Bart van de Warrenburg

3.0k total citations
30 papers, 508 citations indexed

About

Bart van de Warrenburg is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Bart van de Warrenburg has authored 30 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cellular and Molecular Neuroscience, 17 papers in Neurology and 13 papers in Molecular Biology. Recurrent topics in Bart van de Warrenburg's work include Genetic Neurodegenerative Diseases (17 papers), Neurological disorders and treatments (10 papers) and Mitochondrial Function and Pathology (9 papers). Bart van de Warrenburg is often cited by papers focused on Genetic Neurodegenerative Diseases (17 papers), Neurological disorders and treatments (10 papers) and Mitochondrial Function and Pathology (9 papers). Bart van de Warrenburg collaborates with scholars based in Netherlands, France and Malaysia. Bart van de Warrenburg's co-authors include Shahrul Azmin, Jorik Nonnekes, Bart Post, Dineke S. Verbeek, Norlinah Mohamed Ibrahim, Alexandra Dürr, Massimo Pandolfo, Stefanie Wolf, Marina Grisoli and Tanja Schmitz‐Hübsch and has published in prestigious journals such as SHILAP Revista de lepidopterología, NeuroImage and Neurology.

In The Last Decade

Bart van de Warrenburg

28 papers receiving 501 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bart van de Warrenburg Netherlands 13 328 246 211 96 41 30 508
Yaimeé Vázquez‐Mojena Cuba 16 362 1.1× 258 1.0× 214 1.0× 82 0.9× 33 0.8× 31 475
Adriana Moro Brazil 14 265 0.8× 243 1.0× 339 1.6× 51 0.5× 26 0.6× 38 589
Hiroyuki Soma Japan 11 304 0.9× 163 0.7× 313 1.5× 130 1.4× 14 0.3× 21 462
Patricia Greenstein United States 8 229 0.7× 207 0.8× 150 0.7× 106 1.1× 19 0.5× 14 408
Roderick P.P.W.M. Maas Netherlands 12 271 0.8× 183 0.7× 186 0.9× 168 1.8× 21 0.5× 34 507
Yanetza González-Zaldívar Cuba 13 301 0.9× 242 1.0× 159 0.8× 64 0.7× 46 1.1× 29 413
Ajit Kale United States 8 173 0.5× 160 0.7× 235 1.1× 50 0.5× 46 1.1× 12 520
Louise‐Laure Mariani France 14 174 0.5× 278 1.1× 308 1.5× 33 0.3× 81 2.0× 32 629
Antonella Antenora Italy 13 210 0.6× 163 0.7× 145 0.7× 55 0.6× 57 1.4× 22 390
Maria Rakowicz Poland 14 482 1.5× 371 1.5× 296 1.4× 140 1.5× 23 0.6× 32 646

Countries citing papers authored by Bart van de Warrenburg

Since Specialization
Citations

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

Fields of papers citing papers by Bart van de Warrenburg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bart van de Warrenburg. 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 Bart van de Warrenburg. The network helps show where Bart van de Warrenburg may publish in the future.

