Slavé Petrovski

AstraZeneca (United Kingdom) — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

66h-index24.4kcitations234works11.42yr avg
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Research Topics

Genomics and Rare Diseases(99), Genetic Associations and Epidemiology(50), Genetics and Neurodevelopmental Disorders(36), Epilepsy research and treatment(28), Genomic variations and chromosomal abnormalities(22)

Publications213 total

Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance
Molecular Metabolism·2025Open Access
A continuum of inherited telomere dysfunction links TERT rare variants to age-related diseases
Blood·2025Open Access
Whole-genome sequencing of 490,640 UK Biobank participants
Nature·2025· 47 citedOpen Access
Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty
Nature Aging·2025· 2 citedOpen Access
Population-scale sequencing resolves correlates and determinants of latent Epstein-Barr Virus infection
2025· 1 citedOpen Access
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity
2025· 3 citedOpen Access
Mitochondrial metabolism sustains DNMT3A-R882-mutant clonal haematopoiesis
Nature·2025· 25 citedOpen Access
Diverse ancestral representation improves genetic intolerance metrics
Nature Communications·2025· 2 citedOpen Access
Identification of plasma proteomic markers underlying polygenic risk of type 2 diabetes and related comorbidities
Nature Communications·2025· 15 citedOpen Access
Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson’s disease
Cell Reports·2025· 11 citedOpen Access
The contribution of genetic determinants of blood gene expression and splicing to molecular phenotypes and health outcomes
Nature Genetics·2025· 15 citedOpen Access
Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genes
The American Journal of Human Genetics·2025· 6 citedOpen Access
Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases
Nature Communications·2025· 7 citedOpen Access
Narcolepsy as a potential risk factor for Schizophrenia
Translational Psychiatry·2025· 3 citedOpen Access
Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis
Nature Genetics·2025· 8 citedOpen Access
P027: Genetic landscape of ALPL and other genes impacting alkaline phosphatase variation in the UK Biobank
Genetics in Medicine Open·2025Open Access
Novel loci and biomedical consequences of iron homoeostasis variation
Communications Biology·2024· 8 citedOpen Access
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
Nature Communications·2024· 7 citedOpen Access
Diverse ancestral representation improves genetic intolerance metrics
2024Open Access
Causes and Consequences of Clonal Hematopoiesis with Unknown Drivers in 409,553 Whole-Genome Sequenced UK Biobank Participants
Blood·2024· 1 cited
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Frequent Co-authors

David B. Goldstein(22), Quanli Wang(11), Andrew S. Allen(8), Ingrid E. Scheffer(7), Samuel F. Berkovic(7), Erika Kvikstad(6), Erin L. Heinzen(6), Zhong Ren(6), Ryan S. Dhindsa(6), Heiko Runz(6), Paul Nioi(5), Erin N. Smith(5), Sándor Szalma(5), Lyndon J. Mitnaul(5), Joseph D. Szustakowski(5), Christopher D. Whelan(5), Sitharthan Kamalakaran(5), Carolina Haefliger(5), David B. Goldstein(5), J. Wade Davis(5)