Christophe Verthuy

1.6k total citations · 1 hit paper
19 papers, 1.2k citations indexed

About

Christophe Verthuy is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Christophe Verthuy has authored 19 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Immunology, 8 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Christophe Verthuy's work include T-cell and B-cell Immunology (10 papers), Immune Cell Function and Interaction (9 papers) and CAR-T cell therapy research (4 papers). Christophe Verthuy is often cited by papers focused on T-cell and B-cell Immunology (10 papers), Immune Cell Function and Interaction (9 papers) and CAR-T cell therapy research (4 papers). Christophe Verthuy collaborates with scholars based in France, Morocco and United Kingdom. Christophe Verthuy's co-authors include Pierre Ferrier, N. Mathieu, Toby Lawrence, William M. Hempel, Marc Dalod, Gaëlle Bouvier, Salvatore Spicuglia, Philippe Naquet, Françoise Watrin and Thien‐Phong Vu Manh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Experimental Medicine.

In The Last Decade

Christophe Verthuy

18 papers receiving 1.2k citations

Hit Papers

Membrane Cholesterol Efflux Drives Tumor-Associated Macro... 2019 2026 2021 2023 2019 100 200 300
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Membrane Cholesterol Efflux Drives Tumor-Associated Macrophage Reprogramming and Tumor Progression
    2019 347 citations Pieter Goossens, Juan Rodríguez‐Vita et al. Cell Metabolism profile →

Peers

Christophe Verthuy
Kathleen Roderick United States
J Tschopp Switzerland
Marei Dose United States
J C Pena United States
Hatice D. Saatcioglu United States
Taras Kreslavsky United States
Elke Raderschall United States
David G.T. Hesslein United States
Alexandra Schebesta Austria
Mitali Manzur Australia
Kathleen Roderick United States
Christophe Verthuy
Citations per year, relative to Christophe Verthuy Christophe Verthuy (= 1×) peers Kathleen Roderick

Countries citing papers authored by Christophe Verthuy

Since Specialization
Citations

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

Fields of papers citing papers by Christophe Verthuy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christophe Verthuy

