Dimitar Serbezov

Sofia, 1000, Bulgaria

Last Updated: 09/26/2026

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Found 8 publications

RETRACTED: Toncheva et al. Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data. Genes 2023, 14, 727.

RETRACTED: Toncheva et al. Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data. Genes 2023, 14, 727.

Journal: Genes
Published: July 08, 2025

Rare Pathogenic Variants in Pooled Whole-Exome Sequencing Data Suggest Hyperammonemia as a Possible Cause of Dementia Not Classified as Alzheimer's Disease or Frontotemporal Dementia.

Rare Pathogenic Variants in Pooled Whole-Exome Sequencing Data Suggest Hyperammonemia as a Possible Cause of Dementia Not Classified as Alzheimer's Disease or Frontotemporal Dementia.

Journal: Genes
Published: March 13, 2024

RETRACTED: Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data.

RETRACTED: Pathogenic Variants Associated with Rare Monogenic Diseases Established in Ancient Neanderthal and Denisovan Genome-Wide Data.

Journal: Genes
Published: February 15, 2023

Spatio-temporal dynamics of pathogenic variants associated with monogenic disorders reconstructed with ancient DNA.

Spatio-temporal dynamics of pathogenic variants associated with monogenic disorders reconstructed with ancient DNA.

Journal: PloS one
Published: November 09, 2021

Ancient mitochondrial DNA pathogenic variants putatively associated with mitochondrial disease.

Ancient mitochondrial DNA pathogenic variants putatively associated with mitochondrial disease.

Journal: PloS one
Published: May 09, 2020

Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations.

Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations.

Journal: Technology in cancer research & treatment
Published: April 03, 2020

Clinical impact of copy number variation changes in bladder cancer samples.

Clinical impact of copy number variation changes in bladder cancer samples.

Journal: Experimental and therapeutic medicine
Published: November 30, 2019

NGS nominated CELA1, HSPG2, and KCNK5 as candidate genes for predisposition to Balkan endemic nephropathy.

NGS nominated CELA1, HSPG2, and KCNK5 as candidate genes for predisposition to Balkan endemic nephropathy.

Journal: BioMed research international
Published: February 19, 2014
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Last Updated: 09/26/2026