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Contact


Email

slavep@unimelb.edu.au

Credentials


Position
Honorary (Professorial Fellow)
Department of Medicine
Education
PhD
University of Melbourne
Bachelors Degree (Honours)
University of Melbourne
Bachelors Degree
University of Melbourne
ORCID

0000-0002-1527-961X

Prof Slave Petrovski

Honorary (Professorial Fellow)
Department of Medicine

221 Scholarly works
6 Projects

HIGHLIGHTS

  • 2026

    Journal article

    Genetic liability to psoriasis predicts severe disease outcomes
    DOI: 10.1186/s13073-025-01561-2
  • 2026

    Journal article

    Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes
    DOI: 10.1038/s41586-025-10087-x
  • 2026

    Journal article

    Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity
    DOI: 10.1038/s41588-026-02553-7
  • 2018

    Research Grant

    Clinical Utility and Cost-Effectivenmess of Genome Sequencing for Refractory Epilepsy in Children and Adults: A Multicentre Randomised Controlled Trial
  • 2017

    Research Grant

    Detection of Somatic Mutations in Sporadic Epilepsies
  • 2017

    Research Grant

    Integrating Population Genetics, in Silico and Functional Data to Enable Precision Medicine in the Epilepsies
  • 2016

    Journal article

    De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies
    DOI: 10.1016/j.ajhg.2016.06.003
Slave Petrovski

Latest Honours,
Awards and Fellowships


2012
NHMRC Fellowship (NHMRCF)
2011
Epilepsy Society of Australia
2011
AES Grass Foundation Young Investigator Award
2009
Student Travel Grant Victorian Life Sciences Computation Initiative

RECENT SCHOLARLY WORKS

  • 2026

    Journal article

    Quantifying risk modifiers of hereditary hemochromatosis using genomic and electronic health record data
    DOI: 10.1016/j.jhepr.2026.101774
  • 2026

    Journal article

    Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant
    DOI: 10.1001/jamanetworkopen.2026.1452
  • 2026

    Journal article

    Population-scale sequencing resolves determinants of persistent EBV DNA
    DOI: 10.1038/s41586-025-10020-2
  • 2026

    Journal article

    Transcription Factor Binding and Individual Genetic Risk of Valproate Teratogenicity
    DOI: 10.1212/WNL.0000000000214570
  • 2026

    Journal article

    Rare heterozygous missense variants in VSX2 are associated with retinal detachment
    DOI: 10.1371/journal.pgen.1012027
  • 2026

    Journal article

    Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance
    DOI: 10.1016/j.molmet.2025.102301
  • 2025

    Journal article

    GWAS and Replication Analysis of Apparent Treatment-Resistant Hypertension
    DOI: 10.1161/HYPERTENSIONAHA.125.25719

RECENT PROJECTS

  • 2017

    Research Grant

    Detection of Somatic Mutations in Sporadic Epilepsies

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