Radek Vodička

405 total citations
35 papers, 252 citations indexed

About

Radek Vodička is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Physiology. According to data from OpenAlex, Radek Vodička has authored 35 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 9 papers in Physiology. Recurrent topics in Radek Vodička's work include Prenatal Screening and Diagnostics (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Radek Vodička is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Radek Vodička collaborates with scholars based in Czechia, United States and Australia. Radek Vodička's co-authors include Radek Vrtěl, Ladislav Dušek, Jiří Šantavý, Arvind R. Singh, Martin Procházka, Jiřı́ Dostál, I Oborná, Kateřina Menšíková, Kateřina Křížová and Petr Kaňovský and has published in prestigious journals such as Scientific Reports, Gene and Medicine.

In The Last Decade

Radek Vodička

33 papers receiving 245 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Radek Vodička Czechia 8 86 84 64 57 33 35 252
Mengmeng Shi China 10 81 0.9× 43 0.5× 99 1.5× 90 1.6× 4 0.1× 20 289
Oumar Samassékou Canada 9 28 0.3× 129 1.5× 131 2.0× 7 0.1× 11 0.3× 22 241
Daniela L. Buscariollo United States 7 71 0.8× 14 0.2× 149 2.3× 14 0.2× 8 0.2× 20 387
Sukhdeep Singh United States 8 63 0.7× 60 0.7× 335 5.2× 8 0.1× 17 0.5× 8 556
Zamalou Gisèle Ouandaogo France 4 19 0.2× 49 0.6× 156 2.4× 28 0.5× 93 2.8× 4 285
N. A. Skryabin Russia 10 157 1.8× 16 0.2× 184 2.9× 13 0.2× 10 0.3× 46 371
Irén Haltrich Hungary 9 93 1.1× 8 0.1× 103 1.6× 11 0.2× 10 0.3× 33 239
Tatsuhiro Sakamoto Japan 7 41 0.5× 15 0.2× 55 0.9× 10 0.2× 26 0.8× 36 279
Mark A. Garthwaite United States 13 111 1.3× 28 0.3× 176 2.8× 4 0.1× 56 1.7× 15 395

Countries citing papers authored by Radek Vodička

Since Specialization
Citations

This map shows the geographic impact of Radek Vodička's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Radek Vodička with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Radek Vodička more than expected).

Fields of papers citing papers by Radek Vodička

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Radek Vodička. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Radek Vodička. The network helps show where Radek Vodička may publish in the future.

Co-authorship network of co-authors of Radek Vodička

This figure shows the co-authorship network connecting the top 25 collaborators of Radek Vodička. A scholar is included among the top collaborators of Radek Vodička based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Radek Vodička. Radek Vodička is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Menšíková, Kateřina, Radoslav Matěj, Carlo Colosimo, et al.. (2022). Lewy body disease or diseases with Lewy bodies?. npj Parkinson s Disease. 8(1). 3–3. 49 indexed citations
3.
Vodička, Radek, et al.. (2022). Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development. Frontiers in Neuroscience. 16. 817713–817713. 1 indexed citations
4.
Vrtěl, Radek, et al.. (2022). Ovarian tumors and genetic predisposition. PubMed. 87(3). 211–216. 1 indexed citations
5.
Vrtěl, Radek, Václav Hána, Ondřej Souček, et al.. (2021). Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms. Biomedical Papers. 166(1). 63–67. 3 indexed citations
6.
Menšíková, Kateřina, Radek Vodička, Radek Vrtěl, et al.. (2018). New endemic familial parkinsonism in south Moravia, Czech Republic and its genetical background. Medicine. 97(38). e12313–e12313. 4 indexed citations
7.
Fostira, Florentia, Radek Vodička, Radek Vrtěl, et al.. (2017). Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece. Scientific Reports. 7(1). 16697–16697. 23 indexed citations
8.
Menšíková, Kateřina, Radek Vodička, Radek Vrtěl, et al.. (2016). Familial atypical parkinsonism with rare variant in VPS35 and FBXO7 genes. Medicine. 95(46). e5398–e5398. 6 indexed citations
9.
Vodička, Radek, Marek Ľubušký, Ladislav Dušek, et al.. (2015). Clinical Potential of Effective Noninvasive Exclusion of <b><i>KEL1</i></b>-Positive Fetuses in <b><i>KEL1</i></b>-Negative Pregnant Women. Fetal Diagnosis and Therapy. 40(1). 48–53. 2 indexed citations
10.
Menšíková, Kateřina, Petr Kaňovský, Pavel Otruba, et al.. (2015). Familial, autosomal-dominant neurodegenerative parkinsonism with cognitive deterioration spanning five generations in a genetically isolated population of south-eastern Moravia, Czech Republic. Biomedical Papers. 160(1). 158–160. 3 indexed citations
11.
Vrtěl, Radek, et al.. (2013). STAT6 - polymorphisms, haplotypes and epistasis in relation to atopy and asthma. Biomedical Papers. 157(2). 172–180. 12 indexed citations
12.
13.
Vodička, Radek, et al.. (2012). Association of STAT6 and ADAM33 single nucleotide polymorphisms with asthma bronchiale and IgE level and its possible epigenetic background. Biomedical Papers. 156(3). 236–247. 12 indexed citations
14.
Vodička, Radek, et al.. (2011). SEQUENCE RECOMBINATION IN EXON 1 OF THE TSPY GENE IN MEN WITH IMPAIRED FERTILITY. Biomedical Papers. 155(3). 287–298. 3 indexed citations
15.
Kacerovská, Denisa, Radek Vrtěl, Michal Michal, et al.. (2009). TSC2/PKD1 Contiguous Gene Syndrome: A Report of 2 Cases With Emphasis on Dermatopathologic Findings. American Journal of Dermatopathology. 31(6). 532–541. 15 indexed citations
16.
Vodička, Radek, Radek Vrtěl, Ladislav Dušek, et al.. (2008). Refined fluorescent STR quantification of cell‐free fetal DNA during pregnancy in physiological and Down syndrome fetuses. Prenatal Diagnosis. 28(5). 425–433. 10 indexed citations
17.
Vodička, Radek, Radek Vrtěl, Ladislav Dušek, et al.. (2007). TSPY gene copy number as a potential new risk factor for male infertility. Reproductive BioMedicine Online. 14(5). 579–587. 54 indexed citations
18.
Vodička, Radek, et al.. (2006). [Rapid detection of most frequent chromosomal aneuploidies by the multiplex QF PCR method in the first trimester of pregnancy].. PubMed. 71(4). 280–4. 1 indexed citations
19.
Singh, Arvind R., et al.. (2006). Comparative Study of AZF Deletions and TSPY Gene Variation in Czech and Indian Infertile Men. International Journal of Human Genetics. 6(3). 209–217. 1 indexed citations
20.
Vodička, Radek, Radek Vrtěl, Jiřina Zapletalová, et al.. (2004). Refined quantitative fluorescent PCR of Y-chromosome DNA sequences mosaics in Turner's syndrome patients—alternative to real-time PCR. Journal of Biochemical and Biophysical Methods. 60(2). 151–162. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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