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American Journal of Human Genetics|February 24, 2023
The impact of coding germline variants on contralateral breast cancer risk and survivalAnna Morra, Nasim Mavaddat, Taru A Muranen, 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.
Journal of Medical Genetics|September 21, 2011
7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association ConsortiumRoger L Milne, Justo Lorenzo-Bermejo, Barbara Burwinkel, et al.
Journal of the National Cancer Institute|July 2, 2009
Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042Roger L Milne, Javier Benítez, Heli Nevanlinna, et al.
American Journal of Human Genetics|August 3, 2024
Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing datasetAimee L Davidson, Kyriaki Michailidou, Michael T Parsons, et al.
European Journal of Human Genetics : EJHG|January 27, 2023
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European womenGisella Figlioli, Amandine Billaud, Thomas U Ahearn, et al.
Plos One|May 6, 2016
RAD51B in Familial Breast CancerLiisa M Pelttari, Sofia Khan, Mikko Vuorela, et al.
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