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Amy C Sturm

Showing results (81-90 of 114) with videos related to

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JAMIA Open|March 11, 2024
Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran ProgramCharles A Brunette, Thomas Yi, Morgan E Danowski, et al.
Circulation. Genomic and Precision Medicine|March 8, 2021
Clinical Findings and Diagnostic Yield of Arrhythmogenic Cardiomyopathy Through Genomic Screening of Pathogenic or Likely Pathogenic Desmosome Gene VariantsEric D Carruth, Dominik Beer, Amro Alsaid, et al.
Health Affairs (Project Hope)|May 8, 2018
Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The LiteratureMegan C Roberts, W David Dotson, Christopher S DeVore, et al.
Journal of the American Heart Association|May 28, 2015
Use of whole exome sequencing for the identification of Ito-based arrhythmia mechanism and therapyAmy C Sturm, Crystal F Kline, Patric Glynn, et al.
Frontiers in Health Services|May 15, 2023
Designing implementation strategies to improve identification, cascade testing, and management of families with familial hypercholesterolemia: An intervention mapping approachLaney K Jones, Evan M Calvo, Gemme Campbell-Salome, et al.
Circulation|July 1, 2018
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada SyndromeS Mohsen Hosseini, Raymond Kim, Sharmila Udupa, et al.
European Heart Journal|September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic deathRoddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Journal of the American Heart Association|June 29, 2023
Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data ScreeningSamuel S Gidding, H Lester Kirchner, Andrew Brangan, et al.
BMC Pediatrics|May 17, 2020
Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parentsJuliann M Savatt, Jennifer K Wagner, Steven Joffe, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 23, 2015
SCN5A variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmiaHassan Musa, Crystal F Kline, Amy C Sturm, et al.
Pageof 12

Showing results (81-90 of 114) with videos related to

Sort By:
Pageof 12
JAMIA Open|March 11, 2024
Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran ProgramCharles A Brunette, Thomas Yi, Morgan E Danowski, et al.
Circulation. Genomic and Precision Medicine|March 8, 2021
Clinical Findings and Diagnostic Yield of Arrhythmogenic Cardiomyopathy Through Genomic Screening of Pathogenic or Likely Pathogenic Desmosome Gene VariantsEric D Carruth, Dominik Beer, Amro Alsaid, et al.
Health Affairs (Project Hope)|May 8, 2018
Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The LiteratureMegan C Roberts, W David Dotson, Christopher S DeVore, et al.
Journal of the American Heart Association|May 28, 2015
Use of whole exome sequencing for the identification of Ito-based arrhythmia mechanism and therapyAmy C Sturm, Crystal F Kline, Patric Glynn, et al.
Frontiers in Health Services|May 15, 2023
Designing implementation strategies to improve identification, cascade testing, and management of families with familial hypercholesterolemia: An intervention mapping approachLaney K Jones, Evan M Calvo, Gemme Campbell-Salome, et al.
Circulation|July 1, 2018
Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada SyndromeS Mohsen Hosseini, Raymond Kim, Sharmila Udupa, et al.
European Heart Journal|September 24, 2021
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic deathRoddy Walsh, Arnon Adler, Ahmad S Amin, et al.
Journal of the American Heart Association|June 29, 2023
Yield of Familial Hypercholesterolemia Genetic and Phenotypic Diagnoses After Electronic Health Record and Genomic Data ScreeningSamuel S Gidding, H Lester Kirchner, Andrew Brangan, et al.
BMC Pediatrics|May 17, 2020
Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parentsJuliann M Savatt, Jennifer K Wagner, Steven Joffe, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 23, 2015
SCN5A variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmiaHassan Musa, Crystal F Kline, Amy C Sturm, et al.
Pageof 12