Claudia Stendel

2.7k total citations
17 papers, 443 citations indexed

About

Claudia Stendel is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Claudia Stendel has authored 17 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 5 papers in Cell Biology. Recurrent topics in Claudia Stendel's work include Hereditary Neurological Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Cellular transport and secretion (4 papers). Claudia Stendel is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Cellular transport and secretion (4 papers). Claudia Stendel collaborates with scholars based in Germany, United States and Switzerland. Claudia Stendel's co-authors include Jan Senderek, Ueli Suter, Thomas Klopstock, Marni J. Falk, Elizabeth M. McCormick, Estelle Arnaud, Bernhard Lüscher, Rebecca Ganetzky, Andreas Roos and H. O. Kleine and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and Neurology.

In The Last Decade

Claudia Stendel

17 papers receiving 437 citations

Peers

Claudia Stendel

CMN

NEURO

Sonia Nouioua Algeria

Marie Coutelier France

Stefania Magri Italy

Dagmara Kabzińska Poland

Dolores Martínez‐Rubio Spain

Fiorella Speziani United States

Paola Saveri Italy

Vincenzo Lupo Spain

Xingyao Wu United States

Amelie Pandraud United Kingdom

Sonia Nouioua Algeria

Claudia Stendel

298 ×1.1

CMN

164 ×0.7

136 ×1.3

105 ×1.3

NEURO

124 ×1.7

NEURO

Citations per year, relative to Claudia Stendel Claudia Stendel (= 1×) peers Sonia Nouioua

Countries citing papers authored by Claudia Stendel

Since Specialization

Citations

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

Fields of papers citing papers by Claudia Stendel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Stendel

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

All Works

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17 of 17 papers shown

Smeıtınk, Jan, Jan van Es, Mirian C. H. Janssen, et al.. (2024). Phase 2b program with sonlicromanol in patients with mitochondrial disease due to m.3243A>G mutation. Brain. 148(3). 896–907. 3 indexed citations

Kern, Jan Marco, Judith Böhringer, Dagmar Timmann, et al.. (2023). Clinical, Imaging, Genetic, and Disease Course Characteristics in Patients With GM2 Gangliosidosis. Neurology. 102(1). e207898–e207898. 2 indexed citations

Amprosi, Matthias, Elisabetta Indelicato, Wolfgang Nachbauer, et al.. (2022). Mast Syndrome Outside the Amish Community: SPG21 in Europe. Frontiers in Neurology. 12. 799953–799953. 2 indexed citations

Stendel, Claudia, Christiane Neuhofer, & Thomas Klopstock. (2022). Mitochondriale Erkrankungen – Ein Update zu Klinik, Diagnostik und Therapie. 5(1). 73–96. 1 indexed citations

Röeben, Benjamin, Eva Bültmann, Claudia Stendel, & Matthis Synofzik. (2022). Cerebellar Bottom of Fissure Hyperintensities in MT‐ATP6‐Associated Ataxia. Annals of Neurology. 91(3). 438–440. 1 indexed citations

Feil, Katharina, Christine Adrion, Sylvia Boesch, et al.. (2021). Safety and Efficacy of Acetyl-DL-Leucine in Certain Types of Cerebellar Ataxia. JAMA Network Open. 4(12). e2135841–e2135841. 18 indexed citations

Stendel, Claudia, Maria Cristina D’Adamo, Marina Dusl, et al.. (2020). Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia. International Journal of Molecular Sciences. 21(11). 3810–3810. 18 indexed citations

Ganetzky, Rebecca, Claudia Stendel, Elizabeth M. McCormick, et al.. (2019). MT-ATP6mitochondrial disease variants: Phenotypic and biochemical features analysis in 218 published cases and cohort of 14 new cases. Human Mutation. 40(5). 499–515. 74 indexed citations

Stendel, Claudia, Matias Wagner, Guenther Rudolph, & Thomas Klopstock. (2019). Gillespie's Syndrome with Minor Cerebellar Involvement and No Intellectual Disability Associated with a Novel ITPR1 Mutation: Report of a Case and Literature Review. Neuropediatrics. 50(6). 382–386. 8 indexed citations

10.

Stendel, Claudia & Thomas Klopstock. (2016). Mitochondriale Erkrankungen. InFo Neurologie + Psychiatrie. 18(10). 36–48. 1 indexed citations

11.

Koene, Saskia, Jan C.M. Hendriks, Lonneke de Boer, et al.. (2016). International Paediatric Mitochondrial Disease Scale. Journal of Inherited Metabolic Disease. 39(5). 705–712. 13 indexed citations

12.

Horn, Michael, Jorge A. Pereira, Páris Sidiropoulos, et al.. (2012). Myelin is dependent on the Charcot–Marie–Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells. Brain. 135(12). 3567–3583. 56 indexed citations

13.

Stendel, Claudia, Andreas Roos, H. O. Kleine, et al.. (2010). SH3TC2, a protein mutant in Charcot–Marie–Tooth neuropathy, links peripheral nerve myelination to endosomal recycling. Brain. 133(8). 2462–2474. 74 indexed citations

14.

Arnaud, Estelle, Jennifer Zenker, Claudia Stendel, et al.. (2009). SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system. Proceedings of the National Academy of Sciences. 106(41). 17528–17533. 85 indexed citations

15.

Stendel, Claudia, et al.. (2008). Small Rho GTPases are key regulators of peripheral nerve biology in health and disease. Journal of the Peripheral Nervous System. 13(3). 188–199. 9 indexed citations

16.

Kirfel, Jutta, Jan Senderek, Markus Moser, et al.. (2006). Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2. Gene Expression Patterns. 6(8). 978–984. 2 indexed citations

17.

Azzedine, Hamid, N. Ravisé, Christophe Verny, et al.. (2006). Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations. Neurology. 67(4). 602–606. 76 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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