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Roddy Walsh

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Researcher/Lecturer

City, University of London

United Kingdom

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Grant: Open

Novel approaches to investigate the genetic aetiology of Brugada syndrome

Open Date: 2026-04-01

Close Date: 2028-03-01

Articles (20)

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Collaborators (22)

Joel Rämö

University of Helsinki

FINLAND

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Enzo Porrello

University of Melbourne

AUSTRALIA

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A.s Amin

Cardiologist

Amsterdam University Medical Centers

NETHERLANDS

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Richard Redon

INSERM

FRANCE

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Elizabeth Jordan

Ohio State University

UNITED STATES

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Belinda Gray

University of Sydney

AUSTRALIA

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Sally Ann Lynch

IRELAND

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Tomohiko Ai

JAPAN

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James McNamara

Team Leader

Murdoch Childrens Research Institute

AUSTRALIA

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Andrew Glazer

Assistant Professor

Vanderbilt University Medical Center

UNITED STATES

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David-Alexandre Trégouët

Team Director / 1st Class INSERM Research Director

INSERM U1219

FRANCE

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Elizabeth Ormondroyd

UNITED KINGDOM

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David Elliott

Group Leader

Murdoch Childrens Research Institute

AUSTRALIA

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Eduardo Villacorta

University Hospital of Salamanca

SPAIN

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James Pirruccello

University of California, San Francisco

UNITED STATES

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Ray Hershberger

Professor of Medicine/Cardiology/Human Genetics

Ohio State University

UNITED STATES

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Rachel Buchan

Imperial College London

UNITED KINGDOM

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Jamie Vandenberg

Conjoint Professor

University of New South Wales

AUSTRALIA

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Sean Jurgens

Assistant Professor

Amsterdam UMC Locatie AMC Divisie 9

NETHERLANDS

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Lisa Anderson

Honorary Reader

St George’s, University of London

UNITED KINGDOM

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Anuj Goel

University of Oxford

UNITED KINGDOM

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Antonio de Marvao

Imperial College London

UNITED KINGDOM

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Roddy Walsh

Research Interests

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Articles (20)

An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy

Pangenomes aid accurate detection of large insertions and deletions from targeted sequencing: the case of cardiomyopathies

Intermediate Effect Variants in HCM: Integration into Clinical Practice and Family Screening

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy

Genes Associated With Hypertrophic Cardiomyopathy

Titin and the mystery of cardiomyopathy incidence

Redefining the Genetic Architecture of Hypertrophic Cardiomyopathy: Role of Intermediate Effect Variants

Automated patch clamp data improve variant classification and penetrance stratification for SCN5A-Brugada syndrome.

Brugada Syndrome: an exemplar for the genomic basis of sudden death.

Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance

Rare coding variant analysis for human diseases across biobanks and ancestries

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience.

Navigating The Complex Path From Monogenic to Polygenic Clinical Genetic Testing in Hypertrophic Cardiomyopathy.

Top stories on genome-wide association studies.

Emery-Dreifuss muscular dystrophy: a closer look at cardiac complications.

New Insights into the Genetics of Cardiomyopathies.

The Trouble with Trabeculation: How Genetics Can Help to Unravel a Complex and Controversial Phenotype.

Collaborators (22)

Joel Rämö

Enzo Porrello

A.s Amin

Richard Redon

Elizabeth Jordan

Belinda Gray

Sally Ann Lynch

Tomohiko Ai

James McNamara

Andrew Glazer

David-Alexandre Trégouët

Elizabeth Ormondroyd

David Elliott

Eduardo Villacorta

James Pirruccello

Ray Hershberger

Rachel Buchan

Jamie Vandenberg

Sean Jurgens

Lisa Anderson

Anuj Goel

Antonio de Marvao

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