Steffen Syrbe

5.3k total citations
76 papers, 1.2k citations indexed

About

Steffen Syrbe is a scholar working on Molecular Biology, Psychiatry and Mental health and Genetics. According to data from OpenAlex, Steffen Syrbe has authored 76 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 29 papers in Psychiatry and Mental health and 24 papers in Genetics. Recurrent topics in Steffen Syrbe's work include Epilepsy research and treatment (28 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Pharmacological Effects and Toxicity Studies (10 papers). Steffen Syrbe is often cited by papers focused on Epilepsy research and treatment (28 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Pharmacological Effects and Toxicity Studies (10 papers). Steffen Syrbe collaborates with scholars based in Germany, United States and Denmark. Steffen Syrbe's co-authors include Peter Wiedemann, Andreas Reichenbach, Andreas Bringmann, Andreas Merkenschlager, Matthias K. Bernhard, Mike Francke, Johannes Kacza, Astrid Bertsche, Wieland Kieß and Thilo Bertsche and has published in prestigious journals such as Brain, Neurology and PEDIATRICS.

In The Last Decade

Steffen Syrbe

71 papers receiving 1.2k citations

Peers

Steffen Syrbe

PMH

PPCH

GENET

NEURO

Roy Dudley Canada

John H. Livingston United Kingdom

Jiro Ono Japan

Paola Iannetti Italy

Sarenur Gökben Türkiye

Meng‐Han Tsai Taiwan

Raffaello Canapicchi Italy

Keith A. Cauley United States

Yutaka Awaya Japan

Christian Korff Switzerland

Roy Dudley Canada

Steffen Syrbe

491 ×1.1

215 ×0.6

PMH

86 ×0.4

PPCH

118 ×0.5

GENET

197 ×1.0

NEURO

Citations per year, relative to Steffen Syrbe Steffen Syrbe (= 1×) peers Roy Dudley

Countries citing papers authored by Steffen Syrbe

Since Specialization

Citations

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

Fields of papers citing papers by Steffen Syrbe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steffen Syrbe

This figure shows the co-authorship network connecting the top 25 collaborators of Steffen Syrbe. A scholar is included among the top collaborators of Steffen Syrbe 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 Steffen Syrbe. Steffen Syrbe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Bergner, Caroline G., Steffen Syrbe, Robert Wágner, et al.. (2025). KaRhab: an international online registry for cardiac rhabdomyomas. Orphanet Journal of Rare Diseases. 20(1). 44–44.

Nicolai, Joost, Elisabeth A. Cats, Gerhard Kluger, et al.. (2025). Amitriptyline use in individuals with KCNQ2/3 gain‐of‐function variants: A retrospective cohort study. Epilepsia. 66(5). 1628–1640. 2 indexed citations

Mütze, Ulrike, Florian Gleich, Dorothea Haas, et al.. (2024). Vitamin B12 Deficiency Newborn Screening. PEDIATRICS. 154(2). 2 indexed citations

Schröter, Julian, et al.. (2024). A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids. Scientific Data. 11(1). 514–514. 7 indexed citations

Xian, Julie, Shridhar Parthasarathy, Michael J. Boland, et al.. (2024). Early life seizures and epileptic spasms in STXBP1‐related disorders. Epilepsia. 65(3). 805–816. 6 indexed citations

Rotimi, Solomon O., et al.. (2024). Exome sequencing in Nigerian children with early‐onset epilepsy syndromes. Epilepsia Open. 10(1). 222–232. 1 indexed citations

Hofmann, Christoph P., Steffen Syrbe, Joachim Hebe, et al.. (2023). Long‐term use of everolimus for refractory arrhythmia in a child with tuberous sclerosis complex. American Journal of Medical Genetics Part A. 194(5). 3 indexed citations

Klotz, Kerstin Alexandra, Georgia Ramantani, Lena‐Luise Becker, et al.. (2023). Epilepsy surgery in early infancy: A retrospective, multicenter study. Epilepsia Open. 8(3). 1182–1189. 14 indexed citations

Specht, Sabine, Jens H. Westhoff, Andreas Ziegler, et al.. (2023). Fat embolism syndrome in Duchenne muscular dystrophy: Report on a novel case and systematic literature review. European Journal of Paediatric Neurology. 48. 91–100. 3 indexed citations

10.

Schröter, Julian, Saskia Biskup, Kerstin Alexandra Klotz, et al.. (2021). Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders. International Journal of Molecular Sciences. 22(6). 2824–2824. 25 indexed citations

11.

Schröter, Julian, Marjolein H. Willemsen, Thomas Bast, et al.. (2021). Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder. Human Mutation. 42(9). 1094–1100. 12 indexed citations

12.

Rotimi, Solomon O., et al.. (2021). Voltage Gated Sodium Channel Genes in Epilepsy: Mutations, Functional Studies, and Treatment Dimensions. Frontiers in Neurology. 12. 600050–600050. 35 indexed citations

13.

Schröter, Julian, Sven F. Garbade, Georg F. Hoffmann, et al.. (2020). Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies. Genetics in Medicine. 23(3). 516–523. 18 indexed citations

14.

Bernhard, Matthias K., Matthias Krause, & Steffen Syrbe. (2018). Sweaty feet in adolescents—Early use of botulinum type A toxin in juvenile plantar hyperhidrosis. Pediatric Dermatology. 35(6). 784–786. 10 indexed citations

15.

Syrbe, Steffen, Heidrun Kuhrt, Ulrich Gärtner, et al.. (2017). Müller glial cells of the primate foveola: An electron microscopical study. Experimental Eye Research. 167. 110–117. 69 indexed citations

16.

Hornemann, Frauke, Steffen Syrbe, Andreas Merkenschlager, et al.. (2017). Seizure disorders and developmental disorders: impact on life of affected families—a structured interview. European Journal of Pediatrics. 176(8). 1121–1129. 30 indexed citations

17.

Maljevic, Snezana, Matthias K. Bernhard, Astrid Bertsche, et al.. (2016). Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures. Molecular Syndromology. 7(4). 189–196. 14 indexed citations

18.

Bernhard, Matthias K., Steffen Syrbe, Martina Patrizia Neininger, et al.. (2016). Epilepsy in children and adolescents: Disease concepts, practical knowledge, and coping. Epilepsy & Behavior. 59. 77–82. 28 indexed citations

19.

Neininger, Martina Patrizia, Matthias K. Bernhard, Steffen Syrbe, et al.. (2015). Knowledge and attitudes of school teachers, preschool teachers and students in teacher training about epilepsy and emergency management of seizures. Archives of Disease in Childhood. 100(9). 851–855. 34 indexed citations

20.

Merkenschlager, Andreas, et al.. (2013). Wide spectrum of clinical manifestations in children with tuberous sclerosis complex – Follow-up of 20 children. Brain and Development. 36(4). 306–314. 11 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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