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Scientific Reports|August 31, 2019
Two truncating variants in FANCC and breast cancer riskThilo Dörk, Paolo Peterlongo, Arto Mannermaa, et al.
Journal of the National Cancer Institute|December 31, 2010
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studiesXiaohong R Yang, Jenny Chang-Claude, Ellen L Goode, et al.
Nature Genetics|January 24, 2012
Genome-wide association analysis identifies three new breast cancer susceptibility lociMaya Ghoussaini, Olivia Fletcher, Kyriaki Michailidou, et al.
Genome Medicine|January 26, 2023
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestryStefanie H Mueller, Alvina G Lai, Maria Valkovskaya, et al.
American Journal of Human Genetics|June 19, 2021
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer elementJoseph S Baxter, Nichola Johnson, Katarzyna Tomczyk, et al.
Journal of the National Cancer Institute|April 10, 2015
Prediction of breast cancer risk based on profiling with common genetic variantsNasim Mavaddat, Paul D P Pharoah, Kyriaki Michailidou, et al.
Nature Communications|April 17, 2019
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancerManuel A Ferreira, Eric R Gamazon, Fares Al-Ejeh, et al.
Nature Communications|February 18, 2021
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersJuliette Coignard, Michael Lush, Jonathan Beesley, et al.
British Journal of Cancer|February 22, 2019
Genome-wide association study of germline variants and breast cancer-specific mortalityMaria Escala-Garcia, Qi Guo, Thilo Dörk, et al.
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