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  • Effects of the dopamine transporter gene on striatal functional connectivity in youths with attention-deficit/hyperactivity disorder
  • Interactions among variants in P53 apoptotic pathway genes are associated with neurologic deterioration and functional outcome after acute ischemic stroke
  • A circadian rhythm-related MTNR1B genetic variant (rs10830963) modulate body weight change and insulin resistance after 9 months of a high protein/low carbohydrate vs a standard hypocaloric diet
  • Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence
  • HLA-G+ 3196 polymorphism as a risk factor for cell mediated rejection following heart transplant
  • Associations between period 3 gene polymorphisms and sleep-/chronotype-related variables in patients with late-life insomnia
  • The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1,-2 and-3 and Is Associated with Risk for Multiple Sclerosis
  • Familial Analysis of Epistatic and Sex-Dependent Association of Genes of the Renin–Angiotensin–Aldosterone System and Blood Pressure
  • Monoamine Oxidase A Genotype and Methylation Moderate the Association of Maltreatment and Aggressive Behaviour
  • Randomized Controlled Trial of a MUFA or Fiber-rich diet on Hepatic fat in Pre-diabetes
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