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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
LncRNA SERPINB9P1 expression and polymorphisms are associated with ischemic stroke in a Chinese Han population
C5 Variant rs10985126 is Associated with Mortality in Patients with Symptomatic Coronary Artery Disease
Integrated analysis of probability of type 2 diabetes mellitus with polymorphisms and methylation of KCNQ1 gene: a nested case‐control study
Associations Between Genotype and Peripheral Complement Proteins in First-Episode Psychosis: Evidences From C3 and C4