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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

dc.contributor.authorGEMO Study Collaborators
dc.contributor.authorEMBRACE Collaborators
dc.contributor.authorGehrig, Andrea
dc.contributor.authorGeorgoulias, Vassilios
dc.contributor.authorGiles, Graham G
dc.contributor.authorGodwin, A K
dc.contributor.authorGoldberg, Mark S.
dc.contributor.authorGoldgar, David
dc.contributor.authorGonzález-Neira, Anna
dc.contributor.authorGreene, Mark H
dc.contributor.authorGuénel, Pascal
dc.contributor.authorHaeberle, Lothar
dc.date.accessioned2021-05-24T09:08:01Z
dc.date.available2021-05-24T09:08:01Z
dc.date.issued2021-05-14
dc.identifier.citationGEMO Study Collaborators , EMBRACE Collaborators , Gehrig , A , Georgoulias , V , Giles , G G , Godwin , A K , Goldberg , M S , Goldgar , D , González-Neira , A , Greene , M H , Guénel , P & Haeberle , L 2021 , ' A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers ' , Nature Communications , vol. 12 , no. 1 , 1078 . https://doi.org/10.1038/s41467-020-20496-3en
dc.identifier.issn2041-1723
dc.identifier.otherPURE: 193391798
dc.identifier.otherPURE UUID: 4bbfa869-40f9-406e-85c2-b12d4bdfbe9c
dc.identifier.otherJisc: c83574a60a5e4ad7acac30777a3d3d2a
dc.identifier.otherpublisher-id: s41467-020-20496-3
dc.identifier.othermanuscript: 20496
dc.identifier.otherScopus: 85101270098
dc.identifier.urihttps://hdl.handle.net/2164/16526
dc.format.extent22
dc.language.isoeng
dc.relation.ispartofNature Communicationsen
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectR Medicineen
dc.subjectPhysics and Astronomy(all)en
dc.subjectChemistry(all)en
dc.subjectBiochemistry, Genetics and Molecular Biology(all)en
dc.subjectMedical Research Council (MRC)en
dc.subjectCancer Research UKen
dc.subjectOtheren
dc.subjectNational Institute for Health Research (NIHR)en
dc.subjectEuropean Commissionen
dc.subjectEuropean Research Councilen
dc.subjectSupplementary Informationen
dc.subjecthttps://doi.org/10.1038/s41467-020-20496-3en
dc.subject.lccRen
dc.titleA case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medicine, Medical Sciences & Nutritionen
dc.contributor.institutionUniversity of Aberdeen.Centre for Health Data Scienceen
dc.contributor.institutionUniversity of Aberdeen.Clinical Medicineen
dc.contributor.institutionUniversity of Aberdeen.Data Safe Havenen
dc.contributor.institutionUniversity of Aberdeen.Applied Medicineen
dc.contributor.institutionUniversity of Aberdeen.Institute of Medical Sciencesen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1038/s41467-020-20496-3
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85101270098&partnerID=8YFLogxKen


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