Rosa Luna

7.7k total citations
40 papers, 2.0k citations indexed

About

Rosa Luna is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Rosa Luna has authored 40 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Oncology. Recurrent topics in Rosa Luna's work include RNA Research and Splicing (17 papers), RNA modifications and cancer (13 papers) and DNA Repair Mechanisms (11 papers). Rosa Luna is often cited by papers focused on RNA Research and Splicing (17 papers), RNA modifications and cancer (13 papers) and DNA Repair Mechanisms (11 papers). Rosa Luna collaborates with scholars based in Spain, United States and France. Rosa Luna's co-authors include Andrés Aguilera, Cristina González‐Aguilera, Belén Gómez‐González, Marı́a Garcı́a-Rubio, Pablo Huertas, Sónia Barroso, Ana G. Rondón, José A. Pintor‐Toro, Sonia Jimeno and Cristina Tous and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Rosa Luna

38 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rosa Luna Spain 24 1.7k 360 213 169 168 40 2.0k
Douglas A. Holtzman United States 13 1.7k 1.0× 325 0.9× 182 0.9× 217 1.3× 364 2.2× 15 2.1k
David B. Whyte United States 11 1.3k 0.8× 532 1.5× 186 0.9× 74 0.4× 224 1.3× 15 1.8k
Rafael E. Herrera United States 16 2.2k 1.3× 969 2.7× 261 1.2× 190 1.1× 249 1.5× 23 2.6k
Miriam Fuchs United States 10 1.7k 1.0× 419 1.2× 152 0.7× 208 1.2× 117 0.7× 10 2.0k
Mohamed Guermah United States 19 1.9k 1.1× 212 0.6× 199 0.9× 151 0.9× 83 0.5× 23 2.2k
Maria K. Mateyak United States 15 1.9k 1.1× 706 2.0× 303 1.4× 175 1.0× 232 1.4× 18 2.2k
Gonosuke Sonoda United States 17 1.3k 0.7× 369 1.0× 334 1.6× 220 1.3× 185 1.1× 25 2.0k
Nathalie Scamuffa France 16 864 0.5× 176 0.5× 172 0.8× 132 0.8× 211 1.3× 21 1.4k
Zhen-Qiang Pan United States 13 1.2k 0.7× 507 1.4× 229 1.1× 154 0.9× 205 1.2× 15 1.4k
Ruth A. Gjerset United States 23 1.1k 0.6× 527 1.5× 105 0.5× 200 1.2× 75 0.4× 44 1.5k

Countries citing papers authored by Rosa Luna

Since Specialization
Citations

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

Fields of papers citing papers by Rosa Luna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rosa Luna

