Mar Valés‐Gómez

5.2k total citations
74 papers, 4.1k citations indexed

About

Mar Valés‐Gómez is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Mar Valés‐Gómez has authored 74 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Immunology, 19 papers in Molecular Biology and 14 papers in Oncology. Recurrent topics in Mar Valés‐Gómez's work include Immune Cell Function and Interaction (56 papers), T-cell and B-cell Immunology (38 papers) and Extracellular vesicles in disease (12 papers). Mar Valés‐Gómez is often cited by papers focused on Immune Cell Function and Interaction (56 papers), T-cell and B-cell Immunology (38 papers) and Extracellular vesicles in disease (12 papers). Mar Valés‐Gómez collaborates with scholars based in Spain, United States and United Kingdom. Mar Valés‐Gómez's co-authors include Hugh T. Reyburn, Jack L. Strominger, Ofer Mandelboim, Daniel M. Davis, Laszlo Pazmany, Lola Fernández‐Messina, J L Strominger, Sonia Agüera‐González, Omodele Ashiru and Philippe Boutet and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Mar Valés‐Gómez

73 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mar Valés‐Gómez Spain 33 3.1k 1.1k 780 500 365 74 4.1k
Thomas Brocker Germany 38 4.2k 1.4× 1.1k 1.0× 1.1k 1.4× 404 0.8× 297 0.8× 87 5.4k
Matthias Schiemann Germany 35 3.1k 1.0× 1.1k 1.0× 1.2k 1.6× 675 1.4× 176 0.5× 68 4.5k
Christopher D.C. Allen United States 23 3.9k 1.3× 1.0k 0.9× 695 0.9× 274 0.5× 294 0.8× 37 5.2k
Giandomenica Iezzi Switzerland 37 3.2k 1.0× 1.2k 1.1× 1.8k 2.3× 242 0.5× 338 0.9× 72 5.1k
Yosef Refaeli United States 22 1.9k 0.6× 1.4k 1.3× 695 0.9× 463 0.9× 241 0.7× 38 3.7k
Lianjun Shen China 17 1.6k 0.5× 1.4k 1.3× 750 1.0× 264 0.5× 127 0.3× 49 2.8k
Jill E. Slansky United States 37 4.0k 1.3× 2.0k 1.8× 2.5k 3.2× 498 1.0× 298 0.8× 79 6.4k
Jean‐Pierre Abastado France 41 3.1k 1.0× 1.3k 1.2× 1.3k 1.7× 572 1.1× 303 0.8× 95 4.8k
Roberto S. Accolla Italy 41 3.9k 1.3× 1.4k 1.3× 1.2k 1.6× 325 0.7× 279 0.8× 179 5.8k
Giulia Casorati Italy 48 5.8k 1.9× 1.5k 1.3× 2.1k 2.6× 542 1.1× 235 0.6× 131 7.4k

Countries citing papers authored by Mar Valés‐Gómez

Since Specialization
Citations

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

Fields of papers citing papers by Mar Valés‐Gómez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mar Valés‐Gómez. 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 Mar Valés‐Gómez. The network helps show where Mar Valés‐Gómez may publish in the future.

