Fernando Setién

9.9k total citations · 1 hit paper
57 papers, 3.4k citations indexed

About

Fernando Setién is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Fernando Setién has authored 57 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 14 papers in Immunology and 9 papers in Genetics. Recurrent topics in Fernando Setién's work include Epigenetics and DNA Methylation (19 papers), RNA modifications and cancer (12 papers) and Cancer-related gene regulation (11 papers). Fernando Setién is often cited by papers focused on Epigenetics and DNA Methylation (19 papers), RNA modifications and cancer (12 papers) and Cancer-related gene regulation (11 papers). Fernando Setién collaborates with scholars based in Spain, United States and Netherlands. Fernando Setién's co-authors include Manel Esteller, Mario F. Fraga, Santiago Ropero, Esteban Ballestar, Miguel Alaminos, Montse Sánchez‐Céspedes, Alberto Villanueva, Celia Cerrato, Carlos Caldas and Amaia Lujambio and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Fernando Setién

57 papers receiving 3.4k citations

Hit Papers

Genetic Unmasking of an Epigenetically Silenced microRNA ... 2007 2026 2013 2019 2007 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fernando Setién Spain 30 2.7k 1.1k 403 337 324 57 3.4k
Stefan J. Erkeland Netherlands 25 3.2k 1.2× 2.5k 2.3× 496 1.2× 374 1.1× 325 1.0× 57 4.1k
Marian E. Durkin United States 31 2.1k 0.8× 944 0.9× 168 0.4× 455 1.4× 289 0.9× 55 3.0k
Steven Goossens Belgium 26 1.9k 0.7× 649 0.6× 409 1.0× 805 2.4× 242 0.7× 71 3.0k
Matteo Cesaroni United States 23 2.2k 0.8× 606 0.6× 297 0.7× 314 0.9× 186 0.6× 45 2.7k
Ann Kuo United States 13 2.9k 1.1× 357 0.3× 360 0.9× 397 1.2× 705 2.2× 14 3.4k
Mira Jeong United States 28 2.8k 1.0× 593 0.5× 763 1.9× 264 0.8× 416 1.3× 47 4.1k
Diana Bellavia Italy 30 1.9k 0.7× 564 0.5× 850 2.1× 636 1.9× 168 0.5× 57 3.0k
Thomas Mikeska Australia 22 2.0k 0.8× 543 0.5× 314 0.8× 508 1.5× 443 1.4× 45 2.7k
Rachel Deplus Belgium 14 3.1k 1.2× 522 0.5× 268 0.7× 256 0.8× 571 1.8× 18 3.6k
Lluís Morey United States 26 4.1k 1.5× 684 0.6× 234 0.6× 436 1.3× 595 1.8× 41 4.6k

