Kristýna Kolaříková

University Hospital Olomouc — Czech Republic

Medicine · Health Sciences

4h-index130citations16works1.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Parkinson's Disease Mechanisms and Treatments(6), Neurological diseases and metabolism(6), CRISPR and Genetic Engineering(3), Neurological disorders and treatments(2), Lysosomal Storage Disorders Research(2)

Publications16 total

Reply to: Questioning the cycad theory of Kii ALS–PDC causation
Nature Reviews Neurology·2024· 1 citedOpen Access
Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities
Gene·2023· 1 citedOpen Access
Endemic parkinsonism: clusters, biology and clinical features
Nature Reviews Neurology·2023· 11 cited
Ovarian tumors and genetic predisposition
Česká gynekologie·2022· 1 cited
Reply: Matters Arising ‘Lewy body disease or diseases with Lewy bodies?’
npj Parkinson s Disease·2022Open Access
Magnetic fabric study of the Dejvice loess/paleosol sequence (Prague, Czech Republic)
2022Open Access
Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development
Frontiers in Neuroscience·2022· 3 citedOpen Access
High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic
Life·2022· 2 citedOpen Access
Lewy body disease or diseases with Lewy bodies?
npj Parkinson s Disease·2022· 76 citedOpen Access
Evaluating Basic Next-Generation Sequencing Parameters in Relation to True/False Positivity Findings of Rare Variants in an Isolated Population from the Czech Republic South-Eastern Moravia Region with a High Incidence of Parkinsonism
Lecture notes in computer science·2020· 1 cited
Atypical parkinsonism of progressive supranuclear palsy–parkinsonism (PSP-P) phenotype with rare variants in FBXO7 and VPS35 genes associated with Lewy body pathology
Acta Neuropathologica·2018· 22 cited
New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background
Medicine·2018· 9 citedOpen Access
The identification of molecular-genetic background of familial atypical parkinsonism in “Hornacko”, a specific region of the South-Eastern Moravia, Czech Republic
Parkinsonism & Related Disorders·2018
The identification of molecular-genetic background of familial atypical parkinsonism in "Hornacko", a specific region of the South-Eastern Moravia, Czech Republic
Journal of the Neurological Sciences·2017
Next Generation Sequencing Data Analysis Evaluation in Patients with Parkinsonism from a Genetically Isolated Population
Genomics and Computational Biology·2017· 3 citedOpen Access
Vliv imunohistochemické exprese proteinů ERCC1, FLNA a mutačního statusu K - RAS k výskytu vzdálených metastáz u NSCLC
2014

Frequent Co-authors

Radek Vodička(14), Radek Vrtěl(14), Kateřina Menšíková(12), Petr Kaňovský(12), Martin Procházka(11), Pavel Otruba(7), Lucie Tučková(5), Michaela Kaiserová(5), Tereza Bartoníková(5), Radoslav Matěj(4), Carlo Colosimo(4), Raymond L. Rosales(4), Dominik Hraboš(4), Martin Bareš(4), Jiří Ehrmann(3), Petr Hluštı́k(3), Miroslav Vaštík(3), Júlia Štellmachová(3), Martin Nevrlý(2), Sandra Kurčová(2)