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Simon A. S. Pope

Observed names: Pope, S, Pope, SA, Pope, Simon, S Pope, S. Pope, S.A.S. Pope, Simon A S Pope, Simon A. Pope, Simon A.S Pope, Simon A.S. Pope, Simon Alexander Samuel Pope, Simon Pope
Observed institutions: Hôpital Necker-Enfants Malades, University College London Hospitals NHS Foundation Trust, Azienda Ospedaliera Citta' della Salute e della Scienza di Torino, Pitié-Salpêtrière Hospital, National Hospital for Neurology and Neurosurgery, Institut des Maladies Génétiques Imagine, UCL Queen Square Institute of Neurology, Université Pierre-et-Marie-Curie, University College London
ORCID: 0000-0002-2991-3722
Observed ORCID: 0000-0002-2991-3722
OpenAlex ID: A5089377165
Dysregulation of glucose metabolism is an early event in sporadic Parkinson's disease
2013 · Laura Dunn, George FG. Allen, et al. · Neurobiology of Aging · 243
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
2016 · Esther Meyer, Deciphering Developmental Disorders Study, et al. · Nature Genetics · 241
Consequences of long-term oral administration of the mitochondria-targeted antioxidant MitoQ to wild-type mice
2009 · Sergio Rodriguez-Cuenca, Helena M. Cochemé, et al. · Free Radical Biology and Medicine · 218
The large-conductance Ca2+-activated K+ channel is essential for innate immunity
2004 · Jatinder Ahluwalia, Andrew Tinker, et al. · Nature · 206
Loss ofPLA2G6leads to elevated mitochondrial lipid peroxidation and mitochondrial dysfunction
2015 · Kerri J. Kinghorn, Jorge Iván Castillo-Quan, et al. · Brain · 197
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Consensus guideline for the diagnosis and treatment of tetrahydrobiopterin (BH4) deficiencies
2020 · on behalf of the International Working Group on Neurotransmitter related Disorders (iNTD), Thomas Opladen, et al. · Orphanet Journal of Rare Diseases · 162
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Oxidative stress and mitochondrial dysfunction in neurodegeneration; cardiolipin a critical target?
2008 · Simon Pope, John M. Land, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 154
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Missense dopamine transporter mutations associate with adult parkinsonism and ADHD
2014 · Freja H. Hansen, Tina Skjørringe, et al. · Journal of Clinical Investigation · 145
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy
2016 · Niklas Darin, Emma Reid, et al. · The American Journal of Human Genetics · 138
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Metabolic adaptation to chronic hypoxia in cardiac mitochondria
2012 · Lisa C. Heather, Mark A. Cole, et al. · Basic Research in Cardiology · 103
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy
2017 · Andreea Manole, Zane Jaunmuktane, et al. · Brain · 97
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Cerebral folate deficiency: Analytical tests and differential diagnosis
2019 · Simon Pope, Rafael Artuch, et al. · Journal of Inherited Metabolic Disease · 88
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PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation
2019 · Viorica Chelban, Matthew P. Wilson, et al. · Annals of Neurology · 75
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Glial cells are functionally impaired in juvenile neuronal ceroid lipofuscinosis and detrimental to neurons
2017 · Lotta Parviainen, Sybille Dihanich, et al. · Acta Neuropathologica Communications · 71
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Synthesis and analysis of conjugates of the major vitamin E metabolite, α-CEHC
2002 · Simon A.S Pope, Guillaume E Burtin, et al. · Free Radical Biology and Medicine · 69
Gene therapy restores dopamine transporter expression and ameliorates pathology in iPSC and mouse models of infantile parkinsonism
2021 · Joanne Ng, Serena Barral, et al. · Science Translational Medicine · 62
Critical role of complex III in the early metabolic changes following myocardial infarction
2009 · L. C. Heather, C. A. Carr, et al. · Cardiovascular Research · 61
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A New Method for the Analysis of Urinary Vitamin E Metabolites and the Tentative Identification of a Novel Group of Compounds
2000 · S.A.S. Pope, P.T. Clayton, et al. · Archives of Biochemistry and Biophysics · 47
DNAJC6 Mutations Disrupt Dopamine Homeostasis in Juvenile Parkinsonism‐Dystonia
2020 · Joanne Ng, Elisenda Cortès‐Saladelafont, et al. · Movement Disorders · 45
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Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?
2015 · Gabriella A. Horvath, Michelle Demos, et al. · Molecular Genetics and Metabolism · 45
A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy
2009 · Charlotte L. Alston, Monika Morak, et al. · Neuromuscular Disorders · 43
Astrocytes Protect Against Copper-Catalysed Loss of Extracellular Glutathione
2008 · Simon A. S. Pope, Rosemary Milton, et al. · Neurochemical Research · 42
Analysis of human cerebrospinal fluid monoamines and their cofactors by HPLC
2017 · Marta Batllori, Marta Molero-Luis, et al. · Nature Protocols · 38
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Glutamate induces release of glutathione from cultured rat astrocytes – a possible neuroprotective mechanism?
2008 · João Frade, Simon Pope, et al. · Journal of Neurochemistry · 38
Uncovering Genomic Causes of Co-Morbidity in Epilepsy: Gene-Driven Phenotypic Characterization of Rare Microdeletions
2011 · Dalia Kasperavičiūtė, Claudia B. Catarino, et al. · PLoS ONE · 31
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Works count: 84
Citation count: 2,935
H-index: 27
I10-index: 40
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