Ignacio Varela

33.1k total citations · 2 hit papers
54 papers, 3.3k citations indexed

About

Ignacio Varela is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, Ignacio Varela has authored 54 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 15 papers in Cancer Research and 11 papers in Hematology. Recurrent topics in Ignacio Varela's work include Cancer Genomics and Diagnostics (11 papers), Nuclear Structure and Function (10 papers) and Acute Myeloid Leukemia Research (10 papers). Ignacio Varela is often cited by papers focused on Cancer Genomics and Diagnostics (11 papers), Nuclear Structure and Function (10 papers) and Acute Myeloid Leukemia Research (10 papers). Ignacio Varela collaborates with scholars based in Spain, United States and United Kingdom. Ignacio Varela's co-authors include Carlos López-Otı́n, José M.P. Freije, Juan Cadiñanos, Alejandro P. Ugalde, Fernando G. Osorio, Laura González-Silva, Colin L. Stewart, Karl Tryggvason, Alberto M. Pendás and Félix de Carlos Villafranca and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Ignacio Varela

52 papers receiving 3.3k citations

Hit Papers

Targeted gene correction of α1-antitrypsin deficiency in ... 2011 2026 2016 2021 2011 2015 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ignacio Varela Spain 23 2.4k 599 569 386 343 54 3.3k
Borja Sáez United States 22 1.7k 0.7× 772 1.3× 432 0.8× 422 1.1× 423 1.2× 41 2.8k
Frédéric Mazurier France 29 1.6k 0.7× 758 1.3× 457 0.8× 498 1.3× 499 1.5× 67 2.8k
Min Luo China 26 2.3k 1.0× 985 1.6× 882 1.6× 344 0.9× 339 1.0× 55 3.3k
Naoko Minegishi Japan 29 1.4k 0.6× 907 1.5× 394 0.7× 258 0.7× 410 1.2× 74 2.7k
Matthew R. Warr United States 17 1.6k 0.7× 876 1.5× 308 0.5× 383 1.0× 454 1.3× 30 2.9k
Stephen M. Sykes United States 27 2.4k 1.0× 765 1.3× 387 0.7× 996 2.6× 302 0.9× 80 3.6k
Samirkumar B. Amin United States 18 1.3k 0.5× 503 0.8× 686 1.2× 453 1.2× 162 0.5× 43 2.3k
Kimberly Straley United States 16 1.3k 0.5× 358 0.6× 743 1.3× 366 0.9× 470 1.4× 25 3.1k
Peng Ji United States 28 1.4k 0.6× 322 0.5× 274 0.5× 372 1.0× 391 1.1× 112 2.4k
Josée Hébert Canada 33 2.2k 0.9× 947 1.6× 389 0.7× 550 1.4× 257 0.7× 93 3.1k

