Isabel Mérida

6.0k total citations
106 papers, 5.0k citations indexed

About

Isabel Mérida is a scholar working on Molecular Biology, Immunology and Cell Biology. According to data from OpenAlex, Isabel Mérida has authored 106 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 39 papers in Immunology and 22 papers in Cell Biology. Recurrent topics in Isabel Mérida's work include T-cell and B-cell Immunology (24 papers), Immune Cell Function and Interaction (23 papers) and Protein Kinase Regulation and GTPase Signaling (21 papers). Isabel Mérida is often cited by papers focused on T-cell and B-cell Immunology (24 papers), Immune Cell Function and Interaction (23 papers) and Protein Kinase Regulation and GTPase Signaling (21 papers). Isabel Mérida collaborates with scholars based in Spain, United States and Australia. Isabel Mérida's co-authors include Antonia Ávila‐Flores, Silvia Carrasco, Ernesto Merino, Carlos Martı́nez-A, Glen N. Gaulton, D. I. Jones, Manuel Izquierdo, Esther Rincón, Teresa Santos-Mendoza and José M. Mato and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Isabel Mérida

103 papers receiving 5.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabel Mérida Spain 42 3.2k 1.5k 1.1k 751 619 106 5.0k
Peter M. Finan United Kingdom 26 5.2k 1.6× 1.4k 1.0× 954 0.9× 1.2k 1.5× 1.2k 1.9× 40 7.6k
Rosana Kapeller United States 26 4.1k 1.3× 1.0k 0.7× 1.0k 1.0× 1.1k 1.4× 744 1.2× 41 5.9k
Thomas Grewal Australia 43 3.1k 1.0× 784 0.5× 740 0.7× 517 0.7× 1.1k 1.7× 119 4.8k
Yoshimi Homma Japan 41 3.1k 1.0× 1.3k 0.9× 939 0.9× 526 0.7× 475 0.8× 128 5.2k
Kathleen Kelly United States 44 3.6k 1.1× 907 0.6× 845 0.8× 1.2k 1.6× 894 1.4× 88 5.9k
Giovanni Raugei Italy 41 3.8k 1.2× 1.2k 0.8× 794 0.7× 524 0.7× 662 1.1× 117 5.0k
Estela Jacinto United States 27 6.9k 2.2× 1.5k 1.0× 965 0.9× 906 1.2× 895 1.4× 45 8.9k
Jeffrey E. Kudlow United States 51 5.6k 1.8× 1.6k 1.1× 663 0.6× 1.1k 1.5× 758 1.2× 97 7.5k
Graeme R. Guy Singapore 46 3.8k 1.2× 1.4k 0.9× 837 0.8× 1.1k 1.5× 706 1.1× 98 5.6k
J E Niedel United States 31 3.5k 1.1× 1.1k 0.7× 661 0.6× 549 0.7× 347 0.6× 46 5.1k

Countries citing papers authored by Isabel Mérida

Since Specialization
Citations

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

Fields of papers citing papers by Isabel Mérida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabel Mérida

