Jürgen Sperner

2.7k total citations
51 papers, 1.5k citations indexed

About

Jürgen Sperner is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Jürgen Sperner has authored 51 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 11 papers in Neurology and 10 papers in Molecular Biology. Recurrent topics in Jürgen Sperner's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Jürgen Sperner is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Jürgen Sperner collaborates with scholars based in Germany, United Kingdom and United States. Jürgen Sperner's co-authors include Ute Thyen, E. Schwinger, Ulrich Stephani, Rainer Boor, Andreas van Baalen, Bettina A. Moser, Jiong Tao, Vera M. Kalscheuer, Jean‐Pierre Fryns and Martine Raynaud and has published in prestigious journals such as SHILAP Revista de lepidopterología, NeuroImage and Annals of Neurology.

In The Last Decade

Jürgen Sperner

50 papers receiving 1.4k citations

Peers

Countries citing papers authored by Jürgen Sperner

Since Specialization

Citations

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

Fields of papers citing papers by Jürgen Sperner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jürgen Sperner

This figure shows the co-authorship network connecting the top 25 collaborators of Jürgen Sperner. A scholar is included among the top collaborators of Jürgen Sperner 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 Jürgen Sperner. Jürgen Sperner 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	Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet? 2015 ·Epilepsy Research ·Felicitas Becker, Julian Schubert, Sarah Weckhuysen, Arvid Suls, (unknown), Elisabeth Korn‐Merker, (unknown), Jürgen Sperner, J. Helen Cross, Kerstin Hallmann, Christian E. Elger, Wolfram S. Kunz, (unknown), Holger Lerche, Yvonne Weber	5
2	Microdeletion 5q14.3 and anomalies of brain development 2013 ·American Journal of Medical Genetics Part A ·Alrun Hotz, Yorck Hellenbroich, Jürgen Sperner, M Linder-Lucht, Uta Tacke, (unknown), Almuth Caliebe, Inga Nagel, Dawn E. Saunders, G. Wolff, Peter Martin, Déborah Morris-Rosendahl	25
3	Beneficial Prenatal Levodopa Therapy in Autosomal Recessive Guanosine Triphosphate Cyclohydrolase 1 Deficiency 2012 ·Archives of Neurology ·Norbert Brüggemann, Juliane Spiegler, Yorck Hellenbroich, Thomas Opladen, Susanne A. Schneider, Ulrich Stephani, Rainer Boor, Gabriele Gillessen‐Kaesbach, Jürgen Sperner, Christine Klein	19
4	Cerebral hemiatrophy associated with hippocampal sclerosis following a single prolonged febrile seizure 2011 ·European Journal of Pediatrics ·Iren Orosz, Christoph Härtel, Stefan Gottschalk, Katharina von Hof, Christian G. Bien, Jürgen Sperner	3
5	Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region 2010 ·Epilepsia ·(unknown), Ingo Helbig, (unknown), (unknown), Holger Tönnies, Hiltrud Muhle, (unknown), Sascha Vermeer, Rolph Pfundt, Jürgen Sperner, Irina Stefanova, Gabriele Gillessen‐Kaesbach, Sarah von Spiczak, Andreas van Baalen, Rainer Boor, Reiner Siebert, Ulrich Stephani, Almuth Caliebe	65
6	Right-sided vagus nerve stimulation in humans: An effective therapy? 2008 ·Epilepsy Research ·(unknown), Georg Nowak, (unknown), Volker Tronnier, Jürgen Sperner	32
7	Implantation und Komplikation der Vagusnervstimulation 2007 ·Journal für Kardiologie (Krause & Pachernegg GmbH) ·(unknown), G. Nowak, Jürgen Sperner, (unknown)	6
8	Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation 2004 ·The American Journal of Human Genetics ·Jiong Tao, Hilde Van Esch, (unknown), Kirsten Hoffmann, Bettina A. Moser, Martine Raynaud, Jürgen Sperner, Jean‐Pierre Fryns, E. Schwinger, Jozef Gécz, Hans‐Hilger Ropers, Vera M. Kalscheuer	236
9	The clinical outcomes of neonatal and childhood stroke: review of the literature and implications for future research 2004 ·European Journal of Neurology ·Christoph Härtel, Sabrina Schilling, Jürgen Sperner, Ute Thyen	48
10	Frontoethmoidal encephalocele with ocular leakage of cerebrospinal fluid 2004 ·Journal of Neurosurgery Pediatrics ·(unknown), Uwe Kehler, Jan Gliemroth, Dirk Petersen, Jürgen Sperner	1
11	Unmet Health Care Needs and Impact on Families With Children With Disabilities in Germany 2003 ·Ambulatory Pediatrics ·Ute Thyen, Jürgen Sperner, Matthias Morfeld, Christiane Meyer, Ulrike Ravens‐Sieberer	36
12	Clinical and genetic features of myoclonus–dystonia in 3 cases: A video presentation 2003 ·Movement Disorders ·Norman Kock, Meike Kasten, Birgitt Schüle, Katja Hedrich, Karin Wiegers, Kemal Kabakci, Johann Hagenah, Peter P. Pramstaller, Matthias Nitschke, Alexander Münchau, Jürgen Sperner, Christine Klein	11
13	Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia 2002 ·The American Journal of Human Genetics ·B. Müller, Katja Hedrich, Norman Kock, Nataša Dragašević, Marina Svetel, Jennifer Garrels, Olfert Landt, Matthias Nitschke, Peter P. Pramstaller, Wolf Reik, E. Schwinger, Jürgen Sperner, Laurie J. Ozelius, Vladimir Kostić, Christine Klein	102
14	Intracranial hypertension in neuroborreliosis 2002 ·Developmental Medicine & Child Neurology ·Christoph Härtel, Stefan Schilling, (unknown), (unknown), Jürgen Sperner	14
15	Familial pontocerebellar hypoplasia type I with anterior horn cell disease 1999 ·European Journal of Paediatric Neurology ·(unknown), Jürgen Sperner, Irwin Reiss, Hans‐Björn Gehl, E. Reusche	19
16	Epilepsia partialis continua associated with a homoplasmic mitochondrial tRNA^Ser(UCN) mutation 1998 ·Annals of Neurology ·Markus Schuelke, (unknown), G. Stoltenburg, Jürgen Sperner, Arpad von Moers	46
17	Pre-eruptive varicella encephalitis: case report and review of the literature 1998 ·European Journal of Pediatrics ·H Wagner, (unknown), (unknown), K. Kruse, Jürgen Sperner	13
18	Severe transitory encephalopathy with reversible lesions of the claustrum 1996 ·Pediatric Radiology ·Jürgen Sperner, B. Sander, (unknown), Heiko Krude, D. Scheffner	37
19	Clinical, radiological and histological findings in desmoplastic infantile ganglioglioma 1994 ·Child s Nervous System ·Jürgen Sperner, Jack A. Gottschalk, Klaus Neumann, (unknown), W. Lanksch, D. Scheffner	29
20	Cranial ultrasound findings in aspartoacylase deficiency (Canavan disease) 1993 ·Pediatric Radiology ·(unknown), C. Bassir, (unknown), Jürgen Sperner, (unknown), D. Scheffner, Herbert J. Kaufmann	8

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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