Showing results (111-120 of 220) with videos related to
Sort By:
Pageof 22
Salud Publica De Mexico|April 19, 2022
Germline pathogenic variants in Mexican patients with hereditary triple-negative breast cancerYanin Chavarri-Guerra, Cynthia Villarreal-Garza, Ana S Ferrigno, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2017
Somatic TP53 variants frequently confound germ-line testing resultsJeffrey N Weitzel, Elizabeth C Chao, Bita Nehoray, et al.Nature Communications|April 9, 2026
Combining multiplexed assays of variant effect for enhanced BRCA2 variant classificationChunling Hu, Sounak Sahu, Wenan Chen, et al.American Journal of Human Genetics|May 7, 2016
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast CancerKara N Maxwell, Steven N Hart, Joseph Vijai, et al.Cancer Research|May 5, 2023
Profiling the Somatic Mutational Landscape of Breast Tumors from Hispanic/Latina Women Reveals Conserved and Unique CharacteristicsYuan Chun Ding, Hanbing Song, Aaron W Adamson, et al.Nature Communications|August 21, 2025
Whole exome sequencing identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer in Hispanic/Latina womenJovia L Nierenberg, Aaron W Adamson, Donglei Hu, et al.Science Translational Medicine|August 9, 2019
Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancerBradon R McDonald, Tania Contente-Cuomo, Stephen-John Sammut, et al.Journal of Medical Genetics|July 19, 2015
Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countriesAva Kwong, Vivian Y Shin, John C W Ho, et al.Cancer|April 15, 2021
Germline mutations and age at onset of lung adenocarcinomaKaren L Reckamp, Carolyn E Behrendt, Thomas P Slavin, et al.Breast Cancer Research and Treatment|October 15, 2014
Use of risk-reducing surgeries in a prospective cohort of 1,499 BRCA1 and BRCA2 mutation carriersXinglei Chai, Tara M Friebel, Christian F Singer, et al.Pageof 22