Jean‐Marc Chatel

5.5k total citations · 1 hit paper
85 papers, 3.5k citations indexed

About

Jean‐Marc Chatel is a scholar working on Molecular Biology, Food Science and Infectious Diseases. According to data from OpenAlex, Jean‐Marc Chatel has authored 85 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 39 papers in Food Science and 20 papers in Infectious Diseases. Recurrent topics in Jean‐Marc Chatel's work include Probiotics and Fermented Foods (38 papers), Gut microbiota and health (28 papers) and Food Allergy and Anaphylaxis Research (12 papers). Jean‐Marc Chatel is often cited by papers focused on Probiotics and Fermented Foods (38 papers), Gut microbiota and health (28 papers) and Food Allergy and Anaphylaxis Research (12 papers). Jean‐Marc Chatel collaborates with scholars based in France, Brazil and Argentina. Jean‐Marc Chatel's co-authors include Philippe Langella, Vasco Azevedo, Luis G. Bermúdez‐Humarán, Anderson Miyoshi, Rebeca Martín, Harry Sokol, Florian Chain, Karine Adel‐Patient, Philippe Langella and Pascale Kharrat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Jean‐Marc Chatel

83 papers receiving 3.4k citations

Hit Papers

Faecalibacterium: a bacterial genus with promising human ... 2023 2026 2024 2025 2023 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jean‐Marc Chatel France 33 1.8k 1.3k 718 434 427 85 3.5k
Anderson Miyoshi Brazil 40 2.4k 1.4× 1.5k 1.2× 943 1.3× 718 1.7× 478 1.1× 175 5.5k
Hanne Frøkiær Denmark 39 2.0k 1.1× 1.4k 1.1× 566 0.8× 368 0.8× 1.2k 2.8× 129 5.2k
Philippe Langella France 20 1.1k 0.6× 918 0.7× 503 0.7× 311 0.7× 284 0.7× 22 2.0k
Christian U. Riedel Germany 32 2.2k 1.3× 1.5k 1.2× 387 0.5× 361 0.8× 475 1.1× 91 3.7k
Fang He China 33 1.9k 1.1× 1.4k 1.1× 429 0.6× 261 0.6× 570 1.3× 148 3.3k
Flaviano S. Martins Brazil 37 2.2k 1.3× 1.3k 1.0× 525 0.7× 275 0.6× 710 1.7× 123 4.1k
Tomomi Kuwahara Japan 28 3.7k 2.1× 935 0.7× 1.4k 2.0× 760 1.8× 515 1.2× 97 6.0k
Philippe Langella France 24 2.8k 1.6× 998 0.8× 1.1k 1.5× 678 1.6× 298 0.7× 41 4.1k
Jiro Nakayama Japan 41 4.3k 2.4× 2.7k 2.1× 833 1.2× 671 1.5× 1.2k 2.9× 189 6.3k
Marta Wlodarska Canada 13 1.8k 1.0× 697 0.5× 1.0k 1.4× 318 0.7× 293 0.7× 13 3.5k

Countries citing papers authored by Jean‐Marc Chatel

Since Specialization
Citations

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

Fields of papers citing papers by Jean‐Marc Chatel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Marc Chatel. 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 Jean‐Marc Chatel. The network helps show where Jean‐Marc Chatel may publish in the future.

