Katja Kobow

5.8k total citations
40 papers, 1.6k citations indexed

About

Katja Kobow is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Katja Kobow has authored 40 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 25 papers in Genetics and 14 papers in Psychiatry and Mental health. Recurrent topics in Katja Kobow's work include Genetics and Neurodevelopmental Disorders (18 papers), Epigenetics and DNA Methylation (17 papers) and Epilepsy research and treatment (14 papers). Katja Kobow is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Epigenetics and DNA Methylation (17 papers) and Epilepsy research and treatment (14 papers). Katja Kobow collaborates with scholars based in Germany, United States and Australia. Katja Kobow's co-authors include Ingmar Blümcke, Roland Coras, David C. Henshall, Assam El‐Osta, Eric Hahnen, Angelika Mühlebner, Michael Buchfelder, Hermann Stefan, Daniel J. Weigel and Jan Hauke and has published in prestigious journals such as Brain, Annals of Neurology and Scientific Reports.

In The Last Decade

Katja Kobow

39 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katja Kobow Germany 21 706 619 521 454 330 40 1.6k
Johannes C. Baayen Netherlands 24 668 0.9× 693 1.1× 188 0.4× 591 1.3× 388 1.2× 31 1.9k
Angelika Mühlebner Netherlands 24 497 0.7× 792 1.3× 340 0.7× 394 0.9× 482 1.5× 59 1.7k
Joan Liu United Kingdom 22 350 0.5× 606 1.0× 129 0.2× 483 1.1× 351 1.1× 35 1.4k
Lillian Martinian United Kingdom 31 589 0.8× 1.2k 1.9× 320 0.6× 1.1k 2.4× 649 2.0× 50 2.4k
Véronique André United States 25 1.1k 1.5× 1.0k 1.7× 292 0.6× 1.7k 3.8× 508 1.5× 36 2.5k
Donncha F. O’Brien Ireland 16 721 1.0× 315 0.5× 168 0.3× 401 0.9× 222 0.7× 37 1.5k
Romina Combi Italy 19 496 0.7× 349 0.6× 150 0.3× 375 0.8× 77 0.2× 38 1.1k
Rosa Gómez‐Villafuertes Spain 28 704 1.0× 378 0.6× 219 0.4× 526 1.2× 55 0.2× 59 2.2k
Michael A. Farrell Ireland 13 699 1.0× 248 0.4× 216 0.4× 258 0.6× 100 0.3× 24 1.3k
Yunfei Huang United States 17 1.0k 1.5× 165 0.3× 321 0.6× 561 1.2× 76 0.2× 29 1.8k

Countries citing papers authored by Katja Kobow

Since Specialization
Citations

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

Fields of papers citing papers by Katja Kobow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katja Kobow

