Showing results (41-50 of 235) with videos related to

Sort By:
Pageof 24
Journal of the National Cancer Institute|October 16, 2024
Polygenic risk scores stratify breast cancer risk among women with benign breast diseaseMark E Sherman, Stacey J Winham, Robert A Vierkant, et al.
Breast Cancer Research : BCR|December 10, 2016
Prediction of breast cancer risk based on common genetic variants in women of East Asian ancestryWanqing Wen, Xiao-Ou Shu, Xingyi Guo, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Human Molecular Genetics|August 1, 2013
A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer riskKaren A Pooley, Stig E Bojesen, Maren Weischer, et al.
Breast Cancer Research : BCR|May 24, 2019
Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer riskCeline M Vachon, Christopher G Scott, Rulla M Tamimi, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 3, 2014
A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicityGillian C Barnett, Deborah Thompson, Laura Fachal, et al.
Blood|December 22, 2018
Genetic susceptibility to radiation-induced breast cancer after Hodgkin lymphomaAnnemieke W J Opstal-van Winden, Hugoline G de Haan, Michael Hauptmann, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
NPJ Breast Cancer|September 23, 2020
Association of germline variation with the survival of women with <i>BRCA1/2</i> pathogenic variants and breast cancerTaru A Muranen, Sofia Khan, Rainer Fagerholm, et al.
Medrxiv : the Preprint Server for Health Sciences|February 13, 2023
Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selectionAoxing Liu, Giulio Genovese, Yajie Zhao, et al.
Pageof 24