Radek Vrtel

Olomouc, Czech Republic

Last Updated: 09/26/2026

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Found 38 publications

Spectrum of germline variants in a group of patients with ovarian cancer.

Spectrum of germline variants in a group of patients with ovarian cancer.

Journal: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia

Published: May 12, 2026

Reply to: Questioning the cycad theory of Kii ALS-PDC causation.

Reply to: Questioning the cycad theory of Kii ALS-PDC causation.

Journal: Nature reviews. Neurology

Published: February 09, 2024

Genetic Predisposition to Male Breast Cancer.

Genetic Predisposition to Male Breast Cancer.

Journal: Folia biologica

Published: January 01, 2024

Endemic parkinsonism: clusters, biology and clinical features.

Endemic parkinsonism: clusters, biology and clinical features.

Journal: Nature reviews. Neurology

Published: August 07, 2023

Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis.

Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis.

Journal: Ceska gynekologie

Published: June 21, 2023

Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities.

Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities.

Journal: Gene

Published: June 01, 2023

Ovarian tumors and genetic predisposition.

Ovarian tumors and genetic predisposition.

Journal: Ceska gynekologie

Published: July 27, 2022

Screening for congenital defects and genetic diseases of the fetus at University Hospital in Olomouc and sending/ reporting to the National register of reproductive health in the Czech Republic.

Screening for congenital defects and genetic diseases of the fetus at University Hospital in Olomouc and sending/ reporting to the National register of reproductive health in the Czech Republic.

Journal: Ceska gynekologie

Published: July 27, 2022

Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.

Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.

Journal: Diagnostics (Basel, Switzerland)

Published: March 21, 2022

Reply: Matters Arising 'Lewy body disease or diseases with Lewy bodies?'

Reply: Matters Arising 'Lewy body disease or diseases with Lewy bodies?'

Journal: NPJ Parkinson's disease

Published: February 23, 2022

Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.

Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.

Journal: Hormone research in paediatrics

Published: January 07, 2022

High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic.

High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic.

Journal: Life (Basel, Switzerland)

Published: December 21, 2021

Showing 1-12 of 38

Last Updated: 09/26/2026