Kerstin Hallmann

Bonn, NW, Germany

Last Updated: 09/26/2026

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Found 13 publications

Acute effects of anti-seizure medications on network level dynamics: A systematic comparison using multielectrode arrays.

Acute effects of anti-seizure medications on network level dynamics: A systematic comparison using multielectrode arrays.

Journal: Epilepsia

Published: April 14, 2026

Complexity of Inheritance of Pathogenic Mutations Associated with Epilepsy in Consanguine Families from Pakistan.

Complexity of Inheritance of Pathogenic Mutations Associated with Epilepsy in Consanguine Families from Pakistan.

Journal: Genes

Published: December 29, 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

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

Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply.

Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply.

Journal: The Journal of biological chemistry

Published: November 14, 2019

Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.

Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy.

Journal: Epilepsia open

Published: June 23, 2017

Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease.

Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease.

Journal: American journal of human genetics

Published: January 12, 2016

Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy.

Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy.

Journal: Brain : a journal of neurology

Published: July 14, 2015

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Journal: Epilepsy research

Published: November 17, 2014

A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy.

A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy.

Journal: Neurology

Published: November 02, 2014

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

Journal: Brain : a journal of neurology

Published: September 10, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026