Francesca Mateo

2.1k total citations
18 papers, 672 citations indexed

About

Francesca Mateo is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Francesca Mateo has authored 18 papers receiving a total of 672 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Oncology and 4 papers in Cell Biology. Recurrent topics in Francesca Mateo's work include Ubiquitin and proteasome pathways (5 papers), Cancer-related Molecular Pathways (5 papers) and Microtubule and mitosis dynamics (4 papers). Francesca Mateo is often cited by papers focused on Ubiquitin and proteasome pathways (5 papers), Cancer-related Molecular Pathways (5 papers) and Microtubule and mitosis dynamics (4 papers). Francesca Mateo collaborates with scholars based in Spain, United States and Italy. Francesca Mateo's co-authors include Miguel Ángel Pujana, Oriol Bachs, María Jesús Pujol, Eduardo Eyras, Belén Miñana, Babita Singh, Amadís Pagès, Juan Valcárcel, Endre Sebestyén and Núria Canela-Canela and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Francesca Mateo

17 papers receiving 667 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francesca Mateo Spain 13 582 148 144 63 53 18 672
Seiji Tachiiri Japan 10 547 0.9× 224 1.5× 154 1.1× 41 0.7× 49 0.9× 13 736
Shishan Deng China 13 390 0.7× 135 0.9× 177 1.2× 67 1.1× 58 1.1× 31 520
Shih-Ya Wang United States 8 666 1.1× 203 1.4× 136 0.9× 74 1.2× 47 0.9× 9 751
Zhanwen Du United States 13 712 1.2× 130 0.9× 258 1.8× 43 0.7× 36 0.7× 17 867
Dongxue Su China 9 570 1.0× 216 1.5× 112 0.8× 77 1.2× 54 1.0× 12 691
Sudha Mannava United States 9 631 1.1× 207 1.4× 201 1.4× 67 1.1× 25 0.5× 11 757
Boyko S. Atanassov United States 12 618 1.1× 195 1.3× 90 0.6× 43 0.7× 32 0.6× 20 729
Joanna Maria Merchut‐Maya Denmark 9 530 0.9× 273 1.8× 72 0.5× 85 1.3× 35 0.7× 12 687
Blanca Felipe‐Abrio Spain 14 557 1.0× 146 1.0× 292 2.0× 116 1.8× 70 1.3× 17 759
Hongli Hu United States 6 420 0.7× 116 0.8× 149 1.0× 28 0.4× 31 0.6× 6 565

Countries citing papers authored by Francesca Mateo

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Mateo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Mateo

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

All Works

18 of 18 papers shown
1.
Trujillo‐Quintero, Juan Pablo, Anna Brunet‐Vega, Nino Spataro, et al.. (2025). A Novel RHEB Germline Variant Associated With Intellectual Disability and Epilepsy: Expanding the Spectrum of mTORopathies. Clinical Genetics. 108(2). 218–223.
2.
3.
Palomero, Luís, Lubomir Bodnar, Francesca Mateo, et al.. (2020). EVI1 as a Prognostic and Predictive Biomarker of Clear Cell Renal Cell Carcinoma. Cancers. 12(2). 300–300. 9 indexed citations
4.
Çubuk, Cankut, Marta R. Hidalgo, Alicia Amadoz, et al.. (2019). Differential metabolic activity and discovery of therapeutic targets using summarized metabolic pathway models. npj Systems Biology and Applications. 5(1). 7–7. 29 indexed citations
5.
Pellegrino, Benedetta, Alba Llop‐Guevara, Cristina Cruz, et al.. (2019). PARP inhibition increases immune infiltration in homologous recombination repair (HRR)-deficient tumors. Annals of Oncology. 30. v760–v760. 3 indexed citations
6.
Çubuk, Cankut, Marta R. Hidalgo, Alicia Amadoz, et al.. (2018). Gene Expression Integration into Pathway Modules Reveals a Pan-Cancer Metabolic Landscape. Cancer Research. 78(21). 6059–6072. 29 indexed citations
7.
Marín, Silvia, Pedro de Atauri, Francesca Mateo, et al.. (2018). Untargeted metabolomics reveals distinct metabolic reprogramming in endothelial cells co-cultured with CSC and non-CSC prostate cancer cell subpopulations. PLoS ONE. 13(2). e0192175–e0192175. 13 indexed citations
8.
Puig‐Butillé, Joan Anton, Antònia Vinyals, Paula Aguilera, et al.. (2017). AURKA Overexpression Is Driven by FOXM1 and MAPK/ERK Activation in Melanoma Cells Harboring BRAF or NRAS Mutations: Impact on Melanoma Prognosis and Therapy. Journal of Investigative Dermatology. 137(6). 1297–1310. 44 indexed citations
9.
Sebestyén, Endre, Babita Singh, Belén Miñana, et al.. (2016). Large-scale analysis of genome and transcriptome alterations in multiple tumors unveils novel cancer-relevant splicing networks. Genome Research. 26(6). 732–744. 193 indexed citations
10.
Bassi, C., Kathleen Joy O. Khu, Francesca Mateo, et al.. (2016). The acetyltransferase Tip60 contributes to mammary tumorigenesis by modulating DNA repair. Cell Death and Differentiation. 23(7). 1198–1208. 55 indexed citations
11.
Gallastegui, Edurne, et al.. (2013). Histone Deacetylase 3 Regulates Cyclin A Stability. Journal of Biological Chemistry. 288(29). 21096–21104. 27 indexed citations
12.
Mateo, Francesca, Pedro L. Fernández, & Timothy M. Thomson. (2013). Stem cells in prostate cancer.. PubMed. 66(5). 475–86. 6 indexed citations
13.
Guerra‐Rebollo, Marta, Francesca Mateo, Kristin Franke, et al.. (2012). Nucleolar exit of RNF8 and BRCA1 in response to DNA damage. Experimental Cell Research. 318(18). 2365–2376. 25 indexed citations
14.
Mateo, Francesca, et al.. (2010). Nuclear translocation of glyceraldehyde-3-phosphate dehydrogenase is regulated by acetylation. The International Journal of Biochemistry & Cell Biology. 42(10). 1672–1680. 102 indexed citations
15.
Mateo, Francesca, et al.. (2010). Acetylation of cyclin A: a new cell cycle regulatory mechanism. Biochemical Society Transactions. 38(1). 83–86. 16 indexed citations
16.
Mateo, Francesca, Núria Canela-Canela, Annalisa Zecchin, et al.. (2009). The transcriptional co-activator PCAF regulates cdk2 activity. Nucleic Acids Research. 37(21). 7072–7084. 33 indexed citations
17.
Mateo, Francesca, Núria Canela-Canela, Luca Busino, et al.. (2009). Degradation of cyclin A is regulated by acetylation. Oncogene. 28(29). 2654–2666. 49 indexed citations
18.
Canela-Canela, Núria, Mar Orzáez, Raquel Fucho, et al.. (2006). Identification of an Hexapeptide That Binds to a Surface Pocket in Cyclin A and Inhibits the Catalytic Activity of the Complex Cyclin-dependent Kinase 2-Cyclin A. Journal of Biological Chemistry. 281(47). 35942–35953. 38 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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