Max Maurin

11.1k total citations · 2 hit papers
159 papers, 7.3k citations indexed

About

Max Maurin is a scholar working on Molecular Biology, Infectious Diseases and Genetics. According to data from OpenAlex, Max Maurin has authored 159 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 42 papers in Infectious Diseases and 39 papers in Genetics. Recurrent topics in Max Maurin's work include Bacillus and Francisella bacterial research (47 papers), Yersinia bacterium, plague, ectoparasites research (30 papers) and Vector-borne infectious diseases (24 papers). Max Maurin is often cited by papers focused on Bacillus and Francisella bacterial research (47 papers), Yersinia bacterium, plague, ectoparasites research (30 papers) and Vector-borne infectious diseases (24 papers). Max Maurin collaborates with scholars based in France, United States and Morocco. Max Maurin's co-authors include Didier Raoult, Jean‐Marc Rolain, Oleg Mediannikov, Jean‐Louis Mège, Sandrine Boisset, Miklós Gyuranecz, Yvan Caspar, Carole Eldin, Sophie Edouard and Matthieu Million and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Applied and Environmental Microbiology.

In The Last Decade

Max Maurin

155 papers receiving 7.1k citations

Hit Papers

Q Fever 1999 2026 2008 2017 1999 2016 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Max Maurin France 41 3.6k 3.1k 1.6k 1.6k 1.2k 159 7.3k
Stephen F. Porcella United States 58 2.1k 0.6× 4.1k 1.3× 2.9k 1.8× 2.2k 1.4× 1.8k 1.6× 144 9.4k
Véronique Roux France 40 4.7k 1.3× 3.6k 1.2× 1.6k 1.0× 949 0.6× 636 0.5× 73 6.9k
Florence Fenollar France 52 2.9k 0.8× 3.3k 1.1× 1.7k 1.0× 1.4k 0.9× 1.5k 1.3× 288 9.3k
Oleg Mediannikov France 45 5.9k 1.6× 5.5k 1.8× 2.2k 1.4× 719 0.5× 561 0.5× 278 8.7k
Kurt D. Reed United States 34 1.5k 0.4× 2.4k 0.8× 861 0.5× 893 0.6× 1.4k 1.2× 89 4.7k
Leo M. Schouls Netherlands 59 2.9k 0.8× 7.6k 2.5× 1.4k 0.8× 3.5k 2.2× 5.8k 5.0× 178 14.6k
Robert F. Massung United States 48 5.9k 1.6× 5.1k 1.7× 1.6k 1.0× 731 0.5× 902 0.8× 120 7.8k
Michael R. Lappin United States 53 5.8k 1.6× 4.2k 1.4× 1.1k 0.7× 495 0.3× 2.8k 2.4× 348 10.6k
Christopher D. Paddock United States 53 8.3k 2.3× 8.6k 2.8× 3.2k 1.9× 800 0.5× 1.3k 1.2× 222 12.4k
Alan Radford United Kingdom 49 767 0.2× 3.0k 1.0× 782 0.5× 2.6k 1.6× 1.4k 1.2× 260 8.9k

Countries citing papers authored by Max Maurin

Since Specialization
Citations

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

Fields of papers citing papers by Max Maurin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Max Maurin

