Charlotte Hooper

Medicine · Health Sciences

10h-index698citations28works1.82yr avg
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Research Topics

Cardiomyopathy and Myosin Studies(20), Cardiovascular Effects of Exercise(5), Muscle Physiology and Disorders(4), Cardiovascular Function and Risk Factors(2), Genetic Neurodegenerative Diseases(2)

Publications28 total

Plasma Extracellular Vesicle Modulate Immune Cell Transcriptional Responses Following Acute Myocardial Infarction
iScience·2026Open Access
Filamin C dimerisation is regulated by HSPB7
Nature Communications·2025· 4 citedOpen Access
Why Do Emergency Medical Service Employees (Not) Seek Organizational Help for Mental Health Support?: A Systematic Review
International Journal of Environmental Research and Public Health·2025· 3 citedOpen Access
An ALPK3 truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamten
Scientific Reports·2025· 3 citedOpen Access
Modulating TTN gene expression in human iPSC-CMs to investigate mechanisms and therapies in TTN-associated dilated cardiomyopathy
European Heart Journal·2024Open Access
An <i>ALPK3</i> truncation variant causing autosomal dominant hypertrophic cardiomyopathy is partially rescued by mavacamten
2024· 1 cited
Why is early-onset atrial fibrillation uncommon in patients with Duchenne muscular dystrophy? Insights from the <i>mdx</i> mouse
Cardiovascular Research·2024· 1 citedOpen Access
Cardiac stress leads to regulation of Filamin C dimerisation via an ancient phosphorylation-modulated interaction with HSPB7
2024· 2 citedOpen Access
Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2
Cells·2023· 17 citedOpen Access
Functional analysis of a FLNC missense variant associated with hypertrophic cardiomyopathy
Journal of Molecular and Cellular Cardiology·2022· 1 cited
Small change, big impact: A Z-disc missense genetic variant causes dramatic morphological changes in the embryonic heart
Journal of Molecular and Cellular Cardiology·2022
Crucial functions of alpha-actinin 2 in the embryonic heart
Cardiovascular Research·2022
Exploring the contribution of mechano-sensing to cardiomyopathy
Cardiovascular Research·2022Open Access
BS30 Crucial functions of alpha-actinin2 in the embryonic heart
2022Open Access
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant
Basic Research in Cardiology·2021· 29 citedOpen Access
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion
Journal of Molecular and Cellular Cardiology·2018· 42 citedOpen Access
RNAseq reveals mechanisms of cardiomyopathy in Mlp-C58G knock-in mice
Journal of Molecular and Cellular Cardiology·2018
Insights into disease mechanisms of cardiomyopathy in the presence of the CSRP3 C58G mutation
2017
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction
Circulation Cardiovascular Genetics·2016· 80 citedOpen Access
MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy
Nature Communications·2016· 78 citedOpen Access
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Frequent Co-authors

Katja Gehmlich(16), Hugh Watkins(12), Elisabeth Ehler(9), Sophie Broadway‐Stringer(8), Benjamin Davies(7), Julia Beglov(6), Amar J. Azad(6), Matt Kelly(5), Charles Redwood(5), Jacinta I. Kalisch‐Smith(5), Duncan B. Sparrow(5), Mathias Gautel(4), Samuel Y. Boateng(4), Violetta Steeples(4), Gillian Douglas(4), Elizabeth Ormondroyd(3), Kate Thomson(3), Mehroz Ehsan(3), Giulia Poloni(3), Lisa Leinhos(3)