Rajendra K. Agrawal

7.0k total citations · 2 hit papers
77 papers, 5.2k citations indexed

About

Rajendra K. Agrawal is a scholar working on Molecular Biology, Genetics and Structural Biology. According to data from OpenAlex, Rajendra K. Agrawal has authored 77 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Structural Biology. Recurrent topics in Rajendra K. Agrawal's work include RNA and protein synthesis mechanisms (65 papers), RNA modifications and cancer (52 papers) and RNA Research and Splicing (17 papers). Rajendra K. Agrawal is often cited by papers focused on RNA and protein synthesis mechanisms (65 papers), RNA modifications and cancer (52 papers) and RNA Research and Splicing (17 papers). Rajendra K. Agrawal collaborates with scholars based in United States, Germany and Nepal. Rajendra K. Agrawal's co-authors include Joachim Frank, Joachim Frank, Robert A. Grassucci, Manjuli R. Sharma, Pawel A. Penczek, Knud H. Nierhaus, Partha P. Datta, C.M.T. Spahn, Irene S. Gabashvili and T.M. Booth and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Rajendra K. Agrawal

77 papers receiving 5.1k citations

Hit Papers

A ratchet-like inter-subunit reorganization of the riboso... 2000 2026 2008 2017 2000 2000 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rajendra K. Agrawal United States 37 4.6k 1.1k 490 372 341 77 5.2k
Björn Forsberg Sweden 13 3.2k 0.7× 454 0.4× 588 1.2× 425 1.1× 401 1.2× 18 4.8k
I.S. Fernandez United Kingdom 24 2.2k 0.5× 340 0.3× 433 0.9× 185 0.5× 154 0.5× 33 2.8k
Richard Brimacombe Germany 53 6.3k 1.4× 1.4k 1.3× 265 0.5× 345 0.9× 774 2.3× 134 6.7k
Jayati Sengupta India 20 2.6k 0.6× 586 0.5× 221 0.5× 196 0.5× 171 0.5× 70 2.9k
Carsten Sachse Germany 36 3.0k 0.7× 261 0.2× 586 1.2× 350 0.9× 334 1.0× 79 4.5k
Zhiheng Yu United States 33 1.9k 0.4× 1.2k 1.1× 336 0.7× 310 0.8× 193 0.6× 75 3.3k
Lori A. Passmore United Kingdom 37 3.4k 0.8× 322 0.3× 682 1.4× 269 0.7× 119 0.3× 68 4.4k
Andrey V. Zavialov Sweden 23 2.7k 0.6× 1.1k 1.0× 130 0.3× 152 0.4× 363 1.1× 32 3.4k
Irina Gutsche France 32 1.6k 0.3× 413 0.4× 148 0.3× 485 1.3× 345 1.0× 74 2.9k
John Berriman United Kingdom 24 1.5k 0.3× 210 0.2× 409 0.8× 400 1.1× 253 0.7× 43 3.4k

Countries citing papers authored by Rajendra K. Agrawal

Since Specialization
Citations

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

Fields of papers citing papers by Rajendra K. Agrawal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rajendra K. Agrawal. 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 Rajendra K. Agrawal. The network helps show where Rajendra K. Agrawal may publish in the future.