This figure shows the co-authorship network connecting the top 25 collaborators of Katja Kobow. A scholar is included among the top collaborators of Katja Kobow 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 Katja Kobow. Katja Kobow 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.
Coras, Roland, Dorothea Schultheis, Harald Herrmann, et al.. (2025). Human brain tissue with MOGHE carrying somatic SLC35A2 variants reveal aberrant protein expression and protein loss in the white matter. Acta Neuropathologica. 149(1). 23–23. 1 indexed citations
2.
Wagstyl, Konrad, Katja Kobow, Pablo M. Casillas‐Espinosa, et al.. (2024). WONOEP 2022: Neurotechnology for the diagnosis of epilepsy. Epilepsia. 65(8). 2238–2247. 3 indexed citations
3.
Wang, Dandan, Samir Jabari, Ingmar Blümcke, et al.. (2023). The specific DNA methylation landscape in focal cortical dysplasia ILAE type 3D. Acta Neuropathologica Communications. 11(1). 129–129. 3 indexed citations
4.
Sahoo, Satya S., Katja Kobow, Jeffrey Buchhalter, et al.. (2022). Ontology-based feature engineering in machine learning workflows for heterogeneous epilepsy patient records. Scientific Reports. 12(1). 19430–19430. 12 indexed citations
5.
Hartlieb, Till, Sara Baldassari, Nam Suk Sim, et al.. (2021). Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE). Acta Neuropathologica Communications. 9(1). 3–3. 78 indexed citations
6.
Blümcke, Ingmar, Silvia Budday, Annapurna Poduri, et al.. (2021). Neocortical development and epilepsy: insights from focal cortical dysplasia and brain tumours. The Lancet Neurology. 20(11). 943–955. 45 indexed citations
7.
Peixoto-Santos, José Eduardo, Tonicarlo Rodrigues Velasco, Carlos Gilberto Carlotti, et al.. (2020). Histological correlates of hippocampal magnetization transfer images in drug-resistant temporal lobe epilepsy patients. NeuroImage Clinical. 28. 102463–102463. 5 indexed citations
8.
Kobow, Katja, Samir Jabari, Tom Pieper, et al.. (2020). Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay. Acta Neuropathologica. 140(6). 881–891. 19 indexed citations
9.
Niestroj, Lisa‐Marie, Patrick May, Mykyta Artomov, et al.. (2019). Assessment of genetic variant burden in epilepsy-associated brain lesions. European Journal of Human Genetics. 27(11). 1738–1744. 12 indexed citations
10.
Scott, Rod C., et al.. (2018). WONOEP APPRAISAL: The many facets of epilepsy networks. Epilepsia. 59(8). 1475–1483. 22 indexed citations
11.
Groemer, Teja W., et al.. (2017). Epigenetic control of epilepsy target genes contributes to a cellular memory of epileptogenesis in cultured rat hippocampal neurons. Acta Neuropathologica Communications. 5(1). 79–79. 22 indexed citations
12.
Boison, Detlev, et al.. (2016). Dynamic Regulation of the Adenosine Kinase Gene during Early Postnatal Brain Development and Maturation. Frontiers in Molecular Neuroscience. 9. 99–99. 35 indexed citations
13.
Dębski, Konrad J., Asla Pitkänen, Noora Puhakka, et al.. (2016). Etiology matters – Genomic DNA Methylation Patterns in Three Rat Models of Acquired Epilepsy. Scientific Reports. 6(1). 25668–25668. 74 indexed citations
14.
Blümcke, Ingmar, Eleonora Aronica, Albert J. Becker, et al.. (2016). Low-grade epilepsy-associated neuroepithelial tumours — the 2016 WHO classification. Nature Reviews Neurology. 12(12). 732–740. 93 indexed citations
15.
Henshall, David C. & Katja Kobow. (2015). Epigenetics and Epilepsy. Cold Spring Harbor Perspectives in Medicine. 5(12). a022731–a022731. 77 indexed citations
16.
Kobow, Katja, Stéphane Auvin, Frances E. Jensen, et al.. (2012). Finding a better drug for epilepsy: Antiepileptogenesis targets. Epilepsia. 53(11). 1868–1876. 74 indexed citations
17.
Kobow, Katja & Ingmar Blümcke. (2012). The emerging role of DNA methylation in epileptogenesis. Epilepsia. 53(s9). 11–20. 72 indexed citations
18.
Kobow, Katja & Ingmar Blümcke. (2011). The methylation hypothesis: Do epigenetic chromatin modifications play a role in epileptogenesis?. Epilepsia. 52(s4). 15–19. 90 indexed citations
19.
Coras, Roland, Florian A. Siebzehnrübl, E. Pauli, et al.. (2010). Low proliferation and differentiation capacities of adult hippocampal stem cells correlate with memory dysfunction in humans. Brain. 133(11). 3359–3372. 129 indexed citations
20.
Kobow, Katja, Michelle A.T. Hildebrandt, Jan Hauke, et al.. (2009). Increased Reelin Promoter Methylation Is Associated With Granule Cell Dispersion in Human Temporal Lobe Epilepsy. Journal of Neuropathology & Experimental Neurology. 68(4). 356–364. 131 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.

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