Roddy J. Walsh
St. George's University Of London
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 99 publications
An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.
Journal: Circulation
Published: September 08, 2026
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
Intermediate Effect Variants in HCM: Integration into Clinical Practice and Family Screening.
Journal: Circulation
Published: May 04, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.
Journal: Research square
Published: February 06, 2026
Titin and the mystery of cardiomyopathy incidence.
Journal: European heart journal
Published: September 05, 2025
Brugada Syndrome: an exemplar for the genomic basis of sudden death.
Journal: European journal of human genetics : EJHG
Published: August 27, 2025
Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: April 21, 2025
Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.
Journal: Nature genetics
Published: December 05, 2024
Pathogenic germline variants in cancer predisposition genes in patients with multiple primary cancers in an Asian population and the role of extended panel genetic testing.
Journal: ESMO open
Published: November 03, 2024
Last Updated: 09/26/2026