Rajesh S. Gokhale

6.4k total citations
90 papers, 4.9k citations indexed

About

Rajesh S. Gokhale is a scholar working on Molecular Biology, Pharmacology and Cell Biology. According to data from OpenAlex, Rajesh S. Gokhale has authored 90 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 38 papers in Pharmacology and 24 papers in Cell Biology. Recurrent topics in Rajesh S. Gokhale's work include Microbial Natural Products and Biosynthesis (38 papers), melanin and skin pigmentation (19 papers) and Genomics and Phylogenetic Studies (18 papers). Rajesh S. Gokhale is often cited by papers focused on Microbial Natural Products and Biosynthesis (38 papers), melanin and skin pigmentation (19 papers) and Genomics and Phylogenetic Studies (18 papers). Rajesh S. Gokhale collaborates with scholars based in India, United States and France. Rajesh S. Gokhale's co-authors include Debasisa Mohanty, Chaitan Khosla, David E. Cane, Gitanjali Yadav, Vivek T. Natarajan, Pooja Arora, Priti Saxena, Rajan Sankaranarayanan, John R. Jacobsen and Stuart Y. Tsuji and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Rajesh S. Gokhale

88 papers receiving 4.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rajesh S. Gokhale India 39 2.9k 1.9k 785 741 608 90 4.9k
Wulf Blankenfeldt Germany 38 3.1k 1.1× 755 0.4× 188 0.2× 249 0.3× 599 1.0× 147 4.9k
José R. Tormo Spain 36 1.9k 0.6× 965 0.5× 241 0.3× 336 0.5× 420 0.7× 142 5.1k
Jeffrey M. Becker United States 41 4.4k 1.5× 511 0.3× 1.0k 1.3× 697 0.9× 578 1.0× 224 6.4k
Donald R. Kirsch United States 21 2.9k 1.0× 335 0.2× 1.1k 1.4× 776 1.0× 284 0.5× 36 5.1k
Mikio Arisawa Japan 42 3.5k 1.2× 534 0.3× 1.3k 1.7× 984 1.3× 585 1.0× 118 5.2k
Nir Osherov Israel 36 1.8k 0.6× 542 0.3× 1.1k 1.4× 698 0.9× 259 0.4× 98 4.0k
Akira Takatsuki Japan 38 4.1k 1.4× 546 0.3× 284 0.4× 591 0.8× 1.0k 1.7× 151 6.6k
Florence Pojer Switzerland 31 2.4k 0.8× 417 0.2× 944 1.2× 471 0.6× 527 0.9× 57 3.9k
Yasuo Ohnishi Japan 45 4.8k 1.6× 3.6k 1.9× 129 0.2× 247 0.3× 837 1.4× 199 6.8k

Countries citing papers authored by Rajesh S. Gokhale

Since Specialization
Citations

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

Fields of papers citing papers by Rajesh S. Gokhale

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rajesh S. Gokhale. 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 Rajesh S. Gokhale. The network helps show where Rajesh S. Gokhale may publish in the future.

