Thierry Langin

4.4k total citations
83 papers, 3.2k citations indexed

About

Thierry Langin is a scholar working on Plant Science, Cell Biology and Molecular Biology. According to data from OpenAlex, Thierry Langin has authored 83 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Plant Science, 43 papers in Cell Biology and 18 papers in Molecular Biology. Recurrent topics in Thierry Langin's work include Plant Pathogens and Fungal Diseases (43 papers), Plant-Microbe Interactions and Immunity (37 papers) and Plant pathogens and resistance mechanisms (21 papers). Thierry Langin is often cited by papers focused on Plant Pathogens and Fungal Diseases (43 papers), Plant-Microbe Interactions and Immunity (37 papers) and Plant pathogens and resistance mechanisms (21 papers). Thierry Langin collaborates with scholars based in France, United States and Morocco. Thierry Langin's co-authors include Marie‐Josée Daboussi, Pierre Capy, Mireille Sévignac, Valérie Geffroy, Michel Dron, Yves Brygoo, Richard Laugé, Marie Dufresne, Catherine Macadré and Dominique Anxolabéhère and has published in prestigious journals such as Nature Communications, PLoS ONE and The Plant Cell.

In The Last Decade

Thierry Langin

81 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thierry Langin France 36 2.8k 1.1k 1.1k 169 136 83 3.2k
J. B. Rasmussen United States 28 3.4k 1.2× 823 0.7× 657 0.6× 338 2.0× 189 1.4× 79 3.6k
Kar‐Chun Tan Australia 30 1.9k 0.7× 779 0.7× 608 0.5× 157 0.9× 42 0.3× 61 2.3k
Les J. Szabo United States 35 3.6k 1.3× 873 0.8× 2.2k 2.0× 437 2.6× 405 3.0× 86 4.1k
Adrienne R. Hardham Australia 32 3.2k 1.2× 1.1k 1.0× 1.3k 1.2× 43 0.3× 50 0.4× 68 3.6k
Anne E. Dorrance United States 37 3.6k 1.3× 1.1k 1.0× 506 0.5× 122 0.7× 165 1.2× 136 3.7k
Jean‐Benoit Morel France 20 3.0k 1.1× 337 0.3× 1.6k 1.4× 124 0.7× 64 0.5× 38 3.5k
Ksenia V. Krasileva United States 27 3.0k 1.1× 347 0.3× 844 0.8× 333 2.0× 104 0.8× 45 3.3k
Mehdi Kabbage United States 25 2.2k 0.8× 460 0.4× 799 0.7× 49 0.3× 253 1.9× 54 2.6k
Reid D. Frederick United States 38 3.6k 1.3× 905 0.8× 2.3k 2.1× 157 0.9× 34 0.3× 83 4.1k
Yuese Ning China 35 3.3k 1.2× 524 0.5× 1.8k 1.6× 307 1.8× 39 0.3× 73 3.9k

Countries citing papers authored by Thierry Langin

Since Specialization
Citations

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

Fields of papers citing papers by Thierry Langin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thierry Langin

