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Nature Genetics|February 1, 2011
Common variants in ZNF365 are associated with both mammographic density and breast cancer riskSara Lindström, Celine M Vachon, Jingmei Li, 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.
Nature Genetics|April 23, 2002
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutationsHanne Meijers-Heijboer, Ans van den Ouweland, Jan Klijn, et al.
EPJ Data Science|December 20, 2016
Enhancing disease surveillance with novel data streams: challenges and opportunitiesBenjamin M Althouse, Samuel V Scarpino, Lauren Ancel Meyers, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|December 11, 2012
Polymorphisms in inflammation pathway genes and endometrial cancer riskRyan J Delahanty, Yong-Bing Xiang, Amanda Spurdle, et al.
American Journal of Human Genetics|December 23, 2006
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationPatrick S Tarpey, Claire Stevens, Jon Teague, et al.
Breast Cancer Research : BCR|August 16, 2015
A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic densityAnja Rudolph, Peter A Fasching, Sabine Behrens, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 17, 2002
Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage ConsortiumDeborah Thompson, Csilla I Szabo, Jon Mangion, et al.
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