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European Urology Oncology|October 8, 2023
Clinical and Functional Analyses of an African-ancestry Gain-of-function HOXB13 Variant Implicated in Aggressive Prostate CancerMayuko Kanayama, Yidong Chen, Daniel Rabizadeh, et al.
JCO Precision Oncology|August 3, 2023
Retrospective Cohort Study on the Limitations of Direct-to-Consumer Genetic Screening in Hereditary Breast and Ovarian CancerNeelam V Desai, Elizabeth D Barrows, Sarah M Nielsen, et al.
Urology|February 11, 2023
Fumarate Hydratase Variants and Their Association With Paraganglioma/PheochromocytomaShirin Zavoshi, Eric Lu, Paul C Boutros, et al.
Prostate Cancer and Prostatic Diseases|June 20, 2025
Case series exploring hormonal sensitivity in prostate cancer patients harboring the germline African-ancestry HOXB13 X285K variantMayuko Kanayama, Emeline Colomba, Yusra Shao, et al.
World Journal of Oncology|September 27, 2024
Patterns and Frequency of Pathogenic Germline Variants Among Prostate Cancer Patients Utilizing Multi-Gene Panel Genetic TestingRamiz Abu Hijlih, Baha Sharaf, Samer Salah, et al.
JCO Precision Oncology|November 22, 2023
Rate of Pathogenic Germline Variants in Patients With Lung CancerSteven Sorscher, Jaclyn LoPiccolo, Brandie Heald, et al.
Journal of the National Cancer Institute|September 27, 2023
Cascade testing for hereditary cancer: comprehensive multigene panels identify unexpected actionable findings in relativesBrandie Heald, Sara Pirzadeh-Miller, Rachel E Ellsworth, et al.
International Journal of Cancer|August 16, 2014
Tumor genome analysis includes germline genome: are we ready for surprises?Daniel V T Catenacci, Andrea L Amico, Sarah M Nielsen, et al.
World Journal of Oncology|September 27, 2024
Multi-Gene Panel Testing for Hereditary Cancer Predisposition Among Patients Sixty-Five Years and Above Diagnosed With Breast CancerHikmat Abdel-Razeq, Faris Tamimi, Baha Sharaf, et al.
Cancer|November 1, 2021
Fumarate hydratase variant prevalence and manifestations among individuals receiving germline testingEric Lu, Kathryn E Hatchell, Sarah M Nielsen, et al.
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