Dipak Datta

3.3k total citations
84 papers, 2.5k citations indexed

About

Dipak Datta is a scholar working on Molecular Biology, Oncology and Immunology. According to data from OpenAlex, Dipak Datta has authored 84 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 20 papers in Oncology and 13 papers in Immunology. Recurrent topics in Dipak Datta's work include RNA modifications and cancer (10 papers), Immunotherapy and Immune Responses (8 papers) and Epigenetics and DNA Methylation (6 papers). Dipak Datta is often cited by papers focused on RNA modifications and cancer (10 papers), Immunotherapy and Immune Responses (8 papers) and Epigenetics and DNA Methylation (6 papers). Dipak Datta collaborates with scholars based in India, United States and Germany. Dipak Datta's co-authors include Soumitro Pal, David M. Briscoe, Akhilesh Singh, Sanjeev Meena, Anup K. Singh, Olivier Dormond, Aninda Basu, Ana Maria Waaga-Gasser, Rakesh Arya and Mushtaq Ahmad Nengroo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Dipak Datta

82 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dipak Datta India 30 1.1k 691 469 287 177 84 2.5k
Yiqun G. Shellman United States 26 1.6k 1.4× 526 0.8× 415 0.9× 489 1.7× 120 0.7× 57 2.6k
Claudia Ceci Italy 15 1.2k 1.0× 444 0.6× 225 0.5× 329 1.1× 177 1.0× 23 2.1k
Sangtaek Oh South Korea 34 2.7k 2.3× 730 1.1× 472 1.0× 329 1.1× 217 1.2× 93 4.0k
Ravi P. Sahu United States 25 1.2k 1.0× 416 0.6× 293 0.6× 285 1.0× 133 0.8× 89 2.2k
Qizhi Wang China 27 2.0k 1.7× 674 1.0× 376 0.8× 544 1.9× 240 1.4× 135 3.0k
Mukesh K. Agarwal United States 22 1.5k 1.3× 1.2k 1.8× 323 0.7× 459 1.6× 125 0.7× 35 2.8k
Sushil Kumar India 22 1.8k 1.5× 793 1.1× 334 0.7× 509 1.8× 292 1.6× 67 3.4k
Numsen Hail United States 29 1.6k 1.4× 385 0.6× 275 0.6× 326 1.1× 141 0.8× 41 2.4k
Rakesh Naidu Malaysia 27 1.2k 1.1× 484 0.7× 177 0.4× 464 1.6× 139 0.8× 91 2.4k
Carmen Ruiz‐Ruiz Spain 27 1.6k 1.4× 656 0.9× 592 1.3× 361 1.3× 92 0.5× 54 2.5k

Countries citing papers authored by Dipak Datta

Since Specialization
Citations

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

Fields of papers citing papers by Dipak Datta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dipak Datta

