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  • Effect and interaction of PINK1 genetic polymorphisms and environmental factors on blood pressure in COEs-exposed workers
  • CYP2C19 genotype and sodium channel blockers in lacosamide-treated children with epilepsy: two major determinants of trough lacosamide concentration or clinical response
  • Peripheral pathway gene variants in lifelong premature ejaculation: CYP19A1, CYP1A1, and CYP1A2 enzymes polymorphisms in Chinese Han men
  • Downregulated Expression and Hypermethylation of SIRT1 in Patients with Kashin-Beck Disease–Mediated Chondrocyte Apoptosis May Potentially Be Ameliorated by Selenium Supplement
  • Impact of Suppressor of Mothers Against Decapentaplegic (SMAD) 7 Gene Single Nucleotide Polymorphisms on Colorectal Cancer Risk and Prognosis
  • The Mediating Role of Abnormal ZEB1 Methylation in the Association between Nickel Exposure and Non-Syndromic Orofacial Cleft
  • Early-life adversity severity, timing, and context type are associated with SLC6A4 methylation in emerging adults: results from a prospective cohort study
  • Association Between Genetically Determined Serum Corin and the Risk of Stroke in Chinese Adults: A Mendelian Randomization Study
  • Development and validation of cardiometabolic risk predictive models based on LDL oxidation and candidate geromarkers from the MARK-AGE data
  • CXCR7 Genetic Variant Predicts Treatment Response of Pegylated-Interferon α in HBeAg-Positive Chronic Hepatitis B Patients
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