Lev L. Kisselev

7.8k total citations
191 papers, 6.2k citations indexed

About

Lev L. Kisselev is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Lev L. Kisselev has authored 191 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 175 papers in Molecular Biology, 26 papers in Genetics and 21 papers in Plant Science. Recurrent topics in Lev L. Kisselev's work include RNA and protein synthesis mechanisms (129 papers), RNA modifications and cancer (83 papers) and RNA Research and Splicing (49 papers). Lev L. Kisselev is often cited by papers focused on RNA and protein synthesis mechanisms (129 papers), RNA modifications and cancer (83 papers) and RNA Research and Splicing (49 papers). Lev L. Kisselev collaborates with scholars based in Russia, France and Sweden. Lev L. Kisselev's co-authors include Ludmila Frolova, Lyudmila Y. Frolova, Xavier Le Goff, Richard H. Buckingham, Just Justesen, M. Philippe, О. О. Фаворова, Alim S. Seit‐Nebi, Galina A. Zhouravleva and Tatyana Merkulova‐Rainon and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Lev L. Kisselev

186 papers receiving 6.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lev L. Kisselev Russia 42 5.7k 941 461 417 283 191 6.2k
John L. Woolford United States 50 7.0k 1.2× 415 0.4× 433 0.9× 673 1.6× 204 0.7× 109 7.4k
Daniel Bogenhagen United States 45 7.5k 1.3× 1.1k 1.1× 435 0.9× 354 0.8× 223 0.8× 91 8.3k
Alan B. Sachs United States 41 7.8k 1.4× 921 1.0× 577 1.3× 359 0.9× 138 0.5× 62 8.9k
Achilles Dugaiczyk United States 31 2.5k 0.4× 739 0.8× 316 0.7× 278 0.7× 211 0.7× 59 3.3k
David P. Leader United Kingdom 30 1.9k 0.3× 603 0.6× 273 0.6× 442 1.1× 173 0.6× 116 3.5k
Masao Kawakita Japan 38 3.3k 0.6× 508 0.5× 228 0.5× 392 0.9× 105 0.4× 138 4.1k
Toshifumi Inada Japan 50 5.8k 1.0× 1.6k 1.7× 219 0.5× 461 1.1× 538 1.9× 113 6.6k
Anton A. Komar United States 40 4.9k 0.9× 618 0.7× 242 0.5× 386 0.9× 212 0.7× 110 5.9k
Richard R. Sinden United States 42 4.3k 0.7× 1.1k 1.2× 416 0.9× 170 0.4× 420 1.5× 98 4.9k
Sergei M. Mirkin United States 45 7.2k 1.3× 1.5k 1.6× 767 1.7× 283 0.7× 495 1.7× 105 7.7k

Countries citing papers authored by Lev L. Kisselev

Since Specialization
Citations

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

Fields of papers citing papers by Lev L. Kisselev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lev L. Kisselev. 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 Lev L. Kisselev. The network helps show where Lev L. Kisselev may publish in the future.

