О. А. Донцова

1.7k total citations
82 papers, 1.1k citations indexed

About

О. А. Донцова is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, О. А. Донцова has authored 82 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 42 papers in Physiology and 16 papers in Genetics. Recurrent topics in О. А. Донцова's work include Telomeres, Telomerase, and Senescence (40 papers), RNA and protein synthesis mechanisms (20 papers) and RNA modifications and cancer (15 papers). О. А. Донцова is often cited by papers focused on Telomeres, Telomerase, and Senescence (40 papers), RNA and protein synthesis mechanisms (20 papers) and RNA modifications and cancer (15 papers). О. А. Донцова collaborates with scholars based in Russia, Tajikistan and Germany. О. А. Донцова's co-authors include Maria I. Zvereva, Daria M. Shcherbakova, Maria P. Rubtsova, Петр В. Сергиев, Anastasia Chugunova, Elena M. Smekalova, Svetlana Dokudovskaya, O. V. Shpanchenko, Dmitry A. Skvortsov and Nikolai V. Ravin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Molecular Cell.

In The Last Decade

О. А. Донцова

77 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
О. А. Донцова Russia 17 859 361 122 100 71 82 1.1k
Maria P. Rubtsova Russia 18 705 0.8× 171 0.5× 106 0.9× 90 0.9× 23 0.3× 59 972
H. Gut Switzerland 20 1.3k 1.5× 100 0.3× 132 1.1× 96 1.0× 60 0.8× 26 1.6k
Florence Manero France 14 935 1.1× 103 0.3× 36 0.3× 75 0.8× 31 0.4× 21 1.2k
Miranda Wilson United Kingdom 19 652 0.8× 103 0.3× 93 0.8× 65 0.7× 16 0.2× 26 1.2k
Xianmei Yang China 17 634 0.7× 71 0.2× 46 0.4× 118 1.2× 22 0.3× 33 907
Corina Borghouts Germany 20 875 1.0× 91 0.3× 51 0.4× 82 0.8× 274 3.9× 29 1.2k
Nurit Livnat‐Levanon Israel 13 908 1.1× 76 0.2× 70 0.6× 43 0.4× 50 0.7× 20 1.1k
Tzu‐Chien V. Wang Taiwan 28 1.5k 1.7× 366 1.0× 550 4.5× 351 3.5× 19 0.3× 65 1.8k
Jad Abdallah Lebanon 15 388 0.5× 84 0.2× 114 0.9× 41 0.4× 10 0.1× 26 713
Isabel Cuesta Spain 13 1.2k 1.4× 36 0.1× 247 2.0× 80 0.8× 27 0.4× 20 1.5k

Countries citing papers authored by О. А. Донцова

Since Specialization
Citations

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

Fields of papers citing papers by О. А. Донцова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by О. А. Донцова. 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 О. А. Донцова. The network helps show where О. А. Донцова may publish in the future.

