Mathilde Body–Malapel

7.3k total citations · 4 hit papers
50 papers, 5.9k citations indexed

About

Mathilde Body–Malapel is a scholar working on Molecular Biology, Immunology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Mathilde Body–Malapel has authored 50 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 15 papers in Immunology and 9 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Mathilde Body–Malapel's work include Immune Response and Inflammation (12 papers), Pharmacological Receptor Mechanisms and Effects (9 papers) and Cannabis and Cannabinoid Research (7 papers). Mathilde Body–Malapel is often cited by papers focused on Immune Response and Inflammation (12 papers), Pharmacological Receptor Mechanisms and Effects (9 papers) and Cannabis and Cannabinoid Research (7 papers). Mathilde Body–Malapel collaborates with scholars based in France, United States and Belgium. Mathilde Body–Malapel's co-authors include Thirumala‐Devi Kanneganti, Luigi Franchi, Amal O. Amer, Gabriel Núñez, Naohiro Inohara, John Bertin, Nesrin Özören, Jong‐Hwan Park, Ethan Grant and Anthony J. Coyle and has published in prestigious journals such as Nature, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Mathilde Body–Malapel

49 papers receiving 5.8k citations

Hit Papers

Cytosolic flagellin requires Ipaf for activation of caspa... 2006 2026 2012 2019 2006 2006 2006 2020 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathilde Body–Malapel France 28 3.3k 2.8k 656 596 501 50 5.9k
Jong‐Hwan Park South Korea 37 3.3k 1.0× 3.1k 1.1× 939 1.4× 364 0.6× 593 1.2× 167 7.4k
Bin Wang China 42 3.7k 1.1× 1.2k 0.4× 633 1.0× 835 1.4× 365 0.7× 217 7.1k
Michael Loos Germany 39 1.1k 0.3× 3.8k 1.3× 371 0.6× 255 0.4× 323 0.6× 195 6.4k
Lei Shi China 41 2.5k 0.8× 787 0.3× 668 1.0× 217 0.4× 315 0.6× 163 5.5k
Rheinallt M. Jones United States 40 3.7k 1.1× 956 0.3× 455 0.7× 103 0.2× 457 0.9× 100 6.1k
Ryuichi Nakano Japan 33 1.2k 0.4× 646 0.2× 335 0.5× 154 0.3× 412 0.8× 155 3.7k
Ken‐ichi Tanamoto Japan 31 936 0.3× 1.5k 0.5× 297 0.5× 193 0.3× 169 0.3× 117 3.3k
Isamu Sugawara Japan 43 1.5k 0.5× 1.4k 0.5× 1.4k 2.1× 438 0.7× 791 1.6× 187 6.2k
Jianzhong Hu United States 31 2.2k 0.7× 468 0.2× 388 0.6× 174 0.3× 285 0.6× 95 3.6k
Lin Zeng China 40 1.8k 0.5× 475 0.2× 697 1.1× 118 0.2× 152 0.3× 136 4.8k

Countries citing papers authored by Mathilde Body–Malapel

Since Specialization
Citations

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

Fields of papers citing papers by Mathilde Body–Malapel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mathilde Body–Malapel. 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 Mathilde Body–Malapel. The network helps show where Mathilde Body–Malapel may publish in the future.

