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Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Integrated Clinicogenomic Risk Modeling for Metachronous Second Primary CancersJohnathan Amsalem, Irina Ostrovnaya, Andrew R Marderstein, et al.
NPJ Precision Oncology|July 17, 2026
PTCH1 mutations and tumor-agnostic clinical outcomes with hedgehog pathway inhibitors across cancer typesAntoine Desilets, Matteo Repetto, Soo Ryum Yang, et al.
Frontiers in Genetics|March 5, 2014
Genome-wide analysis of the role of copy-number variation in pancreatic cancer riskJason A Willis, Semanti Mukherjee, Irene Orlow, et al.
Annals of Surgery|April 7, 2007
Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical managementJose G Guillem, Emily Glogowski, Harvey G Moore, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 20, 2007
BRCA mutations in women with ductal carcinoma in situKaren Lisa Smith, Muriel Adank, Noah Kauff, et al.
Cancer Discovery|September 1, 2022
Genetic Ancestry Correlates with Somatic Differences in a Real-World Clinical Cancer Sequencing CohortKanika Arora, Thinh N Tran, Yelena Kemel, et al.
Cancer Discovery|September 23, 2016
A Recurrent ERCC3 Truncating Mutation Confers Moderate Risk for Breast CancerJoseph Vijai, Sabine Topka, Danylo Villano, et al.
JCO Precision Oncology|July 12, 2021
Tolerability of Breast Radiotherapy Among Carriers of ATM Germline VariantsLeslie A Modlin, Jessica Flynn, Zhigang Zhang, et al.
JCO Precision Oncology|January 16, 2020
Decision-Making Preferences About Secondary Germline Findings That Arise From Tumor Genomic Profiling Among Patients With Advanced CancersJada G Hamilton, Elyse Shuk, Margaux Genoff Garzon, et al.
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