Co-authorship network of co-authors of Rajesh S. Gokhale

This figure shows the co-authorship network connecting the top 25 collaborators of Rajesh S. Gokhale. A scholar is included among the top collaborators of Rajesh S. Gokhale 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 Rajesh S. Gokhale. Rajesh S. Gokhale 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.
Sharma, Sachin, Qiang Liu, Siddhesh S. Kamat, et al.. (2025). Kupyaphores─Self-Assembling Diisocyanolipopeptide Zn II Ionophores in Mycobacterium tuberculosis Zn II /Cu I/II Homeostasis and Antibacterial Effects. Journal of the American Chemical Society. 147(44). 40652–40663.
2.
Reddy, D. Srinivasa, et al.. (2025). Enzymatic Pathway for Kupyaphore Degradation in Mycobacterium tuberculosis: Mechanism of Metal Homeostasis and Turnover. ACS Chemical Biology. 20(7). 1492–1504.
3.
Ramesh, Remya, Amitesh Anand, Ajay Kumar, et al.. (2023). Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: An effective strategy towards development of potent anti-tubercular agents. European Journal of Medicinal Chemistry. 259. 115633–115633. 7 indexed citations
4.
Chandna, Sudhir, et al.. (2023). Sustained pigmentation causes DNA damage and invokes translesion polymerase Polκ for repair in melanocytes. Nucleic Acids Research. 51(19). 10451–10466. 1 indexed citations
6.
Tanwar, Jyoti, et al.. (2020). Histone variant dictates fate biasing of neural crest cells to melanocyte lineage. Development. 147(5). 17 indexed citations
7.
Varshney, Swati, Shantanu Sengupta, H K Kar, et al.. (2019). Micro RNAs upregulated in Vitiligo skin play an important role in its aetiopathogenesis by altering TRP1 expression and keratinocyte-melanocytes cross-talk. Scientific Reports. 9(1). 10079–10079. 32 indexed citations
8.
Vats, Archana, et al.. (2019). pH‐controlled histone acetylation amplifies melanocyte differentiation downstream of MITF. EMBO Reports. 21(1). e48333–e48333. 23 indexed citations
9.
Jatana, Nidhi, David B. Ascher, Douglas E. V. Pires, Rajesh S. Gokhale, & Lipi Thukral. (2019). Human LC3 and GABARAP subfamily members achieve functional specificity via specific structural modulations. Autophagy. 16(2). 239–255. 51 indexed citations
10.
Motiani, Rajender K., Jyoti Tanwar, Sachin Sharma, et al.. (2018). STIM 1 activation of adenylyl cyclase 6 connects Ca 2+ and cAMP signaling during melanogenesis. The EMBO Journal. 37(5). 57 indexed citations
11.
Maji, Abhijit, Richa Misra, Anupam Mondal, et al.. (2015). Expression profiling of lymph nodes in tuberculosis patients reveal inflammatory milieu at site of infection. Scientific Reports. 5(1). 15214–15214. 38 indexed citations
12.
Jamwal, Shilpa, et al.. (2012). Mycobacterium tuberculosis-Driven Targeted Recalibration of Macrophage Lipid Homeostasis Promotes the Foamy Phenotype. Cell Host & Microbe. 12(5). 669–681. 226 indexed citations
13.
Singh, Archana, Pankaj Sharma, H K Kar, et al.. (2011). HLA Alleles and Amino-Acid Signatures of the Peptide-Binding Pockets of HLA Molecules in Vitiligo. Journal of Investigative Dermatology. 132(1). 124–134. 58 indexed citations
14.
Mohanty, Debasisa, Rajan Sankaranarayanan, & Rajesh S. Gokhale. (2011). Fatty acyl-AMP ligases and polyketide synthases are unique enzymes of lipid biosynthetic machinery in Mycobacterium tuberculosis. Tuberculosis. 91(5). 448–455. 18 indexed citations
15.
Gokhale, Rajesh S., et al.. (2010). Genome scale prediction of substrate specificity for acyl adenylate superfamily of enzymes based on active site residue profiles. BMC Bioinformatics. 11(1). 57–57. 28 indexed citations
16.
Ghosh, Ratna, Pallavi A. Phatale, Subodh Kumar Samrat, et al.. (2008). Dissecting the Functional Role of Polyketide Synthases in Dictyostelium discoideum. Journal of Biological Chemistry. 283(17). 11348–11354. 35 indexed citations
17.
Dhawan, Jyotsna, Rajesh S. Gokhale, & Inder M. Verma. (2005). Bioscience in India: Times Are Changing. Cell. 123(5). 743–745. 3 indexed citations
18.
Yadav, Gitanjali, Rajesh S. Gokhale, & Debasisa Mohanty. (2003). Computational Approach for Prediction of Domain Organization and Substrate Specificity of Modular Polyketide Synthases. Journal of Molecular Biology. 328(2). 335–363. 170 indexed citations
19.
Tsai, Shiou‐Chuan, Larry J. W. Miercke, J. Krucinski, et al.. (2001). Crystal structure of the macrocycle-forming thioesterase domain of the erythromycin polyketide synthase: Versatility from a unique substrate channel. Proceedings of the National Academy of Sciences. 98(26). 14808–14813. 179 indexed citations
20.
Ray, Soumya S., et al.. (1997). Triosephosphate isomerase from Plasmodium falciparum:. the crystal structure provides insights into antimalarial drug design. Structure. 5(6). 751–761. 105 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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