Luisa Luna

1.7k total citations
36 papers, 1.3k citations indexed

About

Luisa Luna is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Luisa Luna has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 8 papers in Cancer Research and 7 papers in Genetics. Recurrent topics in Luisa Luna's work include DNA Repair Mechanisms (25 papers), RNA modifications and cancer (7 papers) and DNA and Nucleic Acid Chemistry (7 papers). Luisa Luna is often cited by papers focused on DNA Repair Mechanisms (25 papers), RNA modifications and cancer (7 papers) and DNA and Nucleic Acid Chemistry (7 papers). Luisa Luna collaborates with scholars based in Norway, United States and United Kingdom. Luisa Luna's co-authors include Magnar Bjørås, Erling Seeberg, Christine Gran Neurauter, Gunn A. Hildrestrand, Veslemøy Rolseth, Silje Zandstra Krokeide, Stefan Krauß, Laurence H. Pearl, Tracey E. Barrett and Rajikala Suganthan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

Luisa Luna

36 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luisa Luna Norway 21 1.1k 189 177 116 97 36 1.3k
X-J Yang China 10 1.1k 1.0× 143 0.8× 158 0.9× 199 1.7× 70 0.7× 19 1.3k
Geneviève P. Delcuve Canada 15 988 0.9× 121 0.6× 182 1.0× 142 1.2× 44 0.5× 21 1.3k
Joel D. Nelson United States 8 851 0.8× 141 0.7× 94 0.5× 121 1.0× 62 0.6× 9 1.1k
Elena Zelin United States 13 1.1k 1.0× 237 1.3× 151 0.9× 157 1.4× 131 1.4× 14 1.4k
Masayoshi Iizuka Japan 15 1.0k 0.9× 90 0.5× 175 1.0× 140 1.2× 48 0.5× 36 1.3k
Haiqing Fu United States 25 1.5k 1.3× 149 0.8× 210 1.2× 292 2.5× 116 1.2× 51 1.7k
Trent Su United States 19 835 0.7× 188 1.0× 125 0.7× 108 0.9× 72 0.7× 28 1.3k
Amandine Bastide France 20 879 0.8× 168 0.9× 61 0.3× 86 0.7× 59 0.6× 27 1.2k
Sarah Hevi United States 10 1.6k 1.4× 122 0.6× 368 2.1× 71 0.6× 68 0.7× 12 1.8k

Countries citing papers authored by Luisa Luna

Since Specialization
Citations

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

Fields of papers citing papers by Luisa Luna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luisa Luna

