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Kate Thomson

Showing results (41-50 of 46) with videos related to

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Journal of the American College of Cardiology|November 9, 2019
Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI HCM RegistryStefan Neubauer, Paul Kolm, Carolyn Y Ho, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.
Heart Rhythm|February 11, 2026
Hypertrophic cardiomyopathy caused by Filamin-C (FLNC) variants has restrictive and extracardiac features and a distinctive ECGCarin de Villiers, Elizabeth Ormondroyd, Kate Thomson, et al.
European Heart Journal|March 5, 2025
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data setsAlexandra Butters, Kate Thomson, Franki Harrington, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2023
Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosureJoshua Nolan, James Buchanan, John Taylor, et al.
European Heart Journal|August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onsetRenee Johnson, Robert A Fletcher, Stacey Peters, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Journal of the American College of Cardiology|November 9, 2019
Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI HCM RegistryStefan Neubauer, Paul Kolm, Carolyn Y Ho, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.
Heart Rhythm|February 11, 2026
Hypertrophic cardiomyopathy caused by Filamin-C (FLNC) variants has restrictive and extracardiac features and a distinctive ECGCarin de Villiers, Elizabeth Ormondroyd, Kate Thomson, et al.
European Heart Journal|March 5, 2025
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data setsAlexandra Butters, Kate Thomson, Franki Harrington, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 22, 2023
Secondary (additional) findings from the 100,000 Genomes Project: Disease manifestation, health care outcomes, and costs of disclosureJoshua Nolan, James Buchanan, John Taylor, et al.
European Heart Journal|August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onsetRenee Johnson, Robert A Fletcher, Stacey Peters, et al.
Pageof 5