Beáta Soltész

772 total citations
31 papers, 594 citations indexed

About

Beáta Soltész is a scholar working on Molecular Biology, Cancer Research and Immunology. According to data from OpenAlex, Beáta Soltész has authored 31 papers receiving a total of 594 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Cancer Research and 5 papers in Immunology. Recurrent topics in Beáta Soltész's work include MicroRNA in disease regulation (11 papers), Extracellular vesicles in disease (7 papers) and Cancer-related molecular mechanisms research (7 papers). Beáta Soltész is often cited by papers focused on MicroRNA in disease regulation (11 papers), Extracellular vesicles in disease (7 papers) and Cancer-related molecular mechanisms research (7 papers). Beáta Soltész collaborates with scholars based in Hungary, Slovakia and United States. Beáta Soltész's co-authors include Bálint Nagy, Melinda Szilágyi, András Penyige, Éva Márton, Tomáš Szemes, Ondrej Pös, Gergely Buglyó, Ròbert Póka, László Maródi and Beáta Tóth and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Methods in enzymology on CD-ROM/Methods in enzymology.

In The Last Decade

Beáta Soltész

30 papers receiving 586 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beáta Soltész Hungary 12 370 316 122 52 51 31 594
Jéssica Rodrigues Plaça Brazil 14 323 0.9× 206 0.7× 75 0.6× 52 1.0× 50 1.0× 28 495
Harekrushna Panda India 11 318 0.9× 222 0.7× 78 0.6× 26 0.5× 60 1.2× 16 549
Yao Xue China 17 673 1.8× 621 2.0× 86 0.7× 47 0.9× 93 1.8× 56 949
Park Sm South Korea 4 494 1.3× 444 1.4× 73 0.6× 27 0.5× 37 0.7× 15 653
Sonia T. Chelbi France 18 341 0.9× 170 0.5× 276 2.3× 78 1.5× 69 1.4× 24 892
Jonathan Digby‐Bell United Kingdom 5 331 0.9× 93 0.3× 55 0.5× 76 1.5× 97 1.9× 17 510
Zhaolei Cui China 15 311 0.8× 265 0.8× 52 0.4× 44 0.8× 137 2.7× 51 539
Tara L. Sander United States 12 433 1.2× 88 0.3× 107 0.9× 36 0.7× 73 1.4× 19 598
Gufeng Xu China 12 313 0.8× 178 0.6× 202 1.7× 40 0.8× 84 1.6× 40 628

