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Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China
Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases
A novel predictive approach for GVHD after allogeneic SCT based on clinical variables and cytokine gene polymorphisms
Cyclooxygenase-2 up-regulates hepatic somatostatin receptor 2 expression
Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES)
PNPLA3 rs738409 polymorphism is associated with liver fibrosis progression in patients with chronic hepatitis C: A repeated measures study
Association of coding and UTR variants in the known regions with wet age-related macular degeneration in Han Chinese population
Maternal Choline Supplementation during Normal Murine Pregnancy Alters the Placental Epigenome: Results of an Exploratory Study
CYP2D6 phenotype, tamoxifen, and risk of contralateral breast cancer in the WECARE Study
Genetic Variability in eIF2α Gene Is Associated with Islet β-Cell Function in the Development of Diabetes in a Chinese Han Population