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Applied Clinical Informatics
|
May 12, 2021
Infobuttons for Genomic Medicine: Requirements and Barriers
Luke 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 Program
Steven 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 Analysis
Carlos 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 testing
Beth 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 mechanisms
Angela 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 interpretation
Min 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 cancer
Silvia 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 management
Sarah 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 Survey
Linda 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 reclassifications
Andrew Folta, Adriana E Sedeño Cortés, Pankhuri Gupta, et al.
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of 12
Search research articles
Search
Showing results (81-90 of 113) with videos related to
Sort By:
Page
of 12
Applied Clinical Informatics
|
May 12, 2021
Infobuttons for Genomic Medicine: Requirements and Barriers
Luke 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 Program
Steven 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 Analysis
Carlos 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 testing
Beth 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 mechanisms
Angela 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 interpretation
Min 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 cancer
Silvia 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 management
Sarah 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 Survey
Linda 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 reclassifications
Andrew Folta, Adriana E Sedeño Cortés, Pankhuri Gupta, et al.
Page
of 12