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JCO Precision Oncology
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September 19, 2024
Detection of Maternal Malignancy After Abnormal Noninvasive Prenatal Testing: A Single-Center Case Series
Mwanasha H Merrill, Sophie R Cahill, Hannah W Pepprock, et al.
JAMA Network Open
|
January 2, 2025
Double CHEK2 Pathogenic and Low-Risk Variants and Associated Cancer Phenotypes
Brittany L Bychkovsky, Nihat B Agaoglu, Carolyn Horton, et al.
American Journal of Medical Genetics. Part A
|
October 11, 2024
Managing CDH1 Cancer Risks in a Child: Complex Decision Making in a Family With Hereditary Diffuse Gastric Cancer
Nihat Bugra Agaoglu, Ozden Hatirnaz Ng, Itir Ebru Zemheri, et al.
Journal of the National Cancer Institute
|
March 13, 2018
Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing
Huma Q Rana, Rebecca Gelman, Holly LaDuca, et al.
Cancer Medicine
|
February 3, 2024
Genomic disparity impacts variant classification of cancer susceptibility genes in Turkish breast cancer patients
Nihat B Agaoglu, Busra Unal, Connor P Hayes, et al.
JCO Oncology Practice
|
May 7, 2026
Video Education With Clinical Genetic Testing Coordinators for the <i>Rapid</i> Evaluation of Patients With Cancers: Real-World Evidence
Jill E Stopfer, Miki Horiguchi, Anu Chittenden, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
August 10, 2022
Impact of Genetic Counseling on Patient-Reported Electronic Cancer Family History Collection
Rebecca A Vanderwall, Alison Schwartz, Lindsay Kipnis, et al.
JCO Precision Oncology
|
September 15, 2022
Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer
Edward D Esplin, Sarah M Nielsen, Sara L Bristow, et al.
Journal of Community Genetics
|
November 20, 2017
A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings
Huma Q Rana, Sarah R Cochrane, Elaine Hiller, et al.
Journal of the National Cancer Institute
|
October 15, 2025
Frequency and clinical features of germline pathogenic variants in sarcoma: a case-control study
Adela Rodriguez-Hernandez, Miki Horiguchi, Carolyn Horton, et al.
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of 8
Search research articles
Search
Showing results (21-30 of 75) with videos related to
Sort By:
Page
of 8
JCO Precision Oncology
|
September 19, 2024
Detection of Maternal Malignancy After Abnormal Noninvasive Prenatal Testing: A Single-Center Case Series
Mwanasha H Merrill, Sophie R Cahill, Hannah W Pepprock, et al.
JAMA Network Open
|
January 2, 2025
Double CHEK2 Pathogenic and Low-Risk Variants and Associated Cancer Phenotypes
Brittany L Bychkovsky, Nihat B Agaoglu, Carolyn Horton, et al.
American Journal of Medical Genetics. Part A
|
October 11, 2024
Managing CDH1 Cancer Risks in a Child: Complex Decision Making in a Family With Hereditary Diffuse Gastric Cancer
Nihat Bugra Agaoglu, Ozden Hatirnaz Ng, Itir Ebru Zemheri, et al.
Journal of the National Cancer Institute
|
March 13, 2018
Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing
Huma Q Rana, Rebecca Gelman, Holly LaDuca, et al.
Cancer Medicine
|
February 3, 2024
Genomic disparity impacts variant classification of cancer susceptibility genes in Turkish breast cancer patients
Nihat B Agaoglu, Busra Unal, Connor P Hayes, et al.
JCO Oncology Practice
|
May 7, 2026
Video Education With Clinical Genetic Testing Coordinators for the <i>Rapid</i> Evaluation of Patients With Cancers: Real-World Evidence
Jill E Stopfer, Miki Horiguchi, Anu Chittenden, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
August 10, 2022
Impact of Genetic Counseling on Patient-Reported Electronic Cancer Family History Collection
Rebecca A Vanderwall, Alison Schwartz, Lindsay Kipnis, et al.
JCO Precision Oncology
|
September 15, 2022
Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer
Edward D Esplin, Sarah M Nielsen, Sara L Bristow, et al.
Journal of Community Genetics
|
November 20, 2017
A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings
Huma Q Rana, Sarah R Cochrane, Elaine Hiller, et al.
Journal of the National Cancer Institute
|
October 15, 2025
Frequency and clinical features of germline pathogenic variants in sarcoma: a case-control study
Adela Rodriguez-Hernandez, Miki Horiguchi, Carolyn Horton, et al.
Page
of 8