Prof Slave Petrovski
Honorary (Professorial Fellow)
Department of Medicine
214 Scholarly works
6 Projects
HIGHLIGHTS
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
Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant
DOI: 10.1001/jamanetworkopen.2026.14522026
Journal article
GWAS and Replication Analysis of Apparent Treatment-Resistant Hypertension.
DOI: 10.1161/HYPERTENSIONAHA.125.257192018
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
Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance
DOI: 10.1016/j.molmet.2025.1023012025
Journal article
Identification of plasma proteomic markers underlying polygenic risk of type 2 diabetes and related comorbidities
DOI: 10.1038/s41467-025-56695-z2025
Journal article
Narcolepsy as a potential risk factor for Schizophrenia
DOI: 10.1038/s41398-025-03259-w2025
Journal article
Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease
DOI: 10.1186/s13024-025-00830-32025
Journal article
Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases
DOI: 10.1038/s41467-025-56944-12025
Journal article
A continuum of inherited telomere dysfunction links TERT rare variants to age-related diseases
DOI: 10.1182/blood-2025-7492025
Journal article
Recessive FANCM cancer syndrome with high cancer risks, chemotherapy toxicity, chromosome fragility, and gonadal failure
DOI: 10.1016/j.gim.2025.101521
RECENT PROJECTS
2017
Research Grant
Detection of Somatic Mutations in Sporadic Epilepsies