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  • Assessment of three essential tremor genetic loci in sporadic Parkinson’s disease in Eastern China
  • Polymorphisms of the Gene Encoding Cytochrome b-245 Beta Chain of NADPH Oxidase: Relationship with Redox Homeostasis Markers and Risk of Type 2 Diabetes Mellitus
  • Autophagy-Related Gene 7 Polymorphisms and Cerebral Palsy in Chinese Infants
  • Replication of Genome-Wide Association Analysis Identifies New Susceptibility Loci at Long Noncoding RNA Regions for Vogt-Koyanagi-Harada Disease
  • L1R2 Polymorphisms are Associated with an Increased Risk of Esophageal Cancer
  • Investigation of the STOX1 polymorphism on lumbar disc herniation
  • Replication of GWAS identifies RTEL1, CDKN2A/B, and PHLDB1 SNPs as risk factors in Portuguese gliomas patients
  • A comprehensive analysis of drug resistance molecular markers and Plasmodium falciparum genetic diversity in two malaria endemic sites in Mali
  • The Association of UNC13B Gene Polymorphisms and Diabetic Kidney Disease in a Chinese Han Population
  • Transgenerational deep sequencing revealed hypermethylation of hippocampal mGluR1 gene with altered mRNA expression of mGluR5 and mGluR3 associated with behavioral changes in Sprague Dawley rats with history of prolonged febrile seizure
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