Stephan Klebe

5.5k total citations
62 papers, 1.7k citations indexed

About

Stephan Klebe is a scholar working on Cellular and Molecular Neuroscience, Neurology and Genetics. According to data from OpenAlex, Stephan Klebe has authored 62 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Cellular and Molecular Neuroscience, 36 papers in Neurology and 16 papers in Genetics. Recurrent topics in Stephan Klebe's work include Hereditary Neurological Disorders (27 papers), Neurological disorders and treatments (18 papers) and Parkinson's Disease Mechanisms and Treatments (18 papers). Stephan Klebe is often cited by papers focused on Hereditary Neurological Disorders (27 papers), Neurological disorders and treatments (18 papers) and Parkinson's Disease Mechanisms and Treatments (18 papers). Stephan Klebe collaborates with scholars based in Germany, France and Austria. Stephan Klebe's co-authors include Günther Deuschl, Henning Stolze, Lars Friege, Giovanni Stévanin, Christel Depienne, Jens Volkmann, Lüdger Schöls, Alexis Brice, Rebecca Schüle and Roland Wenzelburger and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Stephan Klebe

58 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephan Klebe Germany	23	864	755	357	339	288	62	1.7k
Carlo Casali Italy	22	583 0.7×	304 0.4×	284 0.8×	267 0.8×	364 1.3×	46	1.3k
Antonio Emanuele Elia Italy	24	658 0.8×	1.7k 2.2×	338 0.9×	140 0.4×	398 1.4×	63	2.2k
Talakad N. Sathyaprabha India	21	259 0.3×	661 0.9×	173 0.5×	134 0.4×	270 0.9×	42	1.1k
Marcella Masciullo Italy	25	572 0.7×	317 0.4×	236 0.7×	115 0.3×	512 1.8×	57	1.4k
Peter Heywood United Kingdom	14	1.1k 1.3×	882 1.2×	202 0.6×	188 0.6×	457 1.6×	19	2.1k
Hélio A.G. Teive Brazil	23	826 1.0×	771 1.0×	297 0.8×	149 0.4×	579 2.0×	120	1.5k
Bülent Elibol Türkiye	20	755 0.9×	1.0k 1.4×	330 0.9×	112 0.3×	501 1.7×	58	1.8k
Iva Stanković Serbia	26	455 0.5×	1.3k 1.8×	236 0.7×	295 0.9×	149 0.5×	68	1.7k
Peter Bergin New Zealand	13	262 0.3×	145 0.2×	292 0.8×	305 0.9×	141 0.5×	32	1.1k
Jin Whan Cho South Korea	24	445 0.5×	1.2k 1.5×	280 0.8×	166 0.5×	225 0.8×	127	1.7k

Countries citing papers authored by Stephan Klebe

Since Specialization

Citations

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

Fields of papers citing papers by Stephan Klebe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Klebe

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Klebe. A scholar is included among the top collaborators of Stephan Klebe 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 Stephan Klebe. Stephan Klebe 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

Höllerhage, Matthias, Stephan Klebe, Peter Riederer, et al.. (2025). Parkinson's Disease Multidisciplinary Complex Therapy (PD-MCT): appreciation of its current function for the treatment of people with Parkinson’s disease in Germany and the needs of future development. Journal of Neural Transmission. 133(2). 335–345.

Jöckel, Karl‐Heinz, et al.. (2024). Development and validation of TreatHSP-QoL: a patient-reported outcome measure for health-related quality of life in hereditary spastic paraplegia. Orphanet Journal of Rare Diseases. 19(1). 2–2. 2 indexed citations

Klebe, Stephan, Rebecca Schüle, Bjoern M. Eskofier, et al.. (2024). Mobile digital gait analysis captures effects of botulinum toxin in hereditary spastic paraplegia. European Journal of Neurology. 31(8). e16367–e16367. 2 indexed citations

Köhler, Wolfgang, Stephan Klebe, Saskia Biskup, et al.. (2024). Novel variants in CSF1R associated with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). Journal of Neurology. 271(9). 6025–6037.

Hopfner, Franziska, Carsten Buhmann, Joseph Claßen, et al.. (2024). Tips and tricks in tremor treatment. Journal of Neural Transmission. 131(10). 1229–1246.

Tönges, Lars, Carsten Buhmann, Stephan Klebe, et al.. (2022). Blood-based biomarker in Parkinson’s disease: potential for future applications in clinical research and practice. Journal of Neural Transmission. 129(9). 1201–1217. 32 indexed citations

Groh, Janos, Dennis Klein, Winfried Ilg, et al.. (2022). CNS-associated T-lymphocytes in a mouse model of Hereditary Spastic Paraplegia type 11 (SPG11) are therapeutic targets for established immunomodulators. Experimental Neurology. 355. 114119–114119. 7 indexed citations

Kwon, Eun‐Hae, et al.. (2022). SARS-CoV-2, COVID-19 and Parkinson’s Disease—Many Issues Need to Be Clarified—A Critical Review. Brain Sciences. 12(4). 456–456. 7 indexed citations

Beyer, Léon, René Günther, Jan Christoph Koch, et al.. (2020). TDP‐43 as structure‐based biomarker in amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 8(1). 271–277. 20 indexed citations

10.

Weber, Juliane, Lars Frings, Michel Rijntjes, et al.. (2019). Chorea-Acanthocytosis Presenting as Autosomal Recessive Epilepsy in a Family With a Novel VPS13A Mutation. Frontiers in Neurology. 9. 1168–1168. 8 indexed citations

11.

Klebe, Stephan & Dagmar Timmann. (2019). Genetik von Bewegungsstörungen – selten aber wichtig. Der Nervenarzt. 90(2). 197–210. 1 indexed citations

12.

Schlipf, Nina, Christian Beetz, Rebecca Schüle, et al.. (2010). A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42). European Journal of Human Genetics. 18(9). 1065–1067. 16 indexed citations

13.

Lang, Nicolas, et al.. (2010). Axonal integrity of corticospinal projections to the upper limbs in patients with pure hereditary spastic paraplegia. Clinical Neurophysiology. 122(7). 1417–1420. 6 indexed citations

14.

Kuhlenbäumer, Gregor, D. Lorenz, Michael Nothnagel, et al.. (2010). GABAA receptor- and GABA transporter polymorphisms and risk for essential tremor. European Journal of Neurology. 18(8). 1098–1100. 25 indexed citations

15.

Lorenz, Delia, Frank Papengut, Henrik Frederiksen, et al.. (2008). Evaluation of a screening instrument for essential tremor. Movement Disorders. 23(7). 1006–1012. 24 indexed citations

16.

Klebe, Stephan, Alexandra Dürr, Naïma Bouslam, et al.. (2007). Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 854–861. 14 indexed citations

17.

Elleuch, Nizar, Naïma Bouslam, Sylvain Hanein, et al.. (2007). Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families. Neurogenetics. 8(4). 307–315. 15 indexed citations

18.

Klebe, Stephan, Günther Deuschl, & Henning Stolze. (2006). Methylphenidate fails to improve gait and muscle tone in patients with sporadic and hereditary spastic paraplegia. Movement Disorders. 21(9). 1468–1471. 7 indexed citations

19.

Bouslam, Naïma, Ali Benomar, Hamid Azzedine, et al.. (2005). Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28). Annals of Neurology. 57(4). 567–571. 43 indexed citations

20.

Klebe, Stephan, Henning Stolze, F. Kopper, et al.. (2004). Gait analysis of sporadic and hereditary spastic paraplegia. Journal of Neurology. 251(5). 571–578. 48 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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