Enric Esplugues

5.8k total citations · 2 hit papers
31 papers, 3.8k citations indexed

About

Enric Esplugues is a scholar working on Immunology, Cancer Research and Molecular Biology. According to data from OpenAlex, Enric Esplugues has authored 31 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Immunology, 5 papers in Cancer Research and 4 papers in Molecular Biology. Recurrent topics in Enric Esplugues's work include T-cell and B-cell Immunology (19 papers), Immune Cell Function and Interaction (14 papers) and Immunotherapy and Immune Responses (10 papers). Enric Esplugues is often cited by papers focused on T-cell and B-cell Immunology (19 papers), Immune Cell Function and Interaction (14 papers) and Immunotherapy and Immune Responses (10 papers). Enric Esplugues collaborates with scholars based in United States, Spain and Germany. Enric Esplugues's co-authors include Richard A. Flavell, Samuel Huber, Jason S. Weinstein, Begoña Lainez, Nicola Gagliani, William O’Connor, Pilar Lauzurica, Joe Craft, Yajaira Suárez and Carlos Fernández‐Hernando and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Enric Esplugues

31 papers receiving 3.7k citations

Hit Papers

miR-33a/b contribute to the regulation of fatty acid meta... 2011 2026 2016 2021 2011 2011 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
Enric Esplugues United States 24 2.3k 1.1k 600 510 352 31 3.8k
Joseph Barbi United States 24 1.5k 0.7× 1.3k 1.2× 821 1.4× 619 1.2× 392 1.1× 53 3.4k
Raul M. Torres United States 36 3.2k 1.4× 1.5k 1.4× 273 0.5× 492 1.0× 308 0.9× 103 4.9k
Reiko Shinkura Japan 29 1.9k 0.8× 1.3k 1.2× 438 0.7× 416 0.8× 344 1.0× 48 3.1k
Aaron Arvey United States 22 2.7k 1.2× 1.3k 1.2× 435 0.7× 746 1.5× 369 1.0× 27 4.4k
Greg Elson Switzerland 27 1.9k 0.8× 787 0.7× 301 0.5× 702 1.4× 394 1.1× 53 3.1k
Joseph M. Reynolds United States 27 2.5k 1.1× 1.1k 1.1× 298 0.5× 503 1.0× 426 1.2× 48 3.8k
Yury P. Rubtsov Russia 20 3.1k 1.3× 1.2k 1.2× 249 0.4× 690 1.4× 294 0.8× 55 4.7k
Bhanu P. Pappu United States 13 3.1k 1.3× 683 0.6× 456 0.8× 633 1.2× 220 0.6× 14 3.8k
Tomohiro Takahashi Japan 7 2.0k 0.9× 2.4k 2.2× 505 0.8× 626 1.2× 415 1.2× 13 4.1k
Ian R. Rifkin United States 28 4.2k 1.8× 980 0.9× 301 0.5× 572 1.1× 420 1.2× 61 5.4k

