Jesse B G Hayesmoore (Jesse B Hayesmoore)

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 6

Top Topics

Transcription Factor

Hypertrophic Cardiomyopathy

Top Venues

Circulation. Genomic and precision medicine

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Jesse B G Hayesmoore, Michael Bowman, Nora Shannon, Edward Blair, Hugh C Watkins, Kate L Thomson
A Promoter Deletion Confirms That MYBPC3 Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans. Circulation. Genomic and precision medicine 17 (1) (2024)
Jesse B G Hayesmoore, Michael Bowman, Nora Shannon, Edward Blair, Hugh C Watkins, Kate L Thomson
A Promoter Deletion Confirms That MYBPC3 Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans. Circulation. Genomic and precision medicine 17 (1) (2024)
Jesse B G Hayesmoore, Michael Bowman, Nora Shannon, Edward Blair, Hugh C Watkins, Kate L Thomson
Promoter Deletion Confirms That MYBPC3 Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans. Circulation. Genomic and precision medicine (2024)
Jesse B G Hayesmoore, Michael Bowman, Nora Shannon, Edward Blair, Hugh C Watkins, Kate L Thomson
A Promoter Deletion Confirms That MYBPC3 Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans. Circulation. Genomic and precision medicine 17 (1) (2024)
Jesse B G Hayesmoore, Michael Bowman, Nora Shannon, Edward Blair, Hugh C Watkins, Kate L Thomson
A Promoter Deletion Confirms That MYBPC3 Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans. Circulation. Genomic and precision medicine 17 (1) (2024)
Jesse B G Hayesmoore, Zahurul A Bhuiyan, Domenico A Coviello, Desirée du Sart, Matthew Edwards, Maria Iascone, Deborah J Morris-Rosendahl, Katie Sheils, Marjon van Slegtenhorst, Kate L Thomson
EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias. European journal of human genetics : EJHG (2023)