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Nature Reviews. Cardiology
|
September 16, 2021
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
Roddy 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 tachycardia
Roddy Walsh, Nicholas S Peters, Stuart A Cook, et al.
Human Mutation
|
May 15, 2012
Paralogous annotation of disease-causing variants in long QT syndrome genes
James S Ware, Roddy Walsh, Fiona Cunningham, et al.
Genome Medicine
|
February 5, 2015
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity
Dace 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 death
Rebecca 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 Truncation
Leanne 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 Remodeling
Timothy 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 Cardiomyopathy
Upasana 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 significance
Jane Murphy, Claire W Kirk, Deborah M Lambert, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 89) with videos related to
Sort By:
Page
of 9
Nature Reviews. Cardiology
|
September 16, 2021
Minor hypertrophic cardiomyopathy genes, major insights into the genetics of cardiomyopathies
Roddy 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 tachycardia
Roddy Walsh, Nicholas S Peters, Stuart A Cook, et al.
Human Mutation
|
May 15, 2012
Paralogous annotation of disease-causing variants in long QT syndrome genes
James S Ware, Roddy Walsh, Fiona Cunningham, et al.
Genome Medicine
|
February 5, 2015
Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity
Dace 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 death
Rebecca 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 Truncation
Leanne 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 Remodeling
Timothy 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 Cardiomyopathy
Upasana 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 significance
Jane Murphy, Claire W Kirk, Deborah M Lambert, et al.
Page
of 9