Prof Slave Petrovski
Honorary (Professorial Fellow)
Department of Medicine
222 Scholarly works
6 Projects
HIGHLIGHTS
2026
Journal article
Genetic liability to psoriasis predicts severe disease outcomes
DOI: 10.1186/s13073-025-01561-22026
Journal article
Evaluation of Genetics in the Association Between Cardiorespiratory Fitness and Health: Insights from a Genome-Wide Polygenic Score for Cardiorespiratory Fitness in the FinnGen and HUNT cohorts
DOI: 10.1111/sms.702912026
Journal article
Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes
DOI: 10.1038/s41586-025-10087-x2018
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
RECENT SCHOLARLY WORKS
2026
Journal article
Quantifying risk modifiers of hereditary hemochromatosis using genomic and electronic health record data
DOI: 10.1016/j.jhepr.2026.1017742026
Journal article
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity
DOI: 10.1038/s41588-026-02553-72026
Journal article
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant
DOI: 10.1001/jamanetworkopen.2026.14522026
Journal article
Population-scale sequencing resolves determinants of persistent EBV DNA
DOI: 10.1038/s41586-025-10020-22026
Journal article
Transcription Factor Binding and Individual Genetic Risk of Valproate Teratogenicity
DOI: 10.1212/WNL.00000000002145702026
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.2025.1023012026
Journal article
Rare Heterozygous Missense Variants in VSX2 are Associated with Retinal Detachment
DOI: 10.1371/journal.pgen.1012027
RECENT PROJECTS
2017
Research Grant
Detection of Somatic Mutations in Sporadic Epilepsies