Publications by authors named "Kerstin Hallmann"

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Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularization.
Genevieve Trombly, Afaf Milad Said, Alexei P Kudin, Kerstin Hallmann, Anano Kakabadze

Nucleic Acids Res· October 2025

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Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype.
Gábor Zsurka, Maximilian L T Appel, Maximilian Nastaly, Kerstin Hallmann, Niels Hansen

Cells· January 2023

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Large Phenotypic Variation of Individuals from a Family with a Novel Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits.
Randi von Wrede, Martin Schidlowski, Hans-Jürgen Huppertz, Theodor Rüber, Anja Ivo, Kerstin Hallmann

Genes (Basel)· February 2022

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Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply.
Marten Szibor, Zemfira Gizatullina, Timur Gainutdinov, Thomas Endres, Grazyna Debska-Vielhaber, Kerstin Hallmann

J Biol Chem· April 2020

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Functional variants in and may contribute to genetic generalized epilepsy.
Felicitas Becker, Christopher A Reid, Kerstin Hallmann, Han-Shen Tae, A Marie Phillips

Epilepsia Open· September 2017

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Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease.
Guy M Lenk, Krystyna Szymanska, Grazyna Debska-Vielhaber, Malgorzata Rydzanicz, Anna Walczak, Kerstin Hallmann

Am J Hum Genet· July 2016

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Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy.
Kerstin Hallmann, Alexei P Kudin, Gábor Zsurka, Cornelia Kornblum, Jens Reimann

Brain· February 2016

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Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
Felicitas Becker, Julian Schubert, Sarah Weckhuysen, Arvid Suls, Steffen Grüninger, Kerstin Hallmann

Epilepsy Res· August 2015

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A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy.
Kerstin Hallmann, Gábor Zsurka, Susanna Moskau-Hartmann, Janbernd Kirschner, Rudolf Korinthenberg

Neurology· December 2014

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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Dalia Kasperaviciute, Claudia B Catarino, Mar Matarin, Costin Leu, Jan Novy, Kerstin Hallmann

Brain· October 2013

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Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease.
Cornelia Kornblum, Thomas J Nicholls, Tobias B Haack, Susanne Schöler, Viktoriya Peeva, Kerstin Hallmann

Nat Genet· February 2013

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POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts.
Joanna D Stewart, Susanne Schoeler, Kamil S Sitarz, Rita Horvath, Kerstin Hallmann

Biochim Biophys Acta· March 2011

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Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans.
Gábor Zsurka, Tatiana Kudina, Viktoriya Peeva, Kerstin Hallmann, Christian E Elger

BMC Evol Biol· September 2010

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Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
Carolien G F de Kovel, Holger Trucks, Ingo Helbig, Heather C Mefford, Carl Baker, Kerstin Hallmann

Brain· January 2010

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CLCN2 variants in idiopathic generalized epilepsy.
Ailing Kleefuss-Lie, Waltraut Friedl, Sven Cichon, Karsten Haug, Maike Warnstedt, Kerstin Hallmann

Nat Genet· September 2009

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Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Karsten Haug, Maike Warnstedt, Alexi K Alekov, Thomas Sander, Alfredo Ramírez, Kerstin Hallmann

Nat Genet· September 2009

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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies.
Karsten Haug, Maike Warnstedt, Alexi K Alekov, Thomas Sander, Alfredo Ramírez, Kerstin Hallmann

Nat Genet· April 2003

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A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.
Colette Kananura, Karsten Haug, Thomas Sander, Uwe Runge, Wenli Gu, Kerstin Hallmann

Arch Neurol· July 2002

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