Co-authorship network of co-authors of Mathilde Body–Malapel

This figure shows the co-authorship network connecting the top 25 collaborators of Mathilde Body–Malapel. A scholar is included among the top collaborators of Mathilde Body–Malapel 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 Mathilde Body–Malapel. Mathilde Body–Malapel 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.
Djouina, Madjid, Christophe Waxin, Ségolène Caboche, et al.. (2025). Ingestion of environmentally sourced polyvinyl chloride microplastic fragments increases colon inflammation and fibrosis in mice. Environmental Research. 285(Pt 5). 122621–122621.
2.
Djouina, Madjid, et al.. (2024). Recent Progress in Intestinal Toxicity of Microplastics and Nanoplastics: Systematic Review of Preclinical Evidence. SHILAP Revista de lepidopterología. 3(2). 217–233. 6 indexed citations
3.
Djouina, Madjid, Cécile Vignal, Alexandre Dehaut, et al.. (2022). Oral exposure to polyethylene microplastics alters gut morphology, immune response, and microbiota composition in mice. Environmental Research. 212(Pt B). 113230–113230. 88 indexed citations
4.
Djouina, Madjid, Christophe Waxin, Frédéric Leprêtre, et al.. (2022). Gene/environment interaction in the susceptibility of Crohn's disease patients to aluminum. The Science of The Total Environment. 850. 158017–158017. 11 indexed citations
5.
Coll, Patrice, Madjid Djouina, Mathieu Cazaunau, et al.. (2022). Murine in utero exposure to simulated complex urban air pollution disturbs offspring gut maturation and microbiota during intestinal suckling-to-weaning transition in a sex-dependent manner. Particle and Fibre Toxicology. 19(1). 41–41. 14 indexed citations
6.
Djouina, Madjid, Ségolène Caboche, Christophe Waxin, et al.. (2022). Exposure to atmospheric Ag, TiO2, Ti and SiO2 engineered nanoparticles modulates gut inflammatory response and microbiota in mice. Ecotoxicology and Environmental Safety. 236. 113442–113442. 14 indexed citations
7.
Body–Malapel, Mathilde, et al.. (2020). Immunotoxicity and intestinal effects of nano- and microplastics: a review of the literature. Particle and Fibre Toxicology. 17(1). 57–57. 472 indexed citations breakdown →
8.
Vignal, Cécile, Madjid Djouina, Muriel Pichavant, et al.. (2018). Chronic ingestion of deoxynivalenol at human dietary levels impairs intestinal homeostasis and gut microbiota in mice. Archives of Toxicology. 92(7). 2327–2338. 68 indexed citations
9.
Body–Malapel, Mathilde, Madjid Djouina, Christophe Waxin, et al.. (2018). The RAGE signaling pathway is involved in intestinal inflammation and represents a promising therapeutic target for Inflammatory Bowel Diseases. Mucosal Immunology. 12(2). 468–478. 73 indexed citations
10.
Breton, Jérôme, Catherine Daniel, Cécile Vignal, et al.. (2016). Does oral exposure to cadmium and lead mediate susceptibility to colitis? The dark-and-bright sides of heavy metals in gut ecology. Scientific Reports. 6(1). 19200–19200. 55 indexed citations
11.
Leleu‐Chavain, Natascha, Mathilde Body–Malapel, Madjid Djouina, et al.. (2014). Switching cannabinoid response from CB2 agonists to FAAH inhibitors. Bioorganic & Medicinal Chemistry Letters. 24(5). 1322–1326. 11 indexed citations
12.
Leleu‐Chavain, Natascha, Mathilde Body–Malapel, John Spencer, et al.. (2012). Recent Advances in the Development of Selective CB2 Agonists as Promising Anti-Inflammatory Agents. Current Medicinal Chemistry. 19(21). 3457–3474. 31 indexed citations
13.
Muccioli, Giulio G., Mathilde Body–Malapel, Jamal El Bakali, et al.. (2011). New FAAH inhibitors based on 3-carboxamido-5-aryl-isoxazole scaffold that protect against experimental colitis. Bioorganic & Medicinal Chemistry. 19(12). 3777–3786. 38 indexed citations
14.
Zaki, Hasan, Peter Vogel, Mathilde Body–Malapel, Mohamed Lamkanfi, & Thirumala‐Devi Kanneganti. (2010). IL-18 Production Downstream of the Nlrp3 Inflammasome Confers Protection against Colorectal Tumor Formation. The Journal of Immunology. 185(8). 4912–4920. 339 indexed citations
15.
Dharancy, Sébastien, Mathilde Body–Malapel, Alexandre Louvet, et al.. (2009). Neutrophil Migration During Liver Injury Is Under Nucleotide-Binding Oligomerization Domain 1 Control. Gastroenterology. 138(4). 1546–1556.e5. 30 indexed citations
16.
Body–Malapel, Mathilde, Sébastien Dharancy, Dominique Berrebi, et al.. (2008). NOD2: a potential target for regulating liver injury. Laboratory Investigation. 88(3). 318–327. 36 indexed citations
17.
Park, Jong‐Hwan, Yun‐Gi Kim, Christine McDonald, et al.. (2007). RICK/RIP2 Mediates Innate Immune Responses Induced through Nod1 and Nod2 but Not TLRs. The Journal of Immunology. 178(4). 2380–2386. 425 indexed citations
18.
Franchi, Luigi, Amal O. Amer, Mathilde Body–Malapel, et al.. (2006). Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1β in salmonella-infected macrophages. Nature Immunology. 7(6). 576–582. 949 indexed citations breakdown →
19.
Amer, Amal O., Luigi Franchi, Thirumala‐Devi Kanneganti, et al.. (2006). Regulation of Legionella Phagosome Maturation and Infection through Flagellin and Host Ipaf. Journal of Biological Chemistry. 281(46). 35217–35223. 384 indexed citations
20.
Malamut, Georgia, Laurent Dubuquoy, Mathilde Body–Malapel, et al.. (2006). No Evidence for an Involvement of the P38 and JNK Mitogen-Activated Protein in Inflammatory Bowel Diseases. Digestive Diseases and Sciences. 51(8). 1443–1453. 21 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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