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  • Association of uncoupling protein gene polymorphisms with essential hypertension in a northeastern Han Chinese population
  • Association between interferon‐induced helicase (IFIH1) rs1990760 polymorphism and seasonal variation in the onset of type 1 diabetes mellitus
  • Characterizing key nucleotide polymorphisms of hepatitis C virus-disease associations via mass-spectrometric genotyping
  • Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium
  • Association of neural tube defects with gene polymorphisms in one-carbon metabolic pathway
  • TNC Gene Mutation: A Rare Cause for Early-Onset Sensorineural Hearing Loss
  • Polymorphisms in the Glucagon-Like Peptide 1 Receptor (GLP-1R) Gene Are Associated with the Risk of Coronary Artery Disease in Chinese Han Patients with Type …
  • Blood pressure and risk of incident Alzheimer’s disease dementia by antihypertensive medications and APOE ε4 allele
  • Methods and Strategies to Determine Epigenetic Variation in Human Disease
  • A Low glycaemic index diet in pregnancy induces DNA methylation variation in blood of newborns: results from the ROLO randomised controlled trial
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