Natalia Zelinskaya

450 total citations
17 papers, 243 citations indexed

About

Natalia Zelinskaya is a scholar working on Molecular Biology, Parasitology and Molecular Medicine. According to data from OpenAlex, Natalia Zelinskaya has authored 17 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Parasitology and 5 papers in Molecular Medicine. Recurrent topics in Natalia Zelinskaya's work include RNA modifications and cancer (13 papers), RNA and protein synthesis mechanisms (8 papers) and Parasitic Infections and Diagnostics (7 papers). Natalia Zelinskaya is often cited by papers focused on RNA modifications and cancer (13 papers), RNA and protein synthesis mechanisms (8 papers) and Parasitic Infections and Diagnostics (7 papers). Natalia Zelinskaya collaborates with scholars based in United States, Russia and United Kingdom. Natalia Zelinskaya's co-authors include Graeme L. Conn, C.M. Dunham, Carl R. Rankin, Debayan Dey, Maria Garber, Meisam Nosrati, John F. Honek, J.A. Dunkle, Mark S. Dunstan and Eric D. Hoffer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Natalia Zelinskaya

15 papers receiving 239 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalia Zelinskaya United States 11 189 56 35 27 26 17 243
Danielle Carson United Kingdom 7 154 0.8× 32 0.6× 38 1.1× 28 1.0× 13 0.5× 10 293
Ricky Dudley United Kingdom 8 246 1.3× 13 0.2× 16 0.5× 19 0.7× 21 0.8× 8 378
Andrew J. R. Cooper Ireland 8 51 0.3× 20 0.4× 27 0.8× 20 0.7× 27 1.0× 9 160
Daniel G. Mediati Australia 5 102 0.5× 50 0.9× 56 1.6× 58 2.1× 3 0.1× 11 195
Christopher L. Pritchett United States 11 194 1.0× 70 1.3× 81 2.3× 56 2.1× 2 0.1× 13 304
Trevor J. Hird Canada 10 197 1.0× 64 1.1× 23 0.7× 83 3.1× 2 0.1× 12 522
Vanessa Harpin United States 6 54 0.3× 28 0.5× 16 0.5× 57 2.1× 6 0.2× 6 150
Alexander M. Horspool United States 10 106 0.6× 40 0.7× 31 0.9× 43 1.6× 3 0.1× 12 250
Kerri A. Neugebauer United States 8 138 0.7× 12 0.2× 36 1.0× 15 0.6× 2 0.1× 19 256
Alexander S. Mankin United States 5 184 1.0× 48 0.9× 63 1.8× 30 1.1× 5 231

Countries citing papers authored by Natalia Zelinskaya

Since Specialization
Citations

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

Fields of papers citing papers by Natalia Zelinskaya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalia Zelinskaya

This figure shows the co-authorship network connecting the top 25 collaborators of Natalia Zelinskaya. A scholar is included among the top collaborators of Natalia Zelinskaya 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 Natalia Zelinskaya. Natalia Zelinskaya is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Dey, Debayan, et al.. (2025). Basis for selective drug evasion of an aminoglycoside-resistance ribosomal RNA modification. Nature Communications. 16(1). 7992–7992.
2.
3.
Srinivas, Pooja, Meisam Nosrati, Natalia Zelinskaya, et al.. (2023). 30S subunit recognition and G1405 modification by the aminoglycoside-resistance 16S ribosomal RNA methyltransferase RmtC. Proceedings of the National Academy of Sciences. 120(25). e2304128120–e2304128120. 8 indexed citations
4.
Dey, Debayan, Natalia Zelinskaya, Pooja Srinivas, et al.. (2022). 50S subunit recognition and modification by the Mycobacterium tuberculosis ribosomal RNA methyltransferase TlyA. Proceedings of the National Academy of Sciences. 119(14). e2120352119–e2120352119. 17 indexed citations
5.
Nosrati, Meisam, Debayan Dey, Natalia Zelinskaya, et al.. (2019). Functionally critical residues in the aminoglycoside resistance-associated methyltransferase RmtC play distinct roles in 30S substrate recognition. Journal of Biological Chemistry. 294(46). 17642–17653. 33 indexed citations
6.
Zelinskaya, Natalia, et al.. (2015). The Pathogen-Derived Aminoglycoside Resistance 16S rRNA Methyltransferase NpmA Possesses Dual m 1 A1408/m 1 G1408 Specificity. Antimicrobial Agents and Chemotherapy. 59(12). 7862–7865. 5 indexed citations
7.
Zelinskaya, Natalia, et al.. (2015). Heterologous Expression and Functional Characterization of the Exogenously Acquired Aminoglycoside Resistance Methyltransferases RmtD, RmtD2, and RmtG. Antimicrobial Agents and Chemotherapy. 60(1). 699–702. 5 indexed citations
8.
Zelinskaya, Natalia, et al.. (2015). 30S Subunit-Dependent Activation of the Sorangium cellulosum So ce56 Aminoglycoside Resistance-Conferring 16S rRNA Methyltransferase Kmr. Antimicrobial Agents and Chemotherapy. 59(5). 2807–2816. 11 indexed citations
9.
Kuiper, Emily G., Samantha M. Prezioso, Jeffrey Meisner, et al.. (2015). Pseudomonas aeruginosa EftM Is a Thermoregulated Methyltransferase. Journal of Biological Chemistry. 291(7). 3280–3290. 12 indexed citations
10.
Dunkle, J.A., et al.. (2014). Molecular recognition and modification of the 30S ribosome by the aminoglycoside-resistance methyltransferase NpmA. Proceedings of the National Academy of Sciences. 111(17). 6275–6280. 42 indexed citations
11.
Stolboushkina, Elena, С.В. Никонов, Natalia Zelinskaya, et al.. (2013). Crystal Structure of the Archaeal Translation Initiation Factor 2 in Complex with a GTP Analogue and Met-tRNAfMet. Journal of Molecular Biology. 425(6). 989–998. 12 indexed citations
12.
Zelinskaya, Natalia, et al.. (2010). Expression, purification and crystallization of adenosine 1408 aminoglycoside-resistance rRNA methyltransferases for structural studies. Protein Expression and Purification. 75(1). 89–94. 13 indexed citations
13.
Zelinskaya, Natalia, et al.. (2010). Structural insights into the function of aminoglycoside-resistance A1408 16S rRNA methyltransferases from antibiotic-producing and human pathogenic bacteria. Nucleic Acids Research. 38(21). 7791–7799. 29 indexed citations
14.
Dunstan, Mark S., et al.. (2009). Structure of the Thiostrepton Resistance Methyltransferase·S-Adenosyl-l-methionine Complex and Its Interaction with Ribosomal RNA. Journal of Biological Chemistry. 284(25). 17013–17020. 24 indexed citations
15.
Gongadze, G. M., Alexey Korepanov, Elena Stolboushkina, et al.. (2005). The Crucial Role of Conserved Intermolecular H-bonds Inaccessible to the Solvent in Formation and Stabilization of the TL5·5 SrRNA Complex. Journal of Biological Chemistry. 280(16). 16151–16156. 13 indexed citations
16.
Zelinskaya, Natalia, et al.. (2004). Isolation and Characterization of Site-Specific DNA-methyltransferases from Bacillus coagulans K. Biochemistry (Moscow). 69(3). 299–305. 4 indexed citations
17.
Zelinskaya, Natalia, et al.. (2002). Cloning, Purification, and Crystallization of a Bacterial Gene Expression Regulator–Hfq Protein from Escherichia coli. Biochemistry (Moscow). 67(11). 1293–1297. 15 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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