Xavier Deupí

8.5k total citations · 2 hit papers
79 papers, 6.2k citations indexed

About

Xavier Deupí is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Xavier Deupí has authored 79 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 47 papers in Cellular and Molecular Neuroscience and 13 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Xavier Deupí's work include Receptor Mechanisms and Signaling (63 papers), Photoreceptor and optogenetics research (21 papers) and Neuropeptides and Animal Physiology (21 papers). Xavier Deupí is often cited by papers focused on Receptor Mechanisms and Signaling (63 papers), Photoreceptor and optogenetics research (21 papers) and Neuropeptides and Animal Physiology (21 papers). Xavier Deupí collaborates with scholars based in Switzerland, United States and Spain. Xavier Deupí's co-authors include Brian K. Kobilka, Gebhard F. X. Schertler, Christopher G. Tate, M. Madan Babu, AJ Venkatakrishnan, Guillaume Lebon, Leonardo Pardo, Jörg Standfuss, Mireia Olivella and Gayathri Swaminath 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

Xavier Deupí

77 papers receiving 6.1k citations

Hit Papers

Molecular signatures of G-protein-coupled receptors 2007 2026 2013 2019 2013 2007 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xavier Deupí Switzerland 39 5.5k 3.4k 857 526 503 79 6.2k
Arun K. Shukla India 37 5.3k 1.0× 3.1k 0.9× 738 0.9× 619 1.2× 601 1.2× 101 6.1k
Brian T. DeVree United States 13 5.4k 1.0× 3.0k 0.9× 1.0k 1.2× 487 0.9× 514 1.0× 17 5.8k
Isolde Le Trong United States 30 5.8k 1.1× 3.3k 1.0× 752 0.9× 308 0.6× 390 0.8× 55 7.4k
Craig A. Behnke United States 19 5.8k 1.1× 3.4k 1.0× 575 0.7× 284 0.5× 397 0.8× 26 6.8k
Daniel H. Arlow United States 17 5.4k 1.0× 2.2k 0.7× 657 0.8× 550 1.0× 720 1.4× 20 6.1k
Ellen Y. T. Chien United States 16 5.0k 0.9× 2.4k 0.7× 952 1.1× 447 0.8× 614 1.2× 20 5.9k
Jesper Mosolff Mathiesen Denmark 24 4.6k 0.8× 3.0k 0.9× 694 0.8× 362 0.7× 421 0.8× 45 5.2k
Hee‐Jung Choi South Korea 30 9.2k 1.7× 4.2k 1.3× 1.5k 1.7× 659 1.3× 944 1.9× 96 10.4k
David E. Gloriam Denmark 38 6.9k 1.3× 3.7k 1.1× 1.0k 1.2× 592 1.1× 1.2k 2.4× 107 8.6k
Francesca Fanelli Italy 39 4.6k 0.9× 2.5k 0.7× 530 0.6× 310 0.6× 722 1.4× 164 6.1k

