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Genome‑wide methylation analysis reveals differentially methylated CpG sites and altered expression of heart development‑associated genes in fetuses with cardiac defects
Methyl donor micronutrients, CD40-ligand methylation and disease activity in systemic lupus erythematosus: A cross-sectional association study
Genetic variation of rs12918566 affects GRIN2A expression and is associated with spontaneous movement response during sevoflurane anesthesia induction
Inhibitory control mediates the interaction between serotonin transporter gene (5-HTTLPR) and peer victimization on adolescent depressive symptoms
CYP1A2 Genotype Modifies the Effects of Caffeine Compared With Placebo on Muscle Strength in Competitive Male Athletes
Failure of Phenotypic Markers to Accurately Identify Black Bass Species and Associated Hybrids in Mobile River Basin, Alabama
Association of ITPKB, IL1R2 and COQ7 with Parkinson’s disease in Taiwan
Association of single-nucleotide polymorphism on chromosome 9 and ischemic stroke in Heilongjiang province in China
Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children
Association of GTF2I, NFKB1, and TYK2 Regional Polymorphisms With Systemic Sclerosis in a Chinese Han Population