Denis Faure

7.5k total citations · 1 hit paper
127 papers, 5.2k citations indexed

About

Denis Faure is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Denis Faure has authored 127 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Plant Science, 66 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Denis Faure's work include Plant-Microbe Interactions and Immunity (52 papers), Plant Pathogenic Bacteria Studies (48 papers) and Bacterial biofilms and quorum sensing (33 papers). Denis Faure is often cited by papers focused on Plant-Microbe Interactions and Immunity (52 papers), Plant Pathogenic Bacteria Studies (48 papers) and Bacterial biofilms and quorum sensing (33 papers). Denis Faure collaborates with scholars based in France, Morocco and Malaysia. Denis Faure's co-authors include Yves Dessaux, Catherine Grandclément, S. Moréra, Mélanie Tannières, Yves Dessaux, Amélie Cirou, Elise Haudecoeur, Barry J. Shelp, Julien Lang and Xavier Latour and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Denis Faure

126 papers receiving 5.0k citations

Hit Papers

Quorum quenching: role in... 2015 2026 2018 2022 2015 100 200 300 400

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Denis Faure 3.2k 2.6k 606 527 509 127 5.2k
Kim Findlay 5.2k 1.6× 3.5k 1.4× 310 0.5× 391 0.7× 691 1.4× 93 7.6k
Yves Dessaux 2.4k 0.7× 2.8k 1.1× 271 0.4× 274 0.5× 571 1.1× 51 4.7k
Dmitri V. Mavrodi 2.7k 0.8× 2.3k 0.9× 448 0.7× 232 0.4× 558 1.1× 84 5.0k
René De Mot 1.7k 0.5× 2.6k 1.0× 290 0.5× 394 0.7× 652 1.3× 135 4.9k
Leland S. Pierson 2.5k 0.8× 2.8k 1.1× 389 0.6× 360 0.7× 1.1k 2.1× 68 5.2k
Vittorio Venturi 3.4k 1.1× 3.8k 1.5× 561 0.9× 521 1.0× 1.3k 2.5× 180 7.0k
N. T. Keen 5.5k 1.7× 2.6k 1.0× 720 1.2× 754 1.4× 619 1.2× 103 7.4k
John P. Morrissey 2.1k 0.7× 3.5k 1.3× 293 0.5× 703 1.3× 307 0.6× 115 6.3k
Kouhei Ohnishi 1.9k 0.6× 2.0k 0.8× 321 0.5× 276 0.5× 939 1.8× 184 4.6k
Rosa Lanzetta 1.9k 0.6× 2.6k 1.0× 205 0.3× 424 0.8× 328 0.6× 250 6.0k

