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  • A next generation sequencing combined genome-wide association study identifies novel tuberculosis susceptibility loci in Chinese population
  • Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
  • A validation study of the UGT1A4 rs2011404 variant and the risk of anti‐tuberculosis drug‐induced hepatotoxicity in an Eastern Chinese Han population
  • Moderating Role of TSHR and PTPN22 Gene Polymorphisms in Effects of Excessive Fluoride on Thyroid: a School-Based Cross-Sectional Study
  • Hemodialysis-Related Glycemic Disarray Proven by Continuous Glucose Monitoring: Glycemic Markers and Hypoglycemia
  • Variation in biomarker levels of metals, persistent organic pollutants, and omega-3 fatty acids in association with genetic polymorphisms among Inuit in Nunavik, Canada
  • Correlation between TGF-β2/3 promoter DNA methylation and Smad signaling during palatal fusion induced by 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin
  • Identification of the PmWEEP locus controlling weeping traits in Prunus mume through an integrated genome-wide association study and quantitative trait locus mapping
  • The Association of Vitamin D and Gene Variants in the Vitamin D Metabolic Pathway with Preterm Birth
  • (Re-)activity in the caregiving situation: Genetic diversity within Oxytocin–Vasopressin Pathway is associated with salivary oxytocin and vasopressin concentrations in response to contact with a crying infant-simulator
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