Renaud Geslain

747 total citations
23 papers, 564 citations indexed

About

Renaud Geslain is a scholar working on Molecular Biology, Cancer Research and Ecology. According to data from OpenAlex, Renaud Geslain has authored 23 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 2 papers in Cancer Research and 1 paper in Ecology. Recurrent topics in Renaud Geslain's work include RNA and protein synthesis mechanisms (21 papers), RNA modifications and cancer (19 papers) and RNA Research and Splicing (8 papers). Renaud Geslain is often cited by papers focused on RNA and protein synthesis mechanisms (21 papers), RNA modifications and cancer (19 papers) and RNA Research and Splicing (8 papers). Renaud Geslain collaborates with scholars based in United States, France and Spain. Renaud Geslain's co-authors include Tao Pan, Marsha Rich Rosner, Qing Dai, Mariana Pavon-Eternod, Tao Pan, Lluı́s Ribas de Pouplana, Gilbert Eriani, Philip H. Howe, J. Cavarelli and Simon Grelet and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Molecular Cell.

In The Last Decade

Renaud Geslain

23 papers receiving 562 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Renaud Geslain United States 12 538 91 28 23 14 23 564
Koichi Ogami Japan 13 479 0.9× 93 1.0× 31 1.1× 14 0.6× 12 0.9× 21 527
Isabel S. Naarmann‐de Vries Germany 12 387 0.7× 101 1.1× 21 0.8× 13 0.6× 14 1.0× 25 430
Roberto Munita Chile 9 483 0.9× 244 2.7× 21 0.8× 20 0.9× 13 0.9× 14 540
Tomasz W. Turowski United Kingdom 14 573 1.1× 55 0.6× 34 1.2× 24 1.0× 15 1.1× 23 629
Cyrille Girard Germany 12 687 1.3× 69 0.8× 24 0.9× 26 1.1× 9 0.6× 14 738
Chunyang Ni United States 7 342 0.6× 210 2.3× 23 0.8× 20 0.9× 22 1.6× 7 394
Brandy Y. Brewer United States 8 445 0.8× 74 0.8× 33 1.2× 9 0.4× 11 0.8× 8 486
Chyi-Ying A. Chen United States 6 457 0.8× 122 1.3× 25 0.9× 15 0.7× 9 0.6× 6 494
Lindsey Reynolds United States 5 292 0.5× 150 1.6× 32 1.1× 44 1.9× 20 1.4× 7 411
Anna Uzonyi Israel 7 379 0.7× 104 1.1× 22 0.8× 10 0.4× 6 0.4× 10 393

Countries citing papers authored by Renaud Geslain

Since Specialization
Citations

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

Fields of papers citing papers by Renaud Geslain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renaud Geslain

This figure shows the co-authorship network connecting the top 25 collaborators of Renaud Geslain. A scholar is included among the top collaborators of Renaud Geslain 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 Renaud Geslain. Renaud Geslain 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.
Théobald‐Dietrich, Anne, et al.. (2021). Identification of host tRNAs preferentially recognized by the Plasmodium surface protein tRip. Nucleic Acids Research. 49(18). 10618–10629. 5 indexed citations
2.
Schaeffer, Laure, Johana Chicher, Renaud Geslain, et al.. (2020). The nature of the purine at position 34 in tRNAs of 4-codon boxes is correlated with nucleotides at positions 32 and 38 to maintain decoding fidelity. Nucleic Acids Research. 48(11). 6170–6183. 17 indexed citations
3.
Grelet, Simon, et al.. (2018). Metabolic Labeling and Profiling of Transfer RNAs Using Macroarrays. Journal of Visualized Experiments. 2 indexed citations
4.
Grelet, Simon, et al.. (2017). SPOt: A novel and streamlined microarray platform for observing cellular tRNA levels. PLoS ONE. 12(5). e0177939–e0177939. 9 indexed citations
6.
Eriani, Gilbert, et al.. (2016). The Enzymatic Paradox of Yeast Arginyl-tRNA Synthetase: Exclusive Arginine Transfer Controlled by a Flexible Mechanism of tRNA Recognition. PLoS ONE. 11(2). e0148460–e0148460. 6 indexed citations
7.
Strack, Rita, Xiaoyun Wang, Renaud Geslain, et al.. (2016). A dual fluorescent reporter for the investigation of methionine mistranslation in live cells. RNA. 22(3). 467–476. 19 indexed citations
8.
Eriani, Gilbert, et al.. (2015). MIST, a Novel Approach to Reveal Hidden Substrate Specificity in Aminoacyl-tRNA Synthetases. PLoS ONE. 10(6). e0130042–e0130042. 6 indexed citations
9.
Geslain, Renaud & Gilbert Eriani. (2014). Regulation of translation dynamic and neoplastic conversion by tRNA and their pieces. PubMed. 2(1). e28586–e28586. 3 indexed citations
10.
Geslain, Renaud, Shahab Uddin, Hui Liu, et al.. (2012). Distinct functions of erythropoietin and stem cell factor are linked to activation of mTOR kinase signaling pathway in human erythroid progenitors. Cytokine. 61(1). 329–335. 7 indexed citations
11.
Zhou, Donghui, Jiyoung Lee, Casey Frankenberger, et al.. (2012). Anti-tumor effects of an engineered “killer” transfer RNA. Biochemical and Biophysical Research Communications. 427(1). 148–153. 10 indexed citations
12.
Pavon-Eternod, Mariana, et al.. (2009). tRNA over-expression in breast cancer and functional consequences. Nucleic Acids Research. 37(21). 7268–7280. 238 indexed citations
13.
Geslain, Renaud, et al.. (2009). Chimeric tRNAs as tools to induce proteome damage and identify components of stress responses. Nucleic Acids Research. 38(5). e30–e30. 35 indexed citations
14.
Geslain, Renaud & Tao Pan. (2009). Functional Analysis of Human tRNA Isodecoders. Journal of Molecular Biology. 396(3). 821–831. 74 indexed citations
15.
Jones, Thomas, et al.. (2008). An Operational RNA Code for Faithful Assignment of AUG Triplets to Methionine. Molecular Cell. 29(3). 401–407. 6 indexed citations
16.
Farrera‐Sinfreu, Josep, Yaiza Español, Renaud Geslain, et al.. (2008). Solid-Phase Combinatorial Synthesis of a Lysyl-tRNA Synthetase (LysRS) Inhibitory Library. Journal of Combinatorial Chemistry. 10(3). 391–400. 7 indexed citations
17.
Geslain, Renaud, Eric Aeby, Thomas Jones, et al.. (2006). Trypanosoma Seryl-tRNA Synthetase Is a Metazoan-like Enzyme with High Affinity for tRNASec. Journal of Biological Chemistry. 281(50). 38217–38225. 18 indexed citations
18.
Geslain, Renaud & Lluı́s Ribas de Pouplana. (2004). Regulation of RNA function by aminoacylation and editing?. Trends in Genetics. 20(12). 604–610. 26 indexed citations
19.
Geslain, Renaud, Gilbert Bey, J. Cavarelli, & Gilbert Eriani. (2003). Limited Set of Amino Acid Residues in a Class Ia Aminoacyl-tRNA Synthetase Is Crucial for tRNA Binding. Biochemistry. 42(51). 15092–15101. 12 indexed citations
20.
Geslain, Renaud, Franck Martin, B. Delagoutte, et al.. (2000). In vivo selection of lethal mutations reveals two functional domains in arginyl–tRNA synthetase. RNA. 6(3). 434–448. 14 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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