R. Nandini Asha

618 total citations
29 papers, 481 citations indexed

About

R. Nandini Asha is a scholar working on Organic Chemistry, Oncology and Physical and Theoretical Chemistry. According to data from OpenAlex, R. Nandini Asha has authored 29 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 18 papers in Oncology and 6 papers in Physical and Theoretical Chemistry. Recurrent topics in R. Nandini Asha's work include Metal complexes synthesis and properties (18 papers), Synthesis and biological activity (11 papers) and Synthesis and Characterization of Heterocyclic Compounds (9 papers). R. Nandini Asha is often cited by papers focused on Metal complexes synthesis and properties (18 papers), Synthesis and biological activity (11 papers) and Synthesis and Characterization of Heterocyclic Compounds (9 papers). R. Nandini Asha collaborates with scholars based in India, United States and Taiwan. R. Nandini Asha's co-authors include Murugesan Sankarganesh, Shunmugasundaram Gurusamy, Alagarsamy Mathavan, Nattamai Bhuvanesh, Thayalaraj Christopher Jeyakumar, Jeyaraj Dhaveethu Raja, Paulraj Adwin Jose, A. Sakthivel, R. Subramanian and S. Johnson Raja and has published in prestigious journals such as Journal of Molecular Liquids, Journal of Molecular Structure and Optik.

In The Last Decade

R. Nandini Asha

28 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Nandini Asha India 14 287 279 98 77 73 29 481
Naki Çolak Türkiye 14 423 1.5× 304 1.1× 58 0.6× 76 1.0× 96 1.3× 47 621
Wardha Zafar Pakistan 13 547 1.9× 347 1.2× 71 0.7× 92 1.2× 70 1.0× 20 701
Nurcan Karacan Türkiye 15 389 1.4× 229 0.8× 164 1.7× 90 1.2× 67 0.9× 27 536
D. Gayathri India 13 417 1.5× 293 1.1× 127 1.3× 50 0.6× 142 1.9× 79 695
Sali̇ha Alyar Türkiye 17 478 1.7× 279 1.0× 186 1.9× 109 1.4× 51 0.7× 31 657
Jessica Elizabeth Philip India 11 258 0.9× 220 0.8× 50 0.5× 61 0.8× 127 1.7× 12 419
Md. Al‐Amin‐Al‐Azadul Islam Bangladesh 8 288 1.0× 130 0.5× 53 0.5× 114 1.5× 66 0.9× 19 432
Hami̇t Alyar Türkiye 13 340 1.2× 188 0.7× 103 1.1× 164 2.1× 42 0.6× 22 487
Christophe Boldron France 12 207 0.7× 211 0.8× 125 1.3× 83 1.1× 132 1.8× 16 510
Shunmugasundaram Gurusamy India 13 217 0.8× 275 1.0× 109 1.1× 49 0.6× 62 0.8× 20 471

Countries citing papers authored by R. Nandini Asha

Since Specialization
Citations

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

Fields of papers citing papers by R. Nandini Asha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. Nandini Asha. 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 R. Nandini Asha. The network helps show where R. Nandini Asha may publish in the future.

Co-authorship network of co-authors of R. Nandini Asha

This figure shows the co-authorship network connecting the top 25 collaborators of R. Nandini Asha. A scholar is included among the top collaborators of R. Nandini Asha 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 R. Nandini Asha. R. Nandini Asha 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
2.
Sankarganesh, Murugesan, Jeyaraj Dhaveethu Raja, S. Johnson Raja, et al.. (2023). Synthesis, spectral, DFT calculation, antimicrobial, antioxidant, DNA/BSA binding and molecular docking studies of bio-pharmacologically active pyrimidine appended Cu(II) and Zn(II) complexes. Journal of Biomolecular Structure and Dynamics. 41(24). 14914–14928. 10 indexed citations
4.
Parthiban, A., V. Sachithanandam, P. Lalitha, et al.. (2022). Isolation and biological evaluation 7-hydroxy flavone from Avicennia officinalis L: insights from extensive in vitro , DFT, molecular docking and molecular dynamics simulation studies. Journal of Biomolecular Structure and Dynamics. 41(7). 2848–2860. 13 indexed citations
5.
Gurusamy, Shunmugasundaram, R. Nandini Asha, Murugesan Sankarganesh, Thayalaraj Christopher Jeyakumar, & Alagarsamy Mathavan. (2022). Vanillin based colorimetric and fluorometric chemosensor for detection of Cu(II) ion: DFT calculation, DNA / BSA interaction and molecular docking studies. Inorganic Chemistry Communications. 143. 109716–109716. 26 indexed citations
7.
Sankarganesh, Murugesan, et al.. (2022). Bovine serum albumin interaction, molecular docking, anticancer and antimicrobial activities of Co(II) Schiff base complex derived from Nophen ligand. Journal of Biomolecular Structure and Dynamics. 41(5). 1895–1903. 21 indexed citations
9.
Parthiban, A., et al.. (2022). Synthesis, in vitro, in silico and DFT studies of indole curcumin derivatives as potential anticancer agents. Journal of Molecular Structure. 1270. 133885–133885. 16 indexed citations
10.
Asha, R. Nandini, et al.. (2021). Synthesis, structure, Hirshfeld surface, DFT, and molecular docking studies of a new organic cocrystal: creatinine:2,3‐pyridinedicarboxylic acid. Journal of Physical Organic Chemistry. 34(9). 10 indexed citations
11.
Asha, R. Nandini, et al.. (2021). Experimental and theoretical studies of 1,3,5‐tris (bromomethyl)‐2,4,6‐trimethylbenzene with 2‐pyridone. Journal of Physical Organic Chemistry. 34(6). 4 indexed citations
12.
Sankarganesh, Murugesan, et al.. (2021). Spectroscopic studies on DNA interaction and anticancer activities of pharmacologically active pyrimidine derivative mixed ligand Co(II) and Ni(II) complexes. Journal of Molecular Structure. 1252. 132079–132079. 15 indexed citations
13.
Gurusamy, Shunmugasundaram, et al.. (2021). Synthesis, characterization, DNA interaction, BSA/HSA binding activities of VO(IV), Cu(II) and Zn(II) Schiff base complexes and its molecular docking with biomolecules. Journal of Molecular Liquids. 345. 117045–117045. 99 indexed citations
14.
Asha, R. Nandini, et al.. (2021). Synthesis, molecular docking, and in silico ADMET studies of 4-benzyl-1-(2,4,6-trimethyl-benzyl)-piperidine: Potential Inhibitor of SARS-CoV2. Bioorganic Chemistry. 112. 104967–104967. 34 indexed citations
17.
Sankarganesh, Murugesan, Jeyaraj Dhaveethu Raja, Paulraj Adwin Jose, et al.. (2021). Synthesis, characterization, DFT calculation, biological and molecular docking of Cu(II) complex of pyrimidine derived Schiff base ligand. Journal of Saudi Chemical Society. 25(4). 101225–101225. 36 indexed citations
18.
Kumaresan, S., et al.. (2021). Growth, structural, Hirshfeld surface analysis, DFT validation on the crystal structure of 1, 10-Phenanthrolin-1-ium-5,6-dione perchlorate monohydrate. Chemical Data Collections. 33. 100706–100706. 2 indexed citations
19.
Asha, R. Nandini, et al.. (2020). Synthesis, Characterization and Biological Activity of (Phenylthio)Acetic Acid:Theophylline Cocrystal. Journal of Chemical Crystallography. 51(2). 225–234. 7 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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