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Genetic Variations of CYP19A1 Gene and Stroke Susceptibility: A Case-control Study in the Chinese Han Population
Kidney podocyte-associated gene polymorphisms affect tacrolimus concentration in pediatric patients with refractory nephrotic syndrome
A functional variant in CHK1 contributes to increased risk of nasopharyngeal carcinoma in a Han Chinese population
Clinical factors associated with treatment toxicity of pemetrexed plus platinum in elderly patients with non-small cell lung cancer
MASS SPECTROMETRY‐BASED PERSONALIZED DRUG THERAPY
Structural and functional alterations of Nitric Oxide Synthase 3 due to missense variants associate with High-Altitude Pulmonary Edema through Dynamic study
The study on the association of the methylation in the promoter region of brain derived neurotrophic factor with autism spectrum disorders
rs11927381 Polymorphism and Type 2 Diabetes Mellitus: Contribution of Smoking to the Realization of Susceptibility to the Disease
Association study of SLC22A12 gene rs893006 and SLC2A9 gene rs11942223 with hyperuricemia
Neurological safety of oxaliplatin in patients with uncommon variants in Charcot-Marie-tooth disease genes