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Maria E. O'Hanlon

Observed names: Maria E. O’Hanlon, Maria O'Hanlon, Maria O’Hanlon
Institution: The Lily Foundation
ORCID: 0000-0001-8524-4781
Observed ORCID: 0000-0001-8524-4781
OpenAlex ID: A5044019484
Mitochondrial electron transport chain defects modify Parkinson's disease phenotypes in a Drosophila model
2022 · Maria E. O'Hanlon, Clare Tweedy, et al. · Neurobiology of Disease · 13
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2000–2025: Emerging therapies in primary mitochondrial disease: A structured review, horizon scan, and roadmap for the future
2026 · Amel Karaa, Maria Isabel G. Lopez Sanchez, et al. · Therapeutic Advances in Rare Disease
The Lily Foundation: supporting patients, raising awareness and funding research into mitochondrial diseases
2025 · Liz Curtis, Maria E. O'Hanlon, et al. · FEBS Letters
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Mitochondrial electron transport chain defects modify Parkinson's disease phenotypes in a Drosophila model
2022 · Maria E. O'Hanlon, Clare Tweedy, et al. · Newcastle University ePrints (Newcastle Univesity)
Do genetic differences make some people more susceptible to COVID-19?
2021 · Vikki Rand, Maria O’Hanlon
Think Tank: Forty Neuroscientists Explore the Biological Roots of Human Experience edited by David J. Linden
2021 · Maria O'Hanlon · The Biochemist
Works count: 6
Citation count: 13
H-index: 1
I10-index: 1
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