Co-authorship network of co-authors of Lev L. Kisselev

This figure shows the co-authorship network connecting the top 25 collaborators of Lev L. Kisselev. A scholar is included among the top collaborators of Lev L. Kisselev 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 Lev L. Kisselev. Lev L. Kisselev 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
2.
Heurgué‐Hamard, Valérie, Stéphanie Champ, Liliana Mora, et al.. (2004). The Glutamine Residue of the Conserved GGQ Motif in Saccharomyces cerevisiae Release Factor eRF1 Is Methylated by the Product of the YDR140w Gene. Journal of Biological Chemistry. 280(4). 2439–2445. 79 indexed citations
3.
Chavatte, Laurent, Ludmila Frolova, Lev L. Kisselev, & Alain Favre. (2001). The polypeptide chain release factor eRF1 specifically contacts the s4UGA stop codon located in the A site of eukaryotic ribosomes. European Journal of Biochemistry. 268(10). 2896–2904. 51 indexed citations
4.
Брага, Э. А., Elena M. Pugacheva, Igor Bazov, et al.. (1999). Comparative allelotyping epithelial tumors of the short arm of human chromosome 3 in of four different types. FEBS Letters. 454(3). 215–219. 34 indexed citations
5.
Berezovsky, Igor N., et al.. (1999). Amino acid composition of protein termini are biased in different manners. Protein Engineering Design and Selection. 12(1). 23–30. 36 indexed citations
6.
Kholod, Natalia, et al.. (1998). Aminoacylation of tRNA gene transcripts is strongly affected by 3′‐extended and dimeric substrate RNAs. FEBS Letters. 426(1). 135–139. 5 indexed citations
7.
Frolova, Lyudmila Y., Janne L. Simonsen, Tatyana Merkulova‐Rainon, et al.. (1998). Functional expression of eukaryotic polypeptide chain release factors 1 and 3 by means of baculovirus/insect cells and complex formation between the factors. European Journal of Biochemistry. 256(1). 36–44. 65 indexed citations
8.
Кочетов, А. В., et al.. (1996). Comparative Analysis of the Secondary Structure of mRNA Encoded by High- and Low-Expression Eukaryotic Genes.. 124–129.
9.
Mashkova, Tamara D., et al.. (1996). Evidence for Selection in Evolution of Alpha Satellite DNA: The Central Role of CENP-B/pJα Binding Region. Journal of Molecular Biology. 261(3). 334–340. 73 indexed citations
10.
Вартанян, А. А., et al.. (1996). Interferons induce accumulation of diadenosine triphosphate (Ap3A) in human cultured cells. FEBS Letters. 381(1-2). 32–34. 32 indexed citations
11.
Kisselev, Lev L. & Alexey Wolfson. (1994). Aminoacyl-tRNA Synthetases from Higher Eukaryotes,. Progress in nucleic acid research and molecular biology. 48. 83–142. 70 indexed citations
12.
Frolova, L Iu, Xavier Le Goff, Hanne H. Rasmussen, et al.. (1994). A highly conserved eukaryotic protein family possessing properties of polypeptide chain release factor. Nature. 372(6507). 701–703. 332 indexed citations
13.
Arkov, Alexey L., Sergey Korolev, & Lev L. Kisselev. (1993). Termination of translation in bacteria may be modulated via specific interaction between peptide chain release factor 2 and the last peptidyl-tRNASer/Phe. Nucleic Acids Research. 21(12). 2891–2897. 26 indexed citations
14.
Beresten, Sergey, et al.. (1989). Molecular and cellular studies of tryptophanyl‐tRNA synthetase using monoclonal antibodies. European Journal of Biochemistry. 184(3). 575–581. 21 indexed citations
15.
Zabarovsky, Eugene R., et al.. (1989). λSK3 and λSK5, vectors for constructing genomic libraries derived from λEMBL3 and λEMBL4 by insertion oflacgene. Nucleic Acids Research. 17(8). 3310–3310. 1 indexed citations
16.
Kisselev, Lev L., et al.. (1988). Expression of the protooncogenes in psoriatic lesions. Archives of Dermatological Research. 280(1). 8–11. 9 indexed citations
17.
Kisselev, Lev L.. (1985). The Role of the Anticodon in Recognition of tRNA by Aminoacyl-tRNA Synthetases. Progress in nucleic acid research and molecular biology. 32. 237–266. 55 indexed citations
18.
Kisselev, Lev L., et al.. (1979). [18] Tryptophanyl-tRNA synthetase from beef pancreas. Methods in enzymology on CD-ROM/Methods in enzymology. 59. 234–257. 50 indexed citations
19.
Kisselev, Lev L., et al.. (1979). Molecular Enzymology of Beef Pancreas Tryptophanyl-tRNA Synthetase. Cold Spring Harbor Monograph Archive. 235–246. 2 indexed citations
20.
Frolova, L Iu, et al.. (1975). [RNA-directed DNA synthesis in vitro: detection of polydeoxyadenylate in DNA, complementary to antimessenger-DNA].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 225(6). 1442–5. 1 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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