José M. Rojas

2.9k total citations
57 papers, 2.2k citations indexed

About

José M. Rojas is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, José M. Rojas has authored 57 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 11 papers in Oncology and 10 papers in Cancer Research. Recurrent topics in José M. Rojas's work include Protein Kinase Regulation and GTPase Signaling (9 papers), PI3K/AKT/mTOR signaling in cancer (7 papers) and Cancer-related Molecular Pathways (7 papers). José M. Rojas is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (9 papers), PI3K/AKT/mTOR signaling in cancer (7 papers) and Cancer-related Molecular Pathways (7 papers). José M. Rojas collaborates with scholars based in Spain, United States and Switzerland. José M. Rojas's co-authors include Ricardo Sánchez‐Prieto, Yoichi Taya, J. Silvio Gutkind, Eugenio Santos, Natalia J. Martinez, Natasha Zarich, José Luís Oliva, Dolores Pérez‐Sala, Natalia Martínez and Cecilio López‐Galíndez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

José M. Rojas

56 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José M. Rojas Spain 26 1.3k 413 298 287 194 57 2.2k
Katalin Bánki United States 30 1.1k 0.8× 275 0.7× 150 0.5× 1.2k 4.1× 199 1.0× 50 2.9k
Gabriella Miklóssy United States 19 675 0.5× 296 0.7× 105 0.4× 511 1.8× 108 0.6× 28 1.5k
Hyock Joo Kwon United States 21 1.7k 1.3× 314 0.8× 309 1.0× 264 0.9× 343 1.8× 26 3.3k
Bonne M. Thompson United States 20 1.1k 0.8× 240 0.6× 366 1.2× 382 1.3× 215 1.1× 35 2.0k
James E. Weiel United States 18 999 0.8× 148 0.4× 89 0.3× 354 1.2× 103 0.5× 28 1.8k
Ming-Derg Lai Taiwan 32 1.5k 1.1× 519 1.3× 532 1.8× 564 2.0× 165 0.9× 70 2.8k
Luquan Wang United States 18 2.4k 1.8× 1.3k 3.0× 601 2.0× 270 0.9× 235 1.2× 33 3.8k
Long T. Quan United States 5 2.0k 1.5× 548 1.3× 292 1.0× 580 2.0× 157 0.8× 6 2.6k
Debajit K. Biswas United States 19 1.1k 0.8× 665 1.6× 667 2.2× 265 0.9× 288 1.5× 43 1.8k

Countries citing papers authored by José M. Rojas

Since Specialization
Citations

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

Fields of papers citing papers by José M. Rojas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by José M. Rojas. 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 José M. Rojas. The network helps show where José M. Rojas may publish in the future.

