Paloma Sánchez‐Mateos

8.7k total citations · 1 hit paper
92 papers, 7.2k citations indexed

About

Paloma Sánchez‐Mateos is a scholar working on Immunology, Immunology and Allergy and Molecular Biology. According to data from OpenAlex, Paloma Sánchez‐Mateos has authored 92 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Immunology, 37 papers in Immunology and Allergy and 21 papers in Molecular Biology. Recurrent topics in Paloma Sánchez‐Mateos's work include Cell Adhesion Molecules Research (37 papers), Immunotherapy and Immune Responses (30 papers) and Immune cells in cancer (18 papers). Paloma Sánchez‐Mateos is often cited by papers focused on Cell Adhesion Molecules Research (37 papers), Immunotherapy and Immune Responses (30 papers) and Immune cells in cancer (18 papers). Paloma Sánchez‐Mateos collaborates with scholars based in Spain, United States and Mexico. Paloma Sánchez‐Mateos's co-authors include Francisco Sánchez‐Madrid, Ángel L. Corbí, Miguel Á. del Pozo, Amaya Puig‐Kröger, Rafael Samaniego, Natividad Longo, Elena Sierra‐Filardi, Lorena Sánchez-Martı́n, Carlos Cabañas and Miguel R. Campanero and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Paloma Sánchez‐Mateos

87 papers receiving 7.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Biomechanical Remodeling of the Microenvironment by Stromal Caveolin-1 Favors Tumor Invasion and Metastasis

2011 584 citations Rafael Samaniego, Paloma Sánchez‐Mateos et al. profile →

Peers

Paloma Sánchez‐Mateos

IMMUN

ONCOL

Robert C. Fuhlbrigge United States

Santos Mañes Spain

Kensuke Miyake Japan

Tatsuo Kinashi Japan

Margaret L. Hibbs Australia

Beat A. Imhof Switzerland

Geoffrey S. Kansas United States

Ofer Lider Israel

Antonella Stoppacciaro Italy

Daniel F. Legler Switzerland

Robert C. Fuhlbrigge United States

Paloma Sánchez‐Mateos

5.1k ×1.4

IMMUN

2.3k ×1.0

2.8k ×1.5

ONCOL

1.7k ×1.0

643 ×0.7

Citations per year, relative to Paloma Sánchez‐Mateos Paloma Sánchez‐Mateos (= 1×) peers Robert C. Fuhlbrigge

Countries citing papers authored by Paloma Sánchez‐Mateos

Since Specialization

Citations

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

Fields of papers citing papers by Paloma Sánchez‐Mateos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paloma Sánchez‐Mateos. 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 Paloma Sánchez‐Mateos. The network helps show where Paloma Sánchez‐Mateos may publish in the future.

Co-authorship network of co-authors of Paloma Sánchez‐Mateos

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

All Works

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20 of 20 papers shown

Herrero, Cristina, Francisco Díaz‐Crespo, Rafael Samaniego, et al.. (2025). Reprogramming of GM-CSF-dependent alveolar macrophages through GSK3 activity modulation. eLife. 14.

Fernández‐Cruz, Eduardo, et al.. (2024). Lack of Specific Immune Response after Five Doses of mRNA SARS-CoV-2 Vaccine in a Patient with CD4+ T-Cell Lymphopenia but Preserved Responses to CMV. Vaccines. 12(4). 386–386.

García‐Martínez, Elena, et al.. (2024). Chemokine profiling of melanoma–macrophage crosstalk identifies CCL8 and CCL15 as prognostic factors in cutaneous melanoma. The Journal of Pathology. 262(4). 495–504. 9 indexed citations

Rodríguez-Ruiz, María E., Paloma Sánchez‐Mateos, Maite Álvarez, et al.. (2023). Intratumoral BO-112 in combination with radiotherapy synergizes to achieve CD8 T-cell-mediated local tumor control. Journal for ImmunoTherapy of Cancer. 11(1). e005011–e005011. 14 indexed citations

García‐Martínez, Elena, María Eugenia Fernández‐Santos, Amaya Puig‐Kröger, et al.. (2021). CCL20/TNF/VEGFA Cytokine Secretory Phenotype of Tumor-Associated Macrophages Is a Negative Prognostic Factor in Cutaneous Melanoma. Cancers. 13(16). 3943–3943. 16 indexed citations

García‐Martínez, Elena, et al.. (2021). Activin A Sustains the Metastatic Phenotype of Tumor-Associated Macrophages and Is a Prognostic Marker in Human Cutaneous Melanoma. Journal of Investigative Dermatology. 142(3). 653–661.e2. 13 indexed citations

