Florian Stögbauer

3.8k citations

69 papers · 1.8k indexed · h-index 25

Impact in

Neurology top 2%
- Intracranial Aneurysms: Treatment and Complications
- Peripheral Neuropathies and Disorders
- Neurological diseases and metabolism
Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases

Papers in

Cellular and Molecular Neuroscience 23
- Hereditary Neurological Disorders 14
Neurology 10
- Intracranial Aneurysms: Treatment and Complications 9
- Neurological diseases and metabolism 7
- Botulinum Toxin and Related Neurological Disorders 4

Co-authors: E. Bernd Ringelstein Gregor Kuhlenbäumer Peter Young Stefan Evers M. Oelerich Hartmut Halfter Christoph Kellinghaus Tobias Loddenkemper
Journals: Journal of Neurology (5 papers)Neurology (4 papers)Stroke (4 papers)Neuromuscular Disorders (3 papers)Journal of Neurochemistry (3 papers)
Partner nations: Germany Belgium United States

In The Last Decade

Florian Stögbauer

69 papers receiving 1.7k citations

Peers

Countries citing papers authored by Florian Stögbauer

Since Specialization

Citations

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

Fields of papers citing papers by Florian Stögbauer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Florian Stögbauer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Florian Stögbauer Line = papers co-authored together Florian Stögbauer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Use of oxcarbazepine for treatment of refractory status epilepticus Seizure ·Christoph Kellinghaus, Sascha Berning, Florian Stögbauer	2013	14
2	Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene The American Journal of Human Genetics ·Silke Appenzeller, Anja Schirmacher, Hartmut Halfter, Sebastian Bäumer, Manuela Pendziwiat, Vincent Timmerman, Peter De Jonghe, Klára Fekete, Florian Stögbauer, Peter Lüdemann, Biabani, Elgar Susanne Quabius, E. Bernd Ringelstein, Gregor Kuhlenbäumer	2010	23
3	The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case–control studies Human Genetics ·Klaus Berger, Florian Stögbauer, Monika Stoll, Juergen Wellmann, Andreas Huge, Suzanne Cheng, Christof Kessler, Ulrich John, Gerd Assmann, E. Bernd Ringelstein, Harald Funke	2006	65
4	Generalized arteriopathy in patients with cervical artery dissection Neurology ·Wolfgang Völker, Michael Besselmann, Ralf Dittrich, Darius G. Nabavi, Carsten Konrad, Rainer Dziewas, Serjoscha Evers, Stephan Grewe, Stefan C. Krämer, R Bachmann, Florian Stögbauer, E. Bernd Ringelstein, Gregor Kuhlenbäumer	2005	71
5	Electromagnetic fields (GSM 1800) do not alter blood-brain barrier permeability to sucrose in models in vitro with high barrier tightness Bioelectromagnetics ·Helmut Franke, E. Bernd Ringelstein, Florian Stögbauer	2005	40
6	Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women The International Journal of Neuropsychopharmacology ·Katharina Domschke, Christine M. Freitag, Gregor Kuhlenbäumer, Anja Schirmacher, Philipp Sand, Peter Nyhuis, Christian Jacob, Jürgen Fritze, Petra Franke, Marcella Rietschel, Henk Garritsen, Rolf Fimmers, Markus M. Nöthen, Klaus‐Peter Lesch, Florian Stögbauer, Jürgen Deckert	2004	127
7	Placing Nasogastric Tubes and Intracranial Pressure Journal of Neurosurgical Anesthesiology ·Rainer Dziewas, Peter Sörös, Carsten Konrad, Florian Stögbauer, Peter Lüdemann	2003	2
8	Novel German APP V715A mutation associated with presenile Alzheimer's disease Neurobiology of Aging ·Marc Cruts, Bart Dermaut, Samir Kumar‐Singh, R. Rademakers, Marleen Van den Broeck, Christine Van Broeckhoven, Florian Stögbauer	2002	5
9	Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies Muscle & Nerve ·Kristin Ørstavik, Mona Skard Heier, Jovana Šaljić Ratković, Florian Stögbauer	2001	21
10	Internal carotid artery dissection Neurology ·Michael Besselmann, W.T. Bakker, Stephan Lowens, E. Bernd Ringelstein, Florian Stögbauer	2000	12