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

All Works

19 of 19 papers shown
1.
Belghazi, Maya, et al.. (2025). Remodeling of RNA-binding proteome and RNA-mediated regulation as a new layer of control of sporulation. mSystems. 10(9). e0049625–e0049625.
2.
Cherrak, Yassine, Artémis Kosta, Léon Espinosa, et al.. (2023). Acinetobacter type VI secretion system comprises a non-canonical membrane complex. PLoS Pathogens. 19(9). e1011687–e1011687. 6 indexed citations
3.
Ghislat, Ghita, Christophe Verthuy, Pedro J. Ballester, et al.. (2021). NF-κB–dependent IRF1 activation programs cDC1 dendritic cells to drive antitumor immunity. Science Immunology. 6(61). 77 indexed citations
4.
Goossens, Pieter, Juan Rodríguez‐Vita, Anders Etzerodt, et al.. (2019). Membrane Cholesterol Efflux Drives Tumor-Associated Macrophage Reprogramming and Tumor Progression. Cell Metabolism. 29(6). 1376–1389.e4. 347 indexed citations breakdown →
5.
Habbeddine, Mohamed, Christophe Verthuy, Olivia Rastoin, et al.. (2017). Receptor Activator of NF-κB Orchestrates Activation of Antiviral Memory CD8 T Cells in the Spleen Marginal Zone. Cell Reports. 21(9). 2515–2527. 26 indexed citations
6.
Baratin, Myriam, Olivier Demaria, Mohamed Habbeddine, et al.. (2015). Homeostatic NF-κB Signaling in Steady-State Migratory Dendritic Cells Regulates Immune Homeostasis and Tolerance. Immunity. 42(4). 627–639. 118 indexed citations
7.
Bonnet, Marie, Fang Huang, Touati Benoukraf, et al.. (2009). Duality of Enhancer Functioning Mode Revealed in a Reduced TCRβ Gene Enhancer Knockin Mouse Model. The Journal of Immunology. 183(12). 7939–7948. 11 indexed citations
8.
Agherbi, Hanane, et al.. (2009). Polycomb Mediated Epigenetic Silencing and Replication Timing at the INK4a/ARF Locus during Senescence. PLoS ONE. 4(5). e5622–e5622. 108 indexed citations
9.
Mugnier, Bénédicte, Béatrice Nal, Christophe Verthuy, et al.. (2008). Coronin-1A Links Cytoskeleton Dynamics to TCRαβ-Induced Cell Signaling. PLoS ONE. 3(10). e3467–e3467. 63 indexed citations
10.
Storck, Sébastien, Frédéric Delbos, Nicolas Städler, et al.. (2005). Normal Immune System Development in Mice Lacking the Deltex-1 RING Finger Domain. Molecular and Cellular Biology. 25(4). 1437–1445. 22 indexed citations
11.
Mathieu, N., Salvatore Spicuglia, Olivier Cabaud, et al.. (2003). Assessing the Role of the T Cell Receptor β Gene Enhancer in Regulating Coding Joint Formation during V(D)J Recombination. Journal of Biological Chemistry. 278(20). 18101–18109. 25 indexed citations
12.
Huang, Fang, Olivier Cabaud, Christophe Verthuy, Anne‐Odile Hueber, & Pierre Ferrier. (2003). αβ T‐cell development is not affected by inversion of TCRβ gene enhancer sequences: polar enhancement of gene expression regardless of enhancer orientation. Immunology. 109(4). 510–514. 2 indexed citations
13.
Nal, Béatrice, Elodie Mohr, Rebecca Tagett, et al.. (2002). Wdr12, a Mouse Gene Encoding a Novel WD-Repeat Protein with a Notchless-like Amino-terminal Domain. Genomics. 79(1). 77–86. 20 indexed citations
14.
Leduc, Isabelle, William M. Hempel, N. Mathieu, et al.. (2000). T Cell Development in TCRβ Enhancer-Deleted Mice: Implications for αβ T Cell Lineage Commitment and Differentiation. The Journal of Immunology. 165(3). 1364–1373. 33 indexed citations
15.
Mathieu, N., William M. Hempel, Salvatore Spicuglia, Christophe Verthuy, & Pierre Ferrier. (2000). Chromatin Remodeling by the T Cell Receptor (Tcr)-β Gene Enhancer during Early T Cell Development. The Journal of Experimental Medicine. 192(5). 625–636. 132 indexed citations
16.
Mathieu, N., Salvatore Spicuglia, Dominique Payet‐Bornet, et al.. (2000). Definition of a T-Cell Receptor β Gene Core Enhancer of V(D)J Recombination by Transgenic Mapping. Molecular and Cellular Biology. 20(1). 42–53. 35 indexed citations
17.
Leduc, Isabelle, Holger Karsunky, N. Mathieu, et al.. (2000). The Pim-1 kinase stimulates maturation of TCRβ-deficient T cell progenitors: implications for the mechanism of Pim-1 action. International Immunology. 12(10). 1389–1396. 20 indexed citations
18.
Cambiaggi, Anna, Christophe Verthuy, Philippe Naquet, et al.. (1997). Natural killer cell acceptance of H-2 mismatch bone marrow grafts in transgenic mice expressing HLA-Cw3 specific killer cell inhibitory receptor (CD158b). Proceedings of the National Academy of Sciences. 94(15). 8088–8092. 38 indexed citations
19.
Bouvier, Gaëlle, Françoise Watrin, Marianne Naspetti, et al.. (1996). Deletion of the mouse T-cell receptor beta gene enhancer blocks alphabeta T-cell development.. Proceedings of the National Academy of Sciences. 93(15). 7877–7881. 154 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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