Co-authorship network of co-authors of Rajendra K. Agrawal

This figure shows the co-authorship network connecting the top 25 collaborators of Rajendra K. Agrawal. A scholar is included among the top collaborators of Rajendra K. Agrawal 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 Rajendra K. Agrawal. Rajendra K. Agrawal 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.
Koripella, Ravi Kiran, Manjuli R. Sharma, Kelley Hurst-Hess, et al.. (2025). HflX-mediated drug resistance through ribosome splitting and rRNA disordering in mycobacteria. Proceedings of the National Academy of Sciences. 122(6). e2419826122–e2419826122. 1 indexed citations
2.
Li, Yunlong, Manjuli R. Sharma, Howard Gamper, et al.. (2023). Starvation sensing by mycobacterial RelA/SpoT homologue through constitutive surveillance of translation. Proceedings of the National Academy of Sciences. 120(22). e2302006120–e2302006120. 5 indexed citations
3.
Sharma, Manjuli R., et al.. (2023). The structure of a hibernating ribosome in a Lyme disease pathogen. Nature Communications. 14(1). 6961–6961. 4 indexed citations
4.
Koripella, Ravi Kiran, Manjuli R. Sharma, Kalpana Bhargava, et al.. (2020). Structures of the human mitochondrial ribosome bound to EF-G1 reveal distinct features of mitochondrial translation elongation. Nature Communications. 11(1). 3830–3830. 36 indexed citations
5.
Koripella, Ravi Kiran, et al.. (2019). Structural insights into unique features of the human mitochondrial ribosome recycling. Proceedings of the National Academy of Sciences. 116(17). 8283–8288. 29 indexed citations
6.
Li, Yunlong, Manjuli R. Sharma, Ravi Kiran Koripella, et al.. (2018). Zinc depletion induces ribosome hibernation in mycobacteria. Proceedings of the National Academy of Sciences. 115(32). 8191–8196. 59 indexed citations
7.
Agrawal, Rajendra K., et al.. (2018). Percutaneous Renal Biopsy: Comparison of Blind and Real-time Ultrasound Guided Technique. SHILAP Revista de lepidopterología. 1 indexed citations
8.
Kaushal, P.S., Manjuli R. Sharma, T.M. Booth, et al.. (2014). Cryo-EM structure of the small subunit of the mammalian mitochondrial ribosome. Proceedings of the National Academy of Sciences. 111(20). 7284–7289. 55 indexed citations
9.
Lu, Zonghuan, David Barnard, Tanvir R. Shaikh, et al.. (2014). Gas-assisted annular microsprayer for sample preparation for time-resolved cryo-electron microscopy. Journal of Micromechanics and Microengineering. 24(11). 115001–115001. 25 indexed citations
10.
Yokoyama, Takeshi, Tanvir R. Shaikh, Nobuhiro Iwakura, et al.. (2012). Structural insights into initial and intermediate steps of the ribosome‐recycling process. The EMBO Journal. 31(7). 1836–1846. 30 indexed citations
11.
Yassin, Aymen S., Md. Emdadul Haque, Partha P. Datta, et al.. (2011). Insertion domain within mammalian mitochondrial translation initiation factor 2 serves the role of eubacterial initiation factor 1. Proceedings of the National Academy of Sciences. 108(10). 3918–3923. 46 indexed citations
12.
Datta, Partha P., et al.. (2008). A Single Mammalian Mitochondrial Translation Initiation Factor Functionally Replaces Two Bacterial Factors. Molecular Cell. 29(2). 180–190. 78 indexed citations
13.
Barat, Chandana, Partha P. Datta, V. Samuel Raj, et al.. (2007). Progression of the Ribosome Recycling Factor through the Ribosome Dissociates the Two Ribosomal Subunits. Molecular Cell. 27(2). 250–261. 35 indexed citations
14.
Mears, Jason A., Manjuli R. Sharma, Robin R. Gutell, et al.. (2006). A Structural Model for the Large Subunit of the Mammalian Mitochondrial Ribosome. Journal of Molecular Biology. 358(1). 193–212. 73 indexed citations
15.
Hirano, Michio, Lluís Palenzuela, Noah M. Hahn, et al.. (2005). Does Linezolid Cause Lactic Acidosis by Inhibiting Mitochondrial Protein Synthesis?. Clinical Infectious Diseases. 40(12). e113–e116. 91 indexed citations
16.
Sharma, Manjuli R., Emine C. Koc, Partha P. Datta, et al.. (2003). Structure of the Mammalian Mitochondrial Ribosome Reveals an Expanded Functional Role for Its Component Proteins. Cell. 115(1). 97–108. 269 indexed citations
17.
Mears, Jason A., Jamie J. Cannone, Scott M. Stagg, et al.. (2002). Modeling a Minimal Ribosome Based on Comparative Sequence Analysis. Journal of Molecular Biology. 321(2). 215–234. 117 indexed citations
18.
Frank, Joachim & Rajendra K. Agrawal. (2001). Ratchet-like Movements between the Two Ribosomal Subunits: Their Implications in Elongation Factor Recognition and tRNA Translocation. Cold Spring Harbor Symposia on Quantitative Biology. 66(0). 67–76. 31 indexed citations
19.
Agrawal, Rajendra K., C.M.T. Spahn, Pawel A. Penczek, et al.. (2000). Visualization of Trna Movements on theEscherichia coli70s Ribosome during the Elongation Cycle. The Journal of Cell Biology. 150(3). 447–460. 126 indexed citations
20.
Gabashvili, Irene S., Rajendra K. Agrawal, C.M.T. Spahn, et al.. (2000). Solution Structure of the E. coli 70S Ribosome at 11.5 Å Resolution. Cell. 100(5). 537–549. 329 indexed citations breakdown →

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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