Lionel Bénard

1.3k total citations
26 papers, 1.0k citations indexed

About

Lionel Bénard is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Lionel Bénard has authored 26 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Ecology. Recurrent topics in Lionel Bénard's work include RNA and protein synthesis mechanisms (22 papers), RNA Research and Splicing (11 papers) and Bacterial Genetics and Biotechnology (9 papers). Lionel Bénard is often cited by papers focused on RNA and protein synthesis mechanisms (22 papers), RNA Research and Splicing (11 papers) and Bacterial Genetics and Biotechnology (9 papers). Lionel Bénard collaborates with scholars based in France, United States and Russia. Lionel Bénard's co-authors include Ciarán Condon, Nathalie Mathy, Olivier Pellegrini, Tingyi Wen, Claude Portier, Chantal Ehresmann, Bernard Ehresmann, Reed B. Wickner, Flore Eyermann and Antonin Morillon and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Lionel Bénard

25 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lionel Bénard France 19 935 386 246 115 67 26 1.0k
Olivier Pellegrini France 16 996 1.1× 531 1.4× 329 1.3× 60 0.5× 71 1.1× 26 1.1k
Atilio Deana United States 11 1.1k 1.1× 609 1.6× 339 1.4× 40 0.3× 54 0.8× 13 1.2k
Lukas Rajkowitsch Austria 11 762 0.8× 265 0.7× 138 0.6× 49 0.4× 62 0.9× 12 860
Yanan Feng China 14 527 0.6× 294 0.8× 151 0.6× 251 2.2× 30 0.4× 34 804
T. Brendler United States 15 756 0.8× 562 1.5× 110 0.4× 48 0.4× 101 1.5× 21 905
G A Mackie Canada 17 917 1.0× 598 1.5× 302 1.2× 237 2.1× 22 0.3× 19 1.1k
Elizabeth S. Haas United States 17 1.1k 1.1× 320 0.8× 334 1.4× 108 0.9× 22 0.3× 20 1.2k
Chisato Ushida Japan 13 773 0.8× 364 0.9× 279 1.1× 41 0.4× 15 0.2× 35 848
Jesper Johansen Denmark 9 792 0.8× 414 1.1× 238 1.0× 46 0.4× 35 0.5× 11 952
David R. Cheng United States 4 882 0.9× 177 0.5× 99 0.4× 104 0.9× 64 1.0× 6 1.0k

Countries citing papers authored by Lionel Bénard

Since Specialization
Citations

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

Fields of papers citing papers by Lionel Bénard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lionel Bénard

