Nicolas Charles

3.6k total citations
62 papers, 2.4k citations indexed

About

Nicolas Charles is a scholar working on Immunology, Rheumatology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Nicolas Charles has authored 62 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Immunology, 32 papers in Rheumatology and 12 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Nicolas Charles's work include Mast cells and histamine (38 papers), Urticaria and Related Conditions (18 papers) and Systemic Lupus Erythematosus Research (14 papers). Nicolas Charles is often cited by papers focused on Mast cells and histamine (38 papers), Urticaria and Related Conditions (18 papers) and Systemic Lupus Erythematosus Research (14 papers). Nicolas Charles collaborates with scholars based in France, United States and Germany. Nicolas Charles's co-authors include Juan Rivera, Bárbara Dema, Éric Daugas, Ulrich Blank, Gabor G. Illei, Donna Hardwick, Marc Benhamou, Renato C. Monteiro, Christophe Pellefigues and Sangeeta Kumari and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Nicolas Charles

58 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicolas Charles France 26 1.5k 756 433 396 374 62 2.4k
Nataliya Yeremenko Netherlands 28 1.3k 0.9× 1.0k 1.4× 139 0.3× 873 2.2× 41 0.1× 64 2.5k
James Edwards United Kingdom 23 386 0.3× 552 0.7× 69 0.2× 247 0.6× 162 0.4× 52 2.0k
Arturo Genovese Italy 27 1.2k 0.8× 302 0.4× 676 1.6× 469 1.2× 496 1.3× 62 2.3k
Chang‐Youh Tsai Taiwan 32 1.2k 0.8× 1.4k 1.9× 282 0.7× 812 2.1× 81 0.2× 190 3.3k
Shohei Shimajiri Japan 29 465 0.3× 305 0.4× 184 0.4× 752 1.9× 58 0.2× 113 2.3k
Satoru Kikuchi Japan 30 357 0.2× 88 0.1× 217 0.5× 780 2.0× 37 0.1× 153 2.8k
Wei‐Hsuan Yu United States 17 361 0.2× 92 0.1× 56 0.1× 1.5k 3.7× 379 1.0× 31 2.8k
H. van Weelden Netherlands 28 847 0.6× 220 0.3× 130 0.3× 393 1.0× 235 0.6× 63 2.8k
Akio Tanaka Japan 28 262 0.2× 274 0.4× 284 0.7× 847 2.1× 586 1.6× 193 2.7k
Zoltán Nemes Hungary 24 147 0.1× 165 0.2× 279 0.6× 556 1.4× 77 0.2× 59 2.2k

Countries citing papers authored by Nicolas Charles

Since Specialization
Citations

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

Fields of papers citing papers by Nicolas Charles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicolas Charles