Countries citing papers authored by Xavier Deupí

Since Specialization
Citations

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

Fields of papers citing papers by Xavier Deupí

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xavier Deupí

This figure shows the co-authorship network connecting the top 25 collaborators of Xavier Deupí. A scholar is included among the top collaborators of Xavier Deupí 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 Xavier Deupí. Xavier Deupí 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.
Sen, Saumik, Makoto Iwasaki, Gebhard F. X. Schertler, et al.. (2025). Coral anthozoan-specific opsins employ a novel chloride counterion for spectral tuning. eLife. 14.
2.
Guixà-González, Ramón, Lukas Grätz, Michael Hennig, et al.. (2025). Cyclic peptide inhibitors function as molecular glues to stabilize Gq/11 heterotrimers. Proceedings of the National Academy of Sciences. 122(19). e2418398122–e2418398122. 1 indexed citations
3.
Sen, Saumik, Makoto Iwasaki, Gebhard F. X. Schertler, et al.. (2025). Coral anthozoan-specific opsins employ a novel chloride counterion for spectral tuning. eLife. 14. 1 indexed citations
4.
Pamula, Filip, Mitsumasa Koyanagi, Takashi Nagata, et al.. (2024). Active state structures of a bistable visual opsin bound to G proteins. Nature Communications. 15(1). 8928–8928. 3 indexed citations
5.
Wang, Jinling, Roger Benoit, Xavier Deupí, et al.. (2024). Development of radiofluorinated MLN-4760 derivatives for PET imaging of the SARS-CoV-2 entry receptor ACE2. European Journal of Nuclear Medicine and Molecular Imaging. 52(1). 9–21. 5 indexed citations
6.
Tsai, Ching‐Ju, Filip Pamula, Kenneth N. Goldie, et al.. (2021). Structural basis of the activation of the CC chemokine receptor 5 by a chemokine agonist. Science Advances. 7(25). 46 indexed citations
7.
Wilhelm, Patrick, Cornelia Walther, Roger Schibli, et al.. (2020). Distance-Dependent Cellular Uptake of Oligoproline-Based Homobivalent Ligands Targeting GPCRs—An Experimental and Computational Analysis. Bioconjugate Chemistry. 31(10). 2431–2438. 4 indexed citations
8.
Munk, Christian, Eshita Mutt, Vignir Ísberg, et al.. (2019). An online resource for GPCR structure determination and analysis. Nature Methods. 16(2). 151–162. 98 indexed citations
9.
Nagata, Takashi, Mitsumasa Koyanagi, Hisao Tsukamoto, et al.. (2019). The counterion–retinylidene Schiff base interaction of an invertebrate rhodopsin rearranges upon light activation. Communications Biology. 2(1). 180–180. 32 indexed citations
10.
Varma, Niranjan, Eshita Mutt, Valérie Panneels, et al.. (2019). Crystal structure of jumping spider rhodopsin-1 as a light sensitive GPCR. Proceedings of the National Academy of Sciences. 116(29). 14547–14556. 48 indexed citations
11.
Mayer, Daniel, Fred F. Damberger, Ziva Vuckovic, et al.. (2019). Distinct G protein-coupled receptor phosphorylation motifs modulate arrestin affinity and activation and global conformation. Nature Communications. 10(1). 1261–1261. 81 indexed citations
12.
Tsai, Ching‐Ju, Filip Pamula, Rony Nehmé, et al.. (2018). Crystal structure of rhodopsin in complex with a mini-Gosheds light on the principles of G protein selectivity. Science Advances. 4(9). eaat7052–eaat7052. 52 indexed citations
13.
Olivella, Mireia, Marlous Hoogstraat, Ángel González, et al.. (2018). GPCR-SAS: A web application for statistical analyses on G protein-coupled receptors sequences. PLoS ONE. 13(7). e0199843–e0199843. 5 indexed citations
14.
Singhal, Ankita, Ying Guo, Milos Matkovic, et al.. (2016). Structural role of the T94I rhodopsin mutation in congenital stationary night blindness. EMBO Reports. 17(10). 1431–1440. 30 indexed citations
15.
Wu, Wenting, Przemysław Nogły, Jan Rheinberger, et al.. (2015). Batch crystallization of rhodopsin for structural dynamics using an X-ray free-electron laser. Acta Crystallographica Section F Structural Biology Communications. 71(7). 856–860. 13 indexed citations
16.
Jaussi, Rolf, et al.. (2014). Functional map of arrestin-1 at single amino acid resolution. Proceedings of the National Academy of Sciences. 111(5). 1825–1830. 49 indexed citations
17.
Nakaie, Clóvis R., et al.. (2008). Characterization of a conformationally sensitive TOAC spin-labeled substance P. Peptides. 29(11). 1919–1929. 9 indexed citations
18.
Swaminath, Gayathri, Xavier Deupí, Tae Weon Lee, et al.. (2005). Probing the β2 Adrenoceptor Binding Site with Catechol Reveals Differences in Binding and Activation by Agonists and Partial Agonists. Journal of Biological Chemistry. 280(23). 22165–22171. 223 indexed citations
19.
Deupí, Xavier, Mireia Olivella, Cédric Govaerts, et al.. (2004). Ser and Thr Residues Modulate the Conformation of Pro-Kinked Transmembrane α-Helices. Biophysical Journal. 86(1). 105–115. 76 indexed citations
20.
Ballesteros‐Cánovas, Juan Antonio, Xavier Deupí, Mireia Olivella, Eric Haaksma, & Leonardo Pardo. (2000). Serine and Threonine Residues Bend α-Helices in the χ1=g− Conformation. Biophysical Journal. 79(5). 2754–2760. 153 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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