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Association of tripartite motif family-like 2 (TRIML2) polymorphisms with late-onset Alzheimer’s disease risk in a Korean population
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
Human Leukocyte Antigen-G Polymorphisms Association With Cancer Post-Heart Transplantation
Human leukocyte antigen G single-nucleotide polymorphism -201 (CC–CC) donor–recipient genotype matching as a predictor of severe cardiac allograft vasculopathy
Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders
Genetic susceptibility to dyslipidemia and incidence of cardiovascular disease depending on a diet quality index in the Malmö Diet and Cancer cohort
Several type 2 diabetes-associated variants in genes annotated to WNT signaling interact with dietary fiber in relation to incidence of type 2 diabetes
Further evidence for a parent-of-origin effect at the NOP9locus on language-related phenotypes
Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease-causing variants
Analysis of Rare Variants in the Alcohol Dependence Candidate GeneGATA4