Kate Thomson

11PUBLICATIONS
168CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (11)

|Aug 20, 2026
Genotype-Phenotype Correlations Identify Phenotypic Differences in Sarcomere Mutation-Positive Hypertrophic Cardiomyopathy in the NHLBI HCM Registry.

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

Renee Johnson, Robert A Fletcher, Stacey Peters

|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

|Jul 02, 2024
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants.

Joanne G Ma, Matthew J O'Neill, Ebony Richardson

|Jul 13, 2023
EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias.

Jesse B Hayesmoore, Zahurul A Bhuiyan, Domenico A Coviello

|Jan 26, 2021
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.

Andrew R Harper, Anuj Goel, Christopher Grace

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Frequent Collaborators

4 joint publications

James S Ware

4 joint publications

Hugh Watkins

4 joint publications

Elizabeth Ormondroyd

3 joint publications

Carolyn Y Ho