Natalia Shcherbik

1.3k total citations
38 papers, 930 citations indexed

About

Natalia Shcherbik is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Natalia Shcherbik has authored 38 papers receiving a total of 930 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 10 papers in Cell Biology and 8 papers in Genetics. Recurrent topics in Natalia Shcherbik's work include RNA modifications and cancer (15 papers), RNA and protein synthesis mechanisms (13 papers) and Ubiquitin and proteasome pathways (11 papers). Natalia Shcherbik is often cited by papers focused on RNA modifications and cancer (15 papers), RNA and protein synthesis mechanisms (13 papers) and Ubiquitin and proteasome pathways (11 papers). Natalia Shcherbik collaborates with scholars based in United States, Russia and China. Natalia Shcherbik's co-authors include Dimitri G. Pestov, Dale S. Haines, Arnab Ghosh, Minshi Wang, Yevgeniya R. Lapik, Leena Srivastava, Teresa Żołądek, Joseph T. Nickels, Anna Tretiakova and Gary L. Gallia and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Molecular Cell.

In The Last Decade

Natalia Shcherbik

34 papers receiving 925 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 Shcherbik United States 18 737 167 95 83 67 38 930
Dong-Uk Kim South Korea 18 648 0.9× 110 0.7× 84 0.9× 47 0.6× 74 1.1× 39 892
Donna M. Gordon United States 21 753 1.0× 172 1.0× 59 0.6× 80 1.0× 25 0.4× 31 1.1k
Sarah C. Mutka United States 14 493 0.7× 69 0.4× 94 1.0× 86 1.0× 54 0.8× 22 819
Zhuji Fu United States 21 713 1.0× 116 0.7× 65 0.7× 49 0.6× 47 0.7× 26 1.3k
Daisuke Morishita Japan 18 625 0.8× 125 0.7× 242 2.5× 37 0.4× 57 0.9× 55 994
Laurie K. Jackson United States 17 745 1.0× 70 0.4× 71 0.7× 53 0.6× 68 1.0× 23 981
Nurit Livnat‐Levanon Israel 13 908 1.2× 263 1.6× 179 1.9× 293 3.5× 70 1.0× 20 1.1k
Kentaro Kajiwara Japan 14 555 0.8× 308 1.8× 40 0.4× 79 1.0× 21 0.3× 26 731

Countries citing papers authored by Natalia Shcherbik

Since Specialization
Citations

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

Fields of papers citing papers by Natalia Shcherbik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalia Shcherbik

This figure shows the co-authorship network connecting the top 25 collaborators of Natalia Shcherbik. A scholar is included among the top collaborators of Natalia Shcherbik 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 Shcherbik. Natalia Shcherbik 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.
Yu, Lei, et al.. (2025). Alterations in iron levels in the locus coeruleus of a transgenic Alzheimer’s disease rat model. Neuroscience Letters. 850. 138151–138151.
2.
Santerre, Maryline, Charles Allen, Robert Hooper, et al.. (2023). HIV-1 gp120 protein promotes HAND through the calcineurin pathway activation. Mitochondrion. 70. 31–40. 2 indexed citations
3.
Chen, Geng, Yiyang Wang, Tatiana A. Chernova, et al.. (2023). Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells. STAR Protocols. 4(3). 102489–102489.
4.
Allen, Charles, et al.. (2022). SARS-CoV-2 Causes Lung Inflammation through Metabolic Reprogramming and RAGE. Viruses. 14(5). 983–983. 13 indexed citations
5.
6.
Komar, Anton A., et al.. (2021). Cell-free Translation: Preparation and Validation of Translation-competent Extracts from Saccharomyces cerevisiae. BIO-PROTOCOL. 11(18). e4093–e4093. 3 indexed citations
7.
Wang, Yiyang, Geng Chen, Tatiana A. Chernova, et al.. (2021). Regulation of the endocytosis and prion-chaperoning machineries by yeast E3 ubiquitin ligase Rsp5 as revealed by orthogonal ubiquitin transfer. Cell chemical biology. 28(9). 1283–1297.e8. 10 indexed citations
8.
Ghosh, Arnab, et al.. (2021). A translation enhancer element from black beetle virus engages yeast eIF4G1 to drive cap-independent translation initiation. Scientific Reports. 11(1). 2461–2461. 7 indexed citations
9.
Kovalev, Nikolay, et al.. (2020). Iron-mediated degradation of ribosomes under oxidative stress is attenuated by manganese. Journal of Biological Chemistry. 295(50). 17200–17214. 11 indexed citations
10.
Pestov, Dimitri G., et al.. (2017). Endonucleolytic cleavage in the expansion segment 7 of 25S rRNA is an early marker of low-level oxidative stress in yeast. Journal of Biological Chemistry. 292(45). 18469–18485. 27 indexed citations
11.
Shcherbik, Natalia, Tatiana A. Chernova, Yury O. Chernoff, & Dimitri G. Pestov. (2016). Distinct types of translation termination generate substrates for ribosome-associated quality control. Nucleic Acids Research. 44(14). 6840–6852. 18 indexed citations
12.
13.
Shcherbik, Natalia & Dimitri G. Pestov. (2011). The ubiquitin ligase Rsp5 is required for ribosome stability in Saccharomyces cerevisiae. RNA. 17(8). 1422–1428. 17 indexed citations
14.
Shcherbik, Natalia & Dimitri G. Pestov. (2010). Ubiquitin and Ubiquitin-Like Proteins in the Nucleolus: Multitasking Tools for a Ribosome Factory. Genes & Cancer. 1(7). 681–689. 24 indexed citations
15.
Shcherbik, Natalia & Dale S. Haines. (2007). Cdc48pNpl4p/Ufd1p Binds and Segregates Membrane-Anchored/Tethered Complexes via a Polyubiquitin Signal Present on the Anchors. Molecular Cell. 25(3). 385–397. 79 indexed citations
16.
Shcherbik, Natalia & Dale S. Haines. (2004). Ub on the move. Journal of Cellular Biochemistry. 93(1). 11–19. 34 indexed citations
17.
Shcherbik, Natalia, et al.. (2004). A Single PXY Motif Located within the Carboxyl Terminus of Spt23p and Mga2p Mediates a Physical and Functional Interaction with Ubiquitin Ligase Rsp5p. Journal of Biological Chemistry. 279(51). 53892–53898. 39 indexed citations
18.
Shcherbik, Natalia, Teresa Żołądek, Joseph T. Nickels, & Dale S. Haines. (2003). Rsp5p Is Required for ER Bound Mga2p120 Polyubiquitination and Release of the Processed/Tethered Transactivator Mga2p90. Current Biology. 13(14). 1227–1233. 55 indexed citations
19.
Shcherbik, Natalia, Sharad Kumar, & Dale S. Haines. (2002). Substrate proteolysis is inhibited by dominant-negative Nedd4 and Rsp5 mutants harboring alterations in WW domain 1. Journal of Cell Science. 115(5). 1041–1048. 17 indexed citations
20.
Darbinian, Nune, Gary L. Gallia, Mondira Kundu, et al.. (1999). Association of Purα and E2F-1 suppresses transcriptional activity of E2F-1. Oncogene. 18(46). 6398–6402. 47 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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