Sergey Melnikov

4.0k total citations · 1 hit paper
33 papers, 2.2k citations indexed

About

Sergey Melnikov is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Sergey Melnikov has authored 33 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Oncology. Recurrent topics in Sergey Melnikov's work include RNA and protein synthesis mechanisms (25 papers), RNA modifications and cancer (19 papers) and Genomics and Phylogenetic Studies (10 papers). Sergey Melnikov is often cited by papers focused on RNA and protein synthesis mechanisms (25 papers), RNA modifications and cancer (19 papers) and Genomics and Phylogenetic Studies (10 papers). Sergey Melnikov collaborates with scholars based in United States, United Kingdom and France. Sergey Melnikov's co-authors include G. Yusupova, Marat Yusupov, Adam Ben‐Shem, L. Jenner, Nicolas Garreau de Loubresse, Dieter Söll, Yury S. Polikanov, Thomas A. Steitz, Kasidet Manakongtreecheep and Ronald Micura and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Sergey Melnikov

32 papers receiving 2.2k citations

Hit Papers

The Structure of the Eukaryotic Ribosome at 3.0 Å Resolution 2011 2026 2016 2021 2011 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergey Melnikov United States 20 2.0k 219 191 116 95 33 2.2k
Nicolas Garreau de Loubresse France 7 1.6k 0.8× 131 0.6× 144 0.8× 155 1.3× 63 0.7× 7 1.8k
Jinzhong Lin China 23 1.7k 0.8× 186 0.8× 92 0.5× 99 0.9× 112 1.2× 64 2.1k
Yuliya Gordiyenko United Kingdom 21 1.3k 0.6× 213 1.0× 129 0.7× 55 0.5× 99 1.0× 32 1.5k
Laura Spagnolo United Kingdom 13 1.1k 0.6× 139 0.6× 276 1.4× 72 0.6× 97 1.0× 19 1.3k
Shashi Bhushan Singapore 28 2.0k 1.0× 332 1.5× 177 0.9× 216 1.9× 163 1.7× 59 2.4k
Mario Halić Germany 23 1.9k 1.0× 438 2.0× 206 1.1× 266 2.3× 150 1.6× 36 2.2k
J. Basquin Germany 29 2.2k 1.1× 328 1.5× 98 0.5× 138 1.2× 135 1.4× 63 2.5k
Laurie Betts United States 23 1.6k 0.8× 197 0.9× 109 0.6× 102 0.9× 90 0.9× 37 2.2k
Elizabeth J. Grayhack United States 28 2.9k 1.5× 330 1.5× 226 1.2× 187 1.6× 187 2.0× 43 3.2k

Countries citing papers authored by Sergey Melnikov

Since Specialization
Citations

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

Fields of papers citing papers by Sergey Melnikov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergey Melnikov

