL2 expression was identified for association with executive inhibition in children with attention deficit hyperactivity disorder
Association of type 2 diabetes susceptible genes GCKR, SLC30A8, and FTO polymorphisms with gestational diabetes mellitus risk: a meta-analysis
Subclinical thyroid disease and single nucleotide polymorphisms in reproductive-age women in areas of Shanxi Province, China, where iodine exposure is excessive
Association of LACC1, CEBPB-PTPN1, RIPK2 and ADO-EGR2 with ocular Behcet’s disease in a Chinese Han population
A common regulatory variant in SLC35B4 influences the recurrence and survival of prostate cancer
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa
Association between Zinc transporter genes ZIP11 rs11077654 polymorphism with bladder cancer risk in Chinese Han Population
Genetic risk between the CACNA1I gene and schizophrenia in Chinese Uygur population
FABP1 polymorphisms contribute to hepatocellular carcinoma susceptibility in Chinese population with liver cirrhosis: a case-control study