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  • Association between thyroid stimulating hormone receptor gene intron polymorphisms and autoimmune thyroid disease in a Chinese Han population
  • Single nucleotide polymorphisms in the ORM1-like 3 gene associated with childhood asthma in a Chinese population
  • Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson’s disease in Han Chinese population
  • Association of DNMT1 and DNMT3B polymorphisms with breast cancer risk in Han Chinese women from South China
  • Association of MHC class-III gene polymorphisms with ER-positive breast cancer in Chinese Han population
  • Association of PRM1-190C- > A polymorphism with teratozoospermia
  • Replication study of PLCE1 and C20orf54 polymorphism and risk of esophageal cancer in a Chinese population
  • Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet’s disease susceptibility
  • A systematic survey of loss-of-function variants in human protein-coding genes
  • A case-parent triad assessment of folate metabolic genes and the risk of childhood acute lymphoblastic leukemia
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