Rupesh Kumar

1.3k total citations
21 papers, 1.0k citations indexed

About

Rupesh Kumar is a scholar working on Molecular Biology, Organic Chemistry and Molecular Medicine. According to data from OpenAlex, Rupesh Kumar has authored 21 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 3 papers in Organic Chemistry and 3 papers in Molecular Medicine. Recurrent topics in Rupesh Kumar's work include Cancer therapeutics and mechanisms (6 papers), DNA and Nucleic Acid Chemistry (5 papers) and RNA and protein synthesis mechanisms (5 papers). Rupesh Kumar is often cited by papers focused on Cancer therapeutics and mechanisms (6 papers), DNA and Nucleic Acid Chemistry (5 papers) and RNA and protein synthesis mechanisms (5 papers). Rupesh Kumar collaborates with scholars based in United States, India and Netherlands. Rupesh Kumar's co-authors include Dinshaw J. Patel, Feng Jiang, Roger A. Jones, Xiaomei Ye, Sylvie Nonin‐Lecomte, Asif K Suri, Licong Jiang, Norihiro Ikemoto, Valakunja Nagaraja and Samuel J. Danishefsky and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Rupesh Kumar

21 papers receiving 993 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rupesh Kumar United States 15 838 109 104 77 71 21 1.0k
Francis Schaeffer France 22 1.0k 1.2× 173 1.6× 129 1.2× 223 2.9× 70 1.0× 31 1.3k
E. Scott Priestley United States 16 717 0.9× 355 3.3× 83 0.8× 90 1.2× 40 0.6× 34 1.1k
Thomas Hermann France 17 1.1k 1.4× 164 1.5× 158 1.5× 138 1.8× 30 0.4× 18 1.3k
Keehwan Kwon United States 20 668 0.8× 178 1.6× 62 0.6× 107 1.4× 32 0.5× 39 1.1k
Jan Dohnálek Czechia 20 663 0.8× 87 0.8× 48 0.5× 82 1.1× 68 1.0× 73 1.1k
Divita Garg Germany 11 427 0.5× 130 1.2× 103 1.0× 30 0.4× 19 0.3× 19 591
Ken Blount United States 19 1.5k 1.8× 94 0.9× 141 1.4× 315 4.1× 23 0.3× 46 1.8k
Stefan Schmelz Germany 15 541 0.6× 119 1.1× 51 0.5× 130 1.7× 24 0.3× 30 791
Shwu‐Huey Liaw Taiwan 20 602 0.7× 72 0.7× 39 0.4× 59 0.8× 60 0.8× 39 1.2k
José Gallego Spain 23 1.1k 1.4× 179 1.6× 89 0.9× 88 1.1× 26 0.4× 50 1.4k

