Bart P.C. van de Warrenburg

17.3k citations

213 papers · 7.3k indexed · 1 hit paper · h-index 47

Neurology top 0.2%
- Neurological disorders and treatments 64
- Botulinum Toxin and Related Neurological Disorders 39
- Parkinson's Disease Mechanisms and Treatments 35
- Neurological diseases and metabolism 22
- Transcranial Magnetic Stimulation Studies 18
Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases 110
- Hereditary Neurological Disorders 32
Neurology top 0.5%
- Neurological disorders and treatments 64
- Botulinum Toxin and Related Neurological Disorders 39
- Parkinson's Disease Mechanisms and Treatments 35
- Neurological diseases and metabolism 22
- Transcranial Magnetic Stimulation Studies 18
Physical Therapy, Sports Therapy and Rehabilitation top 0.5%
Psychiatry and Mental health top 1%
Molecular Biology
- Mitochondrial Function and Pathology 61

Co-authors: Bastiaan R. Bloem Kailash P. Bhatia Cathérine C.S. Delnooz Roderick P.P.W.M. Maas Judith van Gaalen Nir Giladi Anke H. Snijders Berry Kremer
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Cell (1 paper)Journal of Neuroscience (2 papers)PLoS ONE (2 papers)
Partner nations: Netherlands Germany United Kingdom

In The Last Decade

Bart P.C. van de Warrenburg

199 papers receiving 7.2k citations

Hit Papers

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Peers

Countries citing papers authored by Bart P.C. van de Warrenburg

Since Specialization

Citations

This map shows the geographic impact of Bart P.C. 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 P.C. 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 P.C. van de Warrenburg more than expected).

