Philippe Déterre

4.7k total citations · 1 hit paper
58 papers, 3.8k citations indexed

About

Philippe Déterre is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, Philippe Déterre has authored 58 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 23 papers in Immunology and 19 papers in Oncology. Recurrent topics in Philippe Déterre's work include Chemokine receptors and signaling (18 papers), Receptor Mechanisms and Signaling (14 papers) and Phosphodiesterase function and regulation (10 papers). Philippe Déterre is often cited by papers focused on Chemokine receptors and signaling (18 papers), Receptor Mechanisms and Signaling (14 papers) and Phosphodiesterase function and regulation (10 papers). Philippe Déterre collaborates with scholars based in France, Australia and United Kingdom. Philippe Déterre's co-authors include Marc Chabre, Claude Pfister, Joëlle Bigay, Christophe Combadière, Danièle Paupardin‐Tritsch, Joël Bockaert, Patrice Debré, Patrice Catty, Mylène Robert and Patricia Hermand and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Philippe Déterre

58 papers receiving 3.7k citations

Hit Papers

CX3CR1-dependent subretinal microglia cell accumulation i... 2007 2026 2013 2019 2007 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Déterre France 32 2.1k 873 863 682 427 58 3.8k
Neeraj Agarwal United States 40 3.6k 1.7× 340 0.4× 972 1.1× 508 0.7× 1.1k 2.6× 118 5.2k
David J. Figueroa United States 23 2.0k 0.9× 557 0.6× 758 0.9× 568 0.8× 478 1.1× 44 3.8k
Koji Igarashi Japan 33 3.5k 1.6× 337 0.4× 520 0.6× 559 0.8× 176 0.4× 116 4.8k
Hideaki Bujo Japan 40 2.9k 1.4× 634 0.7× 1.2k 1.3× 324 0.5× 75 0.2× 186 6.5k
Gail M. Seigel United States 35 1.7k 0.8× 211 0.2× 410 0.5× 404 0.6× 1.2k 2.7× 85 3.2k
Fernand Gobeil Canada 31 1.2k 0.6× 351 0.4× 521 0.6× 201 0.3× 187 0.4× 77 2.7k
Barbara Wiggert United States 29 1.7k 0.8× 607 0.7× 382 0.4× 113 0.2× 937 2.2× 78 2.9k
Yingfei Wang United States 32 2.0k 0.9× 380 0.4× 286 0.3× 674 1.0× 70 0.2× 84 3.3k
Shinichi Harada Japan 30 1.5k 0.7× 331 0.4× 304 0.4× 773 1.1× 72 0.2× 129 3.3k
Steven J. Fliesler United States 44 4.3k 2.0× 304 0.3× 1.0k 1.2× 146 0.2× 1.5k 3.5× 157 5.6k

Countries citing papers authored by Philippe Déterre

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Déterre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Déterre

