Etienne Levavasseur

876 total citations
18 papers, 652 citations indexed

About

Etienne Levavasseur is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Etienne Levavasseur has authored 18 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Neurology and 3 papers in Nutrition and Dietetics. Recurrent topics in Etienne Levavasseur's work include Prion Diseases and Protein Misfolding (16 papers), Neurological diseases and metabolism (6 papers) and Trace Elements in Health (3 papers). Etienne Levavasseur is often cited by papers focused on Prion Diseases and Protein Misfolding (16 papers), Neurological diseases and metabolism (6 papers) and Trace Elements in Health (3 papers). Etienne Levavasseur collaborates with scholars based in France, Belgium and Canada. Etienne Levavasseur's co-authors include Martin Leduc, Daniella Checchin, Florian Sennlaub, Sylvain Chemtob, Stéphane Haı̈k, Jean‐Philippe Brandel, Jean‐Jacques Hauw, Claude Carnaud, Pièrre Aucouturier and Samia Hannaoui and has published in prestigious journals such as Nature Communications, The Journal of Immunology and PLoS ONE.

In The Last Decade

Etienne Levavasseur

18 papers receiving 641 citations

Peers

Etienne Levavasseur
Shao-Bin Wang China
Regina Reimann Switzerland
Kirsten A. Wunderlich Germany
H. Kellar-Wood United Kingdom
Maren Kasper Germany
Tina Banzon United States
S. Tout Australia
Meredith Gregory‐Ksander United States
Carla J. Ramos United States
Shunji Nakatake Japan
Shao-Bin Wang China
Etienne Levavasseur
Citations per year, relative to Etienne Levavasseur Etienne Levavasseur (= 1×) peers Shao-Bin Wang

Countries citing papers authored by Etienne Levavasseur

Since Specialization
Citations

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

Fields of papers citing papers by Etienne Levavasseur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Etienne Levavasseur

This figure shows the co-authorship network connecting the top 25 collaborators of Etienne Levavasseur. A scholar is included among the top collaborators of Etienne Levavasseur 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 Etienne Levavasseur. Etienne Levavasseur is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Bélondrade, Maxime, Simon Nicot, Michele Angelo Di Bari, et al.. (2021). Sensitive protein misfolding cyclic amplification of sporadic Creutzfeldt–Jakob disease prions is strongly seed and substrate dependent. Scientific Reports. 11(1). 4058–4058. 8 indexed citations
2.
Bizat, Nicolas, Etienne Levavasseur, Julian Roussel, et al.. (2021). An in vivo Caenorhabditis elegans model for therapeutic research in human prion diseases. Brain. 144(9). 2745–2758. 4 indexed citations
3.
Brandel, J.‐P., Katarína Grznárová, Etienne Levavasseur, et al.. (2019). Amplification techniques and diagnosis of prion diseases. Revue Neurologique. 175(7-8). 458–463. 8 indexed citations
4.
Brandel, J.P., Katarína Grznárová, Etienne Levavasseur, et al.. (2018). Les marqueurs du liquide céphalo-rachidien pour le diagnostic des maladies à prions. 9(3). 186–191. 1 indexed citations
5.
Comoy, Emmanuel, Jacqueline Mikol, Vincent Lebon, et al.. (2017). Experimental transfusion of variant CJD-infected blood reveals previously uncharacterised prion disorder in mice and macaque. Nature Communications. 8(1). 1268–1268. 17 indexed citations
6.
Levavasseur, Etienne, Nicolas Privat, Steve Simoneau, et al.. (2014). Molecular Modeling of Prion Transmission to Humans. Viruses. 6(10). 3766–3777. 8 indexed citations
7.
Hannaoui, Samia, Nicolas Privat, Etienne Levavasseur, et al.. (2013). Cycline Efficacy on the Propagation of Human Prions in Primary Cultured Neurons is Strain-Specific. The Journal of Infectious Diseases. 209(7). 1144–1148. 26 indexed citations
8.
Peoc’h, Katell, Etienne Levavasseur, Émilien Delmont, et al.. (2012). Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders. Human Molecular Genetics. 21(26). 5417–5428. 23 indexed citations
9.
Hannaoui, Samia, Layal Maatouk, Nicolas Privat, et al.. (2012). Prion Propagation and Toxicity Occur In Vitro with Two-Phase Kinetics Specific to Strain and Neuronal Type. Journal of Virology. 87(5). 2535–2548. 33 indexed citations
10.
Brandel, Jean‐Philippe, Craig A. Heath, Mark Head, et al.. (2009). Variant Creutzfeldt–Jakob disease in France and the United Kingdom: Evidence for the same agent strain. Annals of Neurology. 65(3). 249–256. 43 indexed citations
11.
Levavasseur, Etienne, Baptiste Faucheux, Nicolas Privat, et al.. (2008). Correction: Regulating Factors of PrPres Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains. PLoS ONE. 3(9). 1 indexed citations
12.
Levavasseur, Etienne, Baptiste Faucheux, Nicolas Privat, et al.. (2008). Regulating Factors of PrPres Glycosylation in Creutzfeldt-Jakob Disease - Implications for the Dissemination and the Diagnosis of Human Prion Strains. PLoS ONE. 3(7). e2786–e2786. 28 indexed citations
13.
Defaweux, Valérie, et al.. (2007). Oral scrapie infection modifies the homeostasis of Peyer’s patches’ dendritic cells. Histochemistry and Cell Biology. 128(3). 243–251. 12 indexed citations
14.
Levavasseur, Etienne, Pat Metharom, Hideki Nakano, et al.. (2007). Experimental scrapie in ‘plt’ mice: an assessment of the role of dendritic-cell migration in the pathogenesis of prion diseases. Journal of General Virology. 88(8). 2353–2360. 18 indexed citations
15.
Ballerini, Clara, Véronique Bachy, Nicolas Blanchard, et al.. (2006). Functional Implication of Cellular Prion Protein in Antigen-Driven Interactions between T Cells and Dendritic Cells. The Journal of Immunology. 176(12). 7254–7262. 66 indexed citations
16.
Checchin, Daniella, Florian Sennlaub, Etienne Levavasseur, Martin Leduc, & Sylvain Chemtob. (2006). Potential Role of Microglia in Retinal Blood Vessel Formation. Investigative Ophthalmology & Visual Science. 47(8). 3595–3595. 284 indexed citations
17.
Andréoletti, Olivier, Patricia Berthon, Etienne Levavasseur, et al.. (2002). Phenotyping of Protein-Prion (PrPsc)-accumulating Cells in Lymphoid and Neural Tissues of Naturally Scrapie-affected Sheep by Double-labeling Immunohistochemistry. Journal of Histochemistry & Cytochemistry. 50(10). 1357–1370. 57 indexed citations
18.
Levavasseur, Etienne, et al.. (1999). Purification and biochemical characterization of a novel cysteine protease of Entamoeba histolytica. European Journal of Biochemistry. 266(1). 170–180. 15 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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