Fields of papers citing papers by Bart P.C. van de Warrenburg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Bart P.C. van de Warrenburg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bart P.C. van de Warrenburg Line = papers co-authored together Bart P.C. van de Warrenburg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Unravelling the Global Tapestry of Genetic Ataxias: Epidemiology and Genetic Testing Approaches Movement Disorders ·Malco Rossi,Christopher D. Stephen,Joana Damásio,José Luiz Pedroso,Sheng-Han Kuo,Chi‐Ying Lin,Oluwadamilola O. Ojo,Shaimaa I El-Jaafary,Woong‐Woo Lee,Harutyun Madoev,Orlando Graziani Póvoas Barsottini,Achal Kumar Srivastava,Christine Klein,Bart P.C. van de Warrenburg	2025	0
2	The Goal Attainment Scale in Spinocerebellar Ataxia Type 3: Exploration of Feasibility and Content Validity The Cerebellum ·Kristofoor E Leeuwenberg,Roderick P.P.W.M. Maas,Bart P.C. van de Warrenburg	2025	0
3	The pattern and dynamics of white matter alterations in Spinocerebellar ataxia type 1: A diffusion-weighted magnetic resonance imaging study NeuroImage Clinical ·Kirsten Kapteijns,Teije van Prooije,Hao Li,Tom W. J. Scheenen,Anil M Tuladhar,Bart P.C. van de Warrenburg	2025	0
4	Longitudinal Assessment Reveals Stage‐Dependent Utility of Digital Motor Markers in SCA1 Movement Disorders Clinical Practice ·Ilse H. J. Willemse,Teije van Prooije,Kirsten Kapteijns,Bart P.C. van de Warrenburg	2025	0
5	The FGF14 gene is a milestone in ataxia genetics EBioMedicine ·Bart P.C. van de Warrenburg,Erik‐Jan Kamsteeg	2024	3
6	MRI‐ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study Movement Disorders ·Alessandra Scaravilli,Davide Negroni,C. Senatore,Lorenzo Ugga,Mirco Cosottini,Ivana Ricca,Benjamin Bender,Andreas Traschütz,A. Nazlı Başak,Atay Vural,Bart P.C. van de Warrenburg,Alexandra Dürr,Roberta La Piana,Dagmar Timmann,Rebecca Schüle,Matthis Synofzik,Filippo M. Santorelli,Sirio Cocozza	2024	2
7	Content Validity of the Modified Functional Scale for the Assessment and Rating of Ataxia (f-SARA) Instrument in Spinocerebellar Ataxia The Cerebellum ·Michele Potashman,K. Rüdell,Ivanna M. Pavisic,Naomi Suminski,Rinchen Doma,Maggie Heinrich,Linda Abetz‐Webb,Melissa Beiner,Sheng‐Han Kuo,Liana S. Rosenthal,Theresa Zesiwicz,Terry D. Fife,Bart P.C. van de Warrenburg,Giovanni Ristori,Matthis Synofzik,Susan B. Perlman,Jeremy D. Schmahmann,Gilbert L’Italien	2024	8
8	Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update Movement Disorders ·Lara M. Lange,Paulina González-Latapí,Rajasumi Rajalingam,Marina A.J. Tijssen,Darius Ebrahimi‐Fakhari,Carolin Gabbert,Christos Ganos,Rhia Ghosh,Kishore R. Kumar,Anthony E. Lang,Malco Rossi,Sterre van der Veen,Bart P.C. van de Warrenburg,Thomas T. Warner,Katja Lohmann,Christine Klein,Connie Marras,(unknown)	2022	58
9	Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia Journal of Neurology ·Fatemeh Ghorbani,Jelkje de Boer-Bergsma,Corien C. Verschuuren‐Bemelmans,Maartje Pennings,Eddy N. de Boer,Berry Kremer,Els K. Vanhoutte,Jeroen J. de Vries,Raymond van de Berg,Erik‐Jan Kamsteeg,Cleo C. van Diemen,Helga Westers,Bart P.C. van de Warrenburg,Dineke S. Verbeek	2022	14
10	Diagnosis and Management of Ataxia-Telangiectasia in Resource-Limited Settings Nienke J.H. van Os,Koen van Aerde,Judith van Gaalen,Peter Merkus,Laura Silveira‐Moriyama,Tajul A Tajudin,Bart P.C. van de Warrenburg,Corry M.R. Weemaes,Marieke Dekker,Michèl A.A.P. Willemsen	2020	0
11	De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability European Journal of Human Genetics ·Iris G. M. Wijnen,Hermine E. Veenstra‐Knol,Fleur Vansenne,Erica H. Gerkes,Tom de Koning,Yvonne J. Vos,Marina A.J. Tijssen,Deborah A. Sival,Niklas Darín,Els K. Vanhoutte,Mayke Oosterloo,Maartje Pennings,Bart P.C. van de Warrenburg,Erik-Jan Kamsteeg	2020	8
12	Management of rare movement disorders in Europe: outcome of surveys of the European Reference Network for Rare Neurological Diseases European Journal of Neurology ·Cèlia Painous,Nienke J.H. van Os,Anna Delamarre,I. Michailoviene,Marı́a José Martı́,Bart P.C. van de Warrenburg,Wassilios G. Meissner,Algirdas Utkus,Carola Reinhard,Holm Graeßner,Marina A.J. Tijssen	2020	14
13	“Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia American Journal of Neuroradiology ·Belén Pascual,Susanne T. de Bot,Michlene Daniels,Marcondes C. França,Camilo Toro,Mario Riverol,Peter Hedera,Maria Teresa Bassi,Nereo Bresolin,Bart P.C. van de Warrenburg,B. Kremer,Joost Nicolai,Perrine Charles,Jiaqiong Xu,SanjeetKumar Singh,Nicholas J. Patronas,Steve H. Fung,Michael D. Gregory,Joseph C. Masdeu	2019	39
14	Classic ataxia-telangiectasia: the phenotype of long-term survivors Journal of Neurology ·Nienke J.H. van Os,Marcel van Deuren,Corry M.R. Weemaes,Judith van Gaalen,H. Hijdra,A. Malcolm R. Taylor,Bart P.C. van de Warrenburg,Michèl A.A.P. Willemsen	2019	15
15	Integrative network and brain expression analysis reveals mechanistic modules in ataxia Journal of Medical Genetics ·Ilse Eidhof,Bart P.C. van de Warrenburg,Annette Schenck	2018	9
16	Reliability and Validity of the Range of Motion Scale (ROMS) in Patients with Abnormal Postures Pain Medicine ·Diana E. van Rooijen,Stefania Lalli,Johan Marinus,Christian Maihöfner,Candy McCabe,Alex G. Munts,Anton A. van der Plas,Marina A.J. Tijssen,Bart P.C. van de Warrenburg,Alberto Albanese,Jacobus J. van Hilten	2014	3
17	Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6 Brain ·Kathrin Reetz,Ana Sofia Costa,Shahram Mirzazade,Anna Lehmann,Agnes Juzek,Maria Rakowicz,Romana Bogusławska,Lüdger Schöls,Christoph Linnemann,Caterina Mariotti,Marina Grisoli,Alexandra Dürr,Bart P.C. van de Warrenburg,Dagmar Timmann,Massimo Pandolfo,Peter Bauer,Heike Jacobi,Till‐Karsten Hauser,Thomas Klockgether,Jörg B. Schulz,(unknown)	2013	109
18	Cerebellum-dependent associative learning deficits in primary dystonia are normalized by rTMS and practice European Journal of Neuroscience ·Britt S. Hoffland,Panagiotis Kassavetis,Matteo Bologna,James Teo,Kailash P. Bhatia,John C. Rothwell,Mark J. Edwards,Bart P.C. van de Warrenburg	2013	42
19	Antineuronal antibodies in Parkinson's disease Movement Disorders ·Bart P.C. van de Warrenburg,Andrew J. Church,Davide Martino,Paul M. Candler,Kailash P. Bhatia,Gavin Giovannoni,Niall Quinn	2008	15
20	Postural instability in cerebellar ataxia: Correlations of knee, arm and trunk movements to center of mass velocity Neuroscience ·U.M. Küng,Corinne G.C. Horlings,F. Honegger,H.P.H. Kremer,Bastiaan R. Bloem,Bart P.C. van de Warrenburg,J.H.J. Allum	2008	22

About Bart P.C. van de Warrenburg

Bart P.C. van de Warrenburg is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 213 papers that have together received 7.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (110 papers), Neurological disorders and treatments (64 papers), Mitochondrial Function and Pathology (61 papers), Botulinum Toxin and Related Neurological Disorders (39 papers), Parkinson's Disease Mechanisms and Treatments (35 papers), Hereditary Neurological Disorders (32 papers), Neurological diseases and metabolism (22 papers) and Transcranial Magnetic Stimulation Studies (18 papers). The work is most often cited by research in Neurology (3.5k citations), Cellular and Molecular Neuroscience (3.4k citations) and Neurology (1.4k citations). Bart P.C. van de Warrenburg has collaborated with scholars based in Netherlands, Germany and United Kingdom. Frequent co-authors include Bastiaan R. Bloem, Kailash P. Bhatia, Cathérine C.S. Delnooz, Roderick P.P.W.M. Maas, Judith van Gaalen, Nir Giladi, Anke H. Snijders, Berry Kremer, Richard J. Sinke and Michèl A.A.P. Willemsen. Their work appears in journals such as Cell, Journal of Neuroscience and PLoS ONE.

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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