Radhakrishnan Kanagaraj

1.1k total citations
17 papers, 885 citations indexed

About

Radhakrishnan Kanagaraj is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Radhakrishnan Kanagaraj has authored 17 papers receiving a total of 885 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Cancer Research and 4 papers in Oncology. Recurrent topics in Radhakrishnan Kanagaraj's work include DNA Repair Mechanisms (16 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Mitochondrial Function and Pathology (3 papers). Radhakrishnan Kanagaraj is often cited by papers focused on DNA Repair Mechanisms (16 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Mitochondrial Function and Pathology (3 papers). Radhakrishnan Kanagaraj collaborates with scholars based in Switzerland, Czechia and United Kingdom. Radhakrishnan Kanagaraj's co-authors include Pavel Janščák, Kamila Burdová, I. A. Shevelev, Nurten Saydam, Patrick L. Garcia, Cosimo Pinto, Maryna Levikova, Petr Ćejka, Shreya Paliwal and Sybille Schwendener 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

Radhakrishnan Kanagaraj

17 papers receiving 873 citations

Peers

Radhakrishnan Kanagaraj
Venkateswarlu Popuri United States
Steven Raynard United States
Christine Ralf United Kingdom
Christine Magill United Kingdom
Sean Howard United States
Nicole Hustedt Switzerland
Jennifer M. Svendsen United States
Sara K. Binz United States
Inger Tappin United States
Venkateswarlu Popuri United States
Radhakrishnan Kanagaraj
Citations per year, relative to Radhakrishnan Kanagaraj Radhakrishnan Kanagaraj (= 1×) peers Venkateswarlu Popuri

Countries citing papers authored by Radhakrishnan Kanagaraj

Since Specialization
Citations

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

Fields of papers citing papers by Radhakrishnan Kanagaraj

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Radhakrishnan Kanagaraj

This figure shows the co-authorship network connecting the top 25 collaborators of Radhakrishnan Kanagaraj. A scholar is included among the top collaborators of Radhakrishnan Kanagaraj 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 Radhakrishnan Kanagaraj. Radhakrishnan Kanagaraj is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Andrš, Martin, Henriette Stoy, Nagaraja Chappidi, et al.. (2023). Excessive reactive oxygen species induce transcription-dependent replication stress. Nature Communications. 14(1). 1791–1791. 44 indexed citations
2.
Benitez, Anaid, Radhakrishnan Kanagaraj, Monica C. Rodrigo-Brenni, et al.. (2023). GEN1 promotes common fragile site expression. Cell Reports. 42(2). 112062–112062. 6 indexed citations
3.
Kanagaraj, Radhakrishnan, Richard Mitter, Theodoros Kantidakis, et al.. (2022). Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2. Proceedings of the National Academy of Sciences. 119(4). 21 indexed citations
4.
Caballero, Madison, Ana Rita Rebelo, Seungmae Seo, et al.. (2022). Comprehensive analysis of DNA replication timing across 184 cell lines suggests a role forMCM10in replication timing regulation. Human Molecular Genetics. 31(17). 2899–2917. 9 indexed citations
5.
Naščáková, Zuzana, et al.. (2022). DDX17 helicase promotes resolution of R-loop-mediated transcription–replication conflicts in human cells. Nucleic Acids Research. 50(21). 12274–12290. 23 indexed citations
6.
Kanagaraj, Radhakrishnan, et al.. (2021). AU-Rich Element RNA Binding Proteins: At the Crossroads of Post-Transcriptional Regulation and Genome Integrity. International Journal of Molecular Sciences. 23(1). 96–96. 30 indexed citations
7.
Marco, Stefano Di, Radhakrishnan Kanagaraj, Nagaraja Chappidi, et al.. (2017). RECQ5 Helicase Cooperates with MUS81 Endonuclease in Processing Stalled Replication Forks at Common Fragile Sites during Mitosis. Molecular Cell. 66(5). 658–671.e8. 82 indexed citations
8.
Burdová, Kamila, Radhakrishnan Kanagaraj, Maryna Levikova, et al.. (2014). DNA2 Cooperates with the WRN and BLM RecQ Helicases to Mediate Long-range DNA End Resection in Human Cells. Journal of Biological Chemistry. 289(39). 27314–27326. 167 indexed citations
9.
Paliwal, Shreya, et al.. (2013). Human RECQ5 helicase promotes repair of DNA double-strand breaks by synthesis-dependent strand annealing. Nucleic Acids Research. 42(4). 2380–2390. 51 indexed citations
10.
Kanagaraj, Radhakrishnan, Prasanna Parasuraman, Barbara van Loon, et al.. (2012). Involvement of Werner syndrome protein in MUTYH-mediated repair of oxidative DNA damage. Nucleic Acids Research. 40(17). 8449–8459. 22 indexed citations
11.
Schwendener, Sybille, Steven Raynard, Shreya Paliwal, et al.. (2010). Physical Interaction of RECQ5 Helicase with RAD51 Facilitates Its Anti-recombinase Activity. Journal of Biological Chemistry. 285(21). 15739–15745. 83 indexed citations
12.
Kanagaraj, Radhakrishnan, et al.. (2010). RECQ5 helicase associates with the C-terminal repeat domain of RNA polymerase II during productive elongation phase of transcription. Nucleic Acids Research. 38(22). 8131–8140. 62 indexed citations
13.
Kanagaraj, Radhakrishnan, Sybille Schwendener, Alessandro A. Sartori, et al.. (2009). MRE11 complex links RECQ5 helicase to sites of DNA damage. Nucleic Acids Research. 37(8). 2645–2657. 47 indexed citations
14.
Yodh, Jaya G., Benjamin Stevens, Radhakrishnan Kanagaraj, Pavel Janščák, & Taekjip Ha. (2009). BLM helicase measures DNA unwound before switching strands and hRPA promotes unwinding reinitiation. The EMBO Journal. 28(4). 405–416. 66 indexed citations
15.
Ren, Hua, Shuo‐Xing Dou, Xingdong Zhang, et al.. (2008). The zinc-binding motif of human RECQ5β suppresses the intrinsic strand-annealing activity of its DExH helicase domain and is essential for the helicase activity of the enzyme. Biochemical Journal. 412(3). 425–433. 30 indexed citations
16.
Saydam, Nurten, Radhakrishnan Kanagaraj, Patrick L. Garcia, et al.. (2007). Physical and functional interactions between Werner syndrome helicase and mismatch-repair initiation factors. Nucleic Acids Research. 35(17). 5706–5716. 37 indexed citations
17.
Kanagaraj, Radhakrishnan, et al.. (2006). Human RECQ5β helicase promotes strand exchange on synthetic DNA structures resembling a stalled replication fork. Nucleic Acids Research. 34(18). 5217–5231. 105 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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