Maite Huarte

26.8k total citations · 9 hit papers
52 papers, 18.2k citations indexed

About

Maite Huarte is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Maite Huarte has authored 52 papers receiving a total of 18.2k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 35 papers in Cancer Research and 6 papers in Genetics. Recurrent topics in Maite Huarte's work include Cancer-related molecular mechanisms research (34 papers), RNA modifications and cancer (27 papers) and RNA Research and Splicing (26 papers). Maite Huarte is often cited by papers focused on Cancer-related molecular mechanisms research (34 papers), RNA modifications and cancer (27 papers) and RNA Research and Splicing (26 papers). Maite Huarte collaborates with scholars based in Spain, United States and Germany. Maite Huarte's co-authors include Luisa Statello, Ling‐Ling Chen, Chunjie Guo, John L. Rinn, Aviv Regev, Mitchell Guttman, Manuel Garber, Eric S. Lander, Francesco P. Marchese and B Bernstein and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Maite Huarte

51 papers receiving 18.0k citations

Hit Papers

Chromatin signature revea... 2006 2026 2012 2019 2009 2020 2009 2015 2010 1000 2.0k 3.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maite Huarte Spain 32 15.8k 13.4k 1.2k 958 784 52 18.2k
Richard I. Gregory United States 46 14.2k 0.9× 9.4k 0.7× 402 0.3× 839 0.9× 848 1.1× 80 16.2k
Sean M. Grimmond Australia 58 8.1k 0.5× 3.0k 0.2× 651 0.5× 1.3k 1.4× 796 1.0× 178 11.0k
Kun Qu China 41 7.4k 0.5× 4.0k 0.3× 471 0.4× 505 0.5× 1.2k 1.5× 103 9.5k
Jin‐Wu Nam South Korea 27 9.0k 0.6× 7.6k 0.6× 351 0.3× 479 0.5× 974 1.2× 58 11.1k
Philipp Kapranov United States 39 8.0k 0.5× 3.6k 0.3× 411 0.3× 1.2k 1.3× 2.1k 2.7× 94 11.2k
Ahmad M. Khalil United States 27 6.8k 0.4× 5.9k 0.4× 390 0.3× 539 0.6× 249 0.3× 96 8.1k
Lynne E. Maquat United States 73 15.7k 1.0× 2.2k 0.2× 462 0.4× 1.7k 1.8× 756 1.0× 161 18.2k
Ana Kozomara United Kingdom 6 7.6k 0.5× 6.3k 0.5× 260 0.2× 494 0.5× 630 0.8× 6 10.2k
Rosalind C. Lee United States 10 10.9k 0.7× 9.3k 0.7× 339 0.3× 529 0.6× 688 0.9× 10 13.7k

Countries citing papers authored by Maite Huarte

Since Specialization
Citations

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

Fields of papers citing papers by Maite Huarte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maite Huarte

