Mandar V. Deshmukh

929 total citations
30 papers, 724 citations indexed

About

Mandar V. Deshmukh is a scholar working on Molecular Biology, Spectroscopy and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Mandar V. Deshmukh has authored 30 papers receiving a total of 724 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 5 papers in Spectroscopy and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Mandar V. Deshmukh's work include RNA and protein synthesis mechanisms (7 papers), RNA regulation and disease (6 papers) and RNA Interference and Gene Delivery (6 papers). Mandar V. Deshmukh is often cited by papers focused on RNA and protein synthesis mechanisms (7 papers), RNA regulation and disease (6 papers) and RNA Interference and Gene Delivery (6 papers). Mandar V. Deshmukh collaborates with scholars based in India, Germany and United States. Mandar V. Deshmukh's co-authors include Md. Zahid Kamal, Nalam Madhusudhana Rao, Horst Kessler, Rajan Sankaranarayanan, Frank Krämer, Steffen J. Glaser, M. G. Kulkarni, Alankar A. Vaidya, S. Ganapathy and Tanweer Hussain and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Mandar V. Deshmukh

28 papers receiving 715 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mandar V. Deshmukh India 13 496 126 87 77 50 30 724
Heather E. Findlay United Kingdom 15 474 1.0× 82 0.7× 70 0.8× 55 0.7× 89 1.8× 25 692
Margaret Nutley United Kingdom 16 434 0.9× 78 0.6× 184 2.1× 130 1.7× 31 0.6× 28 733
Krisztina Fehér Hungary 19 512 1.0× 138 1.1× 155 1.8× 71 0.9× 83 1.7× 44 946
Andrea Pica Italy 18 554 1.1× 99 0.8× 104 1.2× 233 3.0× 107 2.1× 45 945
Peter Bellstedt Germany 18 389 0.8× 207 1.6× 189 2.2× 163 2.1× 78 1.6× 43 914
Martha D. Bruch United States 17 578 1.2× 240 1.9× 168 1.9× 139 1.8× 49 1.0× 31 1.0k
Joanna Makowska Poland 15 499 1.0× 153 1.2× 102 1.2× 143 1.9× 21 0.4× 53 763
John W. Tomsho United States 12 387 0.8× 104 0.8× 360 4.1× 111 1.4× 52 1.0× 18 805
Giulio Tesei Denmark 17 879 1.8× 66 0.5× 61 0.7× 218 2.8× 76 1.5× 34 1.2k
Sucharita Dey India 11 526 1.1× 73 0.6× 58 0.7× 178 2.3× 34 0.7× 25 686

Countries citing papers authored by Mandar V. Deshmukh

Since Specialization
Citations

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

Fields of papers citing papers by Mandar V. Deshmukh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mandar V. Deshmukh. 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 Mandar V. Deshmukh. The network helps show where Mandar V. Deshmukh may publish in the future.

