Sergey E. Dmitriev

4.8k total citations
85 papers, 3.2k citations indexed

About

Sergey E. Dmitriev is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Plant Science. According to data from OpenAlex, Sergey E. Dmitriev has authored 85 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Molecular Biology, 20 papers in Cardiology and Cardiovascular Medicine and 9 papers in Plant Science. Recurrent topics in Sergey E. Dmitriev's work include RNA and protein synthesis mechanisms (58 papers), RNA Research and Splicing (32 papers) and RNA modifications and cancer (30 papers). Sergey E. Dmitriev is often cited by papers focused on RNA and protein synthesis mechanisms (58 papers), RNA Research and Splicing (32 papers) and RNA modifications and cancer (30 papers). Sergey E. Dmitriev collaborates with scholars based in Russia, United States and Tajikistan. Sergey E. Dmitriev's co-authors include Ivan N. Shatsky, Ilya M. Terenin, Dmitry E. Andreev, Vadim N. Gladyshev, William C. Merrick, Aleksandra S. Anisimova, Vladimir Prassolov, Pavel V. Baranov, Patrick B. F. O’Connor and Maria P. Rubtsova and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Sergey E. Dmitriev

84 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergey E. Dmitriev Russia 35 2.6k 550 351 198 190 85 3.2k
Nahum Sonenberg Canada 19 2.6k 1.0× 497 0.9× 181 0.5× 225 1.1× 239 1.3× 24 3.0k
Tobias von der Haar United Kingdom 27 2.2k 0.9× 120 0.2× 150 0.4× 198 1.0× 139 0.7× 57 2.6k
Gary Loughran Ireland 24 1.7k 0.7× 262 0.5× 141 0.4× 148 0.7× 141 0.7× 41 2.1k
Maria M. Konarska United States 36 5.5k 2.1× 531 1.0× 350 1.0× 408 2.1× 191 1.0× 61 6.2k
Silvano Riva Italy 41 4.1k 1.6× 561 1.0× 345 1.0× 735 3.7× 191 1.0× 98 5.0k
Vincent A. Blomen Netherlands 24 2.5k 1.0× 223 0.4× 326 0.9× 420 2.1× 265 1.4× 31 3.4k
G. Brett Robb United States 25 2.4k 0.9× 192 0.3× 183 0.5× 227 1.1× 222 1.2× 35 3.0k
Hong Sun China 30 3.2k 1.2× 101 0.2× 379 1.1× 358 1.8× 545 2.9× 77 4.2k
Jeff Coller United States 36 7.1k 2.7× 287 0.5× 384 1.1× 474 2.4× 346 1.8× 56 7.8k
Cheng Wu United States 22 1.3k 0.5× 98 0.2× 196 0.6× 179 0.9× 83 0.4× 45 1.7k

Countries citing papers authored by Sergey E. Dmitriev

Since Specialization
Citations

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

Fields of papers citing papers by Sergey E. Dmitriev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sergey E. Dmitriev. 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 Sergey E. Dmitriev. The network helps show where Sergey E. Dmitriev may publish in the future.