Countries citing papers authored by Denis Faure

Since Specialization
Citations

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

Fields of papers citing papers by Denis Faure

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denis Faure

This figure shows the co-authorship network connecting the top 25 collaborators of Denis Faure. A scholar is included among the top collaborators of Denis Faure 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 Denis Faure. Denis Faure 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.
Vigouroux, Armelle, Magali Aumont‐Nicaise, Mohammed Ahmar, et al.. (2023). A highly conserved ligand-binding site for AccA transporters of antibiotic and quorum-sensing regulator in Agrobacterium leads to a different specificity. Biochemical Journal. 481(2). 93–117.
2.
Effantin, Géraldine, et al.. (2023). Dissimilar gene repertoires of Dickeya solani involved in the colonization of lesions and roots of Solanum tuberosum. Frontiers in Plant Science. 14. 1154110–1154110. 6 indexed citations
3.
Effantin, Géraldine, Laetitia Attaiech, Monique Royer, et al.. (2023). A natural single nucleotide mutation in the small regulatory RNA ArcZ of Dickeya solani switches off the antimicrobial activities against yeast and bacteria. PLoS Genetics. 19(4). e1010725–e1010725. 8 indexed citations
4.
Torres, Marta, et al.. (2021). Agrobacterium tumefaciens fitness genes involved in the colonization of plant tumors and roots. New Phytologist. 233(2). 905–918. 26 indexed citations
5.
Lang, Julien, Catherine Grandclément, Delphine Naquin, et al.. (2018). Lifestyle of the biotroph Agrobacterium tumefaciens in the ecological niche constructed on its host plant. New Phytologist. 219(1). 350–362. 21 indexed citations
6.
Vigouroux, Armelle, Abbas El Sahili, Julien Lang, et al.. (2017). Structural basis for high specificity of octopine binding in the plant pathogen Agrobacterium tumefaciens. Scientific Reports. 7(1). 15 indexed citations
7.
Lang, Julien, Armelle Vigouroux, Abbas El Sahili, et al.. (2016). Fitness costs restrict niche expansion by generalist niche-constructing pathogens. The ISME Journal. 11(2). 374–385. 12 indexed citations
8.
Mhedbi-Hajri, Nadia, et al.. (2016). Transcriptome analysis revealed that a quorum sensing system regulates the transfer of the pAt megaplasmid in Agrobacterium tumefaciens. BMC Genomics. 17(1). 661–661. 8 indexed citations
9.
Chan, Kok‐Gan, Teik-Min Chong, Catherine Grandclément, et al.. (2016). Pseudomonas lini Strain ZBG1 Revealed Carboxylic Acid Utilization and Copper Resistance Features Required for Adaptation to Vineyard Soil Environment: A Draft Genome Analysis. PubMed. 4. 26–28. 3 indexed citations
10.
Mondy, Samuel, Sara Planamente, Mohiéddine Moumni, et al.. (2013). Deep sequencing revealed genome-wide single-nucleotide polymorphism and plasmid content of Erwinia amylovora strains isolated in Middle Atlas, Morocco. Research in Microbiology. 164(8). 815–820. 5 indexed citations
11.
Crépin, Alexandre, Corinne Barbey, Valérie Hélias, et al.. (2012). Quorum Sensing Signaling Molecules Produced by Reference and Emerging Soft-Rot Bacteria (Dickeya and Pectobacterium spp.). PLoS ONE. 7(4). e35176–e35176. 45 indexed citations
12.
Chapelle, Emilie, et al.. (2011). Transgenic plants expressing the quorum quenching lactonase AttM do not significantly alter root-associated bacterial populations. Research in Microbiology. 162(9). 951–958. 12 indexed citations
14.
Chevrot, Romain, Ran Rosen, Elise Haudecoeur, et al.. (2006). GABA controls the level of quorum-sensing signal in Agrobacterium tumefaciens. Proceedings of the National Academy of Sciences. 103(19). 7460–7464. 198 indexed citations
15.
Latour, Xavier, et al.. (2004). Involvement of N-acylhomoserine Lactones Throughout Plant Infection by Erwinia carotovora subsp. atroseptica (Pectobacterium atrosepticum). Molecular Plant-Microbe Interactions. 17(11). 1269–1278. 74 indexed citations
17.
Miché, Lucie, et al.. (2001). Detection and activity of insertion sequences in environmental strains of Burkholderia. Environmental Microbiology. 3(12). 766–773. 13 indexed citations
18.
Alexandre, Gladys, et al.. (1996). Population dynamics of a motile and a non-motile Azospirillum lipoferum strain during rice root colonization and motility variation in the rhizosphere. FEMS Microbiology Ecology. 19(4). 271–278. 28 indexed citations
19.
Givaudan, Alain, Aline Effosse, Denis Faure, et al.. (1993). Polyphenol oxidase inAzospirillum lipoferumisolated from rice rhizosphere: Evidence for laccase activity in non-motile strains ofAzospirillum lipoferum. FEMS Microbiology Letters. 108(2). 205–210. 220 indexed citations
20.
Faure, Denis & Alain Deschamps. (1990). Evaluation of the suitability of grape skins for composting.. 24(1). 1–12. 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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