Co-authorship network of co-authors of Jean‐Marc Chatel

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Marc Chatel. A scholar is included among the top collaborators of Jean‐Marc Chatel 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 Jean‐Marc Chatel. Jean‐Marc Chatel 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.
Marthey, Sylvain, Sandrine Auger, Luís Cláudio Lima de Jesus, et al.. (2025). The Microbial Anti-Inflammatory Molecule (MAM) is a key protein processed and exported to Faecalibacterium duncaniae envelope. Gut Microbes. 17(1). 2519695–2519695.
2.
Auger, Sandrine, Loïc Brot, Nicolas Benech, et al.. (2025). Faecalibacterium Diversity in the Gut Microbiome of Crohn's Disease Patients. United European Gastroenterology Journal. 13(8). 1480–1490. 1 indexed citations
3.
Robert, Véronique, Shintaro Maeno, Moriya Ohkuma, et al.. (2025). Faecalibacterium langellae sp. nov. isolated from human faeces. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 75(6).
4.
Jesus, Luís Cláudio Lima de, Andria dos Santos Freitas, Fernanda Alvarenga Lima Barroso, et al.. (2024). Health-promoting effects and safety aspects of Lactobacillus delbrueckii: A food industry species. Trends in Food Science & Technology. 150. 104605–104605. 12 indexed citations
5.
Chatel, Jean‐Marc, Rebeca Martín, Denis Mariat, et al.. (2023). New gene markers for classification and quantification ofFaecalibacteriumspp. in the human gut. FEMS Microbiology Ecology. 99(5). 5 indexed citations
6.
Auger, Sandrine, Virginie Mournetas, Hélène Chiapello, et al.. (2022). Gene co-expression network analysis of the human gut commensal bacterium Faecalibacterium prausnitzii in R-Shiny. PLoS ONE. 17(11). e0271847–e0271847. 6 indexed citations
7.
8.
Breyner, Natália Martins, Christophe Michon, Florian Chain, et al.. (2017). Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii Shows a Protective Effect on DNBS and DSS-Induced Colitis Model in Mice through Inhibition of NF-κB Pathway. Frontiers in Microbiology. 8. 114–114. 165 indexed citations
9.
Mancha-Agresti, Pamela, Mariana Martins Drumond, Fillipe Luiz Rosa Do Carmo, et al.. (2016). A New Broad Range Plasmid for DNA Delivery in Eukaryotic Cells Using Lactic Acid Bacteria: In Vitro and In Vivo Assays. Molecular Therapy — Methods & Clinical Development. 4. 83–91. 24 indexed citations
11.
Azevedo, Marcela de, Clarissa Santos Rocha, Vanessa Bastos Pereira, et al.. (2015). Prospective uses of recombinant Lactococcus lactis expressing both listeriolysin O and mutated internalin A from Listeria monocytogenes as a tool for DNA vaccination. Genetics and Molecular Research. 14(4). 18485–18493. 4 indexed citations
12.
Pontes, Daniela Santos, Marcela de Azevedo, Silvia Innocentin, et al.. (2014). Immune Response Elicited by DNA Vaccination Using Lactococcus lactis Is Modified by the Production of Surface Exposed Pathogenic Protein. PLoS ONE. 9(1). e84509–e84509. 13 indexed citations
13.
LeBlanc, Jean Guy, Camille Aubry, Naima G. Cortes‐Perez, et al.. (2013). Mucosal targeting of therapeutic molecules using genetically modified lactic acid bacteria: an update. FEMS Microbiology Letters. 344(1). 1–9. 64 indexed citations
14.
Bermúdez‐Humarán, Luis G., Camille Aubry, Jean‐Paul Motta, et al.. (2013). Engineering lactococci and lactobacilli for human health. Current Opinion in Microbiology. 16(3). 278–283. 125 indexed citations
15.
Azevedo, Marcela de, Silvia Innocentin, Fernanda Alves Dorella, et al.. (2013). Immunotherapy of allergic diseases using probiotics or recombinant probiotics. Journal of Applied Microbiology. 115(2). 319–333. 31 indexed citations
16.
Chain, Florian, Jean‐Jacques Gratadoux, Sébastien Blugeon, et al.. (2012). Identification of One Novel Candidate Probiotic Lactobacillus plantarum Strain Active against Influenza Virus Infection in Mice by a Large-Scale Screening. Applied and Environmental Microbiology. 79(5). 1491–1499. 87 indexed citations
17.
Pontes, Daniela Santos, et al.. (2011). Lactococcus lactis as a live vector: Heterologous protein production and DNA delivery systems. Protein Expression and Purification. 79(2). 165–175. 113 indexed citations
18.
Chatel, Jean‐Marc, Karine Adel‐Patient, Christophe Créminon, & Jean‐Michel Wal. (1999). Expression of a Lipocalin in Prokaryote and Eukaryote Cells: Quantification and Structural Characterization of Recombinant Bovine β-Lactoglobulin. Protein Expression and Purification. 16(1). 70–75. 18 indexed citations
19.
Oliver, Lisa, Jean‐Marc Chatel, Jean Massoulié, Marc Vigny, & François M. Vallette. (1992). Molecular forms of acetylcholinesterase in dystrophic (mdx) mouse tissues. Neuromuscular Disorders. 2(2). 87–97. 11 indexed citations
20.
Gróf, Pál, S. Bon, Patrick Masson, et al.. (1991). A comparative Raman spectroscopic study of cholinesterases. Biochimie. 73(11). 1375–1386. 12 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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