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Email

nikeisha.caruana@unimelb.edu.au

Credentials


Position
Research Fellow (Bioinformatics)
Department of Biochemistry and Pharmacology
Education
PhD
La Trobe University
Bachelors Degree (Honours)
La Trobe University
ORCID

0000-0002-0817-1686

Dr Nikeisha Caruana

Research Fellow (Bioinformatics)
Department of Biochemistry and Pharmacology

22 Scholarly works
1 Projects

HIGHLIGHTS

  • 2026

    Journal article

    Sprint interval exercise disrupts mitochondrial ultrastructure driving a unique mitochondrial stress response and remodelling in men
    DOI: 10.1038/s41467-025-66625-8
  • 2026

    Journal article

    Clinical proteomics in variant classification: are we there yet?
    DOI: 10.1016/j.pathol.2026.01.227
  • 2026

    Journal article

    Exercise induces temporal but not sex-specific transcriptomic changes in healthy human skeletal muscle
    DOI: 10.7600/jspfsm.75.73
  • 2025

    Journal article

    Untargeted proteomics enables ultra-rapid variant prioritisation in mitochondrial and other rare diseases
    DOI: 10.1186/s13073-025-01467-z
  • 2024

    Journal article

    Fibre-specific mitochondrial protein abundance is linked to resting and post-training mitochondrial content in the muscle of men
    DOI: 10.1038/s41467-024-50632-2
  • 2024

    Journal article

    ACAD9 treatment with bezafibrate and nicotinamide riboside temporarily stabilizes cardiomyopathy and lactic acidosis
    DOI: 10.1016/j.mito.2024.101905
  • 2023

    Research grants (other domestic)

    High Performance Computer Workstations
Nikeisha Caruana

RECENT SCHOLARLY WORKS

  • 2024

    Journal article

    Resistance-only and concurrent exercise induce similar myofibrillar protein synthesis rates and associated molecular responses in moderately active men before and after training
    DOI: 10.1096/fj.202302024R
  • 2024

    Journal article

    Exercise training and changes in skeletal muscle mitochondrial proteins: from blots to “omics”
    DOI: 10.1080/10409238.2024.2383408
  • 2024

    Journal article

    Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts
    DOI: 10.1016/j.rare.2024.100040
  • 2023

    Journal article

    TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease
    DOI: 10.1038/s41467-023-36277-7

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