Radek Vrtěl

1.1k total citations
49 papers, 616 citations indexed

About

Radek Vrtěl is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Radek Vrtěl has authored 49 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Physiology and 16 papers in Genetics. Recurrent topics in Radek Vrtěl's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Tuberous Sclerosis Complex Research (9 papers) and Prenatal Screening and Diagnostics (9 papers). Radek Vrtěl is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Tuberous Sclerosis Complex Research (9 papers) and Prenatal Screening and Diagnostics (9 papers). Radek Vrtěl collaborates with scholars based in Czechia, Denmark and United States. Radek Vrtěl's co-authors include Radek Vodička, Jiří Bártek, Jiřina Bártková, Ladislav Dušek, Jiří Šantavý, Martin Mistrík, Päivi Heikkilä, Heli Nevanlinna, Rainer Fagerholm and Martin Procházka and has published in prestigious journals such as Nature Genetics, Oncogene and Scientific Reports.

In The Last Decade

Radek Vrtěl

47 papers receiving 606 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 Vrtěl Czechia 13 310 157 134 127 64 49 616
Shey‐Cherng Tzou United States 16 130 0.4× 67 0.4× 53 0.4× 84 0.7× 44 0.7× 23 534
Stephan Geley Austria 14 634 2.0× 77 0.5× 40 0.3× 185 1.5× 18 0.3× 16 879
Giuseppina D’Andrilli Italy 13 484 1.6× 93 0.6× 26 0.2× 163 1.3× 78 1.2× 19 714
Soung Jung Kim South Korea 14 400 1.3× 41 0.3× 78 0.6× 50 0.4× 59 0.9× 16 637
Shigeru Daido Japan 9 577 1.9× 48 0.3× 92 0.7× 124 1.0× 58 0.9× 17 966
Éric Jeandidier France 11 226 0.7× 155 1.0× 43 0.3× 35 0.3× 10 0.2× 32 456
Károly Szekeres United States 12 208 0.7× 68 0.4× 75 0.6× 119 0.9× 8 0.1× 18 572
Jason Beliakoff United States 10 455 1.5× 158 1.0× 17 0.1× 86 0.7× 11 0.2× 11 596
Melissa L. Sokolosky United States 6 521 1.7× 43 0.3× 27 0.2× 182 1.4× 14 0.2× 6 697
Anne Aries France 13 460 1.5× 61 0.4× 60 0.4× 119 0.9× 6 0.1× 21 718

Countries citing papers authored by Radek Vrtěl

Since Specialization
Citations

This map shows the geographic impact of Radek Vrtěl'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 Vrtěl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Radek Vrtěl more than expected).

Fields of papers citing papers by Radek Vrtěl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Radek Vrtěl. 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 Vrtěl. The network helps show where Radek Vrtěl may publish in the future.

Co-authorship network of co-authors of Radek Vrtěl

This figure shows the co-authorship network connecting the top 25 collaborators of Radek Vrtěl. A scholar is included among the top collaborators of Radek Vrtěl 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 Vrtěl. Radek Vrtěl 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.
Srovnal, Josef, et al.. (2022). Clinical impact of variants in non-coding regions of SHOX – Current knowledge. Gene. 818. 146238–146238. 2 indexed citations
4.
Souček, Ondřej, Radek Vrtěl, Václav Hána, et al.. (2022). Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features. Hormone Research in Paediatrics. 95(5). 465–475. 2 indexed citations
5.
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
6.
Slabáková, Eva, Lucia Binó, Ján Remšík, et al.. (2019). Generation of human iPSCs from fetal prostate fibroblasts HPrF. Stem Cell Research. 35. 101405–101405. 3 indexed citations
7.
Slabáková, Eva, Lucia Binó, Ján Remšík, et al.. (2018). Generation of human iPSCs from human prostate cancer-associated fibroblasts IBPi002-A. Stem Cell Research. 33. 255–259. 3 indexed citations
8.
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
9.
Bártková, Jiřina, Radek Vrtěl, Dušana Majera, et al.. (2016). DNA damage signalling barrier, oxidative stress and treatment‐relevant DNA repair factor alterations during progression of human prostate cancer. Molecular Oncology. 10(6). 879–894. 46 indexed citations
10.
Mistrík, Martin, Pavel Moudrý, Ján Gurský, et al.. (2016). Tumors overexpressing RNF168 show altered DNA repair and responses to genotoxic treatments, genomic instability and resistance to proteotoxic stress. Oncogene. 36(17). 2405–2422. 44 indexed citations
11.
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
12.
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
13.
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
14.
15.
Kacerovská, Denisa, Katrin Kerl, Michal Michal, et al.. (2012). Giant angiofibromas in tuberous sclerosis complex: A possible role for localized lymphedema in their pathogenesis. Journal of the American Academy of Dermatology. 67(6). 1319–1326. 5 indexed citations
16.
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
17.
Liontos, Michalis, Katerina Niforou, Georgia Velimezi, et al.. (2009). Modulation of the E2F1-Driven Cancer Cell Fate by the DNA Damage Response Machinery and Potential Novel E2F1 Targets in Osteosarcomas. American Journal Of Pathology. 175(1). 376–391. 37 indexed citations
18.
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
19.
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
20.
Verhoef, Senno, Radek Vrtěl, Irene Stolte‐Dijkstra, et al.. (1998). Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene. Human Mutation. 11(S1). S85–S87. 8 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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