Countries citing papers authored by Rupesh Kumar

Since Specialization
Citations

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

Fields of papers citing papers by Rupesh Kumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rupesh Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Rupesh Kumar. A scholar is included among the top collaborators of Rupesh Kumar 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 Rupesh Kumar. Rupesh Kumar 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.
Kumar, Rupesh, et al.. (2022). Intersubunit and intrasubunit interactions driving the MukBEF ATPase. Journal of Biological Chemistry. 298(6). 101964–101964. 1 indexed citations
2.
Kumar, Rupesh, et al.. (2021). The MukB-topoisomerase IV interaction mutually suppresses their catalytic activities. Nucleic Acids Research. 50(5). 2621–2634. 11 indexed citations
3.
Kumar, Rupesh, et al.. (2019). Dissecting DNA Compaction by the Bacterial Condensin MukB. Methods in molecular biology. 2004. 169–180. 2 indexed citations
4.
Kumar, Rupesh, et al.. (2017). The bacterial condensin MukB compacts DNA by sequestering supercoils and stabilizing topologically isolated loops. Journal of Biological Chemistry. 292(41). 16904–16920. 20 indexed citations
5.
Prabhu, Krishnananda, et al.. (2017). Serum butyrylcholinesterase and zinc in breast cancer. Journal of Cancer Research and Therapeutics. 13(2). 367–367. 25 indexed citations
6.
Kumar, Rupesh, et al.. (2017). The MukB–topoisomerase IV interaction is required for proper chromosome compaction. Journal of Biological Chemistry. 292(41). 16921–16932. 14 indexed citations
7.
Ghosh, Soumitra, Adwait Anand Godbole, Wareed Ahmed, et al.. (2016). Transcriptional regulation of topology modulators and transcription regulators of Mycobacterium tuberculosis. Biochemical and Biophysical Research Communications. 475(3). 257–263. 2 indexed citations
8.
Chang, Elizabeth, Sergei Pourmal, Chun Zhou, et al.. (2016). N-Terminal Amino Acid Sequence Determination of Proteins byN-Terminal Dimethyl Labeling: Pitfalls and Advantages When Compared with EdmanDegradation Sequence Analysis. Journal of Biomolecular Techniques JBT. 27(2). 61–74. 9 indexed citations
9.
Kumar, Rupesh, et al.. (2014). Molecular Basis for the Differential Quinolone Susceptibility of Mycobacterial DNA Gyrase. Antimicrobial Agents and Chemotherapy. 58(4). 2013–2020. 24 indexed citations
10.
Rohilla, Ankur, et al.. (2012). Diabetic Retinopathy: Origin and Complications. European Journal of Experimental Biology. 2(1). 4 indexed citations
11.
Marathe, Sandhya Amol, Rupesh Kumar, Parthasarathi Ajitkumar, Valakunja Nagaraja, & Dipshikha Chakravortty. (2012). Curcumin reduces the antimicrobial activity of ciprofloxacin against Salmonella Typhimurium and Salmonella Typhi. Journal of Antimicrobial Chemotherapy. 68(1). 139–152. 67 indexed citations
12.
Kumar, Rupesh, et al.. (2012). Binding of two DNA molecules by type II topoisomerases for decatenation. Nucleic Acids Research. 40(21). 10904–10915. 20 indexed citations
13.
Patel, Dinshaw J., Asif K Suri, Feng Jiang, et al.. (1997). Structure, recognition and adaptive binding in RNA aptamer complexes. Journal of Molecular Biology. 272(5). 645–664. 239 indexed citations
14.
Kumar, Rupesh, Norihiro Ikemoto, & Dinshaw J. Patel. (1997). Solution structure of the calicheamicin γ1-DNA complex. Journal of Molecular Biology. 265(2). 187–201. 54 indexed citations
15.
Kumar, Rupesh, Norihiro Ikemoto, & Dinshaw J. Patel. (1997). Solution structure of the esperamicin A1-DNA complex. Journal of Molecular Biology. 265(2). 173–186. 26 indexed citations
16.
Jiang, Feng, Rupesh Kumar, Roger A. Jones, & Dinshaw J. Patel. (1996). Structural basis of RNA folding and recognition in an AMP–RNA aptamer complex. Nature. 382(6587). 183–186. 207 indexed citations
17.
Jiang, Feng, Radovan Fiala, David Live, Rupesh Kumar, & Dinshaw J. Patel. (1996). RNA Folding Topology and Intermolecular Contacts in the AMP−RNA Aptamer Complex. Biochemistry. 35(40). 13250–13266. 33 indexed citations
18.
Ikemoto, N., Rupesh Kumar, Tao Ling, et al.. (1995). Calicheamicin-DNA complexes: warhead alignment and saccharide recognition of the minor groove.. Proceedings of the National Academy of Sciences. 92(23). 10506–10510. 70 indexed citations
19.
Ye, Xiaomei, Rupesh Kumar, & Dinshaw J. Patel. (1995). Molecular recognition in the bovine immunodeficiency virus Tat peptide-TAR RNA complex. Chemistry & Biology. 2(12). 827–840. 148 indexed citations
20.
Ikemoto, Norihiro, Rupesh Kumar, Peter C. Dedon, Samuel J. Danishefsky, & Dinshaw J. Patel. (1994). Esperamicin A1 Intercalates into Duplex DNA from the Minor Groove. Journal of the American Chemical Society. 116(20). 9387–9388. 20 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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