Pavlína Plevová

714 total citations
34 papers, 398 citations indexed

About

Pavlína Plevová is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Pavlína Plevová has authored 34 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Oncology and 8 papers in Genetics. Recurrent topics in Pavlína Plevová's work include Genetic factors in colorectal cancer (7 papers), BRCA gene mutations in cancer (4 papers) and DNA Repair Mechanisms (3 papers). Pavlína Plevová is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), BRCA gene mutations in cancer (4 papers) and DNA Repair Mechanisms (3 papers). Pavlína Plevová collaborates with scholars based in Czechia, France and Australia. Pavlína Plevová's co-authors include Zdeněk Sedláček, Anna Křepelová, Zdeněk Kolář, Jana Zapletalová, Pavlína Kušnierová, Lenka Foretová, Julie Fleitz, Nicholas K. Foreman, Marie Trková and Leoš Pleva and has published in prestigious journals such as Human Molecular Genetics, European Journal of Cancer and Muscle & Nerve.

In The Last Decade

Pavlína Plevová

31 papers receiving 386 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pavlína Plevová Czechia 11 150 114 114 93 60 34 398
Dong-Il Sun South Korea 8 154 1.0× 41 0.4× 76 0.7× 113 1.2× 42 0.7× 11 485
Hilda Tateossian United Kingdom 11 227 1.5× 48 0.4× 105 0.9× 131 1.4× 100 1.7× 17 515
Shiori Endo Japan 16 309 2.1× 52 0.5× 112 1.0× 91 1.0× 28 0.5× 37 500
JH Choi South Korea 12 159 1.1× 94 0.8× 98 0.9× 14 0.2× 29 0.5× 21 510
U. Häuser Germany 12 153 1.0× 152 1.3× 193 1.7× 378 4.1× 14 0.2× 26 826
Umut Aypar United States 12 273 1.8× 111 1.0× 88 0.8× 9 0.1× 127 2.1× 33 557
Ferenc Fazakas Hungary 12 135 0.9× 82 0.7× 27 0.2× 12 0.1× 22 0.4× 18 348
Sara Nathan United States 11 209 1.4× 39 0.3× 58 0.5× 21 0.2× 21 0.3× 16 483
Thomas F. Barrett United States 12 150 1.0× 70 0.6× 146 1.3× 55 0.6× 12 0.2× 26 495
J.M. Martínez-Peñuela Spain 13 195 1.3× 118 1.0× 215 1.9× 8 0.1× 53 0.9× 35 572

Countries citing papers authored by Pavlína Plevová

Since Specialization
Citations

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

Fields of papers citing papers by Pavlína Plevová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pavlína Plevová