This figure shows the co-authorship network connecting the top 25 collaborators of Rosa Luna. A scholar is included among the top collaborators of Rosa Luna 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 Rosa Luna. Rosa Luna 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.
Luna, Rosa, et al.. (2023). Genetic diversity in creole pigs in south central Peru. Tropical Animal Health and Production. 55(6). 426–426.
2.
3.
Barroso, Sónia, Ana G. Rondón, Mónica Pérez-Alegre, et al.. (2019). Depletion of the MFAP1/SPP381 Splicing Factor Causes R-Loop-Independent Genome Instability. Cell Reports. 28(6). 1551–1563.e7. 14 indexed citations
4.
Luna, Rosa, et al.. (2019). The THO Complex as a Paradigm for the Prevention of Cotranscriptional R-Loops. Cold Spring Harbor Symposia on Quantitative Biology. 84. 105–114. 30 indexed citations
5.
Santos-Pereira, José M., et al.. (2016). Excess of Yra1 RNA-Binding Factor Causes Transcription-Dependent Genome Instability, Replication Impairment and Telomere Shortening. PLoS Genetics. 12(4). e1005966–e1005966. 20 indexed citations
6.
Santos-Pereira, José M., Marı́a Garcı́a-Rubio, Cristina González‐Aguilera, Rosa Luna, & Andrés Aguilera. (2014). A genome-wide function of THSC/TREX-2 at active genes prevents transcription–replication collisions. Nucleic Acids Research. 42(19). 12000–12014. 17 indexed citations
7.
Gallardo, Mercedes, et al.. (2013). R-Loop Mediated Transcription-Associated Recombination in trf4Δ Mutants Reveals New Links between RNA Surveillance and Genome Integrity. PLoS ONE. 8(6). e65541–e65541. 39 indexed citations
8.
Escoubet‐Lozach, Laure, Christopher Benner, Minna U. Kaikkonen, et al.. (2011). Mechanisms Establishing TLR4-Responsive Activation States of Inflammatory Response Genes. PLoS Genetics. 7(12). e1002401–e1002401. 113 indexed citations
9.
González‐Aguilera, Cristina, et al.. (2011). Nab2 functions in the metabolism of RNA driven by polymerases II and III. Molecular Biology of the Cell. 22(15). 2729–2740. 24 indexed citations
10.
Luna, Rosa, Ana G. Rondón, & Andrés Aguilera. (2011). New clues to understand the role of THO and other functionally related factors in mRNP biogenesis. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1819(6). 514–520. 70 indexed citations
11.
Barroso, Sónia, et al.. (2011). Genome Instability and Transcription Elongation Impairment in Human Cells Depleted of THO/TREX. PLoS Genetics. 7(12). e1002386–e1002386. 188 indexed citations
12.
Lorès, Patrick, Orane Visvikis, Rosa Luna, Emmanuel Lemichez, & Gérard Gâcon. (2010). The SWI/SNF protein BAF60b is ubiquitinated through a signalling process involving Rac GTPase and the RING finger protein Unkempt. FEBS Journal. 277(6). 1453–1464. 20 indexed citations
13.
González‐Aguilera, Cristina, Cristina Tous, Belén Gómez‐González, et al.. (2008). The THP1-SAC3-SUS1-CDC31 Complex Works in Transcription Elongation-mRNA Export Preventing RNA-mediated Genome Instability. Molecular Biology of the Cell. 19(10). 4310–4318. 116 indexed citations
14.
Luna, Rosa, Hélène Gaillard, Cristina González‐Aguilera, & Andrés Aguilera. (2008). Biogenesis of mRNPs: integrating different processes in the eukaryotic nucleus. Chromosoma. 117(4). 319–331. 89 indexed citations
15.
Garcı́a-Rubio, Marı́a, Sebastián Chávez, Pablo Huertas, et al.. (2007). Different physiological relevance of yeast THO/TREX subunits in gene expression and genome integrity. Molecular Genetics and Genomics. 279(2). 123–132. 30 indexed citations
16.
Huertas, Pablo, Marı́a Garcı́a-Rubio, Ralf Erik Wellinger, Rosa Luna, & Andrés Aguilera. (2006). An hpr1 Point Mutation That Impairs Transcription and mRNP Biogenesis without Increasing Recombination. Molecular and Cellular Biology. 26(20). 7451–7465. 36 indexed citations
17.
Kim, Tae Hoon, Leah O. Barrera, Chunxu Qu, et al.. (2005). Direct isolation and identification of promoters in the human genome. Genome Research. 15(6). 830–839. 67 indexed citations
18.
Luna, Rosa, et al.. (2005). Interdependence between Transcription and mRNP Processing and Export, and Its Impact on Genetic Stability. Molecular Cell. 18(6). 711–722. 100 indexed citations
19.
Ramos‐Morales, Francisco, Francisco Romero, Rosa Luna, et al.. (2000). Cell cycle regulated expression and phosphorylation of hpttg proto-oncogene product. Oncogene. 19(3). 403–409. 92 indexed citations
20.
Lorès, Patrick, et al.. (1997). Enhanced apoptosis in the thymus of transgenic mice expressing constitutively activated forms of human Rac2GTPase. Oncogene. 15(5). 601–605. 66 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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