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  • Association and Gene–Gene Interactions Study of Late-Onset Alzheimer’s Disease in the Russian Population
  • TP53 mutation in newly diagnosed acute myeloid leukemia and myelodysplastic syndrome
  • Placental cadmium, placental genetic variations, and birth size
  • NOX Subunit Gene Polymorphisms and the Risk of Chronic Artery Disease in Type 2 Diabetes Patients
  • Lrp6 Genotype affects Individual Susceptibility to Nonalcoholic Fatty Liver Disease and Silibinin Therapeutic Response via Wnt/β-catenin-Cyp2e1 Signaling
  • Amalgamation of Auto Machine Learning and Ensemble Approaches to Achieve State-of-the-Art Post-Heart Failure Survival Predictions
  • Combinatorial pharmacogenomic test for successful antidepressant treatment of a major depressive disorder
  • Association of exposure to deoxynivalenol with DNA methylation in white blood cells in children in China
  • CYP3A7, CYP3A4, and CYP3A5 genetic polymorphisms in recipients rather than donors influence tacrolimus concentrations in the early stages after liver transplantation
  • Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome
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