This figure shows the co-authorship network connecting the top 25 collaborators of Isabel Mérida. A scholar is included among the top collaborators of Isabel Mérida 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 Isabel Mérida. Isabel Mérida 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.
2.
Mérida, Isabel, et al.. (2024). Sorting nexin 27–dependent regulation of Lck and CD4 tunes the initial stages of T-cell activation. Journal of Leukocyte Biology. 116(4). 793–806. 1 indexed citations
3.
Ávila‐Flores, Antonia, et al.. (2023). Identification of Host PDZ-Based Interactions with the SARS-CoV-2 E Protein in Human Monocytes. International Journal of Molecular Sciences. 24(16). 12793–12793. 3 indexed citations
4.
Leitner, Judith, et al.. (2021). Diacylglycerol kinase α inhibition cooperates with PD-1-targeted therapies to restore the T cell activation program. Cancer Immunology Immunotherapy. 70(11). 3277–3289. 19 indexed citations
5.
Mérida, Isabel, et al.. (2019). Diacylglycerol Kinase Malfunction in Human Disease and the Search for Specific Inhibitors. Handbook of experimental pharmacology. 259. 133–162. 14 indexed citations
6.
Ávila‐Flores, Antonia, et al.. (2018). Transcriptional Activity of FOXO Transcription Factors Measured by Luciferase Assays. Methods in molecular biology. 1890. 91–102. 5 indexed citations
7.
Tello‐Lafoz, María, et al.. (2017). Sorting nexin 27 interactome in T‐lymphocytes identifies zona occludens‐2 dynamic redistribution at the immune synapse. Traffic. 18(8). 491–504. 17 indexed citations
8.
Mérida, Isabel, et al.. (2017). Diacylglycerol Kinase ζ Limits Cytokine-dependent Expansion of CD8+ T Cells with Broad Antitumor Capacity. EBioMedicine. 19. 39–48. 14 indexed citations
9.
Mérida, Isabel, et al.. (2016). Diacylglycerol kinases in cancer. Advances in Biological Regulation. 63. 22–31. 59 indexed citations
10.
Mérida, Isabel, et al.. (2013). Diacylglycerol metabolism attenuates T-cell receptor signaling and alters thymocyte differentiation. Cell Death and Disease. 4(11). e912–e912. 18 indexed citations
11.
Gharbi, Severine, et al.. (2013). Transient PKCα shuttling to the immunological synapse is governed by (DGK)ζ and regulates L-selectin shedding. Journal of Cell Science. 126(Pt 10). 2176–86. 14 indexed citations
12.
Gharbi, Severine, Esther Rincón, Antonia Ávila‐Flores, et al.. (2011). Diacylglycerol kinase ζ controls diacylglycerol metabolism at the immunological synapse. Molecular Biology of the Cell. 22(22). 4406–4414. 41 indexed citations
13.
Alonso, Roberto, Carla Mazzeo, Mark Marsh, et al.. (2011). Diacylglycerol kinase α regulates the formation and polarisation of mature multivesicular bodies involved in the secretion of Fas ligand-containing exosomes in T lymphocytes. Cell Death and Differentiation. 18(7). 1161–1173. 115 indexed citations
14.
Mérida, Isabel, et al.. (2009). T Cell Receptor-dependent Tyrosine Phosphorylation of β2-Chimaerin Modulates Its Rac-GAP Function in T Cells. Journal of Biological Chemistry. 284(17). 11354–11363. 15 indexed citations
15.
Merino, Ernesto, Antonia Ávila‐Flores, Yasuhito Shirai, et al.. (2008). Lck-Dependent Tyrosine Phosphorylation of Diacylglycerol Kinase α Regulates Its Membrane Association in T Cells. The Journal of Immunology. 180(9). 5805–5815. 31 indexed citations
16.
Shirai, Yasuhito, Keiko Yagi, Naoko Adachi, et al.. (2005). Importance of chroman ring and tyrosine phosphorylation in the subtype‐specific translocation and activation of diacylglycerol kinase α by d‐α‐tocopherol. Genes to Cells. 10(4). 311–319. 48 indexed citations
17.
Martı́n-Puig, Silvia, Julián Aragonés, David Jones, et al.. (2004). Role of diacylglycerol induced by hypoxia in the regulation of HIF-1α activity. Biochemical and Biophysical Research Communications. 315(1). 44–50. 31 indexed citations
18.
Sanjuán, Miguel A. F., Bérengère Pradet‐Balade, D. I. Jones, et al.. (2003). T Cell Activation In Vivo Targets Diacylglycerol Kinase α to the Membrane: A Novel Mechanism for Ras Attenuation. The Journal of Immunology. 170(6). 2877–2883. 93 indexed citations
19.
Ciprés, Angel, Silvia Carrasco, Ernesto Merino, et al.. (2003). Regulation of Diacylglycerol Kinase α by Phosphoinositide 3-Kinase Lipid Products. Journal of Biological Chemistry. 278(37). 35629–35635. 52 indexed citations
20.
Mérida, Isabel, Peter Williamson, Kendall A. Smith, & Glen N. Gaulton. (1993). The Role of Diacylglycerol Kinase Activation and Phosphatidate Accumulation in Interleukin-2-Dependent Lymphocyte Proliferation. DNA and Cell Biology. 12(6). 473–479. 20 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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