Samaniego, Rafael, Alejandra Gutiérrez‐González, Iván Márquez‐Rodas, et al.. (2018). CCL20 Expression by Tumor-Associated Macrophages Predicts Progression of Human Primary Cutaneous Melanoma. Cancer Immunology Research. 6(3). 267–275. 62 indexed citations

Benito, Marta, Diana Peiteado, Alejandro Balsa, et al.. (2017). FRI0062 Synovial fluid treg cells secrete il-17 and at the same time are potent suppressors of tresp cell proliferation, tnf alpha and ifn gamma production. Annals of the Rheumatic Diseases. 76. 501–502.

Martínez‐Moreno, Mónica, Magdalena Leiva, Noemí Aguilera‐Montilla, et al.. (2015). In vivo adhesion of malignant B cells to bone marrow microvasculature is regulated by α4β1 cytoplasmic-binding proteins. Leukemia. 30(4). 861–872. 28 indexed citations

10.

Hernández-Varas, Pablo, Georgina P. Coló, Rubén A. Bartolomé, et al.. (2011). Rap1-GTP-interacting Adaptor Molecule (RIAM) Protein Controls Invasion and Growth of Melanoma Cells. Journal of Biological Chemistry. 286(21). 18492–18504. 32 indexed citations

11.

Sánchez-Martı́n, Lorena, Ana Estecha, Rafael Samaniego, et al.. (2010). The chemokine CXCL12 regulates monocyte-macrophage differentiation and RUNX3 expression. Blood. 117(1). 88–97. 248 indexed citations

12.

Puig‐Kröger, Amaya, Elena Sierra‐Filardi, Ángeles Domínguez‐Soto, et al.. (2009). Folate Receptor β Is Expressed by Tumor-Associated Macrophages and Constitutes a Marker for M2 Anti-inflammatory/Regulatory Macrophages. Cancer Research. 69(24). 9395–9403. 310 indexed citations

13.

Bartolomé, Rubén A., et al.. (2006). Activation of Vav/Rho GTPase Signaling by CXCL12 Controls Membrane-Type Matrix Metalloproteinase–Dependent Melanoma Cell Invasion. Cancer Research. 66(1). 248–258. 109 indexed citations

14.

Riol‐Blanco, Lorena, Noelia Sánchez‐Sánchez, A.L. Torres, et al.. (2005). The Chemokine Receptor CCR7 Activates in Dendritic Cells Two Signaling Modules That Independently Regulate Chemotaxis and Migratory Speed. The Journal of Immunology. 174(7). 4070–4080. 187 indexed citations

15.

Sánchez-Martı́n, Lorena, Noelia Sánchez‐Sánchez, María Dolores Gutiérrez‐López, et al.. (2004). Signaling through the Leukocyte Integrin LFA-1 in T Cells Induces a Transient Activation of Rac-1 That Is Regulated by Vav and PI3K/Akt-1. Journal of Biological Chemistry. 279(16). 16194–16205. 59 indexed citations

16.

Relloso, Miguel, Amaya Puig‐Kröger, Óscar M. Pello, et al.. (2002). DC-SIGN (CD209) Expression Is IL-4 Dependent and Is Negatively Regulated by IFN, TGF-β, and Anti-Inflammatory Agents. The Journal of Immunology. 168(6). 2634–2643. 252 indexed citations

17.

Puig‐Kröger, Amaya, Francisco Sanz‐Rodríguez, Natividad Longo, et al.. (2000). Maturation-Dependent Expression and Function of the CD49d Integrin on Monocyte-Derived Human Dendritic Cells. The Journal of Immunology. 165(8). 4338–4345. 69 indexed citations

18.

Pozo, Miguel Á. del, Paloma Sánchez‐Mateos, & Francisco Sánchez‐Madrid. (1996). Cellular polarization induced by chemokines: a mechanism for leukocyte recruitment?. Immunology Today. 17(3). 127–131. 87 indexed citations

19.

Sánchez‐Mateos, Paloma, Carlos Cabañas, & Francisco Sánchez‐Madrid. (1996). Regulation of integrin function. Seminars in Cancer Biology. 7(3). 99–109. 65 indexed citations

20.

Sánchez‐Mateos, Paloma, et al.. (1989). Expression of a gp33/27,000 MW activation inducer molecule (AIM) on human lymphoid tissues. Induction of cell proliferation on thymocytes and B lymphocytes by anti-AIM antibodies.. PubMed. 68(1). 72–9. 42 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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