Co-authorship network of co-authors of О. А. Донцова

This figure shows the co-authorship network connecting the top 25 collaborators of О. А. Донцова. A scholar is included among the top collaborators of О. А. Донцова 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 О. А. Донцова. О. А. Донцова 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.
Ivanenkov, Yan A., et al.. (2025). Coculture‐Based Screening Revealed Selective Cytostatic Effects of Pyrazol–Azepinoindoles. ChemMedChem. 20(12). e202500052–e202500052.
2.
Донцова, О. А., et al.. (2024). Natural activators of autophagy. 89(1). 5–32. 1 indexed citations
3.
Донцова, О. А., et al.. (2024). Diversity of Molecular Functions of RNA-Binding Ubiquitin Ligases from the MKRN Protein Family. Biochemistry (Moscow). 89(9). 1558–1572. 2 indexed citations
4.
Аверина, О. А., Vadim Kumeiko, Maria V. Marey, et al.. (2023). Mitoregulin Contributes to Creatine Shuttling and Cardiolipin Protection in Mice Muscle. International Journal of Molecular Sciences. 24(8). 7589–7589. 6 indexed citations
5.
Аверина, О. А., Vadim Kumeiko, Maria V. Marey, et al.. (2023). Kidney-Related Function of Mitochondrial Protein Mitoregulin. International Journal of Molecular Sciences. 24(10). 9106–9106. 7 indexed citations
6.
Lp, Sycheva, О. А. Аверина, Петр В. Сергиев, et al.. (2023). Sweet-Tasting Natural Proteins Brazzein and Monellin: Safe Sugar Substitutes for the Food Industry. Foods. 12(22). 4065–4065. 10 indexed citations
7.
Донцова, О. А., et al.. (2023). Post-Transcriptional and Post-Translational Modifications in Telomerase Biogenesis and Recruitment to Telomeres. International Journal of Molecular Sciences. 24(5). 5027–5027. 5 indexed citations
8.
Komarova, Ekaterina S., О. А. Донцова, Д. В. Пышный, Мarsel R. Kabilov, & Петр В. Сергиев. (2023). Flow-Seq Method: Features and Application in Bacterial Translation Studies. PubMed. 14(4). 20–37. 1 indexed citations
9.
Донцова, О. А., et al.. (2023). Deletion of 184–188 Nucleotides of Human Telomerase RNA Does Not Affect the Telomerase Functioning. Doklady Biochemistry and Biophysics. 510(1). 104–109.
10.
Skvortsov, Dmitry A., et al.. (2023). BRD2 and BRD3 genes independently evolved RNA structures to control unproductive splicing. NAR Genomics and Bioinformatics. 6(1). lqad113–lqad113. 2 indexed citations
11.
Сергиев, Петр В., Maria P. Rubtsova, Nikolai V. Ravin, et al.. (2021). Production of a Cloned Offspring and CRISPR/Cas9 Genome Editing of Embryonic Fibroblasts in Cattle. Doklady Biochemistry and Biophysics. 496(1). 48–51. 3 indexed citations
12.
Skvortsov, Dmitry A., et al.. (2020). Multiple competing RNA structures dynamically control alternative splicing in the human ATE1 gene. Nucleic Acids Research. 49(1). 479–490. 21 indexed citations
13.
Yamansarov, Emil Yu., Irina V. Saltykova, С. В. Ковалев, et al.. (2020). Synthesis and Evaluation of New Trivalent Ligands for Hepatocyte Targeting via the Asialoglycoprotein Receptor. Bioconjugate Chemistry. 31(5). 1313–1319. 12 indexed citations
14.
Донцова, О. А., et al.. (2020). The telomeric Cdc13 protein from yeast Hansenula polymorpha. Acta Naturae. 12(1). 84–88. 2 indexed citations
15.
Beletsky, Alexey V., Maria V. Sukhanova, Eugenia S. Mardanova, et al.. (2017). The genome-wide transcription response to telomerase deficiency in the thermotolerant yeast Hansenula polymorpha DL-1. BMC Genomics. 18(1). 492–492. 1 indexed citations
16.
Chugunova, Anastasia, О. А. Донцова, & Петр В. Сергиев. (2016). Methods of genome engineering: a new era of molecular biology. Biochemistry (Moscow). 81(7). 662–677. 7 indexed citations
17.
Beletsky, Alexey V., Maria V. Sukhanova, Eugenia S. Mardanova, et al.. (2015). Expression of genes involved in DNA repair and telomere maintenance in the yeast Hansenula polymorpha DL1 under heat stress. Doklady Biochemistry and Biophysics. 462(1). 185–188. 3 indexed citations
18.
Skvortsov, Dmitry A., et al.. (2015). Telomerase activity in peripheral blood mononuclear cells as a universal scale for quantitative measurement of telomerase activation on the example of liver diseases. Doklady Biochemistry and Biophysics. 462(1). 172–175. 1 indexed citations
19.
Rubtsova, Maria P., et al.. (2013). Endonuclease cleavage is the first event of human telomerase RNA 3’-end processing. FEBS Journal. 280. 47–47. 1 indexed citations
20.
Zvereva, Maria I., Daria M. Shcherbakova, & О. А. Донцова. (2010). Telomerase: Structure, functions, and activity regulation. Biochemistry (Moscow). 75(13). 1563–1583. 175 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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