Alex Pines

2.3k total citations
41 papers, 1.8k citations indexed

About

Alex Pines is a scholar working on Molecular Biology, Oncology and Physiology. According to data from OpenAlex, Alex Pines has authored 41 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 11 papers in Oncology and 5 papers in Physiology. Recurrent topics in Alex Pines's work include DNA Repair Mechanisms (25 papers), RNA modifications and cancer (6 papers) and CRISPR and Genetic Engineering (6 papers). Alex Pines is often cited by papers focused on DNA Repair Mechanisms (25 papers), RNA modifications and cancer (6 papers) and CRISPR and Genetic Engineering (6 papers). Alex Pines collaborates with scholars based in Netherlands, Italy and United States. Alex Pines's co-authors include Leon H.F. Mullenders, Gianluca Tell, Martijn S. Luijsterburg, Mischa G. Vrouwe, Haico van Attikum, Giuseppe Damante, Milena Romanello, Wim Vermeulen, Franco Quadrifoglio and Harry Vrieling and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Alex Pines

41 papers receiving 1.8k citations

Peers

Alex Pines
Aya Kita Japan
Todd M. Savarese United States
Bret B. Friday United States
Eric A. Hanse United States
Don Benjamin Switzerland
Aya Kita Japan
Alex Pines
Citations per year, relative to Alex Pines Alex Pines (= 1×) peers Aya Kita

Countries citing papers authored by Alex Pines

Since Specialization
Citations

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

Fields of papers citing papers by Alex Pines

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alex Pines

This figure shows the co-authorship network connecting the top 25 collaborators of Alex Pines. A scholar is included among the top collaborators of Alex Pines 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 Alex Pines. Alex Pines 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.
Pai, Yun Jin, et al.. (2025). Transcription‐coupled repair: tangled up in convoluted repair. FEBS Journal. 292(20). 5288–5323. 2 indexed citations
2.
Zhou, Di, Anita Salmazo, Marjolein van Sluis, et al.. (2024). STK19 drives transcription-coupled repair by stimulating repair complex stability, RNA Pol II ubiquitylation, and TFIIH recruitment. Molecular Cell. 84(24). 4740–4757.e12. 13 indexed citations
3.
Theil, Arjan F., Gert‐Jan Kremers, Jeroen Demmers, et al.. (2023). Live cell transcription-coupled nucleotide excision repair dynamics revisited. DNA repair. 130. 103566–103566. 4 indexed citations
4.
Theil, Arjan F., Alex Pines, José María Heredia‐Genestar, et al.. (2023). Trichothiodystrophy‐associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation. EMBO Molecular Medicine. 15(11). e17973–e17973. 8 indexed citations
5.
Helfricht, Angela, Cristina Ribeiro-Silva, Anja Raams, et al.. (2023). Different SWI/SNF complexes coordinately promote R-loop- and RAD52-dependent transcription-coupled homologous recombination. Nucleic Acids Research. 51(17). 9055–9074. 23 indexed citations
6.
Kumar, Namrata, Arjan F. Theil, Vera Roginskaya, et al.. (2022). Global and transcription-coupled repair of 8-oxoG is initiated by nucleotide excision repair proteins. Nature Communications. 13(1). 974–974. 51 indexed citations
7.
Pines, Alex, Branislav Mišovic, Bob van de Water, et al.. (2020). Quantitative phosphoproteomics to unravel the cellular response to chemical stressors with different modes of action. Archives of Toxicology. 94(5). 1655–1671. 15 indexed citations
8.
Zhou, Di, Petra Schwertman, Maria Tresini, et al.. (2019). FACT subunit Spt16 controls UVSSA recruitment to lesion-stalled RNA Pol II and stimulates TC-NER. Nucleic Acids Research. 47(8). 4011–4025. 32 indexed citations
9.
Sabatella, Mariangela, Alex Pines, Jana Slyšková, Wim Vermeulen, & Hannes Lans. (2019). ERCC1–XPF targeting to psoralen–DNA crosslinks depends on XPA and FANCD2. Cellular and Molecular Life Sciences. 77(10). 2005–2016. 5 indexed citations
10.
Evans, Mark D., Vilas Mistry, Rajinder Singh, et al.. (2016). Nucleotide excision repair of oxidised genomic DNA is not a source of urinary 8-oxo-7,8-dihydro-2′-deoxyguanosine. Free Radical Biology and Medicine. 99. 385–391. 26 indexed citations
11.
Stechow, Louise von, Dimitris Typas, Jordi Carreras‐Puigvert, et al.. (2015). The E3 Ubiquitin Ligase ARIH1 Protects against Genotoxic Stress by Initiating a 4EHP-Mediated mRNA Translation Arrest. Molecular and Cellular Biology. 35(7). 1254–1268. 33 indexed citations
12.
Typas, Dimitris, et al.. (2014). Insight in the multilevel regulation of NER. Experimental Cell Research. 329(1). 116–123. 20 indexed citations
13.
Pines, Alex, et al.. (2011). Enhanced Nucleotide Excision Repair in Human Fibroblasts Pre‐exposed to Ionizing Radiation. Photochemistry and Photobiology. 88(1). 147–153. 6 indexed citations
14.
Alekseev, Sergey, Martijn S. Luijsterburg, Alex Pines, et al.. (2008). Cellular Concentrations of DDB2 Regulate Dynamic Binding of DDB1 at UV-Induced DNA Damage. Molecular and Cellular Biology. 28(24). 7402–7413. 32 indexed citations
15.
Pines, Alex, Claude Backendorf, Sergey Alekseev, et al.. (2008). Differential activity of UV-DDB in mouse keratinocytes and fibroblasts: Impact on DNA repair and UV-induced skin cancer. DNA repair. 8(2). 153–161. 17 indexed citations
16.
Deganuto, Marta, María Gabriela Pittis, Alex Pines, et al.. (2007). Altered intracellular redox status in Gaucher disease fibroblasts and impairment of adaptive response against oxidative stress. Journal of Cellular Physiology. 212(1). 223–235. 43 indexed citations
17.
Salzano, Anna Maria, Igor Paron, Alex Pines, et al.. (2006). Differential proteomic analysis of nuclear extracts from thyroid cell lines☆. Journal of Chromatography B. 833(1). 41–50. 17 indexed citations
18.
Tell, Gianluca, Alex Pines, Franco Arturi, et al.. (2004). Control of Phosphatase and Tensin Homolog (PTEN) Gene Expression in Normal and Neoplastic Thyroid Cells. Endocrinology. 145(10). 4660–4666. 25 indexed citations
19.
Tell, Gianluca, Alex Pines, Igor Paron, et al.. (2002). Redox Effector Factor-1 Regulates the Activity of Thyroid Transcription Factor 1 by Controlling the Redox State of the N Transcriptional Activation Domain. Journal of Biological Chemistry. 277(17). 14564–14574. 37 indexed citations
20.
Tell, Gianluca, Enrico Crivellato, Alex Pines, et al.. (2001). Mitochondrial localization of APE/Ref-1 in thyroid cells. Mutation Research/DNA Repair. 485(2). 143–152. 68 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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