Countries citing papers authored by Fernando Setién

Since Specialization
Citations

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

Fields of papers citing papers by Fernando Setién

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fernando Setién

This figure shows the co-authorship network connecting the top 25 collaborators of Fernando Setién. A scholar is included among the top collaborators of Fernando Setién 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 Setién. Fernando Setién 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.
Soares, Edilene Siqueira, Marta Soler, Fernando Setién, et al.. (2025). NEAT1-mediated regulation of proteostasis and mRNA localization impacts autophagy dysregulation in Rett syndrome. Nucleic Acids Research. 53(4). 2 indexed citations
2.
García‐Prieto, Carlos A., Gerardo Ferrer, Verónica Dávalos, et al.. (2024). A DNA methylation database of human and mouse hematological malignancy cell lines. Leukemia. 39(2). 512–515. 1 indexed citations
3.
Romero, Octavio A., Juan J. Alburquerque-Béjar, Antonio Gómez, et al.. (2021). SMARCA4 deficient tumours are vulnerable to KDM6A/UTX and KDM6B/JMJD3 blockade. Nature Communications. 12(1). 4319–4319. 36 indexed citations
4.
Hernández, Rosa Elena Huerta, Cristina Jiménez‐Luna, Raúl Ortíz, et al.. (2021). Impact of the Epigenetically Regulated Hoxa-5 Gene in Neural Differentiation from Human Adipose-Derived Stem Cells. Biology. 10(8). 802–802. 2 indexed citations
5.
Soler, Marta, Verónica Dávalos, Fernando Setién, et al.. (2021). The transcribed ultraconserved region uc.160+ enhances processing and A‐to‐I editing of the miR‐376 cluster: hypermethylation improves glioma prognosis. Molecular Oncology. 16(3). 648–664. 4 indexed citations
6.
Solanich, Xavier, Gardenia Vargas‐Parra, Caspar I. van der Made, et al.. (2021). Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19. Frontiers in Immunology. 12. 719115–719115. 74 indexed citations
7.
Palomeras, Sònia, Ángel Díaz‐Lagares, Gemma Viñas, et al.. (2019). Epigenetic silencing of TGFBI confers resistance to trastuzumab in human breast cancer. Breast Cancer Research. 21(1). 79–79. 50 indexed citations
8.
Paz, Alexia Martínez de, David Piñeyro, Anna Martínez‐Cardús, et al.. (2019). Epigenetic inactivation of the splicing RNA-binding protein CELF2 in human breast cancer. Oncogene. 38(45). 7106–7112. 49 indexed citations
9.
Vaclová, Tereza, Gonzalo Goméz-López, Fernando Setién, et al.. (2015). DNA repair capacity is impaired in healthy BRCA1 heterozygous mutation carriers. Breast Cancer Research and Treatment. 152(2). 271–282. 24 indexed citations
10.
Anadon, Carmen M., Sònia Guil, Laia Simó‐Riudalbas, et al.. (2015). Gene amplification-associated overexpression of the RNA editing enzyme ADAR1 enhances human lung tumorigenesis. Oncogene. 35(33). 4407–4413. 95 indexed citations
11.
12.
Taniguchi, Hiroaki, Agustín F. Fernández, Fernando Setién, et al.. (2009). Epigenetic Inactivation of the Circadian Clock Gene BMAL1 in Hematologic Malignancies. Cancer Research. 69(21). 8447–8454. 146 indexed citations
13.
Lopez‐Serra, Lidia, Esteban Ballestar, Santiago Ropero, et al.. (2008). Unmasking of epigenetically silenced candidate tumor suppressor genes by removal of methyl-CpG-binding domain proteins. Oncogene. 27(25). 3556–3566. 47 indexed citations
14.
Lujambio, Amaia, Santiago Ropero, Esteban Ballestar, et al.. (2007). Genetic Unmasking of an Epigenetically Silenced microRNA in Human Cancer Cells. Cancer Research. 67(4). 1424–1429. 729 indexed citations breakdown →
15.
Martínez, Ramón, et al.. (2007). CpG island promoter hypermethylation of the pro-apoptotic gene caspase-8 is a common hallmark of relapsed glioblastoma multiforme. Carcinogenesis. 28(6). 1264–1268. 78 indexed citations
16.
Lopez‐Serra, Lidia, Esteban Ballestar, Mario F. Fraga, et al.. (2006). A Profile of Methyl-CpG Binding Domain Protein Occupancy of Hypermethylated Promoter CpG Islands of Tumor Suppressor Genes in Human Cancer. Cancer Research. 66(17). 8342–8346. 102 indexed citations
17.
Zamorano, José Luís, et al.. (2005). Proteolytic Regulation of Activated STAT6 by Calpains. The Journal of Immunology. 174(5). 2843–2848. 21 indexed citations
18.
Oteo, Marta, et al.. (2001). Structural characterization of two CD1A allelic variants. Human Immunology. 62(10). 1137–1141. 11 indexed citations
19.
Álvarez, Victoria, et al.. (1996). Molecular evolution of the N-formyl peptide and C5a receptors in non-human primates. Immunogenetics. 44(6). 446–452. 31 indexed citations
20.
Álvarez, Victoria, et al.. (1995). Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components. American Journal of Medical Genetics. 55(4). 408–413. 2 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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