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Brian H Shirts

Showing results (81-90 of 113) with videos related to

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Applied Clinical Informatics|May 12, 2021
Infobuttons for Genomic Medicine: Requirements and BarriersLuke V Rasmussen, John J Connolly, Guilherme Del Fiol, et al.
Human Mutation|December 19, 2021
Harmonizing variant classification for return of results in the All of Us Research ProgramSteven M Harrison, Christina A Austin-Tse, Serra Kim, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 6, 2015
Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness AnalysisCarlos J Gallego, Brian H Shirts, Caroline S Bennette, et al.
BMC Primary Care|December 21, 2025
Cost-effectiveness of primary care-based risk assessment and hereditary cancer genetic testingBeth Devine, Sanne E Aalbers, HuiHsuan Chan, et al.
Journal of Medical Genetics|June 26, 2025
Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanismsAngela L Jacobson, Amal AbuRayyan, Suleyman Gulsuner, et al.
American Journal of Human Genetics|June 6, 2025
Insights on improving accessibility and usability of functional data to unlock their potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2019
Characterization of splice-altering mutations in inherited predisposition to cancerSilvia Casadei, Suleyman Gulsuner, Brian H Shirts, et al.
The Journal of Allergy and Clinical Immunology|April 17, 2021
Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical managementSarah K Baxter, Tom Walsh, Silvia Casadei, et al.
JCO Precision Oncology|October 28, 2023
Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice SurveyLinda Rodgers-Fouche, Sanjeevani Arora, Charité Ricker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 21, 2025
Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassificationsAndrew Folta, Adriana E Sedeño Cortés, Pankhuri Gupta, et al.
Pageof 12

Showing results (81-90 of 113) with videos related to

Sort By:
Pageof 12
Applied Clinical Informatics|May 12, 2021
Infobuttons for Genomic Medicine: Requirements and BarriersLuke V Rasmussen, John J Connolly, Guilherme Del Fiol, et al.
Human Mutation|December 19, 2021
Harmonizing variant classification for return of results in the All of Us Research ProgramSteven M Harrison, Christina A Austin-Tse, Serra Kim, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 6, 2015
Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness AnalysisCarlos J Gallego, Brian H Shirts, Caroline S Bennette, et al.
BMC Primary Care|December 21, 2025
Cost-effectiveness of primary care-based risk assessment and hereditary cancer genetic testingBeth Devine, Sanne E Aalbers, HuiHsuan Chan, et al.
Journal of Medical Genetics|June 26, 2025
Long-read DNA and RNA sequencing for inherited polyposis and colorectal cancer: cryptic intronic variants and multiple mutational mechanismsAngela L Jacobson, Amal AbuRayyan, Suleyman Gulsuner, et al.
American Journal of Human Genetics|June 6, 2025
Insights on improving accessibility and usability of functional data to unlock their potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 18, 2019
Characterization of splice-altering mutations in inherited predisposition to cancerSilvia Casadei, Suleyman Gulsuner, Brian H Shirts, et al.
The Journal of Allergy and Clinical Immunology|April 17, 2021
Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical managementSarah K Baxter, Tom Walsh, Silvia Casadei, et al.
JCO Precision Oncology|October 28, 2023
Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice SurveyLinda Rodgers-Fouche, Sanjeevani Arora, Charité Ricker, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 21, 2025
Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassificationsAndrew Folta, Adriana E Sedeño Cortés, Pankhuri Gupta, et al.
Pageof 12