Sven Klimpe

2.3k total citations
24 papers, 1.1k citations indexed

About

Sven Klimpe is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology. According to data from OpenAlex, Sven Klimpe has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 15 papers in Neurology and 7 papers in Neurology. Recurrent topics in Sven Klimpe's work include Hereditary Neurological Disorders (16 papers), Neurological diseases and metabolism (13 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Sven Klimpe is often cited by papers focused on Hereditary Neurological Disorders (16 papers), Neurological diseases and metabolism (13 papers) and Neurogenetic and Muscular Disorders Research (6 papers). Sven Klimpe collaborates with scholars based in Germany, France and Austria. Sven Klimpe's co-authors include Lüdger Schöls, Rebecca Schüle, Jan Kassubek, Konrad J. Werhahn, Thomas Klopstock, Otto W. Witte, Beate Winner, Volker Mall, Thomas Deufel and Michaela Auer‐Grumbach and has published in prestigious journals such as Neurology, The American Journal of Cardiology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Sven Klimpe

24 papers receiving 1.1k citations

Peers

Countries citing papers authored by Sven Klimpe

Since Specialization

Citations

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

Fields of papers citing papers by Sven Klimpe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sven Klimpe

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

#	Work	Indexed citations
1	The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8 2015 ·Orphanet Journal of Rare Diseases ·Amir Jahić, Mukhran Khundadze, Nadine Jaenisch, Rebecca Schüle, Sven Klimpe, Stephan Klebe, Christiane Frahm, Jan Kassubek, Giovanni Stévanin, Lüdger Schöls, Alexis Brice, Christian A. Hübner, Christian Beetz	16
2	A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes 2012 ·Neurogenetics ·Claudia Dufke, Nina Schlipf, Rebecca Schüle, Michael Bonin, Michaela Auer‐Grumbach, Giovanni Stévanin, Christel Depienne, Jan Kassubek, Stephan Klebe, Sven Klimpe, Thomas Klopstock, Susanne Otto, Sven Poths, (unknown), Henning Stolze, Andreas Gal, Lüdger Schöls, Peter Bauer	3
3	The safety and efficacy of add-on levetiracetam in elderly patients with focal epilepsy: A one-year observational study 2011 ·Seizure ·Konrad J. Werhahn, Sven Klimpe, (unknown), Eugen Trinka, Günter Krämer	42
4	Amplicon‐based high‐throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients 2011 ·Clinical Genetics ·(unknown), Rebecca Schüle, Sven Klimpe, (unknown), Matthis Synofzik, Julia Schicks, (unknown), Lüdger Schöls, Peter Bauer	26
5	Disease severity affects quality of life of hereditary spastic paraplegia patients 2011 ·European Journal of Neurology ·Sven Klimpe, Rebecca Schüle, Jan Kassubek, Otto W. Witte, Zacharias Kohl, Stephan Klebe, Thomas Klopstock, (unknown), Kathrin N. Karle, Lüdger Schöls	30
6	Sex Differences in Early Carotid Atherosclerosis (from the Community-Based Gutenberg-Heart Study) 2011 ·The American Journal of Cardiology ·Christoph Sinning, Philipp S. Wild, (unknown), Sandra Wilde, Renate B. Schnabel, Edith Lubos, (unknown), Christoph Bickel, Sven Klimpe, Tommaso Gori, Thomas F. Münzel, Stefan Blankenberg, Christine Espinola–Klein	76
7	A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42) 2010 ·European Journal of Human Genetics ·Nina Schlipf, Christian Beetz, Rebecca Schüle, Giovanni Stévanin, Anne Kjersti Erichsen, Sylvie Forlani, Cécile Zaros, Kathrin N. Karle, Stephan Klebe, Sven Klimpe, Alexandra Dürr, Susanne Otto, Chantal Tallaksen, Olaf Rieß, Alexis Brice, Peter Bauer, Lüdger Schöls	16
