Fernando Calvo

4.3k total citations · 1 hit paper
42 papers, 2.9k citations indexed

About

Fernando Calvo is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Fernando Calvo has authored 42 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 22 papers in Cell Biology and 15 papers in Oncology. Recurrent topics in Fernando Calvo's work include Cancer Cells and Metastasis (13 papers), Cellular Mechanics and Interactions (11 papers) and Protein Kinase Regulation and GTPase Signaling (10 papers). Fernando Calvo is often cited by papers focused on Cancer Cells and Metastasis (13 papers), Cellular Mechanics and Interactions (11 papers) and Protein Kinase Regulation and GTPase Signaling (10 papers). Fernando Calvo collaborates with scholars based in Spain, United Kingdom and United States. Fernando Calvo's co-authors include Erik Sahai, Emad Moeendarbary, Steven Hooper, Guillaume Charras, Piero Crespo, Peter Williamson, Robert P. Jenkins, A. Grande-García, Nil Ege and Kevin J. Harrington and has published in prestigious journals such as Nature Communications, The Journal of Cell Biology and Nature Cell Biology.

In The Last Decade

Fernando Calvo

41 papers receiving 2.9k citations

Hit Papers

Mechanotransduction and YAP-dependent matrix remodelling ... 2013 2026 2017 2021 2013 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
Fernando Calvo Spain 22 1.8k 1.1k 1.0k 467 336 42 2.9k
Ana Cerezo Spain 13 1.1k 0.6× 677 0.6× 841 0.8× 358 0.8× 170 0.5× 16 2.0k
John M. Lamar United States 21 1.2k 0.7× 1.1k 1.0× 649 0.6× 384 0.8× 206 0.6× 38 2.3k
Rachel B. Hazan United States 23 2.3k 1.3× 847 0.8× 1.4k 1.4× 664 1.4× 230 0.7× 30 3.6k
Laurie E. Littlepage United States 26 2.7k 1.5× 860 0.8× 1.5k 1.5× 1.2k 2.5× 412 1.2× 41 4.1k
Elisabeth Génot France 31 1.5k 0.8× 1.1k 1.0× 614 0.6× 498 1.1× 594 1.8× 87 3.1k
Kiyoko Yoshioka Japan 23 1.6k 0.9× 626 0.6× 693 0.7× 339 0.7× 167 0.5× 38 2.4k
Stephanie Hehlgans Germany 29 1.1k 0.7× 450 0.4× 735 0.7× 338 0.7× 236 0.7× 62 2.3k
María Soledad Sosa United States 21 1.4k 0.8× 428 0.4× 1.6k 1.6× 908 1.9× 501 1.5× 32 2.9k
François Lehembre Switzerland 17 1.8k 1.0× 391 0.4× 1.1k 1.0× 362 0.8× 252 0.8× 26 2.5k
Dawn A. Kirschmann United States 29 2.6k 1.5× 475 0.4× 1.2k 1.1× 1.0k 2.2× 409 1.2× 39 3.4k

Countries citing papers authored by Fernando Calvo

Since Specialization
Citations

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

Fields of papers citing papers by Fernando Calvo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fernando Calvo