This figure shows the co-authorship network connecting the top 25 collaborators of Max Maurin. A scholar is included among the top collaborators of Max Maurin 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 Max Maurin. Max Maurin 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
2.
Maurin, Max, et al.. (2024). Tularemia in Pediatric Patients: A Case Series and Review of the Literature. The Pediatric Infectious Disease Journal. 44(2). 180–185. 1 indexed citations
3.
Mostafavi, Ehsan, Saber Esmaeili, Ahmad Mahmoudi, et al.. (2024). The Epidemiological Investigation of Yersinia pestis , Francisella tularensis , and Arenavirus Infections in Small Mammals in Northwestern Iran. Vector-Borne and Zoonotic Diseases. 24(8). 489–498. 1 indexed citations
4.
Guimard, Thomas, Estibaliz Lazaro, Olivia Peuchant, et al.. (2023). Case Studies and Literature Review of Francisella tularensis–Related Prosthetic Joint Infection. Emerging infectious diseases. 29(6). 1118–1126. 5 indexed citations
6.
Moyne, Oriane, Florence Castelli, Dominique Bicout, et al.. (2021). Metabotypes of Pseudomonas aeruginosa Correlate with Antibiotic Resistance, Virulence and Clinical Outcome in Cystic Fibrosis Chronic Infections. Metabolites. 11(2). 63–63. 20 indexed citations
7.
Drissi, Mourad, et al.. (2021). Enterobacter cloacae Complex and CTX-M Extended-Spectrum β-Lactamases in Algeria. Microbial Drug Resistance. 28(3). 346–354. 4 indexed citations
8.
Esmaeili, Saber, et al.. (2019). Epidemiological survey of tularemia in Ilam Province, west of Iran. BMC Infectious Diseases. 19(1). 502–502. 12 indexed citations
9.
Bonnet, Isabelle, H. Meugnier, François Vandenesch, et al.. (2018). High prevalence of spa type t571 among methicillin-susceptible Staphylococcus aureus from bacteremic patients in a French University Hospital. PLoS ONE. 13(10). e0204977–e0204977. 19 indexed citations
10.
Chiquet, Christophe, et al.. (2018). Genetic and Phenotypic Traits of Staphylococcus Epidermidis Strains Causing Postcataract Endophthalmitis Compared to Commensal Conjunctival Flora. American Journal of Ophthalmology. 191. 76–82. 7 indexed citations
11.
Caspar, Yvan, Mylène Maillet, Patricia Pavèse, et al.. (2017). mcr-1 Colistin Resistance in ESBL-Producing Klebsiella pneumoniae, France. Emerging infectious diseases. 23(5). 874–876. 20 indexed citations
12.
Mailles, Alexandra, Bruno Garin‐Bastuji, Jean‐Philippe Lavigne, et al.. (2016). Human brucellosis in France in the 21st century: Results from national surveillance 2004–2013. Médecine et Maladies Infectieuses. 46(8). 411–418. 24 indexed citations
13.
Héquet, Arnaud, Olga Ν. Burchak, Matthieu Jeanty, et al.. (2014). 1‐(1H‐Indol‐3‐yl)ethanamine Derivatives as Potent Staphylococcus aureus NorA Efflux Pump Inhibitors. ChemMedChem. 9(7). 1534–1545. 30 indexed citations
14.
Caspar, Yvan, C. Recule, P Pouzol, et al.. (2013). Psychrobacter arenosusBacteremia after Blood Transfusion, France. Emerging infectious diseases. 19(7). 1118–1120. 16 indexed citations
15.
Kay, Elisabeth, et al.. (2009). Mutational paths towards increased fluoroquinolone resistance in Legionella pneumophila. Journal of Antimicrobial Chemotherapy. 64(2). 284–293. 39 indexed citations
16.
Maurin, Max, Laure Hammer, Jean‐François Timsit, et al.. (2009). Quantitative real-time PCR tests for diagnostic and prognostic purposes in cases of legionellosis. Clinical Microbiology and Infection. 16(4). 379–384. 25 indexed citations
17.
Chiquet, Christophe, et al.. (2007). Diagnostic microbiologique des endophtalmies aiguës. Journal Français d Ophtalmologie. 30(10). 1049–1059. 6 indexed citations
18.
Botelho-Nevers, Élisabeth, Pierre‐Edouard Fournier, Hervé Richet, et al.. (2007). Coxiella burnetii infection of aortic aneurysms or vascular grafts: report of 30 new cases and evaluation of outcome. European Journal of Clinical Microbiology & Infectious Diseases. 26(9). 635–640. 112 indexed citations
19.
Épaulard, Olivier, et al.. (2006). The changing pattern of fusobacterium infections in humans: recent experience with fusobacterium bacteraemia. Clinical Microbiology and Infection. 12(2). 178–181. 24 indexed citations
20.
Sessa, Carmine, et al.. (2005). Abdominal aortic aneurysm and Coxiella burnetii infection: Report of three cases and review of the literature. Journal of Vascular Surgery. 42(1). 153–158. 36 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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