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  • Association between set shifting in attention deficit/hyperactivity disorder (ADHD) and NRXN1 gene
  • Methylation and serum response factor mediated in the regulation of gene ARRDC3 in breast cancer
  • Pharmacogenetics of hypoglycemia associated with sulfonylurea therapy in usual clinical care
  • DNA methylation and mRNA expression of IGF‐1 and MMP‐2 after form‐deprivation myopia in guinea pigs
  • The Effect of Interactions between Folic Acid Supplementation and One Carbon Metabolism Gene Variants on Small-for-Gestational-Age Births in the Screening for Pregnancy Endpoints (SCOPE) Cohort Study
  • “A cleaner break”: Genetic divergence between geographic groups and sympatric phenotypes revealed in ballan wrasse (Labrus bergylta)
  • Association of IRF4 SNP rs12203592 with melanoma‐specific survival
  • Correlation of ATP Binding Cassette Transporter A1 Gene Polymorphisms and Lower Extremity Athero-sclerotic Disease
  • SMARCB1 (INI1)-deficient thyroid carcinoma: A novel entity expanding the spectrum of tumors with INI1 loss
  • Associations of single nucleotide polymorphisms of UCP genes with diabetic retinopathy in Chinese Han population
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