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Kate Thomson

10PUBLICATIONS

159CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cellular nervous systemNeurogeneticsCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)

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Publications (10)

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|Aug 12, 2025

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Renee Johnson, Robert A Fletcher, Stacey Peters

|Mar 25, 2025

Combined RNA Splicing and Patch-Clamp Analysis Reveal Pathogenicity of Splice-Altering Variants in <i>KCNH2</i>-Related LQTS.

Susan Clasper, Gunjan Trivedi, Kate L Thomson

|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

|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 <i>SCN5A</i> Brugada Syndrome-Associated Variants.

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

|Jan 23, 2024

A Promoter Deletion Confirms That <i>MYBPC3</i> Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans.

Jesse B G Hayesmoore, Michael Bowman, Nora Shannon

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Frequent Collaborators

4 joint publications

James S Ware

4 joint publications

Elizabeth Ormondroyd

3 joint publications

Hugh Watkins

2 joint publications

Roddy Walsh

2 joint publications

Francesco Mazzarotto

2 joint publications

Martin Farrall

2 joint publications

Andrew R Harper

2 joint publications

Jesse B Hayesmoore

2 joint publications

Connie R Bezzina

2 joint publications

Rafik Tadros

Frequent Collaborators

4 joint publications

James S Ware

4 joint publications

Elizabeth Ormondroyd

3 joint publications

Hugh Watkins

2 joint publications

Roddy Walsh

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