David Reboutier

738 total citations
25 papers, 558 citations indexed

About

David Reboutier is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, David Reboutier has authored 25 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Plant Science, 11 papers in Molecular Biology and 9 papers in Cell Biology. Recurrent topics in David Reboutier's work include Microtubule and mitosis dynamics (7 papers), Plant Stress Responses and Tolerance (5 papers) and Plant-Microbe Interactions and Immunity (5 papers). David Reboutier is often cited by papers focused on Microtubule and mitosis dynamics (7 papers), Plant Stress Responses and Tolerance (5 papers) and Plant-Microbe Interactions and Immunity (5 papers). David Reboutier collaborates with scholars based in France, United States and Switzerland. David Reboutier's co-authors include Claude Prigent, François Bouteau, Marie‐Bérengère Troadec, Cécile Frankart, Jean‐Pierre Rona, Mathias Brault, Joèl Briand, Christelle Benaud, Kenji Fukasawa and Marie‐Anne Barny and has published in prestigious journals such as Nature Communications, The Journal of Cell Biology and Biochemical and Biophysical Research Communications.

In The Last Decade

David Reboutier

25 papers receiving 545 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Reboutier France 14 311 286 217 49 32 25 558
Jeffrey T. Irelan United States 10 292 0.9× 456 1.6× 75 0.3× 44 0.9× 12 0.4× 11 623
Veerle De Wever Canada 10 102 0.3× 497 1.7× 142 0.7× 60 1.2× 20 0.6× 14 589
Vicky Buck United Kingdom 8 137 0.4× 467 1.6× 230 1.1× 32 0.7× 28 0.9× 8 515
Samuel Roberts United States 6 342 1.1× 978 3.4× 91 0.4× 49 1.0× 25 0.8× 9 1.2k
Manuel Arellano Spain 12 244 0.8× 707 2.5× 313 1.4× 89 1.8× 34 1.1× 13 817
Marie‐Pierre Gulli France 12 142 0.5× 879 3.1× 458 2.1× 40 0.8× 22 0.7× 13 959
Hiroshi Mitsuzawa Japan 17 87 0.3× 650 2.3× 143 0.7× 56 1.1× 21 0.7× 28 718
Marco Geymonat United Kingdom 17 191 0.6× 821 2.9× 514 2.4× 34 0.7× 14 0.4× 28 873
Rafael R. Daga Spain 16 148 0.5× 669 2.3× 447 2.1× 14 0.3× 10 0.3× 38 789
Brian Fleharty United States 8 173 0.6× 720 2.5× 131 0.6× 35 0.7× 32 1.0× 9 882

Countries citing papers authored by David Reboutier

Since Specialization
Citations

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

Fields of papers citing papers by David Reboutier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Reboutier

