Radhakrishnan Sabarinathan

10.8k total citations
45 papers, 2.1k citations indexed

About

Radhakrishnan Sabarinathan is a scholar working on Molecular Biology, Cancer Research and Materials Chemistry. According to data from OpenAlex, Radhakrishnan Sabarinathan has authored 45 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 13 papers in Cancer Research and 9 papers in Materials Chemistry. Recurrent topics in Radhakrishnan Sabarinathan's work include RNA and protein synthesis mechanisms (13 papers), RNA modifications and cancer (11 papers) and Enzyme Structure and Function (9 papers). Radhakrishnan Sabarinathan is often cited by papers focused on RNA and protein synthesis mechanisms (13 papers), RNA modifications and cancer (11 papers) and Enzyme Structure and Function (9 papers). Radhakrishnan Sabarinathan collaborates with scholars based in India, Denmark and Spain. Radhakrishnan Sabarinathan's co-authors include Abel González-Pérez, Núria López-Bigas, Jan Gorodkin, Loris Mularoni, Jordi Deu-Pons, Mikkel Christensen‐Dalsgaard, Henrik Nielsen, Ulf Birkedal, Nicolai Krogh and Ferran Muiños and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Radhakrishnan Sabarinathan

45 papers receiving 2.1k citations

Peers

Radhakrishnan Sabarinathan
Roman Camarda United States
Ivan Mikaélian France
Hui Xie China
Yide Mei China
Hongzhuang Peng United States
El Mustapha Bahassi United States
Yoshiyuki Shibata United States
Zhiao Chen China
Yaoyu E. Wang United States
Roman Camarda United States
Radhakrishnan Sabarinathan
Citations per year, relative to Radhakrishnan Sabarinathan Radhakrishnan Sabarinathan (= 1×) peers Roman Camarda

Countries citing papers authored by Radhakrishnan Sabarinathan

Since Specialization
Citations

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

Fields of papers citing papers by Radhakrishnan Sabarinathan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Radhakrishnan Sabarinathan

This figure shows the co-authorship network connecting the top 25 collaborators of Radhakrishnan Sabarinathan. A scholar is included among the top collaborators of Radhakrishnan Sabarinathan 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 Sabarinathan. Radhakrishnan Sabarinathan 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.
Sabarinathan, Radhakrishnan. (2024). Immunoproteasome as a biomarker for immunotherapy. Nature reviews. Cancer. 25(1). 6–6. 3 indexed citations
2.
Sahoo, Sarthak, et al.. (2023). Prognostic association of immunoproteasome expression in solid tumours is governed by the immediate immune environment. Molecular Oncology. 17(6). 1041–1059. 5 indexed citations
3.
Singh, Anurag Kumar, Radhakrishnan Sabarinathan, Jitendra Thakur, et al.. (2023). Active enhancers strengthen insulation by RNA-mediated CTCF binding at chromatin domain boundaries. Genome Research. 33(1). 1–17. 19 indexed citations
4.
Singh, Anurag Kumar, et al.. (2023). Cis‐regulatory effect of HPV integration is constrained by host chromatin architecture in cervical cancers. Molecular Oncology. 18(5). 1189–1208. 5 indexed citations
5.
Nair, Madhumathy G, et al.. (2023). An androgen receptor regulated gene score is associated with epithelial to mesenchymal transition features in triple negative breast cancers. Translational Oncology. 37. 101761–101761. 10 indexed citations
6.
Singh, Anurag Kumar, Ranveer Singh Jayani, Ashwin Nair, et al.. (2020). A rare variant of African ancestry activates 8q24 lncRNA hub by modulating cancer associated enhancer. Nature Communications. 11(1). 3598–3598. 32 indexed citations
7.
Singh, Anurag Kumar, et al.. (2020). Exome sequencing identifies ARID2 as a novel tumor suppressor in early-onset sporadic rectal cancer. Oncogene. 40(4). 863–874. 23 indexed citations
8.
Tamborero, David, Carlota Rubio-Pérez, Ferran Muiños, et al.. (2018). A Pan-cancer Landscape of Interactions between Solid Tumors and Infiltrating Immune Cell Populations. Clinical Cancer Research. 24(15). 3717–3728. 221 indexed citations
9.
Pich, Oriol, Ferran Muiños, Radhakrishnan Sabarinathan, et al.. (2018). Somatic and Germline Mutation Periodicity Follow the Orientation of the DNA Minor Groove around Nucleosomes. Cell. 175(4). 1074–1087.e18. 81 indexed citations
10.
Frigola, Joan, Radhakrishnan Sabarinathan, Loris Mularoni, et al.. (2017). Reduced mutation rate in exons due to differential mismatch repair. Nature Genetics. 49(12). 1684–1692. 96 indexed citations
11.
Mularoni, Loris, Radhakrishnan Sabarinathan, Jordi Deu-Pons, Abel González-Pérez, & Núria López-Bigas. (2016). OncodriveFML: a general framework to identify coding and non-coding regions with cancer driver mutations. Genome biology. 17(1). 128–128. 177 indexed citations
12.
Vento‐Tormo, Roser, Javier Rodríguez‐Ubreva, Lorenzo de la Rica, et al.. (2016). IL-4 orchestrates STAT6-mediated DNA demethylation leading to dendritic cell differentiation. Genome biology. 17(1). 4–4. 97 indexed citations
13.
Sabarinathan, Radhakrishnan, Loris Mularoni, Jordi Deu-Pons, Abel González-Pérez, & Núria López-Bigas. (2016). Nucleotide excision repair is impaired by binding of transcription factors to DNA. Nature. 532(7598). 264–267. 198 indexed citations
14.
15.
Sabarinathan, Radhakrishnan, Hakim Tafer, Stefan E. Seemann, et al.. (2013). The RNAsnp web server: predicting SNP effects on local RNA secondary structure. Nucleic Acids Research. 41(W1). W475–W479. 109 indexed citations
16.
Sabarinathan, Radhakrishnan, et al.. (2011). Water-mediated ionic interactions in protein structures. Journal of Biosciences. 36(2). 253–263. 21 indexed citations
17.
Sabarinathan, Radhakrishnan, et al.. (2010). ProSTRIP: A method to find similar structural repeats in three-dimensional protein structures. Computational Biology and Chemistry. 34(2). 126–130. 20 indexed citations
18.
Sridhar, Jayavel, Radhakrishnan Sabarinathan, Hong‐Yu Ou, et al.. (2010). sRNAscanner: A Computational Tool for Intergenic Small RNA Detection in Bacterial Genomes. PLoS ONE. 5(8). e11970–e11970. 41 indexed citations
19.
Kumar, Sanjeev, et al.. (2009). BSDD-2.0: Biomolecules Segment Display Device ― An updated web accessible computing resource. Current Science. 97(1). 28–32. 1 indexed citations
20.
Sabarinathan, Radhakrishnan, et al.. (2009). An algorithm to find similar internal sequence repeats. Current Science. 97(9). 1345–1349. 2 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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