Countries citing papers authored by Enric Esplugues

Since Specialization
Citations

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

Fields of papers citing papers by Enric Esplugues

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Enric Esplugues

This figure shows the co-authorship network connecting the top 25 collaborators of Enric Esplugues. A scholar is included among the top collaborators of Enric Esplugues 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 Enric Esplugues. Enric Esplugues 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.
Zhang, Hanming, Diego Sáenz de Urturi, Pablo Fernández‐Tussy, et al.. (2025). Hypercholesterolemia-induced LXR signaling in smooth muscle cells contributes to vascular lesion remodeling and visceral function. Proceedings of the National Academy of Sciences. 122(10). e2417512122–e2417512122. 2 indexed citations
2.
Zhang, Hanming, Lauren A. Biwer, Diego Sáenz de Urturi, et al.. (2024). Abstract 129: Hypercholesterolemia-induced Lxr Signaling In Smc Contributes To Atherosclerotic Lesion Remodeling And Regulates Vascular And Visceral Smc Function. Arteriosclerosis Thrombosis and Vascular Biology. 44(Suppl_1). 1 indexed citations
3.
Sun, Jonathan, Enric Esplugues, Alicia Bort, et al.. (2024). Fatty acid binding protein 5 suppression attenuates obesity-induced hepatocellular carcinoma by promoting ferroptosis and intratumoral immune rewiring. Nature Metabolism. 6(4). 741–763. 33 indexed citations
4.
Meseguer, Salvador, Mari‐Paz Rubio, Begoña Lainez, et al.. (2023). SARS-CoV-2-encoded small RNAs are able to repress the host expression of SERINC5 to facilitate viral replication. Frontiers in Microbiology. 14. 6 indexed citations
5.
Xu, Hao, Theodora Agalioti, Jun Zhao, et al.. (2020). The induction and function of the anti-inflammatory fate of TH17 cells. Nature Communications. 11(1). 3334–3334. 38 indexed citations
6.
Calcinotto, Arianna, Arianna Brevi, Marta Chesi, et al.. (2018). Microbiota-driven interleukin-17-producing cells and eosinophils synergize to accelerate multiple myeloma progression. Nature Communications. 9(1). 4832–4832. 158 indexed citations
7.
Reguant, Anna Pascual, Claudia Baumann, Rebecca Noster, et al.. (2017). TH17 cells express ST2 and are controlled by the alarmin IL-33 in the small intestine. Mucosal Immunology. 10(6). 1431–1442. 56 indexed citations
8.
Weinstein, Jason S., Edward I. Herman, Begoña Lainez, et al.. (2016). TFH cells progressively differentiate to regulate the germinal center response. Nature Immunology. 17(10). 1197–1205. 282 indexed citations
9.
Campisi, Laura, Gaëtan Barbet, Yi Ding, et al.. (2016). Apoptosis in response to microbial infection induces autoreactive TH17 cells. Nature Immunology. 17(9). 1084–1092. 83 indexed citations
10.
Xin, Gang, David Schauder, Begoña Lainez, et al.. (2015). A Critical Role of IL-21-Induced BATF in Sustaining CD8-T-Cell-Mediated Chronic Viral Control. Cell Reports. 13(6). 1118–1124. 108 indexed citations
11.
Paterka, Magdalena, Volker Siffrin, Jan Oliver Voß, et al.. (2015). Gatekeeper role of brain antigen‐presenting CD11c + cells in neuroinflammation. The EMBO Journal. 35(1). 89–101. 44 indexed citations
12.
Shulman, Ziv, Alexander D. Gitlin, Jason S. Weinstein, et al.. (2014). Dynamic signaling by T follicular helper cells during germinal center B cell selection. Science. 345(6200). 1058–1062. 280 indexed citations
13.
Kim, Lark Kyun, Enric Esplugues, Cornelia E. Zorca, et al.. (2014). Oct-1 Regulates IL-17 Expression by Directing Interchromosomal Associations in Conjunction with CTCF in T Cells. Molecular Cell. 54(1). 56–66. 40 indexed citations
14.
Cirera‐Salinas, Daniel, Montse Pauta, Ryan M. Allen, et al.. (2012). Mir-33 regulates cell proliferation and cell cycle progression. Cell Cycle. 11(5). 922–933. 142 indexed citations
15.
Zhang, Wei, John Ferguson, Sok Meng Evelyn Ng, et al.. (2012). Effector CD4+ T Cell Expression Signatures and Immune-Mediated Disease Associated Genes. PLoS ONE. 7(6). e38510–e38510. 15 indexed citations
16.
Esplugues, Enric, Samuel Huber, Nicola Gagliani, et al.. (2011). Control of TH17 cells occurs in the small intestine. Nature. 475(7357). 514–518. 505 indexed citations breakdown →
17.
Vega‐Ramos, Javier, Elisenda Alari‐Pahissa, Juana del Valle-Mendoza, et al.. (2010). CD69 limits early inflammatory diseases associated with immune response to Listeria monocytogenes infection. Immunology and Cell Biology. 88(7). 707–715. 36 indexed citations
18.
Saborit-Villarroya, Ifigènia, Juana del Valle-Mendoza, Xavier Romero, et al.. (2005). The Adaptor Protein 3BP2 Binds Human CD244 and Links this Receptor to Vav Signaling, ERK Activation, and NK Cell Killing. The Journal of Immunology. 175(7). 4226–4235. 43 indexed citations
19.
Sancho, David, Manuel Gómez‐Florit, Enric Esplugues, et al.. (2003). CD69 downregulates autoimmune reactivity through active transforming growth factor-β production in collagen-induced arthritis. Journal of Clinical Investigation. 112(6). 872–882. 157 indexed citations
20.
Martı́n, Margarita, Xavier Romero, Miguel Á. de la Fuente, et al.. (2001). CD84 Functions as a Homophilic Adhesion Molecule and Enhances IFN-γ Secretion: Adhesion Is Mediated by Ig-Like Domain 1. The Journal of Immunology. 167(7). 3668–3676. 114 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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