11	The natural history of hereditary neuralgic amyotrophy in the Dutch population. Neuromuscular Disorders ·Z Dobrzanski, Peter De Jonghe, Teresa Sequeros, Johan A. K. Suykens, A.A.W.M. Gabreëls‐Festen, Maya Yasmin, A. Levy, Gregor Kuhlenbäumer, Sônia Beatriz Balvedi Zackrzevski, Jan Meuleman, A Pou-Serradell, A. Bethani, Andrea Schenone, Florian Stögbauer, Vincent Timmerman, Nens van Alfen, Baziel G.M. van Engelen, Christine Van Broeckhoven	2000	3
12	Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cells Molecular Brain Research ·Hartmut Halfter, Annisa Luthfiyatur Rosyda, Matthias Friedrich, E. Bernd Ringelstein, Florian Stögbauer	2000	8
13	PMP22 Thr118Met is not a clinically relevant CMT1 marker Journal of Neurology ·Peter Young, Florian Stögbauer, G. Fury, Peter De Jonghe, A. Löfgren, Vincent Timmerman, Bernd Rautenstrauß, Konrad Oexle, H. Grehl, Gregor Kuhlenbäumer, Christine Van Broeckhoven, E B Ringelstein, Harald Funke	2000	11
14	Activation of Jak-Stat and MAPK2 Pathways by Oncostatin M Leads to Growth Inhibition of Human Glioma Cells PubMed ·Hartmut Halfter, Matthias Friedrich, Annisa Luthfiyatur Rosyda, E. Bernd Ringelstein, Florian Stögbauer	1999	20
15	Kinetics of 3-[123I]iodo-l-α-methyltyrosine transport in rat C6 glioma cells PubMed ·Burkhard Riemann, Florian Stögbauer, Klaus Kopka, Hartmut Halfter, Nim. RifqiZamzami, Anja Schirmacher, Torsten Kuwert, Matthias Weckesser, E. Bernd Ringelstein, Otmar Schober	1999	24
16	Autosomal dominant burning feet syndrome Journal of Neurology Neurosurgery & Psychiatry ·Florian Stögbauer, Peter R. Young, Gregor Kuhlenbäumer, Reinhard Kiefer, Vincent Timmerman, E B Ringelstein, V. Oesch, J. M. Schröder, Christine Van Broeckhoven, Joachim Weis	1999	17
17	Inhibition of Growth and Induction of Differentiation of Glioma Cell Lines by Oncostatin M (OSM) Growth Factors ·Hartmut Halfter, Ramin Lotfi, Reiner Westermann, Peter Young, E. Bernd Ringelstein, Florian Stögbauer	1998	40
18	Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome Neuroscience Letters ·Florian Stögbauer, Cortney Simons, Heiko Wiebusch, Vincent Timmerman, Gregor Kuhlenbäumer, Eva Nelis, E. Bernd Ringelstein, SABRİYE KARADENİZLİ TAŞKIN, Gerd Assmann, Christine Van Broeckhoven, Harald Funke	1998	14
19	Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25 Human Genetics ·Florian Stögbauer, Peter Young, Vincent Timmerman, Xinjin Fu, E. Bernd Ringelstein, Christine Van Broeckhoven, G Kurlemann	1997	33
20	Four frequently observed polymorphisms in the 3‘‐UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes Clinical Genetics ·Peter Young, Heiko Wiebusch, Florian Stögbauer, Bernd Ringelstein, Gerd Assmann, Harald Funke	1996	1

About Florian Stögbauer

Florian Stögbauer is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Oncology and Psychiatry and Mental health, having authored 69 papers that have together received 1.8k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (14 papers), Intracranial Aneurysms: Treatment and Complications (9 papers), Neurological diseases and metabolism (7 papers), Signaling Pathways in Disease (7 papers), Cytokine Signaling Pathways and Interactions (7 papers), interferon and immune responses (6 papers), Botulinum Toxin and Related Neurological Disorders (4 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Neurology (525 citations), Neurology (184 citations), Cellular and Molecular Neuroscience (377 citations), Psychiatry and Mental health (187 citations) and Behavioral Neuroscience (39 citations). Florian Stögbauer has collaborated with scholars based in Germany, Belgium and United States. Frequent co-authors include E. Bernd Ringelstein, Gregor Kuhlenbäumer, Peter Young, Stefan Evers, M. Oelerich, Hartmut Halfter, Christoph Kellinghaus, Tobias Loddenkemper, Peter De Jonghe and Anja Schirmacher. Their work appears in journals such as Journal of Neurology, Neurology, Stroke, Neuromuscular Disorders and Journal of Neurochemistry.

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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