Co-authorship network of co-authors of José M. Rojas

This figure shows the co-authorship network connecting the top 25 collaborators of José M. Rojas. A scholar is included among the top collaborators of José M. Rojas 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 José M. Rojas. José M. Rojas 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.
Rojas, José M., et al.. (2023). Tercer molar desplazado a fosa pterigomaxilar: reporte de caso. 3(2). 94–98. 1 indexed citations
2.
Baltanás, Fernando C., Natasha Zarich, José M. Rojas, & Eugenio Santos. (2020). SOS GEFs in health and disease. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1874(2). 188445–188445. 60 indexed citations
3.
Rojas, José M., et al.. (2020). Toxicological Characterization and Phospholipase D Activity of the Venom of the Spider Sicarius thomisoides. Toxins. 12(11). 702–702. 4 indexed citations
4.
Domı́nguez, Carmen, Sales Ibiza, Natalia J. Martinez, et al.. (2016). PGA1-induced apoptosis involves specific activation of H-Ras and N-Ras in cellular endomembranes. Cell Death and Disease. 7(7). e2311–e2311. 8 indexed citations
5.
Barbáchano, Antonio, Asunción Fernández‐Barral, Fábio Pereira, et al.. (2015). SPROUTY-2 represses the epithelial phenotype of colon carcinoma cells via upregulation of ZEB1 mediated by ETS1 and miR-200/miR-150. Oncogene. 35(23). 2991–3003. 38 indexed citations
6.
Martínez, Natalia, Gonzalo León‐Espinosa, A. Sánchez, et al.. (2011). Sprouty2 and Spred1-2 Proteins Inhibit the Activation of the ERK Pathway Elicited by Cyclopentenone Prostanoids. PLoS ONE. 6(2). e16787–e16787. 5 indexed citations
7.
Oeste, Clara L., Beatriz Díez-Dacal, Mario Garcı́a de Lacoba, et al.. (2011). The C-Terminus of H-Ras as a Target for the Covalent Binding of Reactive Compounds Modulating Ras-Dependent Pathways. PLoS ONE. 6(1). e15866–e15866. 29 indexed citations
8.
Barbáchano, Antonio, Paloma Ordóñez‐Morán, J.M. Jurado, et al.. (2010). SPROUTY-2 and E-cadherin regulate reciprocally and dictate colon cancer cell tumourigenicity. Oncogene. 29(34). 4800–4813. 60 indexed citations
9.
Hevér, Anikó, Richard B. Roth, Peter Hevezi, et al.. (2007). Human endometriosis is associated with plasma cells and overexpression of B lymphocyte stimulator. Proceedings of the National Academy of Sciences. 104(30). 12451–12456. 189 indexed citations
10.
Martínez, Natalia, Beatriz Domingo, José Luís Oliva, et al.. (2007). Sprouty2 binds Grb2 at two different proline-rich regions, and the mechanism of ERK inhibition is independent of this interaction. Cellular Signalling. 19(11). 2277–2285. 22 indexed citations
11.
González-Santiago, Laura, Yajaira Suárez, Natasha Zarich, et al.. (2006). Aplidin® induces JNK-dependent apoptosis in human breast cancer cells via alteration of glutathione homeostasis, Rac1 GTPase activation, and MKP-1 phosphatase downregulation. Cell Death and Differentiation. 13(11). 1968–1981. 71 indexed citations
12.
Suárez, Yajaira, Laura González-Santiago, Natasha Zarich, et al.. (2006). Plitidepsin Cellular Binding and Rac1/JNK Pathway Activation Depend on Membrane Cholesterol Content. Molecular Pharmacology. 70(5). 1654–1663. 24 indexed citations
13.
Álvaro, Cristina de, Natalia Martínez, José M. Rojas, & Margarita Lorenzo. (2005). Sprouty-2 Overexpression in C2C12 Cells Confers Myogenic Differentiation Properties in the Presence of FGF2. Molecular Biology of the Cell. 16(9). 4454–4461. 46 indexed citations
14.
Rico, Daniel, Héctor Peinado, Natasha Zarich, et al.. (2005). Potentiation of tumor formation by topical administration of 15-deoxy-Δ 12,14 -prostaglandin J 2 in a model of skin carcinogenesis. Carcinogenesis. 27(2). 328–336. 30 indexed citations
15.
Queipo‐Ortuño, María Isabel, et al.. (2004). PCR-DIG ELISA with biotinylated primers is unsuitable for use in whole blood samples from patients with brucellosis. Molecular and Cellular Probes. 18(4). 243–250. 3 indexed citations
16.
Gil, Laura, Marina Pollán, Eva Cristóbal, et al.. (2002). Genetic analysis of RET, GFRα1 and GDNF genes in Spanish families with multiple endocrine neoplasia type 2A. International Journal of Cancer. 99(2). 299–304. 30 indexed citations
17.
Rojas, José M., Carmen Guerrero, Rosana Sáez, et al.. (1999). Isoform-specific insertion near the Grb2-binding domain modulates the intrinsic guanine nucleotide exchange activity of hSos1. Oncogene. 18(9). 1651–1661. 10 indexed citations
18.
Rojas, José M., Juan José R. Coque, Carmen Guerrero, et al.. (1996). A 15 amino acid stretch close to the Grb2-binding domain defines two differentially expressed hSos1 isoforms with markedly different Grb2 binding affinity and biological activity.. PubMed. 12(11). 2291–300. 10 indexed citations
19.
Nájera, Isabel, Douglas D. Richman, Isabel Olivares, et al.. (1994). Natural Occurrence of Drug Resistance Mutations in the Reverse Transcriptase of Human Immunodeficiency Virus Type 1 Isolates. AIDS Research and Human Retroviruses. 10(11). 1479–1488. 74 indexed citations
20.
López‐Galíndez, Cecilio, José M. Rojas, R Nájera, Douglas D. Richman, & Manuel Perucho. (1991). Characterization of genetic variation and 3'-azido-3'-deoxythymidine- resistance mutations of human immunodeficiency virus by the RNase A mismatch cleavage method.. Proceedings of the National Academy of Sciences. 88(10). 4280–4284. 45 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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