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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.
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.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2026
PRANA: A Deep Learning Method for Adapting Polygenic Risk Scores to Diverse Ethnic GroupsHagai Levi, Qin Wang, Manjeet K Bolla, et al.
Plos One|May 6, 2016
RAD51B in Familial Breast CancerLiisa M Pelttari, Sofia Khan, Mikko Vuorela, et al.
Breast Cancer Research : BCR|February 18, 2016
Genetic predisposition to ductal carcinoma in situ of the breastChristos Petridis, Mark N Brook, Vandna Shah, et al.
Scientific Reports|November 16, 2016
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer riskJingjing Liu, Ivona Lončar, J Margriet Collée, et al.
Human Molecular Genetics|July 13, 2016
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expressionAsaf Wyszynski, Chi-Chen Hong, Kristin Lam, et al.
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