Slave Petrovski

BioPharmaceuticals R&D
Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 136 publications

A proteome-wide association study of cardiovascular diseases in 640,000 participants of multiple ancestries.

A proteome-wide association study of cardiovascular diseases in 640,000 participants of multiple ancestries.

Journal: medRxiv : the preprint server for health sciences

Published: August 20, 2026

Atlas of glomerular disease-specific genetic effects on blood transcriptome.

Atlas of glomerular disease-specific genetic effects on blood transcriptome.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Author Correction: Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Author Correction: Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Journal: Nature

Published: March 31, 2026

Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant.

Precision Diagnosis in APOL1 Kidney Disease With the p.N264K M1 Protective Variant.

Journal: JAMA network open

Published: March 11, 2026

Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance.

Cross-species studies implicate the melanocortin 3 receptor more strongly in the control of pubertal development than energy balance.

Journal: Molecular metabolism

Published: September 19, 2025

Population-scale sequencing resolves correlates and determinants of latent Epstein-Barr Virus infection.

Population-scale sequencing resolves correlates and determinants of latent Epstein-Barr Virus infection.

Journal: bioRxiv : the preprint server for biology

Published: August 12, 2025

Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource.

Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource.

Journal: Nature

Published: July 31, 2025

Rare heterozygous missense variants in VSX2 are associated with retinal detachment.

Rare heterozygous missense variants in VSX2 are associated with retinal detachment.

Journal: PLoS genetics

Published: July 18, 2025

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Journal: Nature genetics

Published: June 08, 2025

Population-scale sequencing resolves determinants of persistent EBV DNA.

Population-scale sequencing resolves determinants of persistent EBV DNA.

Journal: Nature

Published: May 23, 2025

Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes.

Journal: Nature

Published: March 21, 2025

Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genes.

Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genes.

Journal: American journal of human genetics

Published: August 28, 2024

Showing 1-12 of 136

Last Updated: 09/26/2026