Florian St�gbauer

762 total citations
8 papers, 481 citations indexed

About

Florian St�gbauer is a scholar working on Cellular and Molecular Neuroscience, Surgery and Neurology. According to data from OpenAlex, Florian St�gbauer has authored 8 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Cellular and Molecular Neuroscience, 2 papers in Surgery and 2 papers in Neurology. Recurrent topics in Florian St�gbauer's work include Hereditary Neurological Disorders (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Neurological diseases and metabolism (2 papers). Florian St�gbauer is often cited by papers focused on Hereditary Neurological Disorders (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Neurological diseases and metabolism (2 papers). Florian St�gbauer collaborates with scholars based in Germany and Belgium. Florian St�gbauer's co-authors include E. Bernd Ringelstein, Carsten Konrad, Rainer Dziewas, Stefan Evers, Michael Besselmann, Peter Young, Johannes Goeke, Anja Schirmacher, Hans‐Joachim Galla and Silvia Fischer and has published in prestigious journals such as Muscle & Nerve, Human Genetics and Journal of Neurology.

In The Last Decade

Florian St�gbauer

8 papers receiving 453 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florian St�gbauer Germany 7 253 169 101 71 61 8 481
Liang-Shong Lee Taiwan 12 172 0.7× 34 0.2× 102 1.0× 32 0.5× 12 0.2× 21 432
Erinç Aktüre United States 15 208 0.8× 58 0.3× 113 1.1× 89 1.3× 3 0.0× 28 579
Yoshikazu Kusano Japan 12 262 1.0× 149 0.9× 77 0.8× 60 0.8× 2 0.0× 25 537
Esther S. Yu United States 9 45 0.2× 33 0.2× 408 4.0× 32 0.5× 16 0.3× 14 754
A. E. Rosenbaum United States 11 131 0.5× 31 0.2× 135 1.3× 83 1.2× 4 0.1× 16 499
Emma Bailey United Kingdom 10 186 0.7× 160 0.9× 88 0.9× 44 0.6× 3 0.0× 24 657
N Heldt France 10 126 0.5× 64 0.4× 65 0.6× 53 0.7× 4 0.1× 27 488
W. Poewe Austria 9 318 1.3× 60 0.4× 51 0.5× 105 1.5× 4 0.1× 22 513
Surajit Basu United Kingdom 13 68 0.3× 41 0.2× 25 0.2× 81 1.1× 4 0.1× 33 349
Don L. Burgio United States 11 46 0.2× 27 0.2× 108 1.1× 12 0.2× 42 0.7× 15 377

Countries citing papers authored by Florian St�gbauer

Since Specialization
Citations

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

Fields of papers citing papers by Florian St�gbauer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Florian St�gbauer. 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 Florian St�gbauer. The network helps show where Florian St�gbauer may publish in the future.

Co-authorship network of co-authors of Florian St�gbauer

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

All Works

8 of 8 papers shown
1.
Konrad, Carsten, Claus Langer, Klaus Berger, et al.. (2004). Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections. Journal of Neurology. 251(10). 1242–1248. 43 indexed citations
2.
Dziewas, Rainer, Carsten Konrad, Stefan Evers, et al.. (2003). Cervical artery dissection?clinical features, risk factors, therapy and outcome in 126 patients. Journal of Neurology. 250(10). 1179–1184. 267 indexed citations
3.
Young, Peter, et al.. (2002). Clinical features and molecular genetics of hereditary peripheral neuropathies. Journal of Neurology. 249(12). 1629–1650. 42 indexed citations
4.
Young, Peter, Korbinian Grote, Otfried Debus, et al.. (2001). Mutation analysis in Charcot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity. Journal of Neurology. 248(5). 410–415. 26 indexed citations
5.
Meuleman, Jan, Dominique Audenaert, Peter R. Young, et al.. (2001). Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA). Human Genetics. 108(5). 390–393. 7 indexed citations
6.
Schirmacher, Anja, Silvia Fischer, Johannes Goeke, et al.. (2000). Electromagnetic fields (1.8 GHz) increase the permeability to sucrose of the blood-brain barrier in vitro. Bioelectromagnetics. 21(5). 338–345. 86 indexed citations
7.
8.
St�gbauer, Florian, Peter Young, Vincent Timmerman, et al.. (1997). Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24q25. Human Genetics. 5(99). 685–687. 1 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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