Ramesh Prasad

606 total citations
28 papers, 410 citations indexed

About

Ramesh Prasad is a scholar working on Molecular Biology, Hematology and Cell Biology. According to data from OpenAlex, Ramesh Prasad has authored 28 papers receiving a total of 410 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Hematology and 4 papers in Cell Biology. Recurrent topics in Ramesh Prasad's work include Blood Coagulation and Thrombosis Mechanisms (8 papers), Protein Structure and Dynamics (4 papers) and Hemophilia Treatment and Research (4 papers). Ramesh Prasad is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (8 papers), Protein Structure and Dynamics (4 papers) and Hemophilia Treatment and Research (4 papers). Ramesh Prasad collaborates with scholars based in India, United States and Russia. Ramesh Prasad's co-authors include Prosenjit Sen, Huan‐Xiang Zhou, Kaushik Das, Ashis K. Mukherjee, Divya Kota, Shabbir A. Ansari, Anindita Bhattacharya, Sanbo Qin, Madhu Rawat and Atul Goel and has published in prestigious journals such as Chemical Reviews, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Ramesh Prasad

28 papers receiving 408 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ramesh Prasad India 11 233 91 57 49 40 28 410
Robert J. Goodson United States 7 228 1.0× 88 1.0× 62 1.1× 36 0.7× 74 1.9× 11 391
Shyemaa Shehata Canada 3 255 1.1× 57 0.6× 27 0.5× 35 0.7× 79 2.0× 4 370
Alison Howarth United Kingdom 10 158 0.7× 77 0.8× 20 0.4× 22 0.4× 40 1.0× 16 285
Olga Lubman United States 11 355 1.5× 46 0.5× 36 0.6× 77 1.6× 85 2.1× 11 517
Lucie Ahn United States 7 286 1.2× 91 1.0× 36 0.6× 26 0.5× 94 2.4× 10 388
Zhenzhen Chen China 12 342 1.5× 140 1.5× 19 0.3× 71 1.4× 82 2.0× 25 500
James N. Psathas United States 7 246 1.1× 67 0.7× 13 0.2× 61 1.2× 88 2.2× 7 405
Damien Destouches France 13 439 1.9× 150 1.6× 29 0.5× 56 1.1× 142 3.5× 21 621
Shuang Wu China 12 179 0.8× 58 0.6× 39 0.7× 64 1.3× 14 0.3× 29 460

Countries citing papers authored by Ramesh Prasad

Since Specialization
Citations

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

Fields of papers citing papers by Ramesh Prasad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ramesh Prasad

This figure shows the co-authorship network connecting the top 25 collaborators of Ramesh Prasad. A scholar is included among the top collaborators of Ramesh Prasad 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 Ramesh Prasad. Ramesh Prasad 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.
Prasad, Ramesh, et al.. (2025). Membrane Association of Intrinsically Disordered Proteins. Annual Review of Biophysics. 54(1). 275–302. 2 indexed citations
2.
Prasad, Ramesh, Nabanita Das, Huajun Qin, et al.. (2025). Mycobacterium tuberculosis CrgA Forms a Dimeric Structure with Its Transmembrane Domain Sandwiched between Cytoplasmic and Periplasmic β-Sheets, Enabling Multiple Interactions with Other Divisome Proteins. Journal of the American Chemical Society. 147(13). 11117–11131. 1 indexed citations
3.
Zhou, Huan‐Xiang, Divya Kota, Sanbo Qin, & Ramesh Prasad. (2024). Fundamental Aspects of Phase-Separated Biomolecular Condensates. Chemical Reviews. 124(13). 8550–8595. 32 indexed citations
4.
Zhang, Yi, et al.. (2024). Amino acid-dependent phase equilibrium and material properties of tetrapeptide condensates. Cell Reports Physical Science. 5(10). 102218–102218. 10 indexed citations
5.
Prasad, Ramesh, Yuan Gao, Jens O. Watzlawik, et al.. (2023). A common pathway for detergent-assisted oligomerization of Aβ42. Communications Biology. 6(1). 1184–1184. 5 indexed citations
6.
Prasad, Ramesh, et al.. (2023). Two gates mediate NMDA receptor activity and are under subunit-specific regulation. Nature Communications. 14(1). 1623–1623. 10 indexed citations
7.
Zhang, Rongfu, Huajun Qin, Ramesh Prasad, et al.. (2023). Dimeric Transmembrane Structure of the SARS-CoV-2 E Protein. Communications Biology. 6(1). 1109–1109. 8 indexed citations
8.
9.
Prasad, Ramesh, et al.. (2022). SpiDec: Computing binodals and interfacial tension of biomolecular condensates from simulations of spinodal decomposition. Frontiers in Molecular Biosciences. 9. 1021939–1021939. 7 indexed citations
10.
Bhattacharya, Anindita, et al.. (2020). MAP Kinase driven actomyosin rearrangement is a crucial regulator of monocyte to macrophage differentiation. Cellular Signalling. 73. 109691–109691. 10 indexed citations
11.
Prasad, Ramesh & Huan‐Xiang Zhou. (2020). Membrane Association and Functional Mechanism of Synaptotagmin-1 in Triggering Vesicle Fusion. Biophysical Journal. 119(6). 1255–1265. 8 indexed citations
12.
Das, Kaushik, Subhojit Paul, Arnab Ghosh, et al.. (2019). Triple-negative breast cancer-derived microvesicles transfer microRNA221 to the recipient cells and thereby promote epithelial-to-mesenchymal transition. Journal of Biological Chemistry. 294(37). 13681–13696. 41 indexed citations
13.
Das, Kaushik, et al.. (2018). Matrix metalloproteinase-2: A key regulator in coagulation proteases mediated human breast cancer progression through autocrine signaling. Biomedicine & Pharmacotherapy. 105. 395–406. 43 indexed citations
14.
Prasad, Ramesh & Prosenjit Sen. (2018). Phosphatidylcholine in the groove of endothelial cell protein C receptor (EPCR) regulates EPCR conformation and protein C recognition. Integrative Biology. 10(11). 696–704. 1 indexed citations
15.
Das, Kaushik, et al.. (2018). The Protease Activated Receptor2 Promotes Rab5a Mediated Generation of Pro-metastatic Microvesicles. Scientific Reports. 8(1). 7357–7357. 25 indexed citations
16.
Prasad, Ramesh, et al.. (2018). Contribution of allosteric disulfide in the structural regulation of membrane-bound tissue factor–factor VIIa binary complex. Journal of Biomolecular Structure and Dynamics. 37(14). 3707–3720. 5 indexed citations
17.
Prasad, Ramesh & Prosenjit Sen. (2017). Molecular determinants involved in differential behaviour between soluble tissue factor and full-length tissue factor towards factor VIIa. Physical Chemistry Chemical Physics. 19(33). 22230–22242. 6 indexed citations
18.
Ansari, Shabbir A., Kaushik Das, Ramesh Prasad, et al.. (2017). Coagulation factor VIIa-mediated protease-activated receptor 2 activation leads to β-catenin accumulation via the AKT/GSK3β pathway and contributes to breast cancer progression. Journal of Biological Chemistry. 292(33). 13688–13701. 27 indexed citations
19.
Prasad, Ramesh, et al.. (2015). Understanding epithelial-mesenchymal transition in oral cancer: Made easy. 1. 23–26. 3 indexed citations
20.
Prasad, Ramesh, et al.. (2013). Parotid lymphoepithelial cysts in human immunodeficiency virus: a review. The Journal of Laryngology & Otology. 127(11). 1046–1049. 10 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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