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Déterre. A scholar is included among the top collaborators of Philippe Déterre 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 Philippe Déterre. Philippe Déterre 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.
Hermand, Patricia, et al.. (2015). Comprehensive analysis of chemokine-induced cAMP-inhibitory responses using a real-time luminescent biosensor. Cellular Signalling. 28(1). 120–129. 11 indexed citations
2.
Kumar, Arun, Kenneth Martin, Elizebeth C. Turner, et al.. (2013). Role of CX3CR1 Receptor in Monocyte/Macrophage Driven Neovascularization. PLoS ONE. 8(2). e57230–e57230. 33 indexed citations
3.
Chabre, Marc, Philippe Déterre, & Bruno Antonny. (2009). The apparent cooperativity of some GPCRs does not necessarily imply dimerization. Trends in Pharmacological Sciences. 30(4). 182–187. 87 indexed citations
4.
Hermand, Patricia, Frédéric Pincet, Stéphanie Carvalho, et al.. (2008). Functional Adhesiveness of the CX3CL1 Chemokine Requires Its Aggregation. Journal of Biological Chemistry. 283(44). 30225–30234. 41 indexed citations
5.
Combadière, Christophe, C. Feumi, William Raoul, et al.. (2007). CX3CR1-dependent subretinal microglia cell accumulation is associated with cardinal features of age-related macular degeneration. Journal of Clinical Investigation. 117(10). 2920–2928. 500 indexed citations breakdown →
6.
Combadière, Christophe & Philippe Déterre. (2007). Les chimiokines : un réseau sophistiqué de guidage cellulaire. médecine/sciences. 23(2). 173–179. 9 indexed citations
7.
Métay, Corinne, Ahidjo Ayouba, Anfumbom Kfutwah, et al.. (2006). A natural CCL5/RANTES variant antagonist for CCR1 and CCR3. Immunogenetics. 58(7). 533–541. 9 indexed citations
8.
Spano, Jean‐Philippe, Fabrice André, Luc Morat, et al.. (2004). Chemokine receptor CXCR4 and early-stage non-small cell lung cancer: pattern of expression and correlation with outcome. Annals of Oncology. 15(4). 613–617. 186 indexed citations
9.
Garin, Alexandre, Nadine Tarantino, Sophie Faure, et al.. (2003). Two Novel Fully Functional Isoforms of CX3CR1 Are Potent HIV Coreceptors. The Journal of Immunology. 171(10). 5305–5312. 29 indexed citations
10.
Berthelier, Valérie, et al.. (2000). Probing ligand‐induced conformational changes of human CD38. European Journal of Biochemistry. 267(10). 3056–3064. 17 indexed citations
11.
Bauvois, Brigitte, et al.. (1999). Upregulation of CD38 Gene Expression in Leukemic B Cells by Interferon Types I and II. Journal of Interferon & Cytokine Research. 19(9). 1059–1066. 40 indexed citations
12.
Goding, James W., Robert Terkeltaub, Michèle Maurice, et al.. (1998). Ecto‐phosphodiesterase/pyrophosphatase of lymphocytes and non‐lymphoid cells: structure and function of the PC‐1 family. Immunological Reviews. 161(1). 11–26. 136 indexed citations
13.
Berthelier, Valérie, et al.. (1996). Report on the 2nd International CD38 Workshop. Research in Immunology. 147(6). 407–411. 2 indexed citations
14.
Brückert, Franz, Patrice Catty, Philippe Déterre, & Claude Pfister. (1994). Activation of Phosphodiesterase by Transducin in Bovine Rod Outer Segments: Characteristics of the Successive Binding of Two Transducins. Biochemistry. 33(42). 12625–12634. 16 indexed citations
15.
Pfister, Claude, et al.. (1993). Interactions of a G-protein with its effector: transducin and cGMP phosphodiesterase in retinal rods. Cellular Signalling. 5(3). 235–251. 44 indexed citations
16.
Catty, Patrice & Philippe Déterre. (1991). Activation and solubilization of the retinal cGMP‐specific phosphodiesterase by limited proteolysis. European Journal of Biochemistry. 199(2). 263–269. 56 indexed citations
17.
Chabre, Marc & Philippe Déterre. (1989). Molecular mechanism of visual transduction. European Journal of Biochemistry. 179(2). 255–266. 249 indexed citations
18.
Chabre, Marc, Joëlle Bigay, Franz Brückert, et al.. (1988). Visual Signal Transduction; The Cycle of Transducin Shuttling between Rhodopsin and cGMP Phosphodiesterase. Cold Spring Harbor Symposia on Quantitative Biology. 53(0). 313–324. 13 indexed citations
19.
Déterre, Philippe, Claude Pfister, Joëlle Bigay, & Marc Chabre. (1987). The retinal phototransduction process: enzymatic cascade and regulation. Biochimie. 69(4). 365–370. 7 indexed citations
20.
Déterre, Philippe, et al.. (1986). Activation of retinal rod cyclic GMP‐phosphodiesterase by transducin: Characterization of the complex formed by phosphodiesterase inhibitor and transducin α‐subunit. Proteins Structure Function and Bioinformatics. 1(2). 188–193. 84 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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