Katalin Štěrbová

3.4k total citations
21 papers, 506 citations indexed

About

Katalin Štěrbová is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Katalin Štěrbová has authored 21 papers receiving a total of 506 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Katalin Štěrbová's work include Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (4 papers). Katalin Štěrbová is often cited by papers focused on Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (4 papers). Katalin Štěrbová collaborates with scholars based in Czechia, United States and Belgium. Katalin Štěrbová's co-authors include Vladimı́r Komárek, Milan Paluš, Z Hrnčíř, Petra Laššuthová, Eva Syková, G Brožek, Markéta Vlčková, Z. Šimonová, Pavel Seeman and Jana Neupauerová and has published in prestigious journals such as Behavioural Brain Research, Brain and Language and Epilepsy Research.

In The Last Decade

Katalin Štěrbová

21 papers receiving 500 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Katalin Štěrbová Czechia 11 174 128 112 83 67 21 506
J. Meier Netherlands 20 510 2.9× 147 1.1× 136 1.2× 66 0.8× 45 0.7× 45 1.1k
Äthan Spiros United States 16 109 0.6× 36 0.3× 277 2.5× 32 0.4× 84 1.3× 37 789
Kang K. L. Liu United States 8 414 2.4× 15 0.1× 98 0.9× 51 0.6× 21 0.3× 11 749
Matthäus Staniek Germany 9 535 3.1× 25 0.2× 221 2.0× 235 2.8× 106 1.6× 9 1.1k
Kevin Aquino Australia 17 1.0k 5.9× 20 0.2× 79 0.7× 60 0.7× 40 0.6× 35 1.2k
I. S. Midzyanovskaya Russia 12 155 0.9× 25 0.2× 124 1.1× 22 0.3× 113 1.7× 32 427
Marie‐Therese Horstmann Germany 5 363 2.1× 18 0.1× 198 1.8× 65 0.8× 106 1.6× 6 621
Klaus Prank Germany 15 98 0.6× 49 0.4× 201 1.8× 63 0.8× 6 0.1× 39 845
Sarah F. Muldoon United States 13 703 4.0× 15 0.1× 124 1.1× 156 1.9× 82 1.2× 40 1.1k
Juan V. Sanchez‐Andrés Spain 17 243 1.4× 126 1.0× 464 4.1× 64 0.8× 10 0.1× 47 1.0k

Countries citing papers authored by Katalin Štěrbová

Since Specialization
Citations

This map shows the geographic impact of Katalin Štěrbová'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 Katalin Štěrbová with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katalin Štěrbová more than expected).

Fields of papers citing papers by Katalin Štěrbová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katalin Štěrbová. 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 Katalin Štěrbová. The network helps show where Katalin Štěrbová may publish in the future.

