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Bart P.C. van de Warrenburg

Bart P.C. van de Warrenburg

D-Index & Metrics

Neuroscience

D-Index
75
Citations
17693
World Ranking
2043
National Ranking
64

Overview

Bart P.C. van de Warrenburg is affiliated with Radboud University in the Netherlands. Their research primarily addresses various aspects of neuroscience, medicine, and biochemistry, with significant contributions in genetics and molecular biology.

The main fields of study covered in their research include:

  • Neuroscience
  • Medicine
  • Biochemistry, Genetics and Molecular Biology

The subfields within these disciplines where they have demonstrated considerable focus are:

  • Neurology
  • Cellular and Molecular Neuroscience
  • Molecular Biology
  • Genetics
  • Psychiatry and Mental Health

The central topics of their work reflect a concentration on neurodegenerative and hereditary neurological disorders, including:

  • Genetic Neurodegenerative Diseases
  • Mitochondrial Function and Pathology
  • Neurological Disorders and Treatments
  • Parkinson's Disease Mechanisms and Treatments
  • Hereditary Neurological Disorders
  • DNA Repair Mechanisms
  • Botulinum Toxin and Related Neurological Disorders

Van de Warrenburg has collaborated frequently with several co-authors, including:

  • Matthis Synofzik
  • Lüdger Schöls
  • Thomas Klockgether
  • Dagmar Timmann
  • Jennifer Faber

Their publishing record features a significant number of papers in various prominent journals. Common venues for their research publications include:

  • Movement Disorders
  • Journal of Neurology
  • The Cerebellum
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Parkinsonism & Related Disorders

Selected recent papers illustrate the scope and focus of their work:

  • Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease, 2021, Neurology
  • Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update, 2022, Movement Disorders
  • How to proceed after "negative" exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques, 2022, Journal of Inherited Metabolic Disease
  • The cerebellar cognitive affective syndrome scale reveals early neuropsychological deficits in SCA3 patients, 2021, Journal of Neurology
  • Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease, 2022, Neurology

Best Publications

  • Neurological gait disorders in elderly people: clinical approach and classification

    Anke H Snijders;Bart P van de Warrenburg;Nir Giladi;Bastiaan R Bloem

  • Postural deformities in Parkinson's disease

    Karen M Doherty;Bart P van de Warrenburg;Maria Cecilia Peralta;Laura Silveira-Moriyama

  • How might physical activity benefit patients with Parkinson disease

    Arlène D. Speelman;Bart P. van de Warrenburg;Marlies van Nimwegen;Giselle M. Petzinger

  • Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

    Connie Marras;Anthony Lang;Bart P. van de Warrenburg;Carolyn M. Sue

  • Spinocerebellar ataxia types 1, 2, 3, and 6 Disease severity and nonataxia symptoms

    T Schmitz-Hübsch;M Coudert;Peter Bauer;P Giunti

  • Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

    Heike Jacobi;Sophie Tezenas du Montcel;Peter Bauer;Paola Giunti

  • Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

    Jörg B. Schulz;Jörg B. Schulz;Johannes Borkert;Stefanie Wolf;Stefanie Wolf;Tanja Schmitz-Hübsch

  • Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis

    Michael A. Van Es;Helenius J. Schelhaas;Paul W J Van Vught;Nicola Ticozzi;Nicola Ticozzi

  • The clinical approach to movement disorders.

    Wilson F. Abdo;Bart P. C. van de Warrenburg;David J. Burn;Niall P. Quinn

  • Network localization of cervical dystonia based on causal brain lesions.

    Daniel T Corp;Daniel T Corp;Juho Joutsa;R Ryan Darby;R Ryan Darby;Cathérine C S Delnooz

  • REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.

    Christian Beetz;Rebecca Schüle;Tine Deconinck;Khanh Nhat Tran-Viet

  • Reliability and validity of the International Cooperative Ataxia Rating Scale: A study in 156 spinocerebellar ataxia patients

    Tanja T. Schmitz-Hübsch;Sophie Tezenas S.T. du Montcel;Laszlo L. Baliko;Sylvia S. Boesch

  • Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

    Sophie Tezenas Du Montcel;Sophie Tezenas Du Montcel;Alexandra Durr;Peter Bauer;Karla P. Figueroa

  • Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.

    Janneke H.M. Schuurs-Hoeijmakers;Michael T. Geraghty;Erik-Jan Kamsteeg;Salma Ben-Salem

  • Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

    Christoph Globas;Sophie Tezenas du Montcel;Laslo Baliko;Syliva Boesch

  • Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

    Isabelle Thiffault;Isabelle Thiffault;Isabelle Thiffault;Nicole I. Wolf;Diane Forget;Kether Guerrero

  • ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

    Sascha Vermeer;Rowdy P. P. Meijer;Benjamin J. Pijl;Janneke Timmermans

  • Movement disorders in spinocerebellar ataxias

    Judith van Gaalen;Paola Giunti;Bart P. van de Warrenburg

  • Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects

    Eunju Seong;Ryan Insolera;Marija Dulovic;Erik Jan Kamsteeg

  • Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6

    Kathrin Reetz;Kathrin Reetz;Ana Sofia Costa;Shahram Mirzazade;Shahram Mirzazade;Anna Lehmann;Anna Lehmann

  • Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

    Hirotaka Iwaki;Cornelis Blauwendraat;Hampton L. Leonard;Jonggeol J. Kim

  • Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort.

    Koen L. I. van Gassen;Charlotte D. C. C. van der Heijden;Susanne T. de Bot;Wilfred F. A. den Dunnen

  • Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

    Anna Duarri;Justyna Jezierska;Michiel Fokkens;Michel Meijer

  • Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

    L. Schöls;C. Globas;T. Schmitz-Hübsch;D. Timmann

Frequent Co-Authors

Ludger Schöls
Ludger Schöls University of Tübingen
Thomas Klockgether
Thomas Klockgether German Center for Neurodegenerative Diseases
Alexandra Durr
Alexandra Durr Sorbonne University
Dagmar Timmann
Dagmar Timmann University of Duisburg-Essen
Alexis Brice
Alexis Brice Institut du Cerveau
Rebecca Schüle
Rebecca Schüle University of Tübingen
Hans Scheffer
Hans Scheffer Radboud University
Massimo Pandolfo
Massimo Pandolfo McGill University
Richard J. Sinke
Richard J. Sinke University Medical Center Groningen
Marina A.J. Tijssen
Marina A.J. Tijssen University Medical Center Groningen

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