Tapan Biswas

2.2k total citations
50 papers, 1.7k citations indexed

About

Tapan Biswas is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Tapan Biswas has authored 50 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 10 papers in Genetics and 8 papers in Oncology. Recurrent topics in Tapan Biswas's work include DNA Repair Mechanisms (15 papers), RNA and protein synthesis mechanisms (10 papers) and DNA and Nucleic Acid Chemistry (9 papers). Tapan Biswas is often cited by papers focused on DNA Repair Mechanisms (15 papers), RNA and protein synthesis mechanisms (10 papers) and DNA and Nucleic Acid Chemistry (9 papers). Tapan Biswas collaborates with scholars based in United States, India and Macao. Tapan Biswas's co-authors include Oleg V. Tsodikov, Sankar Mitra, Rabindra Roy, Sylvie Garneau‐Tsodikova, István Boldogh, Marta Radman‐Livaja, Tom Ellenberger, Tapas K. Hazra, Tadahide Izumi and Shogo Ikeda and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Tapan Biswas

49 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tapan Biswas United States 24 1.3k 307 245 185 173 50 1.7k
Rafael Molina Spain 21 1.0k 0.8× 176 0.6× 68 0.3× 152 0.8× 163 0.9× 71 1.6k
Ye Zhao China 20 1.5k 1.1× 389 1.3× 80 0.3× 62 0.3× 258 1.5× 73 1.7k
Jeyanthy Eswaran United Kingdom 27 1.5k 1.1× 480 1.6× 117 0.5× 106 0.6× 178 1.0× 41 2.4k
Suman Kumar Dhar India 22 1.8k 1.4× 290 0.9× 276 1.1× 221 1.2× 114 0.7× 67 2.5k
Darcie J. Miller United States 23 1.6k 1.2× 252 0.8× 98 0.4× 223 1.2× 120 0.7× 48 2.0k
Olga V. Moroz United Kingdom 21 1.3k 1.0× 148 0.5× 113 0.5× 146 0.8× 106 0.6× 52 1.8k
Anita Changela United States 19 900 0.7× 195 0.6× 166 0.7× 81 0.4× 66 0.4× 23 1.6k
Ejvind Mørtz Denmark 16 995 0.7× 105 0.3× 165 0.7× 133 0.7× 129 0.7× 27 1.7k
Hà Phạm United States 17 944 0.7× 113 0.4× 412 1.7× 357 1.9× 174 1.0× 37 1.5k
N. LaRonde-LeBlanc United States 19 1.0k 0.8× 126 0.4× 182 0.7× 157 0.8× 64 0.4× 21 1.3k

Countries citing papers authored by Tapan Biswas

Since Specialization
Citations

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

Fields of papers citing papers by Tapan Biswas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tapan Biswas

