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Search Results for: Hereditary Genetics

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  • Functional variants in the sucrase–isomaltase gene associate with increased risk of irritable bowel syndrome
  • Telomere length, ZNF208 genetic variants and risk of chronic obstructive pulmonary disease in the Hainan Li population
  • Association of genetic variants in RETN, NAMPT and ADIPOQ gene with glycemic, metabolic traits and diabetes risk in a Chinese population
  • Quantitative genetics validates previous genetic variants and identifies novel genetic players influencing Alzheimer’s disease cerebrospinal fluid biomarkers
  • Role of Functional IFNL4, IFNLR1, IFNA, IFNAR2 Polymorphisms in Hepatitis B virus‐related liver disease in Han Chinese population
  • Segregating polymorphism in the NMDA receptor gene GRIN2A, schizotypy, and mental rotation among healthy individuals
  • Superior cognitive goal maintenance in carriers of genetic markers linked to reduced striatal D2 receptor density (C957T and DRD2/ANKK1-TaqIA)
  • Histone modifier gene mutations in peripheral T-cell lymphoma not otherwise specified
  • Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables
  • Single nucleotide polymorphisms in the MYLKP1 pseudogene are associated with increased colon cancer risk in African Americans
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