Kerstin Hallmann

3.0k total citations
20 papers, 596 citations indexed

About

Kerstin Hallmann is a scholar working on Molecular Biology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Kerstin Hallmann has authored 20 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Psychiatry and Mental health and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Kerstin Hallmann's work include Epilepsy research and treatment (10 papers), Ion channel regulation and function (7 papers) and Mitochondrial Function and Pathology (5 papers). Kerstin Hallmann is often cited by papers focused on Epilepsy research and treatment (10 papers), Ion channel regulation and function (7 papers) and Mitochondrial Function and Pathology (5 papers). Kerstin Hallmann collaborates with scholars based in Germany, United States and United Kingdom. Kerstin Hallmann's co-authors include Ortrud K. Steinlein, Armin Heils, Karsten Haug, Thomas Sander, Johannes Rebstock, Uwe Runge, Wolfram S. Kunz, Christian E. Elger, Gábor Zsurka and Hölger Thiele and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Brain.

In The Last Decade

Kerstin Hallmann

19 papers receiving 590 citations

Peers

Kerstin Hallmann
Bree Hodgson Australia
Maéva Langouët United States
Amanda Lindy United States
Dimira Tambunan United States
Tine Van Dyck Belgium
Evan E. Eichler United States
Bing-Mei Li China
Goryu Fukuma Japan
Simone C. Yendle Australia
Ippei Okada Japan
Bree Hodgson Australia
Kerstin Hallmann
Citations per year, relative to Kerstin Hallmann Kerstin Hallmann (= 1×) peers Bree Hodgson

Countries citing papers authored by Kerstin Hallmann

Since Specialization
Citations

This map shows the geographic impact of Kerstin Hallmann's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kerstin Hallmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kerstin Hallmann more than expected).

Fields of papers citing papers by Kerstin Hallmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerstin Hallmann. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kerstin Hallmann. The network helps show where Kerstin Hallmann may publish in the future.

Co-authorship network of co-authors of Kerstin Hallmann

This figure shows the co-authorship network connecting the top 25 collaborators of Kerstin Hallmann. A scholar is included among the top collaborators of Kerstin Hallmann based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kerstin Hallmann. Kerstin Hallmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kudin, Alexei P., Kerstin Hallmann, Viktoriya Peeva, et al.. (2025). Ligase 3 prevents oxidative strand break-induced mitochondrial DNA loss but is not essential for replicative circularization. Nucleic Acids Research. 53(19). 1 indexed citations
2.
Zsurka, Gábor, Kerstin Hallmann, Niels Hansen, et al.. (2023). Loss of the Immunomodulatory Transcription Factor BATF2 in Humans Is Associated with a Neurological Phenotype. Cells. 12(2). 227–227. 4 indexed citations
3.
Wrede, Randi von, Hans‐Jürgen Huppertz, Theodor Rüber, et al.. (2022). Large Phenotypic Variation of Individuals from a Family with a Novel ASPM Mutation Associated with Microcephaly, Epilepsy, and Behavioral and Cognitive Deficits. Genes. 13(3). 429–429. 1 indexed citations
4.
Szibor, Marten, Zemfira Gizatullina, Thomas Endres, et al.. (2020). Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply. Journal of Biological Chemistry. 295(14). 4383–4397. 46 indexed citations
5.
Hallmann, Kerstin. (2019). Professionalisierung in der performativ-künstlerischen Bildungsarbeit:Westphal, Kristin/Bogerts, Teresa/Uhl, Mareike/Sauer, Ilona (Hg.): Zwischen Kunst und Bildung. Theorie, Vermittlung, Forschung in der zeitgenössischen Theater-, Tanz- und Performancekunst. Oberhausen (Athena) 2018.. Multilingual Matters (Channel View Publications).
6.
Becker, Felicitas, Christopher A. Reid, Kerstin Hallmann, et al.. (2017). Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy. Epilepsia Open. 2(3). 334–342. 21 indexed citations
7.
Lenk, Guy M., Krystyna Szymańska, Grażyna Dębska–Vielhaber, et al.. (2016). Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease. The American Journal of Human Genetics. 99(1). 188–194. 41 indexed citations
8.
Becker, Felicitas, Julian Schubert, Sarah Weckhuysen, et al.. (2015). Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?. Epilepsy Research. 114. 47–51. 5 indexed citations
9.
Hallmann, Kerstin, Alexei P. Kudin, Gábor Zsurka, et al.. (2015). Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy. Brain. 139(2). 338–345. 47 indexed citations
10.
Hallmann, Kerstin, Gábor Zsurka, Janbernd Kirschner, et al.. (2014). A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy. Neurology. 83(23). 2183–2187. 52 indexed citations
11.
Zsurka, Gábor, Tatiana A. Kudina, Viktoriya Peeva, et al.. (2010). Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans. BMC Evolutionary Biology. 10(1). 270–270. 22 indexed citations
12.
Stewart, Joanna D., Kamil S. Sitarz, Rita Horváth, et al.. (2010). POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(3). 321–325. 26 indexed citations
13.
Haug, Karsten, Thomas Sander, Uwe Runge, et al.. (2002). A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions. Archives of Neurology. 59(7). 1137–1137. 215 indexed citations
14.
Haug, Karsten, Kerstin Hallmann, Johannes Rebstock, et al.. (2001). The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy. Epilepsy Research. 47(3). 243–246. 29 indexed citations
15.
Haug, Karsten, Kerstin Hallmann, Steve Horvath, et al.. (2000). No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy. Epilepsy Research. 42(1). 57–62. 8 indexed citations
16.
Haug, Karsten, Thomas Sander, Kerstin Hallmann, et al.. (2000). The voltage-gated sodium channel β2-subunit gene and idiopathic generalized epilepsy. Neuroreport. 11(12). 2687–2689. 15 indexed citations
17.
Biervert, Christian, et al.. (2000). A KCNQ2 Splice Site Mutation Causing Benign Neonatal Convulsions in a Scottish Family. Neuropediatrics. 31(1). 9–12. 33 indexed citations
18.
Kremerskothen, Joachim, Kerstin Hallmann, T. Sander, et al.. (2000). Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy. Molecular and Cellular Probes. 14(4). 255–260. 11 indexed citations
19.
Hallmann, Kerstin, Martina Durner, Thomas Sander, & Ortrud K. Steinlein. (2000). Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy. American Journal of Medical Genetics. 96(1). 8–11. 14 indexed citations
20.
Haug, Karsten, Thomas Sander, Kerstin Hallmann, et al.. (2000). Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy. Epilepsy Research. 39(2). 127–132. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Bree Hodgson Breakdown of academic impact, for papers by Maéva Langouët Breakdown of academic impact, for papers by Amanda Lindy Breakdown of academic impact, for papers by Dimira Tambunan Breakdown of academic impact, for papers by Tine Van Dyck Breakdown of academic impact, for papers by Evan E. Eichler Breakdown of academic impact, for papers by Bing-Mei Li Breakdown of academic impact, for papers by Goryu Fukuma Breakdown of academic impact, for papers by Simone C. Yendle Breakdown of academic impact, for papers by Ippei Okada
Rankless by CCL
2026