Nisheeth Agarwal

1.6k total citations
40 papers, 1.1k citations indexed

About

Nisheeth Agarwal is a scholar working on Infectious Diseases, Molecular Biology and Epidemiology. According to data from OpenAlex, Nisheeth Agarwal has authored 40 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Infectious Diseases, 23 papers in Molecular Biology and 21 papers in Epidemiology. Recurrent topics in Nisheeth Agarwal's work include Tuberculosis Research and Epidemiology (28 papers), Mycobacterium research and diagnosis (20 papers) and RNA and protein synthesis mechanisms (9 papers). Nisheeth Agarwal is often cited by papers focused on Tuberculosis Research and Epidemiology (28 papers), Mycobacterium research and diagnosis (20 papers) and RNA and protein synthesis mechanisms (9 papers). Nisheeth Agarwal collaborates with scholars based in India, United States and Hong Kong. Nisheeth Agarwal's co-authors include William R. Bishai, Eira Choudhary, Radhika Gupta, Preeti Thakur, Tirumalai R. Raghunand, Deborah E. Geiman, Gyanu Lamichhane, Scott T. Nolan, Akhilesh K. Tyagi and Nicole C. Ammerman and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Nisheeth Agarwal

38 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nisheeth Agarwal India 17 652 641 544 203 146 40 1.1k
Christian Chalut France 19 696 1.1× 861 1.3× 566 1.0× 164 0.8× 169 1.2× 42 1.5k
Elias R. Gerrick United States 8 514 0.8× 657 1.0× 419 0.8× 236 1.2× 124 0.8× 12 1.1k
John L. Dahl United States 16 533 0.8× 412 0.6× 559 1.0× 223 1.1× 144 1.0× 26 964
Jeffrey M. Chen Canada 18 707 1.1× 373 0.6× 638 1.2× 116 0.6× 175 1.2× 27 1.1k
James Gomez United States 14 501 0.8× 371 0.6× 420 0.8× 128 0.6× 152 1.0× 19 919
Albel Singh United Kingdom 17 488 0.7× 407 0.6× 424 0.8× 108 0.5× 99 0.7× 30 784
Cara C. Boutte United States 15 600 0.9× 755 1.2× 510 0.9× 395 1.9× 209 1.4× 22 1.3k
Noman Siddiqi United States 11 802 1.2× 422 0.7× 640 1.2× 74 0.4× 193 1.3× 14 1.1k
Andrej Benjak Switzerland 20 790 1.2× 552 0.9× 607 1.1× 169 0.8× 104 0.7× 42 1.3k
Damien Portevin Switzerland 14 758 1.2× 445 0.7× 631 1.2× 85 0.4× 62 0.4× 30 1.2k

Countries citing papers authored by Nisheeth Agarwal

Since Specialization
Citations

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

Fields of papers citing papers by Nisheeth Agarwal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nisheeth Agarwal