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando Calvo. A scholar is included among the top collaborators of Fernando Calvo 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 Fernando Calvo. Fernando Calvo 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.
Javanmardi, Yousef, Andrea Malandrino, Michelle Chen, et al.. (2023). Endothelium and Subendothelial Matrix Mechanics Modulate Cancer Cell Transendothelial Migration. Advanced Science. 10(16). e2206554–e2206554. 16 indexed citations
2.
Hermida‐Prado, Francisco, Maruan Hijazi, Marta Pevida, et al.. (2023). Driving role of head and neck cancer cell secretome on the invasion of stromal fibroblasts: Mechanistic insights by phosphoproteomics. Biomedicine & Pharmacotherapy. 158. 114176–114176. 4 indexed citations
3.
Luxán‐Delgado, Beatriz de, et al.. (2023). Dissecting the functions of cancer-associated fibroblasts to therapeutically target head and neck cancer microenvironment. Biomedicine & Pharmacotherapy. 161. 114502–114502. 7 indexed citations
4.
Farrugia, Aaron J., Javier Rodríguez, José L. Orgaz, et al.. (2020). CDC42EP5/BORG3 modulates SEPT9 to promote actomyosin function, migration, and invasion. The Journal of Cell Biology. 219(9). 45 indexed citations
5.
Ferrari, Nicola, Romana Ranftl, Neil Slaven, et al.. (2019). Dickkopf-3 links HSF1 and YAP/TAZ signalling to control aggressive behaviours in cancer-associated fibroblasts. Nature Communications. 10(1). 130–130. 119 indexed citations
6.
Ranftl, Romana & Fernando Calvo. (2017). Analysis of Breast Cancer Cell Invasion Using an Organotypic Culture System. Methods in molecular biology. 1612. 199–212. 5 indexed citations
7.
Avgustinova, Alexandra, Marjan Iravani, David Robertson, et al.. (2016). Tumour cell-derived Wnt7a recruits and activates fibroblasts to promote tumour aggressiveness. Nature Communications. 7(1). 10305–10305. 126 indexed citations
8.
Calvo, Fernando, Romana Ranftl, Steven Hooper, et al.. (2015). Cdc42EP3/BORG2 and Septin Network Enables Mechano-transduction and the Emergence of Cancer-Associated Fibroblasts. Cell Reports. 13(12). 2699–2714. 102 indexed citations
9.
Herráiz, Cecilia, Fernando Calvo, Pahini Pandya, et al.. (2015). Reactivation of p53 by a Cytoskeletal Sensor to Control the Balance Between DNA Damage and Tumor Dissemination. JNCI Journal of the National Cancer Institute. 108(1). djv289–djv289. 154 indexed citations
10.
Martín, Yaiza del Pozo, Danielle Park, Anassuya Ramachandran, et al.. (2015). Mesenchymal Cancer Cell-Stroma Crosstalk Promotes Niche Activation, Epithelial Reversion, and Metastatic Colonization. Cell Reports. 13(11). 2456–2469. 185 indexed citations
11.
Babu, Sahana Suresh, et al.. (2014). TGFβ-mediated suppression of CD248 in non-cancer cells via canonical Smad-dependent signaling pathways is uncoupled in cancer cells. BMC Cancer. 14(1). 113–113. 13 indexed citations
12.
Calvo, Fernando, Nil Ege, A. Grande-García, et al.. (2013). Mechanotransduction and YAP-dependent matrix remodelling is required for the generation and maintenance of cancer-associated fibroblasts. Nature Cell Biology. 15(6). 637–646. 1076 indexed citations breakdown →
13.
Calvo, Fernando, Victoria Sanz‐Moreno, Lorena Agudo‐Ibáñez, et al.. (2011). RasGRF suppresses Cdc42-mediated tumour cell movement, cytoskeletal dynamics and transformation. Nature Cell Biology. 13(7). 819–826. 64 indexed citations
14.
Calvo, Fernando & Erik Sahai. (2011). Cell communication networks in cancer invasion. Current Opinion in Cell Biology. 23(5). 621–629. 71 indexed citations
15.
Crespo, Piero, Fernando Calvo, & Victoria Sanz‐Moreno. (2011). Ras and Rho GTPases on the move. PubMed. 1(4). 200–204. 5 indexed citations
16.
Calvo, Fernando, Lorena Agudo‐Ibáñez, & Piero Crespo. (2010). The Ras‐ERK pathway: Understanding site‐specific signaling provides hope of new anti‐tumor therapies. BioEssays. 32(5). 412–421. 60 indexed citations
17.
Calvo, Fernando & Piero Crespo. (2009). Structural and Spatial Determinants Regulating TC21 Activation by RasGRF Family Nucleotide Exchange Factors. Molecular Biology of the Cell. 20(20). 4289–4302. 13 indexed citations
18.
Martínez, Susana E., Francisco Lázaro‐Diéguez, Javier Selva, et al.. (2007). Lysophosphatidic acid rescues RhoA activation and phosphoinositides levels in astrocytes exposed to ethanol. Journal of Neurochemistry. 102(4). 1044–1052. 21 indexed citations
19.
Matallanas, David, Victoria Sanz‐Moreno, Imanol Arozarena, et al.. (2005). Distinct Utilization of Effectors and Biological Outcomes Resulting from Site-Specific Ras Activation: Ras Functions in Lipid Rafts and Golgi Complex Are Dispensable for Proliferation and Transformation. Molecular and Cellular Biology. 26(1). 100–116. 107 indexed citations
20.
Arozarena, Imanol, David Matallanas, Marı́a T. Berciano, et al.. (2004). Activation of H-Ras in the Endoplasmic Reticulum by the RasGRF Family Guanine Nucleotide Exchange Factors. Molecular and Cellular Biology. 24(4). 1516–1530. 83 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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