This figure shows the co-authorship network connecting the top 25 collaborators of Thierry Langin. A scholar is included among the top collaborators of Thierry Langin 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 Thierry Langin. Thierry Langin 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.
Gaucher, Matthieu, Marjolaine Rey, Marie-Noëlle Brisset, et al.. (2025). Strong elicitation of plant defense pathways by foliar and collar inoculations of wheat with the Bacillus pumilus strain JM79. Current Plant Biology. 43. 100524–100524.
3.
Suarez‐Fernandez, Marta, Florence Cambon, Andrea Sánchez‐Vallet, et al.. (2024). Stomatal penetration: the cornerstone of plant resistance to the fungal pathogen Zymoseptoria tritici. BMC Plant Biology. 24(1). 736–736. 5 indexed citations
4.
Doré, Jeanne, Marjolaine Rey, Guillaume Meiffren, et al.. (2023). Dimethylpolysulfides production as the major mechanism behind wheat fungal pathogen biocontrol, by Arthrobacter and Microbacterium actinomycetes. Microbiology Spectrum. 11(6). e0529222–e0529222. 11 indexed citations
5.
Lebrun, Marc‐Henri, et al.. (2022). Blocked at the Stomatal Gate, a Key Step of Wheat Stb16q-Mediated Resistance to Zymoseptoria tritici. Frontiers in Plant Science. 13. 921074–921074. 27 indexed citations
6.
Saintenac, Cyrille, Florence Cambon, Lamia Aouini, et al.. (2021). A wheat cysteine-rich receptor-like kinase confers broad-spectrum resistance against Septoria tritici blotch. Nature Communications. 12(1). 433–433. 64 indexed citations
7.
Fabre, Francis, Serge Urbach, Sylvie Roche, Thierry Langin, & Ludovic Bonhomme. (2021). Proteomics-Based Data Integration of Wheat Cultivars Facing Fusarium graminearum Strains Revealed a Core-Responsive Pattern Controlling Fusarium Head Blight. Frontiers in Plant Science. 12. 644810–644810. 11 indexed citations
9.
Panek, Johan, Ludovic Bonhomme, Hicham El Alaoui, et al.. (2015). Cross-talk in host–parasite associations: What do past and recent proteomics approaches tell us?. Infection Genetics and Evolution. 33. 84–94. 9 indexed citations
11.
David, Perrine, Catherine Colas des Francs‐Small, Mireille Sévignac, et al.. (2010). Three highly similar formate dehydrogenase genes located in the vicinity of the B4 resistance gene cluster are differentially expressed under biotic and abiotic stresses in Phaseolus vulgaris. Theoretical and Applied Genetics. 121(1). 87–103. 33 indexed citations
12.
Mehrabi, Rahim, Marie Dufresne, Théo van der Lee, et al.. (2006). The MAP kinase‐encoding gene MgFus3 of the non‐appressorium phytopathogen Mycosphaerella graminicola is required for penetration and in vitro pycnidia formation. Molecular Plant Pathology. 7(4). 269–278. 57 indexed citations
13.
Macadré, Catherine, et al.. (2005). Distinct post-transcriptional modifications result into seven alternative transcripts of the CC–NBS–LRR gene JA1tr of Phaseolus vulgaris. Theoretical and Applied Genetics. 110(5). 895–905. 34 indexed citations
14.
Geffroy, Valérie, et al.. (2003). Characterization of expressed NBS-LRR resistance gene candidates from common bean. Theoretical and Applied Genetics. 106(2). 251–261. 60 indexed citations
15.
Hua‐Van, Aurélie, João Alencar Pamphile, Thierry Langin, & Marie‐Josée Daboussi. (2001). Transposition of autonomous and engineered impala transposons in Fusarium oxysporum and a related species. Molecular and General Genetics MGG. 264(5). 724–731. 34 indexed citations
16.
Creusot, Francine, Catherine Macadré, Catherine Riou, et al.. (1999). Cloning and molecular characterization of three members of the NBS-LRR subfamily located in the vicinity of the Co-2 locus for anthracnose resistance in Phaseolus vulgaris. Genome. 42(2). 254–264. 46 indexed citations
17.
Langin, Thierry, et al.. (1999). Specific expression of the Fusarium transposon Fot1 and effects on target gene transcription. Molecular Microbiology. 31(5). 1373–1383. 18 indexed citations
18.
Diolez, Annick, et al.. (1993). The nia gene of Fusarium oxysporum: isolation, sequence and development of a homologous transformation system. Gene. 131(1). 61–67. 36 indexed citations
20.
Langin, Thierry, et al.. (1988). Hybrid DNA extension and reciprocal exchanges: alternative issues of an early intermediate during meiotic recombination?. Genetics. 119(2). 337–344. 5 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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