A/Prof David Stroud
Associate Professor, Biochemistry & Pharmacology
Department of Biochemistry and Pharmacology
161 Scholarly works
20 Projects
HIGHLIGHTS
2026
Journal article
Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in men
DOI: 10.1038/s41467-025-66625-82026
Journal article
Unraveling a Diagnostic Enigma: A TECPR2 Case Solved Through Multi-Omic Genomics
DOI: 10.1002/ajmg.a.701912026
Journal article
Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval
DOI: 10.1111/cge.702132026
Research grants (other domestic)
Orbitrap Exploris 240 Mass Spectrometer and Vanquish Neo UHPLC
2022
Research grants (ARC, NHMRC, MRFF)
RDMassSpec: Mass-Spectrometry Based Functional Genomics Platform for Solving Rare Genetic Disorders
2022
Research grants (ARC, NHMRC, MRFF)
Developing a Multi-Omics Platform for the Diagnosis of Mitochondrial Disease
2021
Journal article
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemias
DOI: 10.1182/blood.2020010167
RECENT SCHOLARLY WORKS
2026
Journal article
Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy
DOI: 10.1002/ana.782682026
Journal article
ASAP-ID: Proximity Labelling With Small Tags
DOI: 10.1016/j.mcpro.2026.1016162026
Journal article
NAXD Deficiency: Heterogeneous Phenotypes and Positive Response to Niacin Treatment
DOI: 10.1002/jimd.702172026
Journal article
Bi-allelic variants in NDUFA5 cause a mitochondriopathy with complex I deficiency
DOI: 10.1016/j.ajhg.2026.03.0032026
Journal article
Antenatal Presentation of MRPS22-Related Mitochondrial Disease Confirmed With Rapid Proteomics
DOI: 10.1002/jmd2.700922026
Journal article
Functional Characterization of a Novel GPC3 Missense Variant in Simpson–Golabi–Behmel Syndrome
DOI: 10.1002/ajmg.a.642872026
Journal article
Clinical proteomics in variant classification: are we there yet?
DOI: 10.1016/j.pathol.2026.01.227
RECENT PROJECTS
2026
Research grants (ARC, NHMRC, MRFF)
Unravelling Mitochondrial ATAD3 as an Underappreciated Cause of Rare Disease