The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

Natalia Teixeira, Annemieke van der Hout, Jan C. Oosterwijk, Janet R. Vos, Peter Devilee, Klaartje van Engelen, Hanne Meijers-Heijboer, Rob B. van der Luijt, Mieke Kriege, Arjen R. Mensenkamp, Matti A. Rookus, Kees E. van Roozendaal, Marian J. E. Mourits, Geertruida H. de Bock, HEBON

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)848-857
Number of pages10
JournalEuropean Journal of Human Genetics
Volume26
Issue number6
DOIs
Publication statusPublished - 1 Jun 2018

Keywords

  • BREAST-CANCER
  • GERMLINE MUTATIONS
  • SUSCEPTIBILITY
  • METAANALYSIS
  • RELATIVES
  • GENES
  • WOMEN

Cite this

Teixeira, N., van der Hout, A., Oosterwijk, J. C., Vos, J. R., Devilee, P., van Engelen, K., Meijers-Heijboer, H., van der Luijt, R. B., Kriege, M., Mensenkamp, A. R., Rookus, M. A., van Roozendaal, K. E., Mourits, M. J. E., de Bock, G. H., & HEBON (2018). The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position? European Journal of Human Genetics, 26(6), 848-857. https://doi.org/10.1038/s41431-018-0111-9