This figure shows the co-authorship network connecting the top 25 collaborators of Tapan Biswas. A scholar is included among the top collaborators of Tapan Biswas 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 Tapan Biswas. Tapan Biswas 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.
2.
Chakraborty, Anirban, Sravan Gopalkrishnashetty Sreenivasmurthy, W. Allen Miller, et al.. (2024). Fructose-2,6-bisphosphate restores DNA repair activity of PNKP and ameliorates neurodegenerative symptoms in Huntington’s disease. Proceedings of the National Academy of Sciences. 121(39). e2406308121–e2406308121. 2 indexed citations
3.
Biswas, Tapan, et al.. (2021). Discovery of a pre-mRNA structural scaffold as a contributor to the mammalian splicing code. Nucleic Acids Research. 49(12). 7103–7121. 6 indexed citations
4.
England, Whitney, et al.. (2020). Structural disruption of exonic stem–loops immediately upstream of the intron regulates mammalian splicing. Nucleic Acids Research. 48(11). 6294–6309. 18 indexed citations
5.
Mulero, María Carmen, D. Huang, Vivien Ya‐Fan Wang, et al.. (2017). DNA-binding affinity and transcriptional activity of the RelA homodimer of nuclear factor κB are not correlated. Journal of Biological Chemistry. 292(46). 18821–18830. 19 indexed citations
6.
Biswas, Tapan, Rajib Bandopadhyay, & Ajoy Kumar Dutta. (2017). Validating The Discriminating Efficacy Of MR T2 Relaxation Value Of Different Brain Lesions And Comparison With Other Differentiating Factors: Use Of Artificial Neural Network And Principal Component Analysis. 20(1). 2 indexed citations
7.
Buffalo, Cosmo Z., et al.. (2016). Conserved patterns hidden within group A Streptococcus M protein hypervariability recognize human C4b-binding protein. Nature Microbiology. 1(11). 16155–16155. 37 indexed citations
8.
Polley, Smarajit, Dario Oliveira Passos, D. Huang, et al.. (2016). Structural Basis for the Activation of IKK1/α. Cell Reports. 17(8). 1907–1914. 45 indexed citations
9.
Furman, Ran, et al.. (2013). DksA2, a zinc‐independent structural analog of the transcription factor DksA. FEBS Letters. 587(6). 614–619. 30 indexed citations
10.
Biswas, Tapan, Jacob L. Houghton, Sylvie Garneau‐Tsodikova, & Oleg V. Tsodikov. (2012). The structural basis for substrate versatility of chloramphenicol acetyltransferase CATI. Protein Science. 21(4). 520–530. 41 indexed citations
11.
Tsodikov, Oleg V. & Tapan Biswas. (2011). Structural and Thermodynamic Signatures of DNA Recognition by Mycobacterium tuberculosis DnaA. Journal of Molecular Biology. 410(3). 461–476. 16 indexed citations
12.
Biswas, Tapan, Jennifer Small, Omar Vandal, et al.. (2010). Structural Insight into Serine Protease Rv3671c that Protects M. tuberculosis from Oxidative and Acidic Stress. Structure. 18(10). 1353–1363. 29 indexed citations
13.
Biswas, Tapan & Oleg V. Tsodikov. (2010). An easy-to-use tool for planning and modeling a calorimetric titration. Analytical Biochemistry. 406(1). 91–93. 13 indexed citations
14.
Biswas, Tapan, Yi Li, Parag Aggarwal, et al.. (2009). The Tail of KdsC. Journal of Biological Chemistry. 284(44). 30594–30603. 17 indexed citations
15.
Bagwell, Christopher E., Tapan Biswas, Timothy R. Hoover, et al.. (2008). Survival in Nuclear Waste, Extreme Resistance, and Potential Applications Gleaned from the Genome Sequence of Kineococcus radiotolerans SRS30216. PLoS ONE. 3(12). e3878–e3878. 52 indexed citations
16.
Biswas, Tapan, Hideki Aihara, Marta Radman‐Livaja, et al.. (2005). A STRUCTURAL BASIS FOR ALLOSTERIC CONTROL OF DNA RECOMBINATION BY LAMDA INTEGRASE. Geophysical Research Letters. 32(4). 38 indexed citations
17.
Radman‐Livaja, Marta, Christine J. Shaw, Marco A. Azaro, et al.. (2003). Arm Sequences Contribute to the Architecture and Catalytic Function of a λ Integrase-Holliday Junction Complex. Molecular Cell. 11(3). 783–794. 27 indexed citations
18.
Biswas, Tapan, et al.. (2002). Binding of Specific DNA Base-pair Mismatches by N-Methylpurine-DNA Glycosylase and Its Implication in Initial Damage Recognition. Journal of Molecular Biology. 320(3). 503–513. 23 indexed citations
19.
Roy, Rabindra, et al.. (2000). Mutation of a Unique Aspartate Residue Abolishes the Catalytic Activity but Not Substrate Binding of the Mouse N-Methylpurine-DNA Glycosylase (MPG). Journal of Biological Chemistry. 275(6). 4278–4282. 7 indexed citations
20.
Ikeda, Shogo, Tapan Biswas, Rabindra Roy, et al.. (1998). Purification and Characterization of Human NTH1, a Homolog ofEscherichia coli Endonuclease III. Journal of Biological Chemistry. 273(34). 21585–21593. 209 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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