Countries citing papers authored by Beáta Soltész

Since Specialization
Citations

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

Fields of papers citing papers by Beáta Soltész

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beáta Soltész

This figure shows the co-authorship network connecting the top 25 collaborators of Beáta Soltész. A scholar is included among the top collaborators of Beáta Soltész 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 Beáta Soltész. Beáta Soltész 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.
Gombos, G., Ondrej Pös, Gergely Buglyó, et al.. (2023). New Possible Ways to Use Exosomes in Diagnostics and Therapy via JAK/STAT Pathways. Pharmaceutics. 15(7). 1904–1904. 5 indexed citations
2.
Micsík, Tamás, Tamás Tornóczky, Levente Kuthi, et al.. (2023). Alterations of miRNA Expression in Diffuse Hyperplastic Perilobar Nephroblastomatosis: Mapping the Way to Understanding Wilms’ Tumor Development and Differential Diagnosis. International Journal of Molecular Sciences. 24(10). 8793–8793. 5 indexed citations
3.
Buglyó, Gergely, Ondrej Pös, Beáta Soltész, et al.. (2022). Extracellular Nucleic Acids in the Diagnosis and Progression of Colorectal Cancer. Cancers. 14(15). 3712–3712. 6 indexed citations
4.
Buglyó, Gergely, Ondrej Pös, Vanda Repiská, et al.. (2022). Liquid Biopsy as a Source of Nucleic Acid Biomarkers in the Diagnosis and Management of Lynch Syndrome. International Journal of Molecular Sciences. 23(8). 4284–4284. 10 indexed citations
5.
Soltész, Beáta, Ondrej Pös, Jaroslav Budiš, et al.. (2022). Mitochondrial DNA copy number changes, heteroplasmy, and mutations in plasma-derived exosomes and brain tissue of glioblastoma patients. Molecular and Cellular Probes. 66. 101875–101875. 12 indexed citations
6.
Soltész, Beáta, Gergely Buglyó, Melinda Szilágyi, et al.. (2021). The Role of Exosomes in Cancer Progression. International Journal of Molecular Sciences. 23(1). 8–8. 38 indexed citations
7.
Márton, Éva, Beáta Soltész, András Penyige, et al.. (2021). Comparative Analysis of Cell-Free miR-205-5p, let-7f-5p, and miR-483-5p Expression in Ovarian Cell Cultures and Plasma Samples of Patients with Ovarian Cancer. Applied Sciences. 11(4). 1735–1735. 3 indexed citations
8.
Szilágyi, Melinda, Ondrej Pös, Éva Márton, et al.. (2020). Circulating Cell-Free Nucleic Acids: Main Characteristics and Clinical Application. International Journal of Molecular Sciences. 21(18). 6827–6827. 140 indexed citations
9.
Soltész, Beáta, Péter Pikó, János Sándor, et al.. (2020). The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population. PLoS ONE. 15(6). e0234547–e0234547. 15 indexed citations
10.
Dvorská, Dana, Dušan Braný, Bálint Nagy, et al.. (2019). Aberrant Methylation Status of Tumour Suppressor Genes in Ovarian Cancer Tissue and Paired Plasma Samples. International Journal of Molecular Sciences. 20(17). 4119–4119. 26 indexed citations
11.
Penyige, András, Éva Márton, Beáta Soltész, et al.. (2019). Circulating miRNA Profiling in Plasma Samples of Ovarian Cancer Patients. International Journal of Molecular Sciences. 20(18). 4533–4533. 28 indexed citations
12.
Soltész, Beáta, Éva Márton, Melinda Szilágyi, et al.. (2019). Detection of cell-free, exosomal and whole blood mitochondrial DNA copy number in plasma or whole blood of patients with serous epithelial ovarian cancer. Journal of Biotechnology. 298. 76–81. 64 indexed citations
13.
Márton, Éva, András Penyige, Eszter Anna Janka, et al.. (2019). Circulating epithelial-mesenchymal transition-associated miRNAs are promising biomarkers in ovarian cancer. Journal of Biotechnology. 297. 58–65. 34 indexed citations
14.
Soltész, Beáta, Éva Márton, Melinda Szilágyi, et al.. (2019). Expression of CD24 in plasma, exosome and ovarian tissue samples of serous ovarian cancer patients. Journal of Biotechnology. 298. 16–20. 26 indexed citations
15.
16.
Soltész, Beáta, et al.. (2019). PITX2 and NEURL1 SNP polymorphisms in Hungarian atrial fibrillation patients determined by quantitative real-time PCR and melting curve analysis. Journal of Biotechnology. 299. 44–49. 3 indexed citations
17.
Soltész, Beáta, et al.. (2019). Determination of miR-193b rs30236 single nucleotide polymorphism in ovarian cancer patients. European Journal of Gynaecological Oncology. 40(4). 547–550. 2 indexed citations
18.
Soltész, Beáta, et al.. (2019). Identification of miR-146a and miR-196a-2 single nucleotide polymorphisms at patients with high-grade serous ovarian cancer. Journal of Biotechnology. 297. 54–57. 9 indexed citations
19.
Soltész, Beáta, Edit Gyimesi, Árpád Lányi, et al.. (2014). Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene. Journal of Clinical Immunology. 35(1). 26–31. 3 indexed citations
20.
Gulácsy, Vera, Beáta Soltész, Edit Gyimesi, et al.. (2014). A novel large deletion and single nucleotide insertion in the Wiskott–Aldrich syndrome protein gene. European Journal Of Haematology. 95(1). 93–98. 2 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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