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Search Results for: Hereditary Genetics

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  • Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites
  • Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer’s Disease Families
  • An N-Ethyl-N-Nitrosourea (ENU)-Induced Dominant Negative Mutation in the JAK3 Kinase Protects against Cerebral Malaria
  • Association of a Functional Variant in the Wnt Co-Receptor LRP6 with Early Onset Ileal Crohn’s Disease
  • Characterization of Genome-Wide Association-Identified Variants for Atrial Fibrillation in African Americans
  • Genetic Affinities of the Central Indian Tribal Populations
  • A genome-wide scan of ashkenazi jewish Crohn’s disease suggests novel susceptibility Loci
  • The Esophageal Adenocarcinoma Genetics Consortium, Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett’s esophagus
  • Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk
  • Mapping the regulatory sequences controlling 93 breast cancer-associated miRNA genes leads to the identification of two functional promoters of the Hsa-mir-200b cluster, methylation of which is associated with metastasis or hormone receptor status in advanced breast cancer
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