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Search Results for: Hereditary Genetics

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  • Association of a melatonin receptor 1B (MTNR1B) gene variant with fasting glucose and HOMA-B in children and adolescents of high BMI-SDS groups
  • Association of variants in the glucose dependent insulinotropic peptide receptor gene (GIPR) with impaired glucose homeostasis in obese children and adolescents from Berlin
  • The role of ghrelin and ghrelin-receptor gene variants and promoter activity in type 2 diabetes
  • Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus
  • Fine scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locus
  • Dissection of the genetics of Parkinson’s disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
  • A comprehensive study of the association between EGFR and ERBB2 genes and glioma risk
  • Dysbindin gene (DTNBP1) in major depressive disorder (MDD) patients: Lack of association with clinical phenotypes
  • Single-nucleotide polymorphisms in p53 pathway and aggressiveness of prostate cancer in a Caucasian population
  • Procolipase gene: No association with early-onset obesity or fat intake
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