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An analysis of allele, genotype and phenotype frequencies, actionable pharmacogenomic (PGx) variants and phenoconversion in 5408 Australian patients genotyped for CYP2D6, CYP2C19, CYP2C9 and VKORC1 genes
Obesity-related genetic variants and hyperuricemia risk in Chinese men
Association of Single Nucleotide Polymorphisms in PTGS1 and PTGS2 with Aspirin-Induced Urticaria/Angioedema
SERPINE2 rs16865421 polymorphism is associated with a lower risk of chronic obstructive pulmonary disease in Uygur population: a case control study
Increased burden of rare deleterious variants of the KCNQ1 gene in patients with large‑vessel ischemic stroke
Analysis of genetic polymorphisms for age-related macular degeneration (AMD) in Chinese Tujia ethnic minority group
Oxytocin receptor DNA methylation and alterations of brain volumes in maltreated children
Vitamin D deficiency during pregnancy affects the function of Th1/Th2 cells and methylation of IFN-γ gene in offspring rats
MMP20 Single-Nucleotide Polymorphisms Correlate with Susceptibility to Alcohol-Induced Osteonecrosis of the Femoral Head in Chinese Males
Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population