Raman Parkesh

3.0k total citations
49 papers, 2.5k citations indexed

About

Raman Parkesh is a scholar working on Molecular Biology, Spectroscopy and Materials Chemistry. According to data from OpenAlex, Raman Parkesh has authored 49 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Spectroscopy and 11 papers in Materials Chemistry. Recurrent topics in Raman Parkesh's work include Molecular Sensors and Ion Detection (11 papers), Calcium signaling and nucleotide metabolism (9 papers) and Analytical Chemistry and Sensors (7 papers). Raman Parkesh is often cited by papers focused on Molecular Sensors and Ion Detection (11 papers), Calcium signaling and nucleotide metabolism (9 papers) and Analytical Chemistry and Sensors (7 papers). Raman Parkesh collaborates with scholars based in India, Ireland and United States. Raman Parkesh's co-authors include Thorfinnur Gunnlaugsson, T. Clive Lee, Grant C. Churchill, Matthew D. Disney, Paul E. Kruger, Gillian M. Hussey, Frederick M. Pfeffer, Kamal K. Kapoor, Jessica L. Childs‐Disney and Sridhar R. Vasudevan and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Raman Parkesh

48 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raman Parkesh India 26 990 885 648 441 312 49 2.5k
Y. George Zheng United States 36 2.8k 2.9× 692 0.8× 597 0.9× 102 0.2× 212 0.7× 105 3.9k
Yutaka Shindo Japan 25 635 0.6× 437 0.5× 439 0.7× 24 0.1× 169 0.5× 57 1.9k
Akiyo Yamauchi Japan 24 438 0.4× 404 0.5× 300 0.5× 66 0.1× 140 0.4× 64 1.7k
Hyun‐Woo Rhee South Korea 29 2.9k 2.9× 589 0.7× 583 0.9× 51 0.1× 93 0.3× 82 4.5k
Ryosuke Kojima Japan 27 1.4k 1.4× 225 0.3× 1.2k 1.8× 22 0.0× 43 0.1× 63 3.4k
Lei Xu China 24 903 0.9× 511 0.6× 752 1.2× 20 0.0× 125 0.4× 118 2.3k
Changmin Yu China 36 1.6k 1.7× 1.4k 1.5× 1.9k 2.9× 35 0.1× 223 0.7× 96 4.1k
Miae Won South Korea 31 1.2k 1.2× 709 0.8× 1.5k 2.2× 61 0.1× 101 0.3× 71 3.7k
Bowen Ke China 29 1.2k 1.2× 243 0.3× 370 0.6× 36 0.1× 58 0.2× 100 2.5k

Countries citing papers authored by Raman Parkesh

Since Specialization
Citations

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

Fields of papers citing papers by Raman Parkesh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raman Parkesh

This figure shows the co-authorship network connecting the top 25 collaborators of Raman Parkesh. A scholar is included among the top collaborators of Raman Parkesh 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 Raman Parkesh. Raman Parkesh 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
4.
Kapoor, Kamal K., et al.. (2022). Fluorescence “Turn-Off” and Colorimetric Sensor for Fe2+, Fe3+, and Cu2+ Ions Based on a 2,5,7-Triarylimidazopyridine Scaffold. ACS Omega. 7(13). 11114–11125. 65 indexed citations
5.
Kumar, Sunil, et al.. (2021). Chemical Space Exploration of DprE1 Inhibitors Using Chemoinformatics and Artificial Intelligence. ACS Omega. 6(22). 14430–14441. 20 indexed citations
6.
Parkesh, Raman, et al.. (2021). Discovery and characterization of small molecule SIRT3-specific inhibitors as revealed by mass spectrometry. Bioorganic Chemistry. 110. 104768–104768. 9 indexed citations
7.
Kumar, Sunil, et al.. (2020). Exploiting cheminformatic and machine learning to navigate the available chemical space of potential small molecule inhibitors of SARS-CoV-2. Computational and Structural Biotechnology Journal. 19. 424–438. 28 indexed citations
8.
Lokesh, Dhanashree, et al.. (2018). Bifidobacterium adolescentis is intrinsically resistant to antitubercular drugs. Scientific Reports. 8(1). 11897–11897. 34 indexed citations
10.
Agrawal, Pushpa, Pawan Gupta, Kunchithapadam Swaminathan, & Raman Parkesh. (2014). α-Glucan Pathway as a Novel Mtb Drug Target: Structural Insights and Cues for Polypharmcological Targeting of GlgB and GlgE. Current Medicinal Chemistry. 21(35). 4074–4084. 4 indexed citations
11.
Dkhar, Hedwin Kitdorlang, Amandeep Kaur, Ella Bhagyaraj, et al.. (2014). Discovery of Mycobacterium tuberculosis α-1,4-Glucan Branching Enzyme (GlgB) Inhibitors by Structure- and Ligand-based Virtual Screening. Journal of Biological Chemistry. 290(1). 76–89. 19 indexed citations
12.
Brailoiu, G. Cristina, Xīn Gào, Raman Parkesh, et al.. (2010). Acidic NAADP-sensitive Calcium Stores in the Endothelium. Journal of Biological Chemistry. 285(48). 37133–37137. 57 indexed citations
13.
Arredouani, Abdelilah, et al.. (2009). Essential role of NAADP-evoked calcium release in glucose-mediated depolarization, [Ca2+]i spiking and insulin secretion in mouse pancreatic beta cell. Diabetologia. 52. 2 indexed citations
14.
Lewis, Alexander M., Akiko Mizote, Justyn M. Thomas, et al.. (2009). Analogues of the Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) Antagonist Ned-19 Indicate Two Binding Sites on the NAADP Receptor. Journal of Biological Chemistry. 284(50). 34930–34934. 36 indexed citations
15.
Parkesh, Raman, Alexander M. Lewis, Parvinder K. Aley, et al.. (2007). Cell-permeant NAADP: A novel chemical tool enabling the study of Ca2+ signalling in intact cells. Cell Calcium. 43(6). 531–538. 61 indexed citations
16.
Yamasaki, Michiko, et al.. (2007). NAADP Controls Cross-talk between Distinct Ca2+ Stores in the Heart. Journal of Biological Chemistry. 282(20). 15302–15311. 86 indexed citations
17.
Parkesh, Raman, et al.. (2006). Chemo-enzymatic synthesis and biological evaluation of photolabile nicotinic acid adenine dinuclotide phosphate (NAADP+). Organic & Biomolecular Chemistry. 5(3). 441–443. 5 indexed citations
18.
Parkesh, Raman, T. Clive Lee, Thorfinnur Gunnlaugsson, & Wolfgang Gowin. (2005). Microdamage in bone: Surface analysis and radiological detection. Journal of Biomechanics. 39(8). 1552–1556. 16 indexed citations
20.
Lee, T. C., Sahar Mohsin, David Taylor, et al.. (2003). Detecting microdamage in bone. Journal of Anatomy. 203(2). 161–172. 155 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026