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Showing results (651-660 of 672) with videos related to

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Journal of the American College of Cardiology|September 10, 2021
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic CardiomyopathyAntonio de Marvao, Kathryn A McGurk, Sean L Zheng, et al.
Nature|October 8, 2011
Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial functionChris McDermott-Roe, Junmei Ye, Rizwan Ahmed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2020
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditionsXiaolei Zhang, Roddy Walsh, Nicola Whiffin, et al.
American Journal of Human Genetics|May 22, 2021
Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanismsCaroline F Wright, Nicholas M Quaife, Laura Ramos-Hernández, et al.
Journal of the American College of Cardiology|June 2, 2022
Precision Phenotyping of Dilated Cardiomyopathy Using Multidimensional DataUpasana Tayal, Job A J Verdonschot, Mark R Hazebroek, et al.
Circulation|September 26, 2022
Genetic Architecture of Acute Myocarditis and the Overlap With Inherited CardiomyopathyAmrit S Lota, Mark R Hazebroek, Pantazis Theotokis, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
Nature|April 24, 2007
PTC124 targets genetic disorders caused by nonsense mutationsEllen M Welch, Elisabeth R Barton, Jin Zhuo, et al.
Journal of the American College of Cardiology|July 30, 2025
Sex Differences in the Genetic Causes of Dilated CardiomyopathyMassimo Mangino, Kathryn A McGurk, Pantazis Theotokis, et al.
Nature Genetics|February 18, 2025
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settingsSean L Zheng, Sean J Jurgens, Kathryn A McGurk, et al.
Pageof 68

Showing results (651-660 of 672) with videos related to

Sort By:
Pageof 68
Journal of the American College of Cardiology|September 10, 2021
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic CardiomyopathyAntonio de Marvao, Kathryn A McGurk, Sean L Zheng, et al.
Nature|October 8, 2011
Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial functionChris McDermott-Roe, Junmei Ye, Rizwan Ahmed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2020
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditionsXiaolei Zhang, Roddy Walsh, Nicola Whiffin, et al.
American Journal of Human Genetics|May 22, 2021
Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanismsCaroline F Wright, Nicholas M Quaife, Laura Ramos-Hernández, et al.
Journal of the American College of Cardiology|June 2, 2022
Precision Phenotyping of Dilated Cardiomyopathy Using Multidimensional DataUpasana Tayal, Job A J Verdonschot, Mark R Hazebroek, et al.
Circulation|September 26, 2022
Genetic Architecture of Acute Myocarditis and the Overlap With Inherited CardiomyopathyAmrit S Lota, Mark R Hazebroek, Pantazis Theotokis, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
Nature|April 24, 2007
PTC124 targets genetic disorders caused by nonsense mutationsEllen M Welch, Elisabeth R Barton, Jin Zhuo, et al.
Journal of the American College of Cardiology|July 30, 2025
Sex Differences in the Genetic Causes of Dilated CardiomyopathyMassimo Mangino, Kathryn A McGurk, Pantazis Theotokis, et al.
Nature Genetics|February 18, 2025
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settingsSean L Zheng, Sean J Jurgens, Kathryn A McGurk, et al.
Pageof 68