Gabor Zsurka

Bonn, NW, Germany

Last Updated: 09/26/2026

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Found 28 publications

Pyruvate dehydrogenase autoantibodies in autoantibody-negative patients with seizures are associated with reduced pyruvate dehydrogenase activity.

Pyruvate dehydrogenase autoantibodies in autoantibody-negative patients with seizures are associated with reduced pyruvate dehydrogenase activity.

Journal: Epilepsia

Published: January 29, 2026

Single-cell multi-omic analysis of mitochondrial mutational mosaicism and dynamics.

Single-cell multi-omic analysis of mitochondrial mutational mosaicism and dynamics.

Journal: Nature communications

Published: May 10, 2025

Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularization.

Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularization.

Journal: Nucleic acids research

Published: February 05, 2025

The Fate of Oxidative Strand Breaks in Mitochondrial DNA.

The Fate of Oxidative Strand Breaks in Mitochondrial DNA.

Journal: Antioxidants (Basel, Switzerland)

Published: March 31, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Journal: medRxiv : the preprint server for health sciences

Published: March 03, 2023

Functional Assessment of Mitochondrial DNA Maintenance by Depletion and Repopulation Using 2',3'-Dideoxycytidine in Cultured Cells.

Functional Assessment of Mitochondrial DNA Maintenance by Depletion and Repopulation Using 2',3'-Dideoxycytidine in Cultured Cells.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: February 22, 2023

Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype.

Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype.

Journal: Cells

Published: November 22, 2022

Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits.

Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits.

Journal: Genes

Published: December 22, 2021

Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome.

Novel Pathogenic Sequence Variation m.5789T>C Causes NARP Syndrome and Promotes Formation of Deletions of the Mitochondrial Genome.

Journal: Neurology. Genetics

Published: December 08, 2021

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy.

Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy.

Journal: Brain : a journal of neurology

Published: August 18, 2021

Molecular and Functional Effects of Loss of Cytochrome c Oxidase Subunit 8A.

Molecular and Functional Effects of Loss of Cytochrome c Oxidase Subunit 8A.

Journal: Biochemistry. Biokhimiia

Published: March 11, 2021

Replication fork rescue in mammalian mitochondria.

Replication fork rescue in mammalian mitochondria.

Journal: Scientific reports

Published: February 14, 2019

Showing 1-12 of 28

Last Updated: 09/26/2026