This figure shows the co-authorship network connecting the top 25 collaborators of Sergey Melnikov. A scholar is included among the top collaborators of Sergey Melnikov 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 Melnikov. Sergey Melnikov 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.
Williams, Tom A., et al.. (2025). Evolution of drug-binding residues in eukaryotic ribosomes. Cell Reports. 44(9). 116244–116244.
2.
Baslé, Arnaud, et al.. (2025). Structurally heterogeneous ribosomes cooperate in protein synthesis in bacterial cells. Nature Communications. 16(1). 2751–2751. 4 indexed citations
3.
Rybak, Mariia Yu., C. Dingwall, Arnaud Baslé, et al.. (2024). A new family of bacterial ribosome hibernation factors. Nature. 626(8001). 1125–1132. 19 indexed citations
4.
Melnikov, Sergey, et al.. (2024). Hibernating ribosomes as drug targets?. Frontiers in Microbiology. 15. 1436579–1436579. 2 indexed citations
5.
Melnikov, Sergey, et al.. (2024). Rippling life on a dormant planet: hibernation of ribosomes, RNA polymerases, and other essential enzymes. Frontiers in Microbiology. 15. 1386179–1386179. 7 indexed citations
6.
Krahn, Natalie, Jingji Zhang, Sergey Melnikov, et al.. (2023). tRNA shape is an identity element for an archaeal pyrrolysyl-tRNA synthetase from the human gut. Nucleic Acids Research. 52(2). 513–524. 11 indexed citations
7.
Elzen, Antonia van den, et al.. (2023). Ribosomal proteins can hold a more accurate record of bacterial thermal adaptation compared to rRNA. Nucleic Acids Research. 51(15). 8048–8059. 2 indexed citations
8.
Uversky, Vladimir N., et al.. (2023). A Conserved Ribosomal Protein Has Entirely Dissimilar Structures in Different Organisms. Molecular Biology and Evolution. 41(1). 3 indexed citations
9.
Panek, Johan, et al.. (2022). Adaptation to genome decay in the structure of the smallest eukaryotic ribosome. Nature Communications. 13(1). 591–591. 23 indexed citations
10.
Vargas‐Rodriguez, Oscar, Ahmed H. Badran, Kyle Hoffman, et al.. (2021). Bacterial translation machinery for deliberate mistranslation of the genetic code. Proceedings of the National Academy of Sciences. 118(35). 12 indexed citations
11.
Melnikov, Sergey, et al.. (2019). Archaeal Ribosomal Proteins Possess Nuclear Localization Signal-Type Motifs: Implications for the Origin of the Cell Nucleus. Molecular Biology and Evolution. 37(1). 124–133. 12 indexed citations
12.
Melnikov, Sergey, et al.. (2018). Muller’s Ratchet and Ribosome Degeneration in the Obligate Intracellular Parasites Microsporidia. International Journal of Molecular Sciences. 19(12). 4125–4125. 21 indexed citations
13.
Pellegrino, Simone, N. Demeshkina, Eder Mancera-Martínez, et al.. (2018). Structural Insights into the Role of Diphthamide on Elongation Factor 2 in mRNA Reading-Frame Maintenance. Journal of Molecular Biology. 430(17). 2677–2687. 37 indexed citations
14.
Melnikov, Sergey, J. Mailliot, Byung‐Sik Shin, et al.. (2016). Molecular insights into protein synthesis with proline residues. EMBO Reports. 17(12). 1776–1784. 77 indexed citations
15.
Melnikov, Sergey, J. Mailliot, Byung‐Sik Shin, et al.. (2016). Crystal Structure of Hypusine-Containing Translation Factor eIF5A Bound to a Rotated Eukaryotic Ribosome. Journal of Molecular Biology. 428(18). 3570–3576. 49 indexed citations
16.
Melnikov, Sergey, Adam Ben‐Shem, G. Yusupova, & Marat Yusupov. (2015). Insights into the origin of the nuclear localization signals in conserved ribosomal proteins. Nature Communications. 6(1). 7382–7382. 22 indexed citations
17.
Polikanov, Yury S., Sergey Melnikov, Dieter Söll, & Thomas A. Steitz. (2015). Structural insights into the role of rRNA modifications in protein synthesis and ribosome assembly. Nature Structural & Molecular Biology. 22(4). 342–344. 199 indexed citations
18.
Jenner, L., Sergey Melnikov, Nicolas Garreau de Loubresse, et al.. (2012). Crystal structure of the 80S yeast ribosome. Current Opinion in Structural Biology. 22(6). 759–767. 100 indexed citations
19.
Ben‐Shem, Adam, Nicolas Garreau de Loubresse, Sergey Melnikov, et al.. (2011). The Structure of the Eukaryotic Ribosome at 3.0 Å Resolution. Science. 334(6062). 1524–1529. 879 indexed citations breakdown →
20.
Соколов, В. В., et al.. (2008). Effect of prothymosin α and its mutants on the activity of the p53 tumor suppressor. Molecular Biology. 42(4). 598–608. 3 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026