Genetic Modifiers of Ovarian Cancer

Abstract

Individuals with germline mutations in BRCA1 have an elevated but incomplete risk of developing ovarian cancer suggesting the presence of genetic modifiers of ovarian cancer in this population. A genome wide association study (GWAS) for ovarian cancer in BRCA1 mutation carriers was initiated in an effort to identify common genetic variants that modify ovarian cancer risk. Discovery and validation studies have identified several novel modifiers of ovarian cancer risk for BRCA1 mutation carriers that can be used for individualized ovarian cancer risk assessment.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2012
Accession Number
ADA566979

Entities

People

  • Fergus J. Couch

Organizations

  • Mayo Clinic

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Diseases And Disorders
  • Genes
  • Genetic Phenomena
  • Genetics
  • Genome
  • Mutations
  • Neoplasms
  • Ovarian Cancer
  • Parkinson'S Disease
  • Risk
  • Risk Analysis
  • Risk Factors
  • Validation

Fields of Study

  • Biology

Readers

  • Molecular and genetic basis of cancer.

Technology Areas

  • Biotechnology