This figure shows the co-authorship network connecting the top 25 collaborators of Dipak Datta. A scholar is included among the top collaborators of Dipak Datta 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 Dipak Datta. Dipak Datta 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.
Dubey, Amit, Nitesh Singh, Pragya D. Yadav, et al.. (2025). Steroidal Alkaloids from Sarcococca saligna (Buxaceae): In Vitro and In Silico Evaluation of Their Cytotoxic Potential. ACS Omega. 10(41). 48111–48129.
2.
Datta, Dipak, et al.. (2024). Emerging role of EZH2 in solid tumor metastasis. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1880(1). 189253–189253. 2 indexed citations
3.
Rai, S., et al.. (2024). Unravelling a novel CTNND1-RAB6A fusion transcript: Implications in colon cancer cell migration. International Journal of Biological Macromolecules. 262(Pt 2). 129981–129981. 1 indexed citations
4.
Saini, Krishan Kumar, Kiran Tripathi, Priyanka Rai, et al.. (2024). ACSL4-mediated H3K9 and H3K27 hyperacetylation upregulates SNAIL to drive TNBC metastasis. Proceedings of the National Academy of Sciences. 121(52). e2408049121–e2408049121. 3 indexed citations
5.
Roy, Kamalika, Avishek Bhuniya, Saptak Banerjee, et al.. (2023). Terminally Exhausted CD8+ T Cells Resistant to PD-1 Blockade Promote Generation and Maintenance of Aggressive Cancer Stem Cells. Cancer Research. 83(11). 1815–1833. 16 indexed citations
6.
Yadav, Anjali, et al.. (2023). Targeting MALAT1 Augments Sensitivity to PARP Inhibition by Impairing Homologous Recombination in Prostate Cancer. Cancer Research Communications. 3(10). 2044–2061. 11 indexed citations
7.
Nengroo, Mushtaq Ahmad, et al.. (2022). Demystifying the CXCR4 conundrum in cancer biology: Beyond the surface signaling paradigm. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1877(5). 188790–188790. 21 indexed citations
8.
Tiwari, Ritika, Vipul Bhatia, Anjali Yadav, et al.. (2020). Androgen deprivation upregulates SPINK1 expression and potentiates cellular plasticity in prostate cancer. Nature Communications. 11(1). 384–384. 57 indexed citations
9.
Gour, Jitendra, Srikanth Gatadi, Ravikumar Akunuri, et al.. (2019). Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles. Organic & Biomolecular Chemistry. 17(35). 8153–8165. 3 indexed citations
10.
Avula, Srinivasa Rao, Akhilesh Singh, Lakhwinder Singh, et al.. (2017). Discovery of a Novel Small-Molecule Inhibitor that Targets PP2A–β-Catenin Signaling and Restricts Tumor Growth and Metastasis. Molecular Cancer Therapeutics. 16(9). 1791–1805. 18 indexed citations
11.
Yadav, Navneet Kumar, Rakesh Arya, Kapil Dev, et al.. (2017). Alcoholic Extract of Eclipta alba Shows In Vitro Antioxidant and Anticancer Activity without Exhibiting Toxicological Effects. Oxidative Medicine and Cellular Longevity. 2017(1). 9094641–9094641. 34 indexed citations
12.
Mishra, Tripti, Rakesh Arya, Sanjeev Meena, et al.. (2016). Isolation, Characterization and Anticancer Potential of Cytotoxic Triterpenes from Betula utilis Bark. PLoS ONE. 11(7). e0159430–e0159430. 57 indexed citations
13.
Singh, Anup K., et al.. (2014). Exosomes: Emerging Players of Intercellular Communication in Tumor Microenvironment. PubMed. 2(3). e26–e26. 19 indexed citations
14.
Basu, Aninda, Tao Liu, Pallavi Banerjee, et al.. (2012). Effectiveness of a combination therapy using calcineurin inhibitor and mTOR inhibitor in preventing allograft rejection and post-transplantation renal cancer progression. Cancer Letters. 321(2). 179–186. 11 indexed citations
15.
Hoerning, André, Dipak Datta, Caroline N. Jones, et al.. (2011). Subsets of human CD4+ regulatory T cells express the peripheral homing receptor CXCR3. European Journal of Immunology. 41(8). 2291–2302. 61 indexed citations
16.
Ravi, V., et al.. (2010). Hepatoprotective Activity of Bombax ceiba Linn against Isoniazid and Rifampicin-induced Toxicity in Experimental Rats. 3(3). 19–26. 36 indexed citations
17.
Datta, Dipak, Alan G. Contreras, Aninda Basu, et al.. (2009). Calcineurin Inhibitors Activate the Proto-Oncogene Ras and Promote Protumorigenic Signals in Renal Cancer Cells. Cancer Research. 69(23). 8902–8909. 54 indexed citations
18.
Basu, Aninda, Alan G. Contreras, Dipak Datta, et al.. (2008). Overexpression of Vascular Endothelial Growth Factor and the Development of Post-Transplantation Cancer. Cancer Research. 68(14). 5689–5698. 56 indexed citations
19.
Dormond, Olivier, Alan G. Contreras, Esther Meijer, et al.. (2008). CD40-Induced Signaling in Human Endothelial Cells Results in mTORC2- and Akt-Dependent Expression of Vascular Endothelial Growth Factor In Vitro and In Vivo. The Journal of Immunology. 181(11). 8088–8095. 44 indexed citations
20.
Datta, Dipak, Christopher Geehan, Martin Grimm, et al.. (2006). Ras-induced Modulation of CXCL10 and Its Receptor Splice Variant CXCR3-B in MDA-MB-435 and MCF-7 Cells: Relevance for the Development of Human Breast Cancer. Cancer Research. 66(19). 9509–9518. 142 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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