Amy K. Reeve

Wellcome Centre for Mitochondrial Research — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

33h-index6.5kcitations63works2.02yr avg
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Research Topics

Mitochondrial Function and Pathology(52), Metabolism and Genetic Disorders(35), Genetic Neurodegenerative Diseases(20), Parkinson's Disease Mechanisms and Treatments(12), ATP Synthase and ATPases Research(12)

Publications63 total

A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disorders
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease·2024· 3 citedOpen Access
3D Reconstruction of the Mitochondrial Network within the Neuronal Soma from SBF-SEM Volume Data
Methods in molecular biology·2024· 1 cited
A stagewise response to mitochondrial dysfunction in mitochondrial DNA maintenance disorders
2023Open Access
Parkinson’s disease neurons exhibit alterations in mitochondrial quality control proteins
npj Parkinson s Disease·2023· 40 citedOpen Access
Single Cell Analysis of Mitochondrial DNA Deletions
Methods in molecular biology·2023· 3 cited
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's Disease
Movement Disorders·2021· 30 citedOpen Access
3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampus
Cell Reports·2021· 128 citedOpen Access
Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease
npj Parkinson s Disease·2021· 30 citedOpen Access
3D Neuronal Mitochondrial Morphology in Axons, Dendrites, and Somata of the Aging Mouse Hippocampus
2021· 10 citedOpen Access
Hippocampal network hyperexcitability in young transgenic mice expressing human mutant alpha-synuclein
Neurobiology of Disease·2020· 24 citedOpen Access
Mitochondrial dysfunction impairs osteogenesis, increases osteoclast activity, and accelerates age related bone loss
Scientific Reports·2020· 159 citedOpen Access
Complex I reductions in the nucleus basalis of Meynert in Lewy body dementia: the role of Lewy bodies
Acta Neuropathologica Communications·2020· 22 citedOpen Access
The rise and rise of mitochondrial DNA mutations
Open Biology·2020· 208 citedOpen Access
Author response for "The rise and rise of mitochondrial DNA mutations"
2020
Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls
Acta Neuropathologica·2019· 16 citedOpen Access
Investigation of mitochondrial biogenesis defects in single substantia nigra neurons using post-mortem human tissues
Neurobiology of Disease·2019· 41 citedOpen Access
Understanding mitochondrial DNA maintenance disorders at the single muscle fibre level
Nucleic Acids Research·2019· 26 citedOpen Access
Mitochondrial Dysfunction in Parkinson’s Disease—Cause or Consequence?
Biology·2019· 254 citedOpen Access
Subcellular origin of mitochondrial DNA deletions in human skeletal muscle
Annals of Neurology·2018· 120 citedOpen Access
Clonally expanded mtDNA deletions in human skeletal muscle originate as a proliferative perinuclear niche
Neuromuscular Disorders·2018
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Frequent Co-authors

Douglass M. Turnbull(39), Robert W. Taylor(16), Kim J. Krishnan(13), Amy E. Vincent(10), Chun Chen(7), Nichola Z. Lax(7), Evelyn Jaros(6), Laura C. Greaves(6), Philippa D. Hepplewhite(6), Christopher M. Morris(5), Eve M. Simcox(5), G. Campbell(5), Alasdair Blain(5), Daniel Erskine(5), Richard Reynolds(4), Don Mahad(4), Anna L. Smith(4), Martin Picard(4), Karolina A. Rygiel(4), Andreas Bender(3)