Countries citing papers authored by Ignacio Varela

Since Specialization
Citations

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

Fields of papers citing papers by Ignacio Varela

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ignacio Varela

This figure shows the co-authorship network connecting the top 25 collaborators of Ignacio Varela. A scholar is included among the top collaborators of Ignacio Varela 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 Ignacio Varela. Ignacio Varela 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.
García-Gutiérrez, Lucia, Virginia G. de Yébenes, Rosa Blanco, et al.. (2023). MYC directly transactivates CR2/CD21, the receptor of the Epstein–Barr virus, enhancing the viral infection of Burkitt lymphoma cells. Oncogene. 42(45). 3358–3370. 6 indexed citations
2.
Varela, Ignacio, et al.. (2022). Role of SWI/SNF chromatin remodeling genes in lung cancer development. Biochemical Society Transactions. 50(3). 1143–1150. 9 indexed citations
3.
Moreno-Rodriguez, Thaidy, Laura González-Silva, Carlos Revilla, et al.. (2021). ARID2 deficiency promotes tumor progression and is associated with higher sensitivity to chemotherapy in lung cancer. Oncogene. 40(16). 2923–2935. 24 indexed citations
4.
Casar, Berta, Anna Esteve‐Codina, Marta Gut, et al.. (2021). PLCγ1/PKCθ Downstream Signaling Controls Cutaneous T-Cell Lymphoma Development and Progression. Journal of Investigative Dermatology. 142(5). 1391–1400.e15. 8 indexed citations
5.
Angrigiani, Claudio, et al.. (2021). The Deltopectoral/Internal Mammary Artery Perforator Flap Revisited. Annals of Plastic Surgery. 88(1). 88–92. 5 indexed citations
6.
Barrios, Oriol de, Juan L. Trincado, Antonio Agraz-Doblás, et al.. (2020). HDAC7 is a major contributor in the pathogenesis of infant t(4;11) proB acute lymphoblastic leukemia. Leukemia. 35(7). 2086–2091. 9 indexed citations
7.
Lange, Sebastian, Thomas Engleitner, Sebastian Mueller, et al.. (2020). Analysis pipelines for cancer genome sequencing in mice. Nature Protocols. 15(2). 266–315. 16 indexed citations
8.
Lafita‐Navarro, M. Carmen, Judit Liaño-Pons, Andrea Quintanilla, et al.. (2020). The MNT transcription factor autoregulates its expression and supports proliferation in MYC-associated factor X (MAX)-deficient cells. Journal of Biological Chemistry. 295(7). 2001–2017. 11 indexed citations
9.
Bueno, Clara, Fernando J. Calero‐Nieto, Xiaonan Wang, et al.. (2019). Enhanced hemato-endothelial specification during human embryonic differentiation through developmental cooperation between AF4-MLL and MLL-AF4 fusions. Haematologica. 104(6). 1189–1201. 14 indexed citations
10.
Agraz-Doblás, Antonio, Clara Bueno, Rachael Bashford-Rogers, et al.. (2019). Unraveling the cellular origin and clinical prognostic markers of infant B-cell acute lymphoblastic leukemia using genome-wide analysis. Haematologica. 104(6). 1176–1188. 60 indexed citations
11.
Osorio, Fernando G., Axel Rosendahl Huber, Rurika Oka, et al.. (2018). Somatic Mutations Reveal Lineage Relationships and Age-Related Mutagenesis in Human Hematopoiesis. Cell Reports. 25(9). 2308–2316.e4. 151 indexed citations
12.
Torices, Silvia, Lorena Álvarez‐Rodríguez, Lara Grande, et al.. (2015). A Truncated Variant of ASCC1, a Novel Inhibitor of NF-κB, Is Associated with Disease Severity in Patients with Rheumatoid Arthritis. The Journal of Immunology. 195(11). 5415–5420. 18 indexed citations
13.
McKerrell, Thomas, Naomi Park, Thaidy Moreno-Rodriguez, et al.. (2015). Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis. Cell Reports. 10(8). 1239–1245. 357 indexed citations breakdown →
14.
Portillo, Isidro Prieto del, et al.. (2014). El paciente con cáncer en la unidad de vigilancia intensiva. Nuevas perspectivas. Revista Clínica Española. 214(7). 403–409. 2 indexed citations
15.
Bolli, Niccolò, Nicla Manes, Thomas McKerrell, et al.. (2014). Characterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol. Haematologica. 100(2). 214–222. 37 indexed citations
16.
Ugalde, Alejandro P., Andrew Ramsay, Jorge de la Rosa, et al.. (2011). Aging and chronic DNA damage response activate a regulatory pathway involving miR‐29 and p53. The EMBO Journal. 30(11). 2219–2232. 198 indexed citations
17.
Varela, Ignacio, Christiaan Klijn, P. J. Stephens, et al.. (2010). Somatic structural rearrangements in genetically engineered mouse mammary tumors. Genome biology. 11(10). R100–R100. 19 indexed citations
18.
Espada, Jesús, Ignacio Varela, Ignacio Flores, et al.. (2008). Nuclear envelope defects cause stem cell dysfunction in premature-aging mice. The Journal of Cell Biology. 181(1). 27–35. 133 indexed citations
19.
Varela, Ignacio, Juan Cadiñanos, Alberto M. Pendás, et al.. (2005). Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation. Nature. 437(7058). 564–568. 367 indexed citations
20.
Cadiñanos, Juan, Ignacio Varela, Carlos López-Otı́n, & José M.P. Freije. (2005). From Immature Lamin to Premature Aging: Molecular Pathways and Therapeutic Opportunities. Cell Cycle. 4(12). 1732–1735. 25 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

Rankless by CCL
2026