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  • Interaction of Multiple Gene Variants and their Effects on Schizophrenia Phenotypes
  • Polymorphisms in UGT1A1 gene predispose South Indians to pigmentous gallstones
  • Lack of association between SREBF-1c gene polymorphisms and risk of non-alcoholic fatty liver disease in a Chinese Han population
  • IGF2BP2 rs11705701 polymorphisms are associated with prediabetes in a Chinese population: A population-based case-control study
  • Whole exome sequencing of extreme age-related macular degeneration phenotype
  • Loss-of-function variants influence the human serum metabolome
  • Genetic variants of SOX9 contribute to susceptibility of gliomas among Chinese population
  • Association of DYRK1A polymorphisms with sporadic Parkinson’s disease in Chinese Han population
  • Association of genetic variants in the CART gene with glioma susceptibility in a Chinese population
  • A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease
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