Co-authorship network of co-authors of Mandar V. Deshmukh

This figure shows the co-authorship network connecting the top 25 collaborators of Mandar V. Deshmukh. A scholar is included among the top collaborators of Mandar V. Deshmukh 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 Mandar V. Deshmukh. Mandar V. Deshmukh 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.
Behera, Prafulla K., et al.. (2025). Chemical shift assignments of N-terminal dsRNA binding domains dsRBD1 and dsRBD2 of Arabidopsis thaliana DRB5. Biomolecular NMR Assignments. 19(1). 95–100.
2.
Paul, J. W. M., et al.. (2025). Conformational Plasticity in dsRNA-Binding Domains Drives Functional Divergence in RNA Recognition. Journal of the American Chemical Society. 147(20). 17088–17100. 2 indexed citations
3.
Paul, J. W. M. & Mandar V. Deshmukh. (2024). Chemical shift assignment of dsRBD1 and dsRBD2 of Arabidopsis thaliana DRB3, an essential protein involved in RNAi-mediated antiviral defense. Biomolecular NMR Assignments. 18(1). 99–104. 1 indexed citations
4.
Deshmukh, Mandar V., et al.. (2024). Key arginine residues in R2D2 dsRBD1 and dsRBD2 lead the siRNA recognition in Drosophila melanogaster RNAi pathway. Biophysical Chemistry. 310. 107247–107247.
5.
Deshmukh, Mandar V., et al.. (2023). Chemical shift assignments of dsRBD1 and linker region of R2D2, a siRNA binding protein in the Drosophila RNAi pathway. Biomolecular NMR Assignments. 17(2). 211–215. 1 indexed citations
6.
Deshmukh, Mandar V., et al.. (2021). A Glimpse of “Dicer Biology” Through the Structural and Functional Perspective. Frontiers in Molecular Biosciences. 8. 643657–643657. 33 indexed citations
7.
Parveen, Sadiya, et al.. (2019). Structural and mechanistic insights into EchAMP: A antimicrobial protein from the Echidna milk. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1861(6). 1260–1274. 3 indexed citations
8.
9.
Sarkar, Parijat, et al.. (2018). Constrained dynamics of the sole tryptophan in the third intracellular loop of the serotonin 1 A receptor. Biophysical Chemistry. 240. 34–41. 12 indexed citations
10.
Deshmukh, Mandar V., et al.. (2017). DRB4 dsRBD1 drives dsRNA recognition in Arabidopsis thaliana tasi/siRNA pathway. Nucleic Acids Research. 45(14). 8551–8563. 14 indexed citations
11.
Deshmukh, Mandar V., et al.. (2016). Recent excitements in protein NMR: Large proteins and biologically relevant dynamics. Journal of Biosciences. 41(4). 787–803. 5 indexed citations
12.
Sahu, Bhubanananda, et al.. (2014). Backbone and stereospecific 13C methyl Ile (δ1), Leu and Val side-chain chemical shift assignments of Crc. Biomolecular NMR Assignments. 9(1). 75–79. 3 indexed citations
13.
Haque, Asfarul S., et al.. (2014). Delineating the reaction mechanism of reductase domains of Nonribosomal Peptide Synthetases from mycobacteria. Journal of Structural Biology. 187(3). 207–214. 12 indexed citations
14.
Deshmukh, Mandar V., et al.. (2014). Chemical shift assignments of DRB4 (1–153), a dsRNA binding protein in A. thaliana RNAi pathway. Biomolecular NMR Assignments. 9(2). 253–256. 4 indexed citations
15.
Kamal, Md. Zahid, Shoeb Ahmad, Trivikram R. Molugu, et al.. (2011). In Vitro Evolved Non-Aggregating and Thermostable Lipase: Structural and Thermodynamic Investigation. Journal of Molecular Biology. 413(3). 726–741. 74 indexed citations
16.
Marelli, Udaya Kiran, et al.. (2011). Backbone and sidechain methyl Ile (δ1), Leu and Val chemical shift assignments of RDE-4 (1–243), an RNA interference initiation protein in C. elegans. Biomolecular NMR Assignments. 6(2). 143–146. 2 indexed citations
17.
Deshmukh, Mandar V., Brittnee N. Jones, Jeremy Flinders, et al.. (2008). mRNA Decapping Is Promoted by an RNA-Binding Channel in Dcp2. Molecular Cell. 29(3). 324–336. 87 indexed citations
18.
Deshmukh, Mandar V., et al.. (2007). Backbone and sidechain methyl Ile (δ1), Leu and Val resonance assignments of the catalytic domain of the yeast mRNA decapping enzyme, Dcp2. Biomolecular NMR Assignments. 1(1). 17–18. 2 indexed citations
19.
Deshmukh, Mandar V., Michael John, M.P. Coles, et al.. (2006). Inter-domain orientation and motions in VAT-N explored by residual dipolar couplings and15N backbone relaxation. Magnetic Resonance in Chemistry. 44(S1). S89–S100. 7 indexed citations
20.
Deshmukh, Mandar V., et al.. (2005). NMR Studies Reveal Structural Differences between the Gallium and Yttrium Complexes of DOTA-d-Phe-Tyr3-octreotide. Journal of Medicinal Chemistry. 48(5). 1506–1514. 39 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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