8	Evaluating the effect of spastin splice mutations by quantitative allele‐specific expression assay 2010 ·European Journal of Neurology ·Sven Klimpe, Arne Zibat, Ulrich Zechner, (unknown), Moneef Shoukier, Simone M. Sauter, D. V. Krishna Pantakani, (unknown)	6
9	Recruitment of motor cortex inhibition differentiates between generalized and focal epilepsy 2009 ·Epilepsy Research ·Sven Klimpe, (unknown), (unknown), Konrad J. Werhahn	18
10	Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots 2008 ·Journal of the Neurological Sciences ·Christian Beetz, Rebecca Schüle, Stephan Klebe, Sven Klimpe, Thomas Klopstock, Arnaud Lacour, Susanne Otto, Anne‐Dorte Sperfeld, Bart van de Warrenburg, Lüdger Schöls, Thomas Deufel	14
11	Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia 2008 ·Neurogenetics ·Rebecca Schüle, (unknown), Kathrin N. Karle, (unknown), Stephan Klebe, Sven Klimpe, Michaela Auer‐Grumbach, Andrew H. Crosby, Christian A. Hübner, Lüdger Schöls, Thomas Deufel, Christian Beetz	35
12	SPG10 is a rare cause of spastic paraplegia in European families 2008 ·Journal of Neurology Neurosurgery & Psychiatry ·Rebecca Schüle, B Kremer, Jan Kassubek, Michaela Auer‐Grumbach, Vladimir Kostić, Thomas Klopstock, Sven Klimpe, Otto W. Witte, Sylvia Boesch, Bart P.C. van de Warrenburg, Lüdger Schöls	39
13	Does the Recruitment of Excitation and Inhibition in the Motor Cortex Differ? 2007 ·Journal of Clinical Neurophysiology ·Konrad J. Werhahn, (unknown), (unknown), Sven Klimpe	21
14	Analysis of correlation between the recruitment of excitation and inhibition in the motor cortex 2007 ·Clinical Neurophysiology ·(unknown), (unknown), (unknown), Sven Klimpe, (unknown)	1
15	Antiepileptic drug use in nursing home residents: A cross-sectional, regional study 2006 ·Seizure ·(unknown), Sven Klimpe, Konrad J. Werhahn	34
16	The Spastic Paraplegia Rating Scale (SPRS) 2006 ·Neurology ·Rebecca Schüle, (unknown), Sven Klimpe, Jan Kassubek, Thomas Klopstock, Volker Mall, Otto W. Witte, Beate Winner, Lüdger Schöls	193
17	Decreased Dopamine D2/D3‐Receptor Binding in Temporal Lobe Epilepsy: An [¹⁸F]Fallypride PET Study 2006 ·Epilepsia ·Konrad J. Werhahn, Christian Landvogt, Sven Klimpe, Hans‐Georg Buchholz, Igor Yakushev, Thomas Siessmeier, Wibke Müller‐Forell, Markus Piel, Frank Rösch, Martin Gläser, Mathias Schreckenberger, Peter Bartenstein	74
18	High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia 2006 ·Neurology ·Christian Beetz, Anders O.H. Nygren, (unknown), Michaela Auer‐Grumbach, Kelly Burk, G. Heide, Jan Kassubek, Sven Klimpe, Thomas Klopstock, Friedmar R. Kreuz, Otto W. Witte, Rebecca Schüle, Lüdger Schöls, (unknown), Thomas Deufel	105
19	Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A 2004 ·Neurogenetics ·Annette Abel, Núria Fonknechten, Anne Höfer, Alexandra D�rr, Corinne Cruaud, Thomas Voit, Jean Weissenbach, Alexis Brice, Sven Klimpe, Georg Auburger, Jamïlé Hazan	38
20	Mutation analysis of thespastingene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia 2002 ·Human Mutation ·Simone M. Sauter, Bianca Miterski, Sven Klimpe, Dominikus Bönsch, Lüdger Schöls, (unknown), (unknown), H. C. Hopf, Wolfgang Engel, Thomas Deufel, Jörg T. Epplen, Jürgen Neesen	74

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