This figure shows the co-authorship network connecting the top 25 collaborators of Nicolas Charles. A scholar is included among the top collaborators of Nicolas Charles 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 Nicolas Charles. Nicolas Charles 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.
Simon, Quentin, F. Gaillard, Delphine Bachelet, et al.. (2025). Immune characterization of lupus nephritis patients undergoing dialysis. Journal of Translational Autoimmunity. 10. 100290–100290.
2.
Jourde‐Chiche, Noémie, et al.. (2024). Anti-dsDNA IgE: a potential non-invasive test for prediction of lupus nephritis relapse. RMD Open. 10(2). e004255–e004255. 2 indexed citations
3.
Charles, Nicolas, Inge Kortekaas Krohn, Emek Kocatürk, et al.. (2023). Autoreactive IgE: Pathogenic role and therapeutic target in autoimmune diseases. Allergy. 78(12). 3118–3135. 7 indexed citations
4.
Gaillard, F., Delphine Bachelet, Cécile Couchoud, et al.. (2023). Lupus activity and outcomes in lupus patients undergoing maintenance dialysis. Lara D. Veeken. 63(3). 780–786. 3 indexed citations
5.
Mageau, Arthur, Valentine Marie Ferré, P. Nicaise‐Roland, et al.. (2022). Impact of BNT162b2 mRNA anti-SARS-CoV-2 vaccine on interferon-alpha production by plasmacytoid dendritic cells and autoreactive T cells in patients with systemic lupus erythematosus: The COVALUS project. Journal of Autoimmunity. 134. 102987–102987. 7 indexed citations
6.
Charles, Nicolas. (2021). Autoimmunity, IgE and FcεRI-bearing cells. Current Opinion in Immunology. 72. 43–50. 18 indexed citations
7.
Vibhushan, Shamila, Alaa El‐Ghoneimi, Marc Benhamou, et al.. (2020). Mast Cell Chymase and Kidney Disease. International Journal of Molecular Sciences. 22(1). 302–302. 17 indexed citations
8.
Saidoune, Fanny, Guillaume Even, Anh‐Thu Gaston, et al.. (2020). Effects of BAFF Neutralization on Atherosclerosis Associated With Systemic Lupus Erythematosus. Arthritis & Rheumatology. 73(2). 255–264. 24 indexed citations
9.
Ibarra-Sánchez, Alfredo, Shamila Vibhushan, Nicolas Charles, et al.. (2019). TLR4 Receptor Induces 2-AG–Dependent Tolerance to Lipopolysaccharide and Trafficking of CB2 Receptor in Mast Cells. The Journal of Immunology. 202(8). 2360–2371. 23 indexed citations
10.
Msallam, Rasha, Magnus Åbrink, Gunnar Pejler, et al.. (2018). Mast Cell Degranulation Exacerbates Skin Rejection by Enhancing Neutrophil Recruitment. Frontiers in Immunology. 9. 2690–2690. 22 indexed citations
11.
Mkaddem, Sanae Ben, Héloïse Flament, Dimitri Titeca‐Beauport, et al.. (2017). Lyn and Fyn function as molecular switches that control immunoreceptors to direct homeostasis or inflammation. Nature Communications. 8(1). 246–246. 82 indexed citations
12.
Dema, Bárbara, Christophe Pellefigues, Fanny Saidoune, et al.. (2017). Basophils contribute to pristane-induced Lupus-like nephritis model. Scientific Reports. 7(1). 7969–7969. 29 indexed citations
13.
Launay, Pierre, et al.. (2017). Phospholipid scramblase 1 amplifies anaphylactic reactions in vivo. PLoS ONE. 12(3). e0173815–e0173815. 7 indexed citations
14.
Dema, Bárbara, Nicolas Charles, Christophe Pellefigues, et al.. (2014). Immunoglobulin E plays an immunoregulatory role in lupus. The Journal of Experimental Medicine. 211(11). 2159–2168. 73 indexed citations
15.
Moura, Ivan Cruz, Yumi Yamashita, Jörg Scheffel, et al.. (2014). Regulation of the Tyrosine Phosphorylation of Phospholipid Scramblase 1 in Mast Cells That Are Stimulated through the High-Affinity IgE Receptor. PLoS ONE. 9(10). e109800–e109800. 7 indexed citations
16.
Pellefigues, Christophe & Nicolas Charles. (2013). The deleterious role of basophils in systemic lupus erythematosus. Current Opinion in Immunology. 25(6). 704–711. 25 indexed citations
17.
Liang, Genqing, Tolga Barker, Zhihui Xie, et al.. (2012). Naive T cells sense the cysteine protease allergen papain through protease-activated receptor 2 and propel TH2 immunity. Journal of Allergy and Clinical Immunology. 129(5). 1377–1386.e13. 45 indexed citations
18.
Charles, Nicolas, Donna Hardwick, Éric Daugas, Gabor G. Illei, & Juan Rivera. (2010). Basophils and the T helper 2 environment can promote the development of lupus nephritis. Nature Medicine. 16(6). 701–707. 274 indexed citations
19.
Alexia, Catherine, et al.. (2008). Phospholipid Scramblase 1 Modulates a Selected Set of IgE Receptor-mediated Mast Cell Responses through LAT-dependent Pathway. Journal of Biological Chemistry. 283(37). 25514–25523. 30 indexed citations
20.
Iwaki, Shoko, Jiřı́ Špička, Christine Tkaczyk, et al.. (2007). Kit- and FcɛRI-induced differential phosphorylation of the transmembrane adaptor molecule NTAL/LAB/LAT2 allows flexibility in its scaffolding function in mast cells. Cellular Signalling. 20(1). 195–205. 52 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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