This figure shows the co-authorship network connecting the top 25 collaborators of Lionel Bénard. A scholar is included among the top collaborators of Lionel Bénard 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 Lionel Bénard. Lionel Bénard 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.
Panozzo, Cristina, et al.. (2024). RNA Blotting by Electrotransfer and RNA Detection. Methods in molecular biology. 2863. 29–41.
2.
Navickas, Albertas, et al.. (2020). No-Go Decay mRNA cleavage in the ribosome exit tunnel produces 5′-OH ends phosphorylated by Trl1. Nature Communications. 11(1). 122–122. 28 indexed citations
3.
Gilet, Jules, et al.. (2019). Additional Layer of Regulation via Convergent Gene Orientation in Yeasts. Molecular Biology and Evolution. 37(2). 365–378. 8 indexed citations
4.
Sinturel, Flore, Albertas Navickas, Maxime Wéry, et al.. (2015). Cytoplasmic Control of Sense-Antisense mRNA Pairs. Cell Reports. 12(11). 1853–1864. 25 indexed citations
5.
Vieira, Neide, Sónia Barbosa, Thierry Delaveau, et al.. (2014). Role of the DHH1 Gene in the Regulation of Monocarboxylic Acids Transporters Expression in Saccharomyces cerevisiae. PLoS ONE. 9(11). e111589–e111589. 25 indexed citations
6.
Mathy, Nathalie, Peggy Mervelet, Lionel Bénard, et al.. (2009). Bacillus subtilis ribonucleases J1 and J2 form a complex with altered enzyme behaviour. Molecular Microbiology. 75(2). 489–498. 99 indexed citations
7.
Mathy, Nathalie, et al.. (2009). Ribosomes initiating translation of the hbs mRNA protect it from 5′‐to‐3′ exoribonucleolytic degradation by RNase J1. Molecular Microbiology. 71(6). 1538–1550. 53 indexed citations
8.
Sinturel, Flore, Olivier Pellegrini, Song Xiang, et al.. (2009). Real-time fluorescence detection of exoribonucleases. RNA. 15(11). 2057–2062. 19 indexed citations
9.
Pellegrini, Olivier, Nathalie Mathy, Ciarán Condon, & Lionel Bénard. (2008). Chapter 9 In Vitro Assays of 5′ to 3′‐Exoribonuclease Activity. Methods in enzymology on CD-ROM/Methods in enzymology. 448. 167–183. 18 indexed citations
10.
Mathy, Nathalie, et al.. (2007). 5′-to-3′ Exoribonuclease Activity in Bacteria: Role of RNase J1 in rRNA Maturation and 5′ Stability of mRNA. Cell. 129(4). 681–692. 280 indexed citations
11.
Todeschini, Anne‐Laure, Ciarán Condon, & Lionel Bénard. (2005). Sodium-induced GCN4 Expression Controls the Accumulation of the 5′ to 3′ RNA Degradation Inhibitor, 3′-Phosphoadenosine 5′-Phosphate. Journal of Biological Chemistry. 281(6). 3276–3282. 17 indexed citations
12.
13.
Morillon, Antonin, Lionel Bénard, Mathias Springer, & Pascale Lesage. (2002). Differential Effects of Chromatin and Gcn4 on the 50-Fold Range of Expression among Individual Yeast Ty1 Retrotransposons. Molecular and Cellular Biology. 22(7). 2078–2088. 56 indexed citations
14.
Bénard, Lionel, et al.. (1999). The Ski7 Antiviral Protein Is an EF1-α Homolog That Blocks Expression of Non-Poly(A) mRNA in Saccharomyces cerevisiae. Journal of Virology. 73(4). 2893–2900. 44 indexed citations
15.
Bénard, Lionel, et al.. (1998). Identification in a pseudoknot of a U⋅G motif essential for the regulation of the expression of ribosomal protein S15. Proceedings of the National Academy of Sciences. 95(5). 2564–2567. 31 indexed citations
16.
Bénard, Lionel, et al.. (1996). Pseudoknot and translational control in the expression of the S15 ribosomal protein. Biochimie. 78(7). 568–576. 12 indexed citations
17.
Ehresmann, Chantal, Claude Philippe, Éric Westhof, et al.. (1995). A pseudoknot is required for efficient translational initiation and regulation of the Escherichia coli rpsO gene coding for ribosomal protein S15. Biochemistry and Cell Biology. 73(11-12). 1131–1140. 19 indexed citations
18.
Philippe, Claude, Lionel Bénard, Flore Eyermann, et al.. (1994). Structural elements ofrpsOmRNA involved in the modulation of translational initiation and regulation ofE.coliribosomal protein S15. Nucleic Acids Research. 22(13). 2538–2546. 20 indexed citations
19.
Bénard, Lionel, L. Dondon, M. Grunberg‐Manago, et al.. (1994). Mutational analysis of the pseudoknot structure of the S15 translational operator from Escherichia coli. Molecular Microbiology. 14(1). 31–40. 19 indexed citations
20.
Eyermann, Flore, et al.. (1993). Ribosomal protein S15 from Escherichia coli modulates its own translation by trapping the ribosome on the mRNA initiation loading site.. Proceedings of the National Academy of Sciences. 90(10). 4394–4398. 102 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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