Publications by authors named "Jesse Hayesmoore"

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A tandem duplication of exon 42 of the gene is a likely benign variant.
Jesse B G Hayesmoore, Ruth Newbury-Ecob, Sarah Durell, Amy Dillon, Farah Kanani

J Med Genet· January 2025

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A Promoter Deletion Confirms That Haploinsufficiency Is Sufficient to Cause Hypertrophic Cardiomyopathy in Humans.
Jesse B G Hayesmoore, Michael Bowman, Nora Shannon, Edward Blair, Hugh Watkins

Circ Genom Precis Med· February 2024

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EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias.
Jesse B Hayesmoore, Zahurul A Bhuiyan, Domenico A Coviello, Desirée du Sart, Matthew Edwards

Eur J Hum Genet· September 2023

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Reevaluation of the South Asian Intronic Deletion in Hypertrophic Cardiomyopathy.
Andrew R Harper, Michael Bowman, Jesse B G Hayesmoore, Helen Sage, Silvia Salatino

Circ Genom Precis Med· June 2020

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Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield.
Kate L Thomson, Elizabeth Ormondroyd, Andrew R Harper, Tim Dent, Karen McGuire, Jesse B G Hayesmoore

Genet Med· July 2019

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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters.
Victoria Harrison, Lyndsey Connell, Jesse Hayesmoore, Joanna McParland, Michael G Pike

Am J Med Genet A· November 2011

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The effect of age and the H1c MAPT haplotype on MAPT expression in human brain.
Jesse B G Hayesmoore, Nicholas J Bray, William C Cross, Michael J Owen, Michael C O'Donovan

Neurobiol Aging· October 2009

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