Co-authorship network of co-authors of Katalin Štěrbová

This figure shows the co-authorship network connecting the top 25 collaborators of Katalin Štěrbová. A scholar is included among the top collaborators of Katalin Štěrbová 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 Katalin Štěrbová. Katalin Štěrbová 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.
Ramos‐Mondragón, Roberto, Shuyun Wang, Xiaotan T. Qiao, et al.. (2025). Altered cardiac excitability and arrhythmia in models of SCN1B-linked developmental and epileptic encephalopathy. JCI Insight. 10(17). 1 indexed citations
2.
Bělohlávková, Anežka, Alena Jahodová, Martin Kudr, et al.. (2024). Brivaracetam use in children with epilepsy: A retrospective multicenter study. Seizure. 121. 243–252. 4 indexed citations
3.
Sedláčková, Lucie, Katalin Štěrbová, Markéta Vlčková, et al.. (2023). Yield of exome sequencing in patients with developmental and epileptic encephalopathies and inconclusive targeted gene panel. European Journal of Paediatric Neurology. 48. 17–29. 3 indexed citations
4.
Chen, Chunling, Julie Ziobro, Samantha L. Hodges, et al.. (2023). Epilepsy and sudden unexpected death in epilepsy in a mouse model of human SCN1B-linked developmental and epileptic encephalopathy. Brain Communications. 5(6). fcad283–fcad283. 7 indexed citations
5.
Zieg, Jakub, M. Balaščaková, Katalin Štěrbová, et al.. (2023). Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 49(1). 11–11. 4 indexed citations
6.
Štěrbová, Katalin, et al.. (2022). A unique coincidence of a 17q12 deletion and duplication in a Czech family led to a refined genotype–phenotype correlation. American Journal of Medical Genetics Part A. 191(3). 870–877. 1 indexed citations
7.
8.
Sedláčková, Lucie, Petra Laššuthová, Katalin Štěrbová, et al.. (2021). Severe neurodevelopmental disorder with intractable seizures due to a novel SLC1A4 homozygous variant. European Journal of Medical Genetics. 64(9). 104263–104263. 7 indexed citations
9.
Bělohlávková, Anežka, Katalin Štěrbová, Cornelia Betzler, et al.. (2020). Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration. European Journal of Paediatric Neurology. 28. 81–88. 4 indexed citations
10.
Muir, Alison M., Candace T. Myers, Nancy Nguyen, et al.. (2019). Genetic heterogeneity in infantile spasms. Epilepsy Research. 156. 106181–106181. 42 indexed citations
11.
Laššuthová, Petra, Katalin Štěrbová, Markéta Vlčková, et al.. (2018). Detection rate of causal variants in severe childhood epilepsy is highest in patients with seizure onset within the first four weeks of life. Orphanet Journal of Rare Diseases. 13(1). 71–71. 22 indexed citations
12.
Laššuthová, Petra, Katalin Štěrbová, Jana Haberlová, et al.. (2018). UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood. Neuropediatrics. 50(1). 57–60. 15 indexed citations
13.
Štěrbová, Katalin, Markéta Vlčková, Petr Klement, et al.. (2018). Neonatal Onset of Epilepsy of Infancy with Migrating Focal Seizures Associated with a Novel GABRB3 Variant in Monozygotic Twins. Neuropediatrics. 49(3). 204–208. 14 indexed citations
14.
Prchalová, Darina, Markéta Havlovičová, Katalin Štěrbová, et al.. (2017). Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report. BMC Medical Genetics. 18(1). 62–62. 23 indexed citations
15.
Neupauerová, Jana, Katalin Štěrbová, Markéta Vlčková, et al.. (2017). Two Novel Variants Affecting CDKL5 Transcript Associated with Epileptic Encephalopathy. Genetic Testing and Molecular Biomarkers. 21(10). 613–618. 10 indexed citations
16.
Komárek, Vladimı́r, et al.. (2015). Structural alterations of the language connectome in children with specific language impairment. Brain and Language. 151. 35–41. 21 indexed citations
17.
Hrdlička, Michal, et al.. (2008). Nonlinear analysis of the sleep EEG in children with pervasive developmental disorder.. PubMed. 29(4). 512–7. 17 indexed citations
18.
Štěrbová, Katalin, et al.. (2007). Epileptiform activity in children with developmental dysphasia: quantification of discharges in overnight sleep video-EEG.. PubMed. 9 Suppl 1. S28–35. 10 indexed citations
19.
Šimonová, Z., Katalin Štěrbová, G Brožek, Vladimı́r Komárek, & Eva Syková. (2003). Postnatal hypobaric hypoxia in rats impairs water maze learning and the morphology of neurones and macroglia in cortex and hippocampus. Behavioural Brain Research. 141(2). 195–205. 43 indexed citations
20.
Paluš, Milan, Vladimı́r Komárek, Z Hrnčíř, & Katalin Štěrbová. (2001). Synchronization as adjustment of information rates: Detection from bivariate time series. Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics. 63(4). 46211–46211. 245 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 J. Meier Breakdown of academic impact, for papers by Äthan Spiros Breakdown of academic impact, for papers by Kang K. L. Liu Breakdown of academic impact, for papers by Matthäus Staniek Breakdown of academic impact, for papers by Kevin Aquino Breakdown of academic impact, for papers by I. S. Midzyanovskaya Breakdown of academic impact, for papers by Marie‐Therese Horstmann Breakdown of academic impact, for papers by Klaus Prank Breakdown of academic impact, for papers by Sarah F. Muldoon Breakdown of academic impact, for papers by Juan V. Sanchez‐Andrés
Rankless by CCL
2026