Co-authorship network of co-authors of Mar Valés‐Gómez

This figure shows the co-authorship network connecting the top 25 collaborators of Mar Valés‐Gómez. A scholar is included among the top collaborators of Mar Valés‐Gómez 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 Mar Valés‐Gómez. Mar Valés‐Gómez 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.
Esteso, Gloria, et al.. (2024). Selective expansion of anti-tumor innate lymphocytes in long-term cultures after a single BCG pulse. Methods in cell biology. 190. 203–221. 1 indexed citations
3.
González, Álvaro, et al.. (2024). Extracellular vesicles in cancer: challenges and opportunities for clinical laboratories. Critical Reviews in Clinical Laboratory Sciences. 61(6). 435–457. 10 indexed citations
4.
Casasnovas, José M., et al.. (2024). Elevated levels of cell-free NKG2D-ligands modulate NKG2D surface expression and compromise NK cell function in severe COVID-19 disease. Frontiers in Immunology. 15. 1273942–1273942. 2 indexed citations
5.
Haller, R. De, Michael D. Miller, Iris Kufferath, et al.. (2024). Immune evasion by proteolytic shedding of natural killer group 2, member D ligands in Helicobacter pylori infection. Frontiers in Immunology. 15. 1282680–1282680. 11 indexed citations
6.
López‐Guerrero, José Antonio, Mar Valés‐Gómez, Francesc E. Borràs, et al.. (2023). Standardising the preanalytical reporting of biospecimens to improve reproducibility in extracellular vesicle research – A GEIVEX study. SHILAP Revista de lepidopterología. 2(4). e76–e76. 16 indexed citations
7.
Robles‐Vera, Iñaki, Santiago Uranga, Ana Belén Gómez, et al.. (2023). Intravenous administration of BCG in mice promotes natural killer and T cell-mediated antitumor immunity in the lung. Nature Communications. 14(1). 6090–6090. 18 indexed citations
8.
Uranga, Santiago, Ana Belén Gómez, Denise Nardelli‐Haefliger, et al.. (2022). Novel intravesical bacterial immunotherapy induces rejection of BCG-unresponsive established bladder tumors. Journal for ImmunoTherapy of Cancer. 10(7). e004325–e004325. 13 indexed citations
9.
López‐Cobo, Sheila, Ana Rodríguez‐Galán, Irene Fernández‐Delgado, et al.. (2022). Natural killer (NK) cell-derived extracellular-vesicle shuttled microRNAs control T cell responses. eLife. 11. 57 indexed citations
10.
Royo, Félix, Mikel Azkargorta, José Luis Lavín, et al.. (2021). Extracellular Vesicles From Liver Progenitor Cells Downregulates Fibroblast Metabolic Activity and Increase the Expression of Immune-Response Related Molecules. Frontiers in Cell and Developmental Biology. 8. 613583–613583. 3 indexed citations
11.
Esteso, Gloria, Nacho Aguiló, Esther Julián, et al.. (2021). Natural Killer Anti-Tumor Activity Can Be Achieved by In Vitro Incubation With Heat-Killed BCG. Frontiers in Immunology. 12. 622995–622995. 18 indexed citations
12.
Martínez‐Fleta, Pedro, Arántzazu Alfranca, Isidoro González‐Álvaro, et al.. (2020). SARS-CoV-2 Cysteine-like Protease Antibodies Can Be Detected in Serum and Saliva of COVID-19–Seropositive Individuals. The Journal of Immunology. 205(11). 3130–3140. 32 indexed citations
13.
Ashiru, Omodele, Gloria Esteso, Eva M. García‐Cuesta, et al.. (2019). BCG Therapy of Bladder Cancer Stimulates a Prolonged Release of the Chemoattractant CXCL10 (IP10) in Patient Urine. Cancers. 11(7). 940–940. 13 indexed citations
14.
Valés‐Gómez, Mar, et al.. (2018). NKG2H-Expressing T Cells Negatively Regulate Immune Responses. Frontiers in Immunology. 9. 390–390. 12 indexed citations
15.
García‐Cuesta, Eva M., Gloria Esteso, Omodele Ashiru, et al.. (2017). Characterization of a human anti-tumoral NK cell population expanded after BCG treatment of leukocytes. OncoImmunology. 6(4). e1293212–e1293212. 27 indexed citations
16.
García‐Cuesta, Eva M., Sheila López‐Cobo, Mario Álvarez‐Maestro, et al.. (2015). NKG2D is a Key Receptor for Recognition of Bladder Cancer Cells by IL-2-Activated NK Cells and BCG Promotes NK Cell Activation. Frontiers in Immunology. 6. 284–284. 36 indexed citations
17.
Valés‐Gómez, Mar. (2015). The Impact of Glycosyl-Phosphatidyl-Inositol Anchored MICA Alleles on Novel NKG2D-Based Therapies. Frontiers in Immunology. 6. 193–193. 10 indexed citations
18.
Ashiru, Omodele, Philippe Boutet, Lola Fernández‐Messina, et al.. (2010). Natural Killer Cell Cytotoxicity Is Suppressed by Exposure to the Human NKG2D Ligand MICA*008 That Is Shed by Tumor Cells in Exosomes. Cancer Research. 70(2). 481–489. 340 indexed citations
19.
Pozo, David, et al.. (2006). CD161 (Human NKR-P1A) Signaling in NK Cells Involves the Activation of Acid Sphingomyelinase. The Journal of Immunology. 176(4). 2397–2406. 68 indexed citations
20.
Reyburn, Hugh T., Ofer Mandelboim, Mar Valés‐Gómez, et al.. (1997). Human NK cells: their ligands, receptors and functions. Immunological Reviews. 155(1). 119–125. 76 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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