This figure shows the co-authorship network connecting the top 25 collaborators of Nisheeth Agarwal. A scholar is included among the top collaborators of Nisheeth Agarwal 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 Nisheeth Agarwal. Nisheeth Agarwal 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.
Rai, S.B., et al.. (2025). Cloning, expression, purification, and characterization of glutamate decarboxylase (Rv3432c) from Mycobacterium tuberculosis. International Microbiology. 28(7). 1603–1616. 3 indexed citations
2.
Giri, Samir, et al.. (2025). Functional flexibility of a type III polyketide synthase in Mycobacterium marinum. iScience. 28(8). 113129–113129.
3.
Bhaskar, Ashima, et al.. (2024). Depletion of essential mycobacterial gene glmM reduces pathogen survival and induces host-protective immune responses against tuberculosis. Communications Biology. 7(1). 949–949. 1 indexed citations
5.
Chakraborti, Soumyananda, et al.. (2024). Discovery of potent antimycobacterial agents targeting lumazine synthase (RibH) of Mycobacterium tuberculosis. Scientific Reports. 14(1). 12170–12170. 2 indexed citations
6.
Pal, Mohinder, et al.. (2023). The physiological effect of rimI/rimJ silencing by CRISPR interference in Mycobacterium smegmatis mc2155. Archives of Microbiology. 205(5). 211–211. 1 indexed citations
7.
Kumar, Yashwant, et al.. (2023). ResR/McdR-regulated protein translation machinery contributes to drug resilience in Mycobacterium tuberculosis. Communications Biology. 6(1). 708–708.
8.
Chaudhary, Deepika, Mardiana Marzuki, Saqib Kidwai, et al.. (2022). Identification of small molecules targeting homoserine acetyl transferase from Mycobacterium tuberculosis and Staphylococcus aureus. Scientific Reports. 12(1). 13801–13801. 7 indexed citations
9.
Dwivedy, Abhisek, et al.. (2021). De novo histidine biosynthesis protects Mycobacterium tuberculosis from host IFN-γ mediated histidine starvation. Communications Biology. 4(1). 410–410. 28 indexed citations
10.
Agarwal, Nisheeth & Radhika Gupta. (2021). History, evolution and classification of CRISPR-Cas associated systems. Progress in molecular biology and translational science. 179. 11–76. 21 indexed citations
11.
Agarwal, Nisheeth. (2020). Construction of a novel CRISPRi-based tool for silencing of multiple genes in Mycobacterium tuberculosis. Plasmid. 110. 102515–102515. 7 indexed citations
12.
Gupta, Radhika, et al.. (2020). The unfoldase ClpC1 of Mycobacterium tuberculosis regulates the expression of a distinct subset of proteins having intrinsically disordered termini. Journal of Biological Chemistry. 295(28). 9455–9473. 31 indexed citations
13.
Thakur, Preeti, et al.. (2018). Regulation and overexpression studies of YidC in Mycobacterium tuberculosis. Scientific Reports. 8(1). 17114–17114. 6 indexed citations
14.
Dwivedy, Abhisek, et al.. (2017). Characterization of a secretory hydrolase from Mycobacterium tuberculosis sheds critical insight into host lipid utilization by M. tuberculosis. Journal of Biological Chemistry. 292(27). 11326–11335. 33 indexed citations
15.
Thakur, Preeti, et al.. (2016). The preprotein translocase YidC controls respiratory metabolism in Mycobacterium tuberculosis. Scientific Reports. 6(1). 24998–24998. 14 indexed citations
16.
Choudhary, Eira, et al.. (2015). Gene silencing by CRISPR interference in mycobacteria. Nature Communications. 6(1). 6267–6267. 188 indexed citations
17.
Choudhary, Eira, William R. Bishai, & Nisheeth Agarwal. (2014). Expression of a Subset of Heat Stress Induced Genes of Mycobacterium tuberculosis Is Regulated by 3',5'-Cyclic AMP. PLoS ONE. 9(2). e89759–e89759. 20 indexed citations
18.
Larsson, Christer, Brian Luna, Nicole C. Ammerman, et al.. (2012). Gene Expression of Mycobacterium tuberculosis Putative Transcription Factors whiB1-7 in Redox Environments. PLoS ONE. 7(7). e37516–e37516. 57 indexed citations
19.
Maïga, Mamoudou, Nisheeth Agarwal, Nicole C. Ammerman, et al.. (2012). Successful Shortening of Tuberculosis Treatment Using Adjuvant Host-Directed Therapy with FDA-Approved Phosphodiesterase Inhibitors in the Mouse Model. PLoS ONE. 7(2). e30749–e30749. 54 indexed citations
20.
Agarwal, Nisheeth, Gyanu Lamichhane, Radhika Gupta, Scott T. Nolan, & William R. Bishai. (2009). Cyclic AMP intoxication of macrophages by a Mycobacterium tuberculosis adenylate cyclase. Nature. 460(7251). 98–102. 178 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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