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Replication of previous genome-wide association studies of HKDC1, BACE2, SLC16A11 and TMEM163 SNPs in a gestational diabetes mellitus case–control sample from Han Chinese population
Glutamate ionotropic receptor NMDA type subunit 2A (GRIN 2A) gene polymorphism (rs4998386) and Parkinson’s disease susceptibility: A meta‐analysis
The research of ion channel‐related gene polymorphisms with atrial fibrillation in the Chinese Han population
Genetic predictors of match performance in sub-elite Australian football players: A pilot study
GENETIC AND ENVIRONMENT INTERACTIONS CONTRIBUTE TO LONGEVITY: A CASE-CONTROL STUDY WITH CENTENARIANS
Genetic Variants in EGFR/PLCE1 Pathway Are Associated with Prognosis of Esophageal Squamous Cell Carcinoma after Radical Resection
Genetic variations associated with telomere length confer risk of gastric cardia adenocarcinoma
Genome‐wide association study of psoriasis in an Egyptian population
Deleterious mutations in DNA repair gene FANCC exist in BRCA1/2-negative Chinese familial breast and/or ovarian cancer patients
The effect of combined patching and citalopram on visual acuity in adults with amblyopia: a randomized, crossover, placebo-controlled trial