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Nature Genetics|November 6, 2021
The context-specific role of germline pathogenicity in tumorigenesisPreethi Srinivasan, Chaitanya Bandlamudi, Philip Jonsson, 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.
Nature Medicine|October 16, 2023
Neoplasia risk in patients with Lynch syndrome treated with immune checkpoint blockadeEmily C Harrold, Michael B Foote, Benoit Rousseau, et al.
Cell Stem Cell|June 18, 2013
Molecular profiling of human mammary gland links breast cancer risk to a p27(+) cell population with progenitor characteristicsSibgat Choudhury, Vanessa Almendro, Vanessa F Merino, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 27, 2017
Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine studyArezou A Ghazani, Nelly M Oliver, Joseph P St Pierre, et al.
The New England Journal of Medicine|July 20, 2016
Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate CancerColin C Pritchard, Joaquin Mateo, Michael F Walsh, et al.
Human Molecular Genetics|October 11, 2019
Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathwaysGeffen Kleinstern, Huihuang Yan, Michelle A T Hildebrandt, et al.
JCO Precision Oncology|September 22, 2023
Germline Pathogenic Variants and Genetic Counseling by Ancestry in Patients With Epithelial Ovarian CancerTiffany Y Sia, Anna Maio, Yelena M Kemel, et al.
Nature Genetics|July 15, 2025
Germline genetic variation impacts clonal hematopoiesis landscape and progression to malignancyJie Liu, Duc Tran, Liying Xue, et al.
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