This figure shows the co-authorship network connecting the top 25 collaborators of Maite Huarte. A scholar is included among the top collaborators of Maite Huarte 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 Maite Huarte. Maite Huarte 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.
Guerrero, Georgina, et al.. (2025). The lncRNA DUBR is regulated by CTCF and coordinates chromatin landscape and gene expression in hematopoietic cells. Nucleic Acids Research. 53(4). 1 indexed citations
2.
Goñi, Enrique, Jovanna González, Amaya Abad, et al.. (2024). Uncovering functional lncRNAs by scRNA-seq with ELATUS. Nature Communications. 15(1). 9709–9709. 5 indexed citations
3.
Statello, Luisa, et al.. (2024). The chromatin-associated lncREST ensures effective replication stress response by promoting the assembly of fork signaling factors. Nature Communications. 15(1). 978–978. 4 indexed citations
4.
Arcas, Aída, Luisa Statello, Enrique Goñi, et al.. (2024). YTHDC1 m6A-dependent and m6A-independent functions converge to preserve the DNA damage response. The EMBO Journal. 43(16). 3494–3522. 3 indexed citations
5.
Goñi, Enrique, Igor Ruiz de los Mozos, Aída Arcas, et al.. (2023). ORC1 binds to cis-transcribed RNAs for efficient activation of replication origins. Nature Communications. 14(1). 4447–4447. 13 indexed citations
6.
Statello, Luisa, Chunjie Guo, Ling‐Ling Chen, & Maite Huarte. (2021). Author Correction: Gene regulation by long non-coding RNAs and its biological functions. Nature Reviews Molecular Cell Biology. 22(2). 159–159. 99 indexed citations
7.
Mitra, Sanhita, Somsundar Veppil Muralidharan, Subazini Thankaswamy Kosalai, et al.. (2020). Subcellular Distribution of p53 by the p53-Responsive lncRNA NBAT1 Determines Chemotherapeutic Response in Neuroblastoma. Cancer Research. 81(6). 1457–1471. 25 indexed citations
8.
Aldaz, Paula, Jaione Auzmendi-Iriarte, Ander Saenz‐Antoñanzas, et al.. (2018). PR-LncRNA signature regulates glioma cell activity through expression of SOX factors. Scientific Reports. 8(1). 12746–12746. 11 indexed citations
9.
Li, Li, Pieter C. Van Breugel, Fabricio Loayza‐Puch, et al.. (2018). LncRNA-OIS1 regulates DPP4 activation to modulate senescence induced by RAS. Nucleic Acids Research. 46(8). 4213–4227. 42 indexed citations
10.
Huarte, Maite. (2016). p53 partners with RNA in the DNA damage response. Nature Genetics. 48(11). 1298–1299. 12 indexed citations
11.
Yoon, Je‐Hyun, Kotb Abdelmohsen, Subramanya Srikantan, et al.. (2013). LincRNA-p21 Suppresses Target mRNA Translation. Molecular Cell. 50(2). 303–303. 9 indexed citations
12.
Yoon, Je‐Hyun, Kotb Abdelmohsen, Subramanya Srikantan, et al.. (2012). LincRNA-p21 Suppresses Target mRNA Translation. Molecular Cell. 47(4). 648–655. 792 indexed citations breakdown →
13.
Rinn, John L. & Maite Huarte. (2011). To repress or not to repress: This is the guardian's question. Trends in Cell Biology. 21(6). 344–353. 46 indexed citations
14.
Qi, Hank H., Madathia Sarkissian, Gangqing Hu, et al.. (2010). Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development. Nature. 466(7305). 503–507. 234 indexed citations
15.
Huarte, Maite & John L. Rinn. (2010). Large non-coding RNAs: missing links in cancer?. Human Molecular Genetics. 19(R2). R152–R161. 412 indexed citations
16.
Khalil, Ahmad M., Mitchell Guttman, Maite Huarte, et al.. (2009). Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression. Proceedings of the National Academy of Sciences. 106(28). 11667–11672. 2331 indexed citations breakdown →
17.
Huarte, Maite. (2009). Journal club. Nature. 459(7246). 487–487. 3 indexed citations
18.
Iwase, Shigeki, Fei Lan, Peter Bayliss, et al.. (2007). The X-Linked Mental Retardation Gene SMCX/JARID1C Defines a Family of Histone H3 Lysine 4 Demethylases. Cell. 128(6). 1077–1088. 529 indexed citations breakdown →
19.
Affar, El Bachir, Frédérique Gay, Yujiang Geno Shi, et al.. (2006). Essential Dosage-Dependent Functions of the Transcription Factor Yin Yang 1 in Late Embryonic Development and Cell Cycle Progression. Molecular and Cellular Biology. 26(9). 3565–3581. 161 indexed citations
20.
Pérez-González, Alicia, Ariel Rodríguez-Frandsen, Maite Huarte, Íñigo J. Salanueva, & Amelia Nieto. (2006). hCLE/CGI-99, a Human Protein that Interacts with the Influenza Virus Polymerase, Is a mRNA Transcription Modulator. Journal of Molecular Biology. 362(5). 887–900. 43 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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