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Francesco Mazzarotto

Showing results (11-20 of 41) with videos related to

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Pacing and Clinical Electrophysiology : PACE|February 20, 2024
Ion channel dysfunction and fibrosis in atrial fibrillation: Two sides of the same coinGianmarco Arabia, Maria Giulia Bellicini, Angelica Cersosimo, et al.
Nature Reviews. Genetics|October 7, 2024
Genome-wide association testing beyond SNPsLaura Harris, Ellen M McDonagh, Xiaolei Zhang, et al.
European Journal of Preventive Cardiology|November 9, 2019
Sex-related differences in exercise performance and outcome of patients with hypertrophic cardiomyopathyLuca Ghiselli, Alberto Marchi, Carlo Fumagalli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single centerFrancesco Mazzarotto, Francesca Girolami, Beatrice Boschi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samplesRoddy Walsh, Kate L Thomson, James S Ware, et al.
JMIR Medical Informatics|February 2, 2022
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine LearningMatej Pičulin, Tim Smole, Bojan Žunkovič, et al.
Computers in Biology and Medicine|July 19, 2021
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathyTim Smole, Bojan Žunkovič, Matej Pičulin, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2021
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretationAndrea D Thompson, Adam S Helms, Anamika Kannan, et al.
Frontiers in Physiology|November 24, 2022
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiencyJosè Manuel Pioner, Lorenzo Santini, Chiara Palandri, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Pacing and Clinical Electrophysiology : PACE|February 20, 2024
Ion channel dysfunction and fibrosis in atrial fibrillation: Two sides of the same coinGianmarco Arabia, Maria Giulia Bellicini, Angelica Cersosimo, et al.
Nature Reviews. Genetics|October 7, 2024
Genome-wide association testing beyond SNPsLaura Harris, Ellen M McDonagh, Xiaolei Zhang, et al.
European Journal of Preventive Cardiology|November 9, 2019
Sex-related differences in exercise performance and outcome of patients with hypertrophic cardiomyopathyLuca Ghiselli, Alberto Marchi, Carlo Fumagalli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 8, 2018
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single centerFrancesco Mazzarotto, Francesca Girolami, Beatrice Boschi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 18, 2016
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samplesRoddy Walsh, Kate L Thomson, James S Ware, et al.
JMIR Medical Informatics|February 2, 2022
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine LearningMatej Pičulin, Tim Smole, Bojan Žunkovič, et al.
Computers in Biology and Medicine|July 19, 2021
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathyTim Smole, Bojan Žunkovič, Matej Pičulin, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 30, 2021
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretationAndrea D Thompson, Adam S Helms, Anamika Kannan, et al.
Frontiers in Physiology|November 24, 2022
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiencyJosè Manuel Pioner, Lorenzo Santini, Chiara Palandri, et al.
Pageof 5