David Arthur Stroud

33PUBLICATIONS
224CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Exercise physiologyGene mappingElectrochemical energy storage and conversion
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Publications (33)

|Jun 09, 2026
Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.

|May 11, 2026
Unraveling a Diagnostic Enigma: A TECPR2 Case Solved Through Multi-Omic Genomics.

|Dec 01, 2025
Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in men.

J Botella, E Perri, N J Caruana

|Oct 22, 2025
Functional Characterization of a Novel GPC3 Missense Variant in Simpson-Golabi-Behmel Syndrome.

Teresa Zhao, Kirsten Allan, Juliet Taylor

|Aug 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders.

Sara M Fielder, Marisa W Friederich, Daniella H Hock

|Aug 15, 2025
Complex II assembly drives metabolic adaptation to OXPHOS dysfunction.

Roopasingam Kugapreethan, Sheik Nadeem Elahee Doomun, Joanna Sacharz

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Frequent Collaborators

10 joint publications

David R Thorburn

9 joint publications

John Christodoulou

7 joint publications

Daniella Helena Hock

6 joint publications

Michael T Ryan