This figure shows the co-authorship network connecting the top 25 collaborators of Pavlína Plevová. A scholar is included among the top collaborators of Pavlína Plevová 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 Pavlína Plevová. Pavlína Plevová 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.
Plevová, Pavlína. (2019). An Update on Inherited Colon Cancer and Gastrointestinal Polyposis. Klinicka onkologie. 32(Suppl 2). 97–108. 5 indexed citations
2.
Pleva, Leoš, Pavlína Kušnierová, Pavlína Plevová, et al.. (2017). The APOE ε2 allele is associated with increased plasma apolipoprotein E levels in patients with coronary artery disease. Cor et Vasa. 59(3). e235–e239. 1 indexed citations
3.
Plevová, Pavlína, et al.. (2017). Familial hematuria: A review. Medicina. 53(1). 1–10. 10 indexed citations
4.
Pleva, Leoš, Pavlína Kušnierová, Pavlína Plevová, et al.. (2015). Increased levels of MMP-3, MMP-9 and MPO represent predictors of in-stent restenosis, while increased levels of ADMA, LCAT, ApoE and ApoD predict bare metal stent patency. Biomedical Papers. 159(4). 586–594. 15 indexed citations
5.
Kušnierová, Pavlína, et al.. (2015). Reference intervals of plasma matrix metalloproteinases 2, 3, and 9 and serum asymmetric dimethylarginine levels. Scandinavian Journal of Clinical and Laboratory Investigation. 75(6). 508–513. 7 indexed citations
6.
Pleva, Leoš, et al.. (2015). The rs1803274 polymorphism of the BCHE gene is associated with an increased risk of coronary in-stent restenosis. BMC Cardiovascular Disorders. 15(1). 135–135. 10 indexed citations
7.
Plevová, Pavlína, et al.. (2013). Breast Cancer in Monozygotic Twins. Klinicka onkologie. 26(3). 213–217. 3 indexed citations
8.
Brožková, Dana Šafka, Radim Mazanec, Jana Haberlová, et al.. (2011). Four novel point mutations in the PMP22 gene with phenotypes of HNPP and Dejerine–Sottas neuropathy. Muscle & Nerve. 44(5). 819–821. 7 indexed citations
9.
Plevová, Pavlína, et al.. (2010). CCND1 and ZNF217 gene amplification is equally frequent in BRCA1 and BRCA2 associated and non-BRCA breast cancer. Neoplasma. 57(4). 325–332. 8 indexed citations
10.
Petrák, B., Pavlína Plevová, Jiřı́ Novotný, & Lenka Foretová. (2009). [Neurofibromatosis von Recklinghausen].. PubMed. 22 Suppl. S38–44. 3 indexed citations
11.
Plevová, Pavlína, Jan Bouchal, Anna Křepelová, et al.. (2007). PML and TRF2 protein expression in hereditary and sporadic colon cancer.. PubMed. 54(4). 269–77. 3 indexed citations
12.
Škarda, Jozef, Eddie Fridman, Pavlína Plevová, et al.. (2006). PROGNOSTIC VALUE OF hMLH1 AND hMSH2 IMMUNOHISTOCHEMICAL EXPRESSION IN NON-SMALL CELL LUNG CANCER. A TISSUE MICROARRAY STUDY. Biomedical Papers. 150(2). 255–259. 7 indexed citations
13.
Trková, Marie, Julie Fleitz, Anna Křepelová, et al.. (2005). Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations. European Journal of Cancer. 41(11). 1597–1603. 54 indexed citations
14.
Plevová, Pavlína, Anna Křepelová, Eva Sedlákova, et al.. (2004). Immunohistochemical detection of the hMLH1 and hMSH2 proteins in hereditary non-polyposis colon cancer and sporadic colon cancer.. PubMed. 51(4). 275–84. 17 indexed citations
15.
Plevová, Pavlína, et al.. (2004). Expression of the hMLH1 and hMSH2 proteins in normal tissues: relationship to cancer predisposition in hereditary non-polyposis colon cancer. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 446(2). 112–119. 11 indexed citations
16.
Plevová, Pavlína, Anna Křepelová, Eva Sedlákova, et al.. (2003). 286 Immunohistochemical detection of the hMLH1 and hMSH2 proteins in hereditary and sporadic colon cancer tissues. European Journal of Cancer Supplements. 1(5). S88–S88.
17.
Kolář, Zdeněk, Jana Dvořáčková, Pavlína Plevová, et al.. (2002). [What is the real importance of evaluating the expression of c-erbB-2 (HER-2/neu) in carcinoma of the breast and prostate? (A short review)].. PubMed. 38 Suppl 1. 15–9. 1 indexed citations
18.
Plevová, Pavlína. (2002). Modulation of radiotherapy-and chemotherapy-induced normal tissue response as prophylaxis of their side effects. Radiology and Oncology. 36(1). 2 indexed citations
19.
Plevová, Pavlína. (2002). Radiotherapy-and chemotherapy-induced normal tissue damage: the role of cytokines and adhesion molecules. Radiology and Oncology. 36(2). 2 indexed citations
20.
Plevová, Pavlína. (1999). Prevention and treatment of chemotherapy- and radiotherapy-induced oral mucositis: a review. Oral Oncology. 35(5). 453–470. 102 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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