Co-authorship network of co-authors of Sergey E. Dmitriev

This figure shows the co-authorship network connecting the top 25 collaborators of Sergey E. Dmitriev. A scholar is included among the top collaborators of Sergey E. Dmitriev 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 Sergey E. Dmitriev. Sergey E. Dmitriev 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.
Gladyshev, Vadim N., et al.. (2024). AgeMeta: Quantitative Gene Expression Database of Mammalian Aging. Biochemistry (Moscow). 89(2). 313–321. 2 indexed citations
2.
Gushchin, Vladimir А., Andrei E. Siniavin, Evgeny V. Usachev, et al.. (2024). Major Role of S-Glycoprotein in Providing Immunogenicity and Protective Immunity in mRNA Lipid Nanoparticle Vaccines Based on SARS-CoV-2 Structural Proteins. Vaccines. 12(4). 379–379. 2 indexed citations
3.
Konopleva, M., Elena V. Shmendel, М. А. Маслов, et al.. (2024). Novel Efficient Lipid-Based Delivery Systems Enable a Delayed Uptake and Sustained Expression of mRNA in Human Cells and Mouse Tissues. Pharmaceutics. 16(5). 684–684. 6 indexed citations
4.
Rozenberg, Julian M., et al.. (2024). Forced Overexpression and Knockout Analysis of SLC30A and SLC39A Family Genes Suggests Their Involvement in Establishing Resistance to Cisplatin in Human Cancer Cells. International Journal of Molecular Sciences. 25(22). 12049–12049. 1 indexed citations
5.
Burakov, Anton V., Ilya M. Terenin, Dmitry A. Bykov, et al.. (2023). A Solitary Stalled 80S Ribosome Prevents mRNA Recruitment to Stress Granules. Biochemistry (Moscow). 88(11). 1786–1799. 6 indexed citations
6.
Zhang, Bohan, David E. Lee, Alexandre Trapp, et al.. (2023). Multi-omic rejuvenation and lifespan extension on exposure to youthful circulation. Nature Aging. 3(8). 948–964. 56 indexed citations
7.
Dmitriev, Sergey E., et al.. (2023). Cell death or survival: Insights into the role of mRNA translational control. Seminars in Cell and Developmental Biology. 154(Pt B). 138–154. 17 indexed citations
8.
Slavokhotova, Anna A., et al.. (2022). Enteroviruses Manipulate the Unfolded Protein Response through Multifaceted Deregulation of the Ire1-Xbp1 Pathway. Viruses. 14(11). 2486–2486. 11 indexed citations
9.
Macedo, Joana Catarina, Madalena Costa, Vladimir Ustiyan, et al.. (2022). In vivo cyclic induction of the FOXM1 transcription factor delays natural and progeroid aging phenotypes and extends healthspan. Nature Aging. 2(5). 397–411. 36 indexed citations
10.
Egorov, Artyom A., et al.. (2021). A standard knockout procedure alters expression of adjacent loci at the translational level. Nucleic Acids Research. 49(19). 11134–11144. 7 indexed citations
11.
Anisimova, Aleksandra S., Mark Meerson, Maxim V. Gerashchenko, et al.. (2020). Multifaceted deregulation of gene expression and protein synthesis with age. Proceedings of the National Academy of Sciences. 117(27). 15581–15590. 80 indexed citations
12.
Dmitriev, Sergey E., et al.. (2020). A Quick Guide to Small-Molecule Inhibitors of Eukaryotic Protein Synthesis. Biochemistry (Moscow). 85(11). 1389–1421. 41 indexed citations
13.
Gladyshev, Vadim N., et al.. (2020). CTELS: A Cell-Free System for the Analysis of Translation Termination Rate. Biomolecules. 10(6). 911–911. 8 indexed citations
14.
Anisimova, Aleksandra S., Artyom A. Egorov, Maria D. Logacheva, et al.. (2019). Translatome and transcriptome analysis of TMA20 (MCT-1) and TMA64 (eIF2D) knockout yeast strains. SHILAP Revista de lepidopterología. 23. 103701–103701. 13 indexed citations
15.
Schwartz, A. M., Anna V. Klepikova, Ilya E. Vorontsov, et al.. (2016). Early B-cell factor 1 (EBF1) is critical for transcriptional control of SLAMF1 gene in human B cells. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1859(10). 1259–1268. 18 indexed citations
16.
Schwartz, A. M., Kirill V. Korneev, Marcela Covic, et al.. (2014). Upstream open reading frames regulate translation of the long isoform of SLAMF1 mRNA that encodes costimulatory receptor CD150. Biochemistry (Moscow). 79(12). 1405–1411. 6 indexed citations
17.
Andreev, Dmitry E., Sergey E. Dmitriev, Ilya M. Terenin, & Ivan N. Shatsky. (2013). Cap-independent translation initiation of Apaf-1 mRNA based on a scanning mechanism is determined by some features of the secondary structure of its 5′ untranslated region. Biochemistry (Moscow). 78(2). 157–165. 15 indexed citations
18.
Andreev, Dmitry E., et al.. (2012). Glycyl-tRNA synthetase specifically binds to the poliovirus IRES to activate translation initiation. Nucleic Acids Research. 40(12). 5602–5614. 48 indexed citations
19.
Dmitriev, Sergey E., Ilya M. Terenin, Dmitry E. Andreev, et al.. (2010). GTP-independent tRNA Delivery to the Ribosomal P-site by a Novel Eukaryotic Translation Factor. Journal of Biological Chemistry. 285(35). 26779–26787. 128 indexed citations
20.
Andreev, Dmitry E., Vasili Hauryliuk, Ilya M. Terenin, et al.. (2007). The bacterial toxin RelE induces specific mRNA cleavage in the A site of the eukaryote ribosome. RNA. 14(2). 233–239. 38 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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