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Breast Cancer Research : BCR|August 19, 2021
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatmentAnna Morra, Maria Escala-Garcia, Jonathan Beesley, et al.British Journal of Cancer|August 3, 2021
Mendelian randomisation study of smoking exposure in relation to breast cancer riskHanla A Park, Sonja Neumeyer, Kyriaki Michailidou, et al.Breast Cancer Research : BCR|January 5, 2022
Common variants in breast cancer risk loci predispose to distinct tumor subtypesThomas U Ahearn, Haoyu Zhang, Kyriaki Michailidou, et al.Scientific Reports|August 31, 2019
Two truncating variants in FANCC and breast cancer riskThilo Dörk, Paolo Peterlongo, Arto Mannermaa, et al.Science (New York, N.Y.)|September 6, 2005
The transcriptional landscape of the mammalian genomeP Carninci, T Kasukawa, S Katayama, 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.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.Nature Genetics|May 20, 2020
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analysesHaoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, et al.Nature|August 5, 2021
Genetic insights into biological mechanisms governing human ovarian ageingKatherine S Ruth, Felix R Day, Jazib Hussain, et al.NPJ Breast Cancer|November 9, 2019
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancerGisella Figlioli, Massimo Bogliolo, Irene Catucci, et al.Pageof 53