Victoria L. Harvey

University College London Hospitals NHS Foundation Trust — United Kingdom

Neuroscience · Life Sciences

63h-index18.7kcitations1.6kworks2.92yr avg
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Research Topics

Neuroscience and Neuropharmacology Research(109), Ion channel regulation and function(46), Receptor Mechanisms and Signaling(40), Pharmacological Effects and Toxicity Studies(39), Epilepsy research and treatment(36)

Publications1.3k total

Clinical–Radiological Spectrum of Cerebral Amyloid Angiopathy‐Related Inflammation
Annals of Neurology·2025· 2 citedOpen Access
Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study
Annals of Neurology·2025Open Access
Propolis compound inhibits profibrotic TGF-β1/SMAD signalling in human fibroblasts
Scientific Reports·2025· 3 citedOpen Access
Review for "Phosphoinositide- and Collybistin-Dependent Synaptic Clustering of Gephyrin"
2025
Pathogenic ultra-rare variants in <i>SLC6A1, SLC6A11, GAD1 and GAD2</i> are new &amp; recurrent GABAergic loci for GGE syndromes
2025Open Access
Milestone Review: Unlocking the Proteomics of Glycine Receptor Complexes
Journal of Neurochemistry·2025· 3 citedOpen Access
Author response for "Milestone Review: Unlocking the Proteomics of Glycine Receptor Complexes"
2025
The emerging role of glycine receptor α2 subunit defects in neurodevelopmental disorders
Frontiers in Molecular Neuroscience·2025Open Access
Inflammation in Cerebral Amyloid Angiopathy‐Related Transient Focal Neurological Episodes
Annals of Neurology·2025· 12 citedOpen Access
Pathogenic Ultra-Rare Variants in SLC6A1, SLC6A11, GAD1 and GAD2 are New &amp;amp; Recurrent GABAergic Loci for Genetic Generalised Epilepsy
SSRN Electronic Journal·2025Open Access
Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia
Genetics in Medicine Open·2024· 2 citedOpen Access
Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability
Genetics in Medicine·2024· 2 citedOpen Access
Sulcal Hyperintensity as an Early Imaging Finding in Cerebral Amyloid Angiopathy–Related Inflammation
Neurology·2024· 16 citedOpen Access
Assessment of the in vitro acaricidal activity of Bravecto® (fluralaner) and a proposed orange oil-based formulation vehicle for the treatment of Sarcoptes scabiei
Parasites & Vectors·2024· 1 citedOpen Access
Dual Role of Dysfunctional Asc-1 Transporter in Distinct Human Pathologies, Human Startle Disease, and Developmental Delay
eNeuro·2023· 8 citedOpen Access
Dopamine-mediated striatal activity and function is enhanced in GlyRα2 knockout animals
iScience·2023· 8 citedOpen Access
Developing carbon dioxide removal policy and anticipatory perspectives in the United Kingdom and United States
Energy Research & Social Science·2023· 16 citedOpen Access
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder
Genetics in Medicine·2023· 7 citedOpen Access
Pharmacokinetic and pharmacodynamic considerations for treating sarcoptic mange with cross-relevance to Australian wildlife
International Journal for Parasitology Drugs and Drug Resistance·2023· 10 citedOpen Access
Drug Resistance
2023· 1 cited
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Frequent Co-authors

Kirsten Harvey(20), Trevor G. Smart(8), Mark I. Rees(7), Maya Topf(6), Nicholas Wood(5), Heinrich Betz(5), Emma Deas(5), Ulrike Müller(4), Sonia Gandhi(4), Bodo Laube(4), Brian R. Pearce(4), Patrick M. Abou‐Sleiman(3), Miratul M. K. Muqit(3), Daniel G. Healy(3), David S. Latchman(3), Andrew J. Lees(3), Heinz Wässle(3), Céline Fuchs(3), Eloisa Carta(3), Ian Duguid(3)