Ann E. Davidson

Moorfields Eye Hospital NHS Foundation Trust — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index1.6kcitations40works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(12), Cardiomyopathy and Myosin Studies(10), Neurogenetic and Muscular Disorders Research(8), CRISPR and Genetic Engineering(6), Animal Genetics and Reproduction(5)

Publications40 total

Influence of inflammatory and metabolic factors on keratoconus risk: a causal inference analysis
Eye·2026Open Access
Integrated monogenic and polygenic risk predicts disease progression in Fuchs endothelial corneal dystrophy
2026Open Access
O6 The UK platform for nucleic acid therapies – target selection guidelines
2026Open Access
A Rapid <scp>F0 CRISPR</scp> Screen in Zebrafish to Identify Regulator Genes of Neuronal Development in the Enteric Nervous System
Neurogastroenterology & Motility·2025Open Access
A New Transgenic Tool to Study the Ret Signaling Pathway in the Enteric Nervous System
International Journal of Molecular Sciences·2022· 9 citedOpen Access
A rapid F0 CRISPR screen in zebrafish to identify regulators of neuronal development in the enteric nervous system
2021· 7 citedOpen Access
561 A RAPID CRISPR/CAS9 GENOME EDITING SCREEN TO IDENTIFY NEW REGULATORS OF NEURONAL DIFFERENTIATION AND SPECIFICATION IN THE ENTERIC NERVOUS SYSTEM
Gastroenterology·2020
Inhibition of PIK3C2B as a treatment strategy for myotubular myopathy
Neuromuscular Disorders·2016
PIK3C2B inhibition improves function and prolongs survival in myotubular myopathy animal models
Journal of Clinical Investigation·2016· 101 citedOpen Access
Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye
Journal of Visualized Experiments·2015· 21 citedOpen Access
Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye
Journal of Visualized Experiments·2015· 4 cited
Brittle Cornea Syndrome ZNF469 Mutation Carrier Phenotype and Segregation Analysis of Rare ZNF469 Variants in Familial Keratoconus
Investigative Ophthalmology & Visual Science·2015· 45 cited
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy
Journal of Clinical Investigation·2015· 31 citedOpen Access
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy
Journal of Clinical Investigation·2014· 200 citedOpen Access
G.P.46
Neuromuscular Disorders·2014
Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy
Human Molecular Genetics·2014· 67 citedOpen Access
Supplementary Material for: Detailed Assessment of Renal Function in a Proband with Harboyan Syndrome Caused by a Novel Homozygous <b><i>SLC4A11 </i></b>Nonsense Mutation
Figshare·2014Open Access
Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations
Journal of Visualized Experiments·2013· 7 cited
Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations
Journal of Visualized Experiments·2013· 21 citedOpen Access
P9.17 Function of CCDC78 in muscle development and muscle disease
Neuromuscular Disorders·2013
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Frequent Co-authors

James J. Dowling(16), Stephen C. Ekker(6), Eric J. Horstick(5), A. E. Stuart(5), Darius Balčiūnas(4), Spencer Hermanson(4), Sridhar Sivasubbu(4), Xingli Li(4), Eva L. Feldman(4), Elizabeth M. Gibbs(4), William R. Telfer(3), Alan H. Beggs(3), Jonathan Volpatti(3), Julia Ganz(3), Nora R. W. Straquadine(3), Perry B. Hackett(2), Michaela Yuen(2), Sarah A. Sandaradura(2), Alla S. Kostyukova(2), Natalia Moroz(2)