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dc.contributor.author | NBCS Collaborators | |
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dc.contributor.author | Yang, XR | |
dc.contributor.author | Har Yip, C | |
dc.contributor.author | Yoo, K-Y | |
dc.contributor.author | Yu, J-C | |
dc.contributor.author | Zheng, W | |
dc.contributor.author | Zheng, Y | |
dc.contributor.author | Zhu, B | |
dc.contributor.author | Ziogas, A | |
dc.contributor.author | Ziv, E | |
dc.contributor.author | ABCTB Investigators | |
dc.contributor.author | ConFab/AOCS Investigators | |
dc.contributor.author | Lakhani, SR | |
dc.contributor.author | Antoniou, AC | |
dc.contributor.author | Droit, A | |
dc.contributor.author | Andrulis, IL | |
dc.contributor.author | Amos, CI | |
dc.contributor.author | Couch, FJ | |
dc.contributor.author | Pharoah, PDP | |
dc.contributor.author | Chang-Claude, J | |
dc.contributor.author | Hall, P | |
dc.contributor.author | Hunter, DJ | |
dc.contributor.author | Milne, RL | |
dc.contributor.author | García-Closas, M | |
dc.contributor.author | Schmidt, MK | |
dc.contributor.author | Chanock, SJ | |
dc.contributor.author | Dunning, AM | |
dc.contributor.author | Edwards, SL | |
dc.contributor.author | Bader, GD | |
dc.contributor.author | Chenevix-Trench, G | |
dc.contributor.author | Simard, J | |
dc.contributor.author | Kraft, P | |
dc.contributor.author | Easton, DF | |
dc.date.accessioned | 2018-07-11T15:23:24Z | |
dc.date.issued | 2017-11 | |
dc.identifier.citation | Nature, 2017, 551 (7678), pp. 92 - 94 | |
dc.identifier.issn | 0028-0836 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/2042 | |
dc.identifier.eissn | 1476-4687 | |
dc.identifier.doi | 10.1038/nature24284 | |
dc.description.abstract | Breast cancer risk is influenced by rare coding variants in susceptibility genes, such as BRCA1, and many common, mostly non-coding variants. However, much of the genetic contribution to breast cancer risk remains unknown. Here we report the results of a genome-wide association study of breast cancer in 122,977 cases and 105,974 controls of European ancestry and 14,068 cases and 13,104 controls of East Asian ancestry. We identified 65 new loci that are associated with overall breast cancer risk at P < 5 × 10 -8 . The majority of credible risk single-nucleotide polymorphisms in these loci fall in distal regulatory elements, and by integrating in silico data to predict target genes in breast cells at each locus, we demonstrate a strong overlap between candidate target genes and somatic driver genes in breast tumours. We also find that heritability of breast cancer due to all single-nucleotide polymorphisms in regulatory features was 2-5-fold enriched relative to the genome-wide average, with strong enrichment for particular transcription factor binding sites. These results provide further insight into genetic susceptibility to breast cancer and will improve the use of genetic risk scores for individualized screening and prevention. | |
dc.format | Print-Electronic | |
dc.format.extent | 92 - 94 | |
dc.language | eng | |
dc.language.iso | eng | |
dc.rights.uri | https://www.rioxx.net/licenses/all-rights-reserved | |
dc.subject | NBCS Collaborators | |
dc.subject | ABCTB Investigators | |
dc.subject | ConFab/AOCS Investigators | |
dc.subject | Humans | |
dc.subject | Breast Neoplasms | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Transcription Factors | |
dc.subject | Risk Assessment | |
dc.subject | Binding Sites | |
dc.subject | Regulatory Sequences, Nucleic Acid | |
dc.subject | Multifactorial Inheritance | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | Computer Simulation | |
dc.subject | Asian Continental Ancestry Group | |
dc.subject | European Continental Ancestry Group | |
dc.subject | Asia | |
dc.subject | Europe | |
dc.subject | Female | |
dc.subject | Genome-Wide Association Study | |
dc.subject | Genetic Loci | |
dc.title | Association analysis identifies 65 new breast cancer risk loci. | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2017-09-17 | |
rioxxterms.versionofrecord | 10.1038/nature24284 | |
rioxxterms.licenseref.uri | https://www.rioxx.net/licenses/all-rights-reserved | |
rioxxterms.licenseref.startdate | 2017-11 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | Nature | |
pubs.issue | 7678 | |
pubs.notes | Not known | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Complex Trait Genetics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Functional Genetic Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Complex Trait Genetics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Functional Genetic Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology | |
pubs.publication-status | Published | |
pubs.volume | 551 | |
pubs.embargo.terms | Not known | |
icr.researchteam | Complex Trait Genetics | |
icr.researchteam | Functional Genetic Epidemiology | |
icr.researchteam | Aetiological Epidemiology | |
dc.contributor.icrauthor | Fletcher, Olivia | |
dc.contributor.icrauthor | Orr, Nicholas | |
dc.contributor.icrauthor | Schoemaker, Minouk | |
dc.contributor.icrauthor | Jones, Michael | |
dc.contributor.icrauthor | Swerdlow, Anthony | |