Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer.

Research output: Contribution to journalArticle

Abstract

Although familial susceptibility to glioma is known, the genetic basis for this susceptibility remains unidentified in the majority of glioma-specific families. An alternative approach to identifying such genes is to examine cancer pedigrees, which include glioma as one of several cancer phenotypes, to determine whether common chromosomal modifications might account for the familial aggregation of glioma and other cancers.

Details

Authors
  • Ulrika Andersson
  • Carl Wibom
  • Kristina Cederquist
  • Steina Aradottir
  • Georgina N Armstrong
  • Sanjay Shete
  • Ching C Lau
  • Matthew N Bainbridge
  • Elizabeth B Claus
  • Jill Barnholtz-Sloan
  • Rose Lai
  • Dora Il'yasova
  • Richard S Houlston
  • Joellen Schildkraut
  • Jonine L Bernstein
  • Sara H Olson
  • Robert B Jenkins
  • Daniel H Lachance
  • Margaret Wrensch
  • Faith G Davis
  • Ryan Merrell
  • Christoffer Johansen
  • Siegal Sadetzki
  • Melissa L Bondy
  • Beatrice S Melin
Organisations
Research areas and keywords

Subject classification (UKÄ) – MANDATORY

  • Cancer and Oncology
Original languageEnglish
Pages (from-to)1333-1340
JournalNeuro-Oncology
Volume16
Issue number10
Publication statusPublished - 2014
Publication categoryResearch
Peer-reviewedYes