Kathryn E Hatchell - JoVE Visualize

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Epilepsia Open|December 10, 2023

Early genetic testing in pediatric epilepsy: Diagnostic and cost implicationsShanna M Swartwood, Ana Morales, Kathryn E Hatchell, et al.

Preventive Medicine|May 8, 2023

Racial disparities in cascade testing for cancer predisposition genesNawal M Kassem, Sandra K Althouse, Patrick O Monahan, et al.

Urology|February 11, 2023

Fumarate Hydratase Variants and Their Association With Paraganglioma/PheochromocytomaShirin Zavoshi, Eric Lu, Paul C Boutros, 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.

Journal of the Peripheral Nervous System : JPNS|August 14, 2024

Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathyJennifer Roggenbuck, Ana Morales, Colin A Ellis, 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.

American Journal of Human Genetics|January 30, 2025

Experience using conventional compared to ancestry-based population descriptors in clinical genomics laboratoriesKathryn E Hatchell, Sarah R Poll, Emily M Russell, 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.

JAMA Network Open|October 24, 2022

Comparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal CancerChad Moretz, Stacey DaCosta Byfield, Kathryn E Hatchell, et al.

JAMA Cardiology|August 10, 2022

Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic TestingLisa M Dellefave-Castillo, Allison L Cirino, Thomas E Callis, et al.

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Showing results (11-20 of 31) with videos related to

Sort By:

Pageof 4

Epilepsia Open|December 10, 2023

Early genetic testing in pediatric epilepsy: Diagnostic and cost implicationsShanna M Swartwood, Ana Morales, Kathryn E Hatchell, et al.

Preventive Medicine|May 8, 2023

Racial disparities in cascade testing for cancer predisposition genesNawal M Kassem, Sandra K Althouse, Patrick O Monahan, et al.

Urology|February 11, 2023

Fumarate Hydratase Variants and Their Association With Paraganglioma/PheochromocytomaShirin Zavoshi, Eric Lu, Paul C Boutros, 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.

Journal of the Peripheral Nervous System : JPNS|August 14, 2024

Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathyJennifer Roggenbuck, Ana Morales, Colin A Ellis, 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.

American Journal of Human Genetics|January 30, 2025

Experience using conventional compared to ancestry-based population descriptors in clinical genomics laboratoriesKathryn E Hatchell, Sarah R Poll, Emily M Russell, 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.

JAMA Network Open|October 24, 2022

Comparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal CancerChad Moretz, Stacey DaCosta Byfield, Kathryn E Hatchell, et al.

JAMA Cardiology|August 10, 2022

Assessment of the Diagnostic Yield of Combined Cardiomyopathy and Arrhythmia Genetic TestingLisa M Dellefave-Castillo, Allison L Cirino, Thomas E Callis, et al.

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