Richard D Bagnall

17PUBLICATIONS
196CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)NeurogeneticsCancer genetics
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Publications (17)

|Apr 04, 2026
DMPK 3' untranslated repeat expansions in unexplained sudden cardiac death in the young.

Zoe Ward, Jackson O'Neill, Rachael Stiles

|Aug 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Renee Johnson, Robert A Fletcher, Stacey Peters

|Apr 21, 2025
Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.

Sophie Hespe, Emma S Singer, Chloe Reuter

|Mar 05, 2025
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data sets.

Alexandra Butters, Kate Thomson, Franki Harrington

|Aug 12, 2024
ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy.

Sophie Hespe, Amber Waddell, Babken Asatryan

|Dec 20, 2023
A case series of patients with filamin-C truncating variants attending a specialized cardiac genetic clinic.

Sophie Hespe, Julia C Isbister, Johan Duflou

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