Co-authorship network of co-authors of Bart van de Warrenburg

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

All Works

20 of 20 papers shown
1.
Pennings, Maartje, Rowdy Meijer, Monique M. Gerrits, et al.. (2023). Copy number variants from 4800 exomes contribute to ~7% of genetic diagnoses in movement disorders, muscle disorders and neuropathies. European Journal of Human Genetics. 31(6). 654–662. 12 indexed citations
2.
Gan, Kok Beng, Nasharuddin Zainal, Norlinah Mohamed Ibrahim, et al.. (2023). Automated Gait Analysis Based on a Marker-Free Pose Estimation Model. Sensors. 23(14). 6489–6489. 22 indexed citations
3.
Warrenburg, Bart van de, et al.. (2022). A Guide for the Differential Diagnosis of Multiple System Atrophy in Clinical Practice. Journal of Parkinson s Disease. 12(7). 2015–2027. 7 indexed citations
4.
Parodi, Livia, Mathieu Barbier, Maxime Jacoupy, et al.. (2022). The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4. Genetics in Medicine. 24(11). 2308–2317. 2 indexed citations
5.
Corominas, Jordi, Maartje Pennings, Rowdy Meijer, et al.. (2021). Systematic analysis of short tandem repeats in 38,095 exomes provides an additional diagnostic yield. Genetics in Medicine. 23(8). 1569–1573. 22 indexed citations
6.
Azmin, Shahrul, et al.. (2021). Pharmacological and non-pharmacological management of spinocerebellar ataxia: A systematic review. Journal of Neurology. 269(5). 2315–2337. 27 indexed citations
7.
Kessels, Roy P. C., et al.. (2021). Neurocognitive Changes in Spinocerebellar Ataxia Type 3: A Systematic Review with a Narrative Design. The Cerebellum. 21(2). 314–327. 19 indexed citations
8.
Rossi, Malco, Sterre van der Veen, Marcelo Merello, Marina A.J. Tijssen, & Bart van de Warrenburg. (2020). Myoclonus‐Ataxia Syndromes: A Diagnostic Approach. Movement Disorders Clinical Practice. 8(1). 9–24. 11 indexed citations
9.
Post, Bart, et al.. (2020). Young Onset Parkinson’s Disease: A Modern and Tailored Approach. Journal of Parkinson s Disease. 10(s1). S29–S36. 67 indexed citations
10.
Rietveld, Anke, Judith van Gaalen, Christiaan G. J. Saris, et al.. (2020). Inclusion body myositis in patients with spinocerebellar ataxia types 3 and 6. Journal of Neurology Neurosurgery & Psychiatry. 91(8). 876–878. 3 indexed citations
11.
Takada, Sanami, Erik‐Jan Kamsteeg, Sjoert Pegge, et al.. (2020). The Phenotypic Spectrum of PNKP-Associated Disease and the Absence of Immunodeficiency and Cancer Predisposition in a Dutch Cohort. Pediatric Neurology. 113. 26–32. 6 indexed citations
12.
Azizan, Elena, et al.. (2020). Frequency of Spinocerebellar Ataxia type 1, 2, 3,6 and 7 and clinical profile of Spinocerebellar Ataxia type 3 in Malaysia. SHILAP Revista de lepidopterología. 7(1). 11–11. 4 indexed citations
13.
Gan‐Or, Ziv, Jennifer A. Ruskey, Bart van de Warrenburg, et al.. (2018). CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia. European Journal of Medical Genetics. 62(12). 103605–103605. 18 indexed citations
14.
Gan‐Or, Ziv, et al.. (2018). CAPN1: novel mutations expanding the phenotype of hereditary spastic paraparesis. (P6.039). Neurology. 90(15_supplement). 1 indexed citations
15.
Eidhof, Ilse, Michaela Fencková, Dei M. Elurbe, et al.. (2017). High-throughput Analysis of Locomotor Behavior in the <em>Drosophila </em>Island Assay. Journal of Visualized Experiments. 7 indexed citations
16.
Delnooz, Cathérine C.S., et al.. (2013). Two Task-Specific Dystonias in One Hand. SHILAP Revista de lepidopterología. 3. 1 indexed citations
17.
Verbeek, Dineke S. & Bart van de Warrenburg. (2011). Genetics of the Dominant Ataxias. Seminars in Neurology. 31(5). 461–469. 23 indexed citations
18.
Schulz, Jörg B., Stefanie Wolf, Tanja Schmitz‐Hübsch, et al.. (2009). Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6. NeuroImage. 49(1). 158–168. 131 indexed citations
19.
Beetz, Christian, Rebecca Schüle, Stephan Klebe, et al.. (2008). Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspots. Journal of the Neurological Sciences. 268(1-2). 131–135. 14 indexed citations
20.
Warrenburg, Bart van de, et al.. (2000). Paroxysmal Leg Weakness and Hearing Loss in a Patient with Subarachnoid Hemorrhage. European Neurology. 44(3). 186–187. 1 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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