Rubén Agrelo

1.2k total citations
17 papers, 879 citations indexed

About

Rubén Agrelo is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Rubén Agrelo has authored 17 papers receiving a total of 879 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Surgery. Recurrent topics in Rubén Agrelo's work include Epigenetics and DNA Methylation (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and DNA Repair Mechanisms (3 papers). Rubén Agrelo is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and DNA Repair Mechanisms (3 papers). Rubén Agrelo collaborates with scholars based in Spain, Austria and Uruguay. Rubén Agrelo's co-authors include Manel Esteller, Mario F. Fraga, Anton Wutz, Fernando Setién, Jesús Espada, María J. Artiga, Antoni Castells, Michel Herranz, Santiago Ropero and Abdallah Souabni and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Rubén Agrelo

17 papers receiving 869 citations

Peers

Rubén Agrelo

GENET

ONCOL

PFM

Dorota Piekutowska‐Abramczuk Poland

Bartolomeo Augello Italy

Moonsook Lee United States

Charlie Degui Chen China

Daniel Savic United States

Rocío Acuña‐Hidalgo United States

Eric Bareke Canada

J. Barra France

Nicola Vickaryous Australia

Maxime Vallée France

Dorota Piekutowska‐Abramczuk Poland

Rubén Agrelo

773 ×1.1

181 ×0.8

GENET

86 ×0.6

67 ×0.6

ONCOL

32 ×0.5

PFM

Citations per year, relative to Rubén Agrelo Rubén Agrelo (= 1×) peers Dorota Piekutowska‐Abramczuk

Countries citing papers authored by Rubén Agrelo

Since Specialization

Citations

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

Fields of papers citing papers by Rubén Agrelo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rubén Agrelo

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

All Works

Sort: Min cites: Since: Top N: Style:

17 of 17 papers shown

Preussner, Jens, et al.. (2017). Promoter hypermethylation as a mechanism for Lamin A/C silencing in a subset of neuroblastoma cells. PLoS ONE. 12(4). e0175953–e0175953. 18 indexed citations

Agrelo, Rubén, et al.. (2015). A novel Werner Syndrome mutation: pharmacological treatment by read-through of nonsense mutations and epigenetic therapies. Epigenetics. 10(4). 329–341. 16 indexed citations

Agrelo, Rubén, Hiroyuki Kishimoto, Maria Novatchkova, et al.. (2013). SATB1 collaborates with loss of p16 in cellular transformation. Oncogene. 32(48). 5492–5500. 15 indexed citations

Agrelo, Rubén, et al.. (2012). From aging to cancer: a DNA methylation journey. 3(1). 4–4. 3 indexed citations

Agrelo, Rubén. (2011). X Inactivation and Progenitor Cancer Cells. Cancers. 3(2). 2169–2175. 3 indexed citations

Agrelo, Rubén & Anton Wutz. (2009). X inactivation and disease. Seminars in Cell and Developmental Biology. 21(2). 194–200. 14 indexed citations

Agrelo, Rubén & Anton Wutz. (2009). Cancer progenitors and epigenetic contexts: AnXisting connection. Epigenetics. 4(8). 568–570. 10 indexed citations

Agrelo, Rubén, Abdallah Souabni, Maria Novatchkova, et al.. (2009). SATB1 Defines the Developmental Context for Gene Silencing by Xist in Lymphoma and Embryonic Cells. Developmental Cell. 16(4). 507–516. 153 indexed citations

Agrelo, Rubén & Anton Wutz. (2009). ConteXt of change—X inactivation and disease. EMBO Molecular Medicine. 2(1). 6–15. 19 indexed citations

10.

Fraga, Mario F., Rubén Agrelo, & Manel Esteller. (2007). Cross‐Talk between Aging and Cancer. Annals of the New York Academy of Sciences. 1100(1). 60–74. 187 indexed citations

11.

Agrelo, Rubén. (2006). A new molecular model of cellular aging based on Werner syndrome. Medical Hypotheses. 68(4). 770–780. 5 indexed citations

12.

Castells, Antoni, Artemio Payá, Cristina Alenda, et al.. (2006). Cyclooxygenase 2 Expression in Colorectal Cancer with DNA Mismatch Repair Deficiency. Clinical Cancer Research. 12(6). 1686–1692. 28 indexed citations

13.

Agrelo, Rubén, Wen‐Hsing Cheng, Fernando Setién, et al.. (2006). Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer. Proceedings of the National Academy of Sciences. 103(23). 8822–8827. 188 indexed citations

14.

Agrelo, Rubén, Fernando Setién, Jesús Espada, et al.. (2005). Inactivation of the Lamin A/C Gene by CpG Island Promoter Hypermethylation in Hematologic Malignancies, and Its Association With Poor Survival in Nodal Diffuse Large B-Cell Lymphoma. Journal of Clinical Oncology. 23(17). 3940–3947. 111 indexed citations

15.

Pellisé, María, Antoni Castells, Àngels Ginès, et al.. (2004). Detection of Lymph Node Micrometastases by Gene Promoter Hypermethylation in Samples Obtained by Endosonography- Guided Fine-Needle Aspiration Biopsy. Clinical Cancer Research. 10(13). 4444–4449. 51 indexed citations

16.

Pellisé, María, Antoni Castells, Àngels Ginès, et al.. (2004). Detection of Lymph Node Micrometastases by Gene Promoter Hypermethylation in Samples Obtained by Endosonography-Guided Fine-Needle Aspiration Biopsy (EUS-FNA). Gastrointestinal Endoscopy. 59(5). P108–P108. 1 indexed citations

17.

Ballestar, Esteban, Santiago Ropero, Miguel Alaminos, et al.. (2004). The impact of MECP2 mutations in the expression patterns of Rett syndrome patients. Human Genetics. 116(1-2). 91–104. 57 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.

Explore authors with similar magnitude of impact