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Author

Vladimír Haň

Observed names: Han, Vladimir, Háň, Vladimír, V. Han, V. Haň, Vladimir Han
ORCID: 0000-0003-1942-3778
Observed ORCID: 0000-0003-1942-3778
OpenAlex ID: A5032488458
Monogenic variants in dystonia: an exome-wide sequencing study
2020 · Michael Zech, Robert Jech, et al. · The Lancet Neurology · 212
Differences in MDS ‐ UPDRS Scores Based on Hoehn and Yahr Stage and Disease Duration
2017 · Matej Skorvanek, Pablo Martinez‐Martin, et al. · Movement Disorders Clinical Practice · 149
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Psychiatric co-morbidity is highly prevalent in idiopathic cervical dystonia and significantly influences health-related quality of life: Results of a controlled study
2016 · M. Smit, A. Kuiper, et al. · Parkinsonism & Related Disorders · 96
Relationship between the MDS-UPDRS and Quality of Life: A large multicenter study of 3206 patients
2018 · Matej Skorvanek, Pablo Martinez-Martin, et al. · Parkinsonism & Related Disorders · 82
Paroxysmal exercise‐induced dystonia within the phenotypic spectrum of ECHS1 deficiency
2016 · Simone Olgiati, Matej Skorvanek, et al. · Movement Disorders · 79
Relationship between the non-motor items of the MDS–UPDRS and Quality of Life in patients with Parkinson's disease
2015 · Matej Skorvanek, Jaroslav Rosenberger, et al. · Journal of the Neurological Sciences · 69
Fatigue, Sleep Disturbances, and Their Influence on Quality of Life in Cervical Dystonia Patients
2016 · Marenka Smit, Arwen S. J. Kamphuis, et al. · Movement Disorders Clinical Practice · 49
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The Clinical Syndrome of Paroxysmal Exercise‐Induced Dystonia: Diagnostic Outcomes and an Algorithm
2014 · Roberto Erro, Maria Stamelou, et al. · Movement Disorders Clinical Practice · 45
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Prevalence of non‐motor symptoms and their association with quality of life in cervical dystonia
2020 · Vladimir Han, Matej Skorvanek, et al. · Acta Neurologica Scandinavica · 41
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Neurodevelopmental disorder associated with IRF2BPL gene mutation: Expanding the phenotype?
2019 · Matej Skorvanek, Petr Dusek, et al. · Parkinsonism & Related Disorders · 32
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia
2021 · Matej Skorvanek, Irena Rektorova, et al. · Parkinsonism & Related Disorders · 31
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Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series
2021 · Ivana Dzinovic, Matej Škorvánek, et al. · Parkinsonism & Related Disorders · 28
Scoring Algorithm‐Based Genomic Testing in Dystonia: A Prospective Validation Study
2021 · Michael Zech, Robert Jech, et al. · Movement Disorders · 26
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Clinically relevant copy-number variants in exome sequencing data of patients with dystonia
2021 · Michael Zech, Sylvia Boesch, et al. · Parkinsonism & Related Disorders · 23
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia
2019 · Kamal Khan, Michael Zech, et al. · Genetics in Medicine · 23
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Prevalence of Prodromal Parkinson’s Disease as Defined by MDS Research Criteria among Elderly Patients Undergoing Colonoscopy
2017 · Matej Skorvanek, Zuzana Ladomirjakova, et al. · Journal of Parkinson s Disease · 21
α‐Synuclein antibody 5G4 identifies manifest and prodromal Parkinson's disease in colonic mucosa
2018 · Matej Skorvanek, Ellen Gelpi, et al. · Movement Disorders · 17
The Frequency and Self‐perceived Impact on Daily Life of Motor and Non‐motor Symptoms in Cervical Dystonia
2017 · Marenka Smit, Anna L. Bartels, et al. · Movement Disorders Clinical Practice · 17
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A Recurrent VPS16 p.Arg187* Nonsense Variant in Early‐Onset Generalized Dystonia
2021 · Miriama Ostrozovicova, Robert Jech, et al. · Movement Disorders · 15
Alzheimer’s Disease-Associated SNP rs708727 in SLC41A1 May Increase Risk for Parkinson’s Disease: Report from Enlarged Slovak Study
2022 · Michal Cibulka, Maria Brodnanova, et al. · International Journal of Molecular Sciences · 14
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Prevalence of Fabry Disease among Patients with Parkinson’s Disease
2022 · Alexandra Lackova, Christian Beetz, et al. · Parkinson s Disease · 11
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Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystonia
2020 · Michael Zech, Theresa Brunet, et al. · Parkinsonism & Related Disorders · 10
Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion
2019 · Petra Dosekova, Andrzej Dubiel, et al. · European Journal of Medical Genetics · 10
Deep Brain Stimulation for VPS16 ‐Related Dystonia: A Multicenter Study
2025 · Tatiana Svorenova, Luigi M. Romito, et al. · Annals of Neurology · 9
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Dystonia as a prominent feature of TCF20-associated neurodevelopmental disorder: Expanding the phenotype
2022 · Tatiana Svorenova, Luigi M. Romito, et al. · Parkinsonism & Related Disorders · 9
Works count: 49
Citation count: 1,158
H-index: 17
I10-index: 23
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