학술논문

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Document Type
article
Author
Mueller, Stefanie HLai, Alvina GValkovskaya, MariaMichailidou, KyriakiBolla, Manjeet KWang, QinDennis, JoeLush, MichaelAbu-Ful, ZomorudaAhearn, Thomas UAndrulis, Irene LAnton-Culver, HodaAntonenkova, Natalia NArndt, VolkerAronson, Kristan JAugustinsson, AnnelieBaert, ThaisFreeman, Laura E BeaneBeckmann, Matthias WBehrens, SabineBenitez, JavierBermisheva, MarinaBlomqvist, CarlBogdanova, Natalia VBojesen, Stig EBonanni, BernardoBrenner, HermannBrucker, Sara YBuys, Saundra SCastelao, Jose EChan, Tsun LChang-Claude, JennyChanock, Stephen JChoi, Ji-YeobChung, Wendy KColonna, Sarah VCornelissen, StenCouch, Fergus JCzene, KamilaDaly, Mary BDevilee, PeterDörk, ThiloDossus, LaureDwek, MiriamEccles, Diana MEkici, Arif BEliassen, A HeatherEngel, ChristophEvans, D GarethFasching, Peter AFletcher, OliviaFlyger, HenrikGago-Dominguez, ManuelaGao, Yu-TangGarcía-Closas, MontserratGarcía-Sáenz, José AGenkinger, JeanineGentry-Maharaj, AleksandraGrassmann, FelixGuénel, PascalGündert, MelanieHaeberle, LotharHahnen, EricHaiman, Christopher AHåkansson, NiclasHall, PerHarkness, Elaine FHarrington, Patricia AHartikainen, Jaana MHartman, MikaelHein, AlexanderHo, Weang-KeeHooning, Maartje JHoppe, ReinerHopper, John LHoulston, Richard SHowell, AnthonyHunter, David JHuo, DezhengIto, HidemiIwasaki, MotokiJakubowska, AnnaJanni, WolfgangJohn, Esther MJones, Michael EJung, AudreyKaaks, RudolfKang, DaeheeKhusnutdinova, Elza KKim, Sung-WonKitahara, Cari MKoutros, StellaKraft, PeterKristensen, Vessela NKubelka-Sabit, KaterinaKurian, Allison WKwong, AvaLacey, James VLambrechts, DietherLe Marchand, Loic
Source
Genome Medicine. 15(1)
Subject
Breast Cancer
Genetics
Clinical Research
Cancer
Aetiology
2.1 Biological and endogenous factors
Humans
Female
Breast Neoplasms
Genetic Predisposition to Disease
Black People
Genetic Testing
Genome-Wide Association Study
Polymorphism
Single Nucleotide
Formins
Breast cancer susceptibility
Diverse ancestry
Rare variants
Gene regulation
Genome-wide association study
NBCS Collaborators
CTS Consortium
ABCTB Investigators
Clinical Sciences
Language
Abstract
BackgroundLow-frequency variants play an important role in breast cancer (BC) susceptibility. Gene-based methods can increase power by combining multiple variants in the same gene and help identify target genes.MethodsWe evaluated the potential of gene-based aggregation in the Breast Cancer Association Consortium cohorts including 83,471 cases and 59,199 controls. Low-frequency variants were aggregated for individual genes' coding and regulatory regions. Association results in European ancestry samples were compared to single-marker association results in the same cohort. Gene-based associations were also combined in meta-analysis across individuals with European, Asian, African, and Latin American and Hispanic ancestry.ResultsIn European ancestry samples, 14 genes were significantly associated (q