This figure shows the co-authorship network connecting the top 25 collaborators of David Reboutier. A scholar is included among the top collaborators of David Reboutier 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 David Reboutier. David Reboutier 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.
2.
Reboutier, David, Stéphane Deschamps, Agnès Méreau, et al.. (2022). The RNA-binding proteins CELF1 and ELAVL1 cooperatively control the alternative splicing of CD44. Biochemical and Biophysical Research Communications. 626. 79–84. 6 indexed citations
3.
Taylor, William R., Stéphane Deschamps, David Reboutier, et al.. (2022). The Splicing Factor PTBP1 Represses TP63 γ Isoform Production in Squamous Cell Carcinoma. Cancer Research Communications. 2(12). 1669–1683. 2 indexed citations
4.
Tran, Daniel, Arnaud Lehner, Patrice Meimoun, et al.. (2021). Biphasic activation of survival and death pathways in Arabidopsis thaliana cultured cells by sorbitol-induced hyperosmotic stress. Plant Science. 305. 110844–110844. 1 indexed citations
5.
Bouteau, François, David Reboutier, Daniel Tran, & Patrick Laurenti. (2020). Ion Transport in Plant Cell Shrinkage During Death. Frontiers in Cell and Developmental Biology. 8. 566606–566606. 6 indexed citations
6.
Courthéoux, Thibault, David Reboutier, Thibaut Vazeille, et al.. (2019). Microtubule nucleation during central spindle assembly requires NEDD1 phosphorylation on serine 405 by Aurora A. Journal of Cell Science. 132(10). 11 indexed citations
7.
Reboutier, David, et al.. (2019). Modeling ocular lens disease in Xenopus. Developmental Dynamics. 249(5). 610–621. 12 indexed citations
8.
Bertolin, Giulia, et al.. (2016). A FRET biosensor reveals spatiotemporal activation and functions of aurora kinase A in living cells. Nature Communications. 7(1). 12674–12674. 47 indexed citations
9.
Reboutier, David, Christelle Benaud, & Claude Prigent. (2015). Aurora A’s Functions During Mitotic Exit: The Guess Who Game. Frontiers in Oncology. 5. 290–290. 12 indexed citations
10.
Reboutier, David, et al.. (2013). Aurora A is involved in central spindle assembly through phosphorylation of Ser 19 in P150Glued. The Journal of Cell Biology. 201(1). 65–79. 45 indexed citations
11.
Reboutier, David & François Bouteau. (2008). Harpins and ion channels modulations. Plant Signaling & Behavior. 3(5). 314–316. 8 indexed citations
12.
Reboutier, David, Mathieu Piednoël, Stéphanie Boisnard, et al.. (2008). Combination of different molecular mechanisms leading to fluconazole resistance in a Candida lusitaniae clinical isolate. Diagnostic Microbiology and Infectious Disease. 63(2). 188–193. 18 indexed citations
13.
Barny, Marie‐Anne, Tristan Boureau, Alexandre Degrave, et al.. (2008). TYPE III EFFECTORS OF E. AMYLOVORA: SYNERGISTIC AND ANTAGONISTIC EFFECTS. Acta Horticulturae. 215–220. 1 indexed citations
14.
Gauthier, Adrien, Olivier Lamotte, David Reboutier, et al.. (2007). Cryptogein-Induced Anion Effluxes. Plant Signaling & Behavior. 2(2). 86–95. 31 indexed citations
15.
Reboutier, David, Cécile Frankart, Joèl Briand, et al.. (2007). The HrpNea Harpin from Erwinia amylovora Triggers Differential Responses on the Nonhost Arabidopsis thaliana Cells and on the Host Apple Cells. Molecular Plant-Microbe Interactions. 20(1). 94–100. 38 indexed citations
17.
Reboutier, David, Cécile Frankart, Régine Vedel, et al.. (2005). A CFTR chloride channel activator prevents HrpNea-induced cell death in Arabidopsis thaliana suspension cells. Plant Physiology and Biochemistry. 43(6). 567–572. 13 indexed citations
18.
Bouizgarne, Brahim, Hayat El‐Maarouf‐Bouteau, Cécile Frankart, et al.. (2005). Early physiological responses of Arabidopsis thaliana cells to fusaric acid: toxic and signalling effects. New Phytologist. 169(1). 209–218. 90 indexed citations
19.
Zhang, Zongshen, Javier A. Ramírez, David Reboutier, et al.. (2005). Brassinosteroids Regulate Plasma Membrane Anion Channels in Addition to Proton Pumps During Expansion of Arabidopsis thaliana Cells. Plant and Cell Physiology. 46(9). 1494–1504. 26 indexed citations
20.
Reboutier, David, Michele Wolfe Bianchi, Mathias Brault, et al.. (2002). The Indolic Compound Hypaphorine Produced by Ectomycorrhizal Fungus Interferes with Auxin Action and Evokes Early Responses in Nonhost Arabidopsis thaliana. Molecular Plant-Microbe Interactions. 15(9). 932–938. 41 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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