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Overview

Marina A.J. Tijssen is affiliated with the University Medical Center Groningen in the Netherlands. Their research primarily spans the fields of Medicine and Neuroscience, with significant expertise in Neurology, Cellular and Molecular Neuroscience, Rheumatology, Psychiatry and Mental Health, and Genetics. The scientist's publications address a range of topics related to neurological disorders and treatments, genetic neurodegenerative diseases, glycogen storage diseases and myoclonus, Parkinson's disease mechanisms and treatments, botulinum toxin and related neurological disorders, psychosomatic disorders and their treatments, and genetics and neurodevelopmental disorders.

Frequent co-authors collaborating with Marina A.J. Tijssen include:

  • Tom J. de Koning (19 joint publications)
  • Martje E. van Egmond (17 joint publications)
  • A.M. Madelein van der Stouwe (16 joint publications)
  • Sterre van der Veen (14 joint publications)
  • Jan Willem J. Elting (14 joint publications)

The scholar's work is often published in key journals such as:

  • Parkinsonism & Related Disorders (17 publications)
  • Movement Disorders (15 publications)
  • Movement Disorders Clinical Practice (10 publications)
  • Journal of Neurology Neurosurgery & Psychiatry (7 publications)
  • NeuroImage Clinical (5 publications)

Notable recent papers by Marina A.J. Tijssen include:

  • "Neuroimaging in Functional Neurological Disorder: State of the Field and Research Agenda," 2021, published in NeuroImage Clinical
  • "Outcome measurement in functional neurological disorder: a systematic review and recommendations," 2020, published in Journal of Neurology Neurosurgery & Psychiatry
  • "Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update," 2022, published in Movement Disorders
  • "Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities," 2020, published in Annals of Neurology
  • "A Statement of the MDS on Biological Definition, Staging, and Classification of Parkinson's Disease," 2023, published in Movement Disorders

Best Publications

  • Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism

    Patricia de Carvalho Aguiar;Patricia de Carvalho Aguiar;Kathleen J Sweadner;John T Penniston;Jacek Zaremba

  • Dopamine-dependent changes in the functional connectivity between basal ganglia and cerebral cortex in humans

    D Williams;M Tijssen;G van Bruggen;A Bosch

  • The phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene

    Allison Brashear;William B. Dobyns;Patricia de Carvalho Aguiar;Michel Borg

  • Double-blind clinical trial of thalamic stimulation in patients with Tourette syndrome.

    Linda Ackermans;Annelien Duits;Chris van der Linden;Marina A. Tijssen

  • Different Functional Loops between Cerebral Cortex and the Subthalmic Area in Parkinson's Disease

    Noa Fogelson;David Williams;Marina Tijssen;Gerard van Bruggen

  • Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.

    Mark I. Rees;Mark I. Rees;Kirsten Harvey;Brian R. Pearce;Seo-Kyung Chung;Seo-Kyung Chung

  • The anatomical basis of dystonia : current view using neuroimaging

    Stéphane Lehéricy;Stéphane Lehéricy;Marina A.J. Tijssen;Marie Vidailhet;Ryuji Kaji

  • Clinical spectrum of ataxia-telangiectasia in adulthood

    M. M. M. Verhagen;W. F. Abdo;M. A. A. P. Willemsen;F. B. L. Hogervorst

  • Deep brain stimulation in Tourette's syndrome: two targets?

    Linda Ackermans;Yasin Temel;Danielle Cath;Chris van der Linden

  • Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene

    Katja Lohmann;Robert A. Wilcox;Susen Winkler;Alfredo Ramirez;Alfredo Ramirez

  • Structural, functional and molecular imaging of the brain in primary focal dystonia-A review

    Evelien Zoons;Jan Booij;Aart J. Nederveen;J. M. Dijk

  • Neuroimaging in Functional Neurological Disorder: State of the Field and Research Agenda.

    David L Perez;Timothy R Nicholson;Ali A Asadi-Pooya;Indrit Bègue

  • Sepiapterin Reductase Deficiency: A Treatable Mimic of Cerebral Palsy

    Jennifer Friedman;Jennifer Friedman;Emmanuel Roze;Jose E. Abdenur;Richard Chang

  • Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update

    Unknown

  • The relationship between oscillatory activity and motor reaction time in the parkinsonian subthalamic nucleus

    David Williams;Andrea Kühn;Andrea Kühn;Andreas Kupsch;Marina Tijssen

  • Acute posthypoxic myoclonus after cardiopulmonary resuscitation

    Aline Bouwes;Daniel van Poppelen;Johannes H. T. M. Koelman;Michael A. Kuiper

  • Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

    Rahel T. Florian;Florian Kraft;Elsa Leitão;Sabine Kaya

  • Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

    Mark A. Corbett;Thessa Kroes;Liana Veneziano;Mark F. Bennett;Mark F. Bennett

  • Behavioural cues are associated with modulations of synchronous oscillations in the human subthalamic nucleus.

    David Williams;Andrea Kühn;Andreas Kupsch;Marina Tijssen

  • Outcome measurement in functional neurological disorder: a systematic review and recommendations

    Susannah Pick;David Anderson;Ali Asadi-Pooya;Ali Asadi-Pooya;Selma Aybek

  • DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation.

    Justus L. Groen;Katja Ritz;Maria Fiorella Contarino;Bart P. van de Warrenburg

  • Propriospinal myoclonus: clinical reappraisal and review of literature.

    Sandra M. A. van der Salm;Roberto Erro;Carla Cordivari;Mark J. Edwards

  • Familial cortical myoclonic tremor with epilepsy: A single syndromic classification for a group of pedigrees bearing common features

    Anne-Fleur Van Rootselaar;Ivo N. van Schaik;Arn M.J.M. van den Maagdenberg;Johannes H.T.M. Koelman

  • Local field potentials and oscillatory activity of the internal globus pallidus in myoclonus-dystonia.

    Elisabeth M.J. Foncke;Lo J. Bour;Johannes D. Speelman;Johannes H.T.M. Koelman

Frequent Co-Authors

Johannes H.T.M. Koelman
Johannes H.T.M. Koelman University of Amsterdam
Anne-Fleur van Rootselaar
Anne-Fleur van Rootselaar University of Amsterdam
Frank Baas
Frank Baas Leiden University Medical Center
Danielle C. Cath
Danielle C. Cath Utrecht University
Peter Brown
Peter Brown University of Oxford
Natasha M. Maurits
Natasha M. Maurits University of Groningen
Lo J. Bour
Lo J. Bour University of Amsterdam
Jon Stone
Jon Stone University of Edinburgh
Christine Klein
Christine Klein University of Lübeck

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