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Physical Review Letters|July 30, 2011
Extended magnetic reconnection across the dayside magnetopauseM W Dunlop, Q-H Zhang, Y V Bogdanova, et al.Journal of Medical Genetics|June 18, 2020
Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancerHonglin Song, Ed M Dicks, Jonathan Tyrer, et al.Cancers|July 14, 2023
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer CasesGisella Figlioli, Amandine Billaud, Qin Wang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer riskTaru A Muranen, Dario Greco, Carl Blomqvist, et al.Human Genetics|December 2, 2015
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association ConsortiumJieping Lei, Anja Rudolph, Kirsten B Moysich, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 9, 2016
Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC CarriersMarjanka K Schmidt, Frans Hogervorst, Richard van Hien, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 10, 2010
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controlsOlivia Fletcher, Nichola Johnson, Isabel dos Santos Silva, et al.Oncotarget|October 30, 2016
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21Yosr Hamdi, Penny Soucy, Véronique Adoue, et al.JAMA Oncology|January 27, 2022
Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes, Nasim Mavaddat, Leila Dorling, et al.Journal of the National Cancer Institute|October 10, 2022
Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk LociAmber A DeVries, Joe Dennis, Jonathan P Tyrer, et al.Pageof 18