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  • Association of ABCB1 promoter methylation with aspirin exposure, platelet function, and clinical outcomes in Chinese intracranial artery stenosis patients
  • Association of ARHGAP22 gene polymorphisms with the risk of type 2 diabetic retinopathy
  • Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians
  • Association of BUD13 polymorphisms with metabolic syndrome in Chinese population: a case-control study
  • Association of common genetic variants in VEGFA with biliary atresia susceptibility in Northwestern Han Chinese
  • Association of Common Variants in TGFA with Increased Risk of Knee Osteoarthritis Susceptibility
  • Association between SNPs in Long Non-coding RNAs and the Risk of Female Breast Cancer in a Chinese Population
  • Association of donor and recipient SUMO4 rs237025 genetic variant with new-onset diabetes mellitus after liver transplantation in a Chinese population
  • Association between SOD2 rs6917589, rs2842980, rs5746136 and rs4880 polymorphisms and primary open angle glaucoma in a northern Chinese population
  • Association of Endothelial Nitric Oxide Synthase Gene Polymorphism with Susceptibility and Nephritis Development of Henoch-Schönlein Purpura in Chinese Han Children
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