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Large-scale genotyping identifies 41 new loci associated with breast cancer risk

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

DOI

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  • Kyriaki Michailidou
  • Per Hall
  • Anna Gonzalez-Neira
  • Maya Ghoussaini
  • Joe Dennis
  • Roger L Milne
  • Marjanka K Schmidt
  • Jenny Chang-Claude
  • Stig E Bojesen
  • Manjeet K Bolla
  • Qin Wang
  • Ed Dicks
  • Andrew Roger Lee
  • Clare Turnbull
  • Nazneen Rahman
  • Olivia Fletcher
  • Julian Peto
  • Lorna Gibson
  • Isabel Dos Santos Silva
  • Heli Nevanlinna
  • Taru A Muranen
  • Kristiina Aittomäki
  • Carl Blomqvist
  • Kamila Czene
  • Astrid Irwanto
  • Jianjun Liu
  • Quinten Waisfisz
  • Hanne Meijers-Heijboer
  • Muriel Adank
  • Rob B van der Luijt
  • Rebecca Hein
  • Norbert Dahmen
  • Lars Beckman
  • Alfons Meindl
  • Rita K Schmutzler
  • Bertram Müller-Myhsok
  • Peter Lichtner
  • John L Hopper
  • Melissa C Southey
  • Enes Makalic
  • Daniel F Schmidt
  • Andre G Uitterlinden
  • Albert Hofman
  • David J Hunter
  • Stephen J Chanock
  • Daniel Vincent
  • François Bacot
  • Børge G Nordestgaard
  • Sune F Nielsen
  • Henrik Flyger
  • Breast and Ovarian Cancer Susceptibility Collaboration
Vis graf over relationer
Breast cancer is the most common cancer among women. Common variants at 27 loci have been identified as associated with susceptibility to breast cancer, and these account for ∼9% of the familial risk of the disease. We report here a meta-analysis of 9 genome-wide association studies, including 10,052 breast cancer cases and 12,575 controls of European ancestry, from which we selected 29,807 SNPs for further genotyping. These SNPs were genotyped in 45,290 cases and 41,880 controls of European ancestry from 41 studies in the Breast Cancer Association Consortium (BCAC). The SNPs were genotyped as part of a collaborative genotyping experiment involving four consortia (Collaborative Oncological Gene-environment Study, COGS) and used a custom Illumina iSelect genotyping array, iCOGS, comprising more than 200,000 SNPs. We identified SNPs at 41 new breast cancer susceptibility loci at genome-wide significance (P <5 × 10(-8)). Further analyses suggest that more than 1,000 additional loci are involved in breast cancer susceptibility.
OriginalsprogEngelsk
TidsskriftNature Genetics
Vol/bind45
Udgave nummer4
Sider (fra-til)353-61, 361e1-2
ISSN1061-4036
DOI
StatusUdgivet - apr. 2013

ID: 38625951