This figure shows the co-authorship network connecting the top 25 collaborators of Luisa Luna. A scholar is included among the top collaborators of Luisa 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 Luisa Luna. Luisa 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, Luisa, Anna Lång, Stig Ove Bøe, et al.. (2024). Depletion of the m1A writer TRMT6/TRMT61A reduces proliferation and resistance against cellular stress in bladder cancer. Frontiers in Oncology. 13. 1334112–1334112. 11 indexed citations
2.
Rolseth, Veslemøy, Luisa Luna, Ann‐Karin Olsen, et al.. (2017). No cancer predisposition or increased spontaneous mutation frequencies in NEIL DNA glycosylases-deficient mice. Scientific Reports. 7(1). 4384–4384. 35 indexed citations
3.
Fernández, José Francisco Díaz, et al.. (2015). Carcinoma adenoescamoso de la vesícula biliar, una rara variedad histológica. Revista Colombiana de Cirugía. 30(3). 246–252. 2 indexed citations
4.
Yang, Mingyi, Luisa Luna, Jan Sörbo, et al.. (2014). Human OXR1 maintains mitochondrial DNA integrity and counteracts hydrogen peroxide-induced oxidative stress by regulating antioxidant pathways involving p21. Free Radical Biology and Medicine. 77. 41–48. 58 indexed citations
5.
Krokeide, Silje Zandstra, Jon K. Laerdahl, Luisa Luna, et al.. (2013). Human NEIL3 is mainly a monofunctional DNA glycosylase removing spiroimindiohydantoin and guanidinohydantoin. DNA repair. 12(12). 1159–1164. 80 indexed citations
6.
Rollag, Halvor, et al.. (2012). The Chromatin Remodeling Factor SMARCB1 Forms a Complex with Human Cytomegalovirus Proteins UL114 and UL44. PLoS ONE. 7(3). e34119–e34119. 12 indexed citations
7.
Yndestad, Arne, Christine Gran Neurauter, Erik Øie, et al.. (2009). Up-regulation of myocardial DNA base excision repair activities in experimental heart failure. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 666(1-2). 32–38. 13 indexed citations
8.
Dale, Hege Avsnes, et al.. (2008). Characterization of Human Cytomegalovirus Uracil DNA Glycosylase (UL114) and Its Interaction with Polymerase Processivity Factor (UL44). Journal of Molecular Biology. 381(2). 276–288. 28 indexed citations
9.
Krokeide, Silje Zandstra, Nils Bolstad, Jon K. Laerdahl, Magnar Bjørås, & Luisa Luna. (2008). Expression and purification of NEIL3, a human DNA glycosylase homolog. Protein Expression and Purification. 65(2). 160–164. 24 indexed citations
10.
Rolseth, Veslemøy, Elise Rundén‐Pran, Christine Gran Neurauter, et al.. (2008). Base excision repair activities in organotypic hippocampal slice cultures exposed to oxygen and glucose deprivation. DNA repair. 7(6). 869–878. 12 indexed citations
11.
Hildrestrand, Gunn A., Dzung B. Diep, David Kunke, et al.. (2007). The capacity to remove 8-oxoG is enhanced in newborn neural stem/progenitor cells and decreases in juvenile mice and upon cell differentiation. DNA repair. 6(6). 723–732. 18 indexed citations
12.
Hildrestrand, Gunn A., Veslemøy Rolseth, Magnar Bjørås, & Luisa Luna. (2007). Human NEIL1 localizes with the centrosomes and condensed chromosomes during mitosis. DNA repair. 6(10). 1425–1433. 5 indexed citations
13.
Bjørås, Magnar, et al.. (2006). Human cytomegalovirus infection modulates DNA base excision repair in fibroblast cells. Virology. 348(2). 389–397. 12 indexed citations
14.
Olsen, Petter Angell, et al.. (2005). Genomic sequence correction by single‐stranded DNA oligonucleotides: role of DNA synthesis and chemical modifications of the oligonucleotide ends. The Journal of Gene Medicine. 7(12). 1534–1544. 53 indexed citations
15.
Luna, Luisa. (2005). Dynamic relocalization of hOGG1 during the cell cycle is disrupted in cells harbouring the hOGG1-Cys326 polymorphic variant. Nucleic Acids Research. 33(6). 1813–1824. 79 indexed citations
16.
Luna, Luisa, et al.. (2004). Product inhibition and magnesium modulate the dual reaction mode of hOgg1. DNA repair. 4(3). 381–387. 39 indexed citations
17.
Dantzer, Françoise, Magnar Bjørås, Luisa Luna, Arne Klungland, & Erling Seeberg. (2003). Comparative analysis of 8-oxoG:C, 8-oxoG:A, A:C and C:C DNA repair in extracts from wild type or 8-oxoG DNA glycosylase deficient mammalian and bacterial cells. DNA repair. 2(6). 707–718. 17 indexed citations
18.
Bjørås, Magnar, Erling Seeberg, Luisa Luna, Laurence H. Pearl, & Tracey E. Barrett. (2002). Reciprocal “flipping” underlies substrate recognition and catalytic activation by the human 8-oxo-guanine DNA glycosylase. Journal of Molecular Biology. 317(2). 171–177. 98 indexed citations
19.
20.
Luna, Luisa, et al.. (1995). Structural Organization and Mapping of the Human TCF11 Gene. Genomics. 27(2). 237–244. 32 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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