Sylvain Armando

1.4k total citations
9 papers, 741 citations indexed

About

Sylvain Armando is a scholar working on Molecular Biology, Oncology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sylvain Armando has authored 9 papers receiving a total of 741 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Oncology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sylvain Armando's work include Receptor Mechanisms and Signaling (6 papers), Chemokine receptors and signaling (4 papers) and Neuropeptides and Animal Physiology (2 papers). Sylvain Armando is often cited by papers focused on Receptor Mechanisms and Signaling (6 papers), Chemokine receptors and signaling (4 papers) and Neuropeptides and Animal Physiology (2 papers). Sylvain Armando collaborates with scholars based in Canada, United States and France. Sylvain Armando's co-authors include Michel Bouvier, Jeffrey Benovic, Olimpia Meucci, John M. Busillo, Rajarshi Sengupta, Julie Quoyer, Jiansong Luo, Yong Ren, Alexandre Beautrait and Stéphane A. Laporte and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Sylvain Armando

9 papers receiving 737 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sylvain Armando Canada 9 557 239 203 153 64 9 741
Sabrina T. Exum United States 15 901 1.6× 396 1.7× 79 0.4× 162 1.1× 80 1.3× 16 1.2k
David M. Nanus United States 13 442 0.8× 133 0.6× 350 1.7× 88 0.6× 79 1.2× 27 902
Alicia Salcedo Spain 7 487 0.9× 169 0.7× 98 0.5× 59 0.4× 47 0.7× 8 604
Cary Esselens Spain 10 444 0.8× 145 0.6× 208 1.0× 71 0.5× 150 2.3× 14 836
Tau Benned‐Jensen Denmark 14 368 0.7× 162 0.7× 166 0.8× 173 1.1× 39 0.6× 22 651
Moulay Driss Rochdi Canada 14 552 1.0× 195 0.8× 70 0.3× 70 0.5× 132 2.1× 15 817
Robert Breese United States 10 364 0.7× 138 0.6× 128 0.6× 147 1.0× 71 1.1× 13 806
Valérie Pawlowski France 12 404 0.7× 141 0.6× 213 1.0× 47 0.3× 39 0.6× 17 752
Vanessa L. Wehbi United States 13 717 1.3× 273 1.1× 142 0.7× 105 0.7× 122 1.9× 14 931
Elena Lastraioli Italy 16 850 1.5× 161 0.7× 150 0.7× 54 0.4× 103 1.6× 40 1.1k

Countries citing papers authored by Sylvain Armando

Since Specialization
Citations

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

Fields of papers citing papers by Sylvain Armando

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvain Armando

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

All Works

9 of 9 papers shown
1.
Schuetz, Doris A., Tomasz Maciej Stępniewski, Yoon Namkung, et al.. (2021). Discovery of a dual Ras and ARF6 inhibitor from a GPCR endocytosis screen. Nature Communications. 12(1). 4688–4688. 10 indexed citations
2.
Beautrait, Alexandre, Justine S. Paradis, Brandon Zimmerman, et al.. (2017). A new inhibitor of the β-arrestin/AP2 endocytic complex reveals interplay between GPCR internalization and signalling. Nature Communications. 8(1). 15054–15054. 122 indexed citations
3.
Namkung, Yoon, Sylvain Armando, Dominic Devost, et al.. (2015). Quantifying biased signaling in GPCRs using BRET-based biosensors. Methods. 92. 5–10. 34 indexed citations
4.
Armando, Sylvain, Julie Quoyer, Yann Percherancier, et al.. (2014). The chemokine CXC4 and CC2 receptors form homo‐ and heterooligomers that can engage their signaling G‐protein effectors and βarrestin. The FASEB Journal. 28(10). 4509–4523. 48 indexed citations
5.
Quoyer, Julie, Jay M. Janz, Jiansong Luo, et al.. (2013). Pepducin targeting the C-X-C chemokine receptor type 4 acts as a biased agonist favoring activation of the inhibitory G protein. Proceedings of the National Academy of Sciences. 110(52). E5088–97. 133 indexed citations
6.
Yagi, Hiroshi, Wenfu Tan, Patrícia Dillenburg-Pilla, et al.. (2011). A Synthetic Biology Approach Reveals a CXCR4-G 13 -Rho Signaling Axis Driving Transendothelial Migration of Metastatic Breast Cancer Cells. Science Signaling. 4(191). ra60–ra60. 115 indexed citations
7.
Martel, Catherine, Karine Boulay, Billy Breton, et al.. (2010). Multimerization of Staufen1 in live cells. RNA. 16(3). 585–597. 41 indexed citations
8.
Busillo, John M., Sylvain Armando, Rajarshi Sengupta, et al.. (2010). Site-specific Phosphorylation of CXCR4 Is Dynamically Regulated by Multiple Kinases and Results in Differential Modulation of CXCR4 Signaling. Journal of Biological Chemistry. 285(10). 7805–7817. 224 indexed citations
9.
Armando, Sylvain, et al.. (2007). Neurosphere-derived neural cells show region-specific behaviour in vitro. Neuroreport. 18(15). 1539–1542. 14 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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