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A prospective study of the impact of AGTR1 A1166C on the effects of candesartan in patients with heart failure
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
New genetic evidence of affinities and discontinuities between bronze age Siberian populations
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
Genotyping of the ABCG2 gene using Matrix‐Associated Laser Desorption/Ionisation, Time‐of‐Flight Mass Spectrometry
LncRNA CDKN2BAS rs2157719 genetic variant contributes to medulloblastoma predisposition
ADGRV1 is implicated in myoclonic epilepsy
ANKRD9 is associated with tumor suppression as a substrate receptor subunit of ubiquitin ligase