Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

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

Andersson, Ulrika ; Wibom, Carl ; Cederquist, Kristina ; Aradottir, Steina LU ; Borg, Åke LU ; Armstrong, Georgina N ; Shete, Sanjay ; Lau, Ching C ; Bainbridge, Matthew N and Claus, Elizabeth B , et al. (2014) In Neuro-Oncology 16(10). p.1333-1340
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.
Please use this url to cite or link to this publication:
author
; ; ; ; ; ; ; ; and , et al. (More)
; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; and (Less)
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Neuro-Oncology
volume
16
issue
10
pages
1333 - 1340
publisher
Oxford University Press
external identifiers
  • pmid:24723567
  • wos:000343671000005
  • scopus:84901614478
  • pmid:24723567
ISSN
1523-5866
DOI
10.1093/neuonc/nou052
language
English
LU publication?
yes
id
ba0f17fe-da6a-4d93-a3c0-95043069c3bc (old id 4430315)
alternative location
http://www.ncbi.nlm.nih.gov/pubmed/24723567?dopt=Abstract
date added to LUP
2016-04-01 10:13:11
date last changed
2022-04-12 03:12:59
@article{ba0f17fe-da6a-4d93-a3c0-95043069c3bc,
  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.}},
  author       = {{Andersson, Ulrika and Wibom, Carl and Cederquist, Kristina and Aradottir, Steina and Borg, Åke and Armstrong, Georgina N and Shete, Sanjay and Lau, Ching C and Bainbridge, Matthew N and Claus, Elizabeth B and Barnholtz-Sloan, Jill and Lai, Rose and Il'yasova, Dora and Houlston, Richard S and Schildkraut, Joellen and Bernstein, Jonine L and Olson, Sara H and Jenkins, Robert B and Lachance, Daniel H and Wrensch, Margaret and Davis, Faith G and Merrell, Ryan and Johansen, Christoffer and Sadetzki, Siegal and Bondy, Melissa L and Melin, Beatrice S}},
  issn         = {{1523-5866}},
  language     = {{eng}},
  number       = {{10}},
  pages        = {{1333--1340}},
  publisher    = {{Oxford University Press}},
  series       = {{Neuro-Oncology}},
  title        = {{Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer.}},
  url          = {{http://dx.doi.org/10.1093/neuonc/nou052}},
  doi          = {{10.1093/neuonc/nou052}},
  volume       = {{16}},
  year         = {{2014}},
}