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Roddy Walsh

Showing results (21-30 of 89) with videos related to

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Nature Reviews. Cardiology|September 16, 2021
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathiesRoddy Walsh, Joost A Offerhaus, Rafik Tadros, et al.
Journal of Medical Genetics|October 19, 2013
Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardiaRoddy Walsh, Nicholas S Peters, Stuart A Cook, et al.
Human Mutation|May 15, 2012
Paralogous annotation of disease-causing variants in long QT syndrome genesJames S Ware, Roddy Walsh, Fiona Cunningham, et al.
Genome Medicine|February 5, 2015
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicityDace Ruklisa, James S Ware, Roddy Walsh, et al.
European Journal of Human Genetics : EJHG|November 14, 2025
Brugada Syndrome: an exemplar for the genomic basis of sudden deathRebecca L M Griffiths, Roddy Walsh, Marta Futema, et al.
Journal of the American Heart Association|April 21, 2020
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?Francesco Mazzarotto, Iacopo Olivotto, Beatrice Boschi, et al.
JAMA Cardiology|July 21, 2016
Recovery of Cardiac Function in Cardiomyopathy Caused by Titin TruncationLeanne E Felkin, Roddy Walsh, James S Ware, et al.
Circulation. Cardiovascular Imaging|August 10, 2016
Moderate Physical Activity in Healthy Adults Is Associated With Cardiac RemodelingTimothy J W Dawes, Ben Corden, Sorcha Cotter, et al.
Journal of the American College of Cardiology|May 13, 2017
Truncating Variants in Titin Independently Predict Early Arrhythmias in Patients With Dilated CardiomyopathyUpasana Tayal, Simon Newsome, Rachel Buchan, et al.
Irish Journal of Medical Science|March 15, 2024
Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significanceJane Murphy, Claire W Kirk, Deborah M Lambert, et al.
Pageof 9

Showing results (21-30 of 89) with videos related to

Sort By:
Pageof 9
Nature Reviews. Cardiology|September 16, 2021
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathiesRoddy Walsh, Joost A Offerhaus, Rafik Tadros, et al.
Journal of Medical Genetics|October 19, 2013
Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardiaRoddy Walsh, Nicholas S Peters, Stuart A Cook, et al.
Human Mutation|May 15, 2012
Paralogous annotation of disease-causing variants in long QT syndrome genesJames S Ware, Roddy Walsh, Fiona Cunningham, et al.
Genome Medicine|February 5, 2015
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicityDace Ruklisa, James S Ware, Roddy Walsh, et al.
European Journal of Human Genetics : EJHG|November 14, 2025
Brugada Syndrome: an exemplar for the genomic basis of sudden deathRebecca L M Griffiths, Roddy Walsh, Marta Futema, et al.
Journal of the American Heart Association|April 21, 2020
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?Francesco Mazzarotto, Iacopo Olivotto, Beatrice Boschi, et al.
JAMA Cardiology|July 21, 2016
Recovery of Cardiac Function in Cardiomyopathy Caused by Titin TruncationLeanne E Felkin, Roddy Walsh, James S Ware, et al.
Circulation. Cardiovascular Imaging|August 10, 2016
Moderate Physical Activity in Healthy Adults Is Associated With Cardiac RemodelingTimothy J W Dawes, Ben Corden, Sorcha Cotter, et al.
Journal of the American College of Cardiology|May 13, 2017
Truncating Variants in Titin Independently Predict Early Arrhythmias in Patients With Dilated CardiomyopathyUpasana Tayal, Simon Newsome, Rachel Buchan, et al.
Irish Journal of Medical Science|March 15, 2024
Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significanceJane Murphy, Claire W Kirk, Deborah M Lambert, et al.
Pageof 9