Roddy Walsh

37PUBLICATIONS
234CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Gene mappingNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (37)

|Sep 08, 2026
An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.

|Feb 06, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.

Daria R Kramarenko, Poeya Haydarlou, George J Powell

|Nov 18, 2025
Automated patch clamp data improve variant classification and penetrance stratification for SCN5A-Brugada syndrome.

Matthew J O'Neill, Joanne G Ma, Jessa L Aldridge

|Nov 14, 2025
Brugada Syndrome: an exemplar for the genomic basis of sudden death.

Rebecca L M Griffiths, Roddy Walsh, Marta Futema

|Aug 29, 2025
Redefining the Genetic Architecture of Hypertrophic Cardiomyopathy: Role of Intermediate-Effect Variants.

Soledad García Hernandez, Luis de la Higuera Romero, Adrian Fernandez

|Feb 18, 2025
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Rafik Tadros, Sean L Zheng, Christopher Grace

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Frequent Collaborators

14 joint publications

Connie R Bezzina

13 joint publications

James Ware

12 joint publications

Sean Jurgens

9 joint publications

Rafik Tadros