N. Selvamurugan

15.7k total citations · 1 hit paper
197 papers, 12.6k citations indexed

About

N. Selvamurugan is a scholar working on Molecular Biology, Biomedical Engineering and Biomaterials. According to data from OpenAlex, N. Selvamurugan has authored 197 papers receiving a total of 12.6k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Molecular Biology, 84 papers in Biomedical Engineering and 54 papers in Biomaterials. Recurrent topics in N. Selvamurugan's work include Bone Tissue Engineering Materials (82 papers), Bone Metabolism and Diseases (57 papers) and MicroRNA in disease regulation (33 papers). N. Selvamurugan is often cited by papers focused on Bone Tissue Engineering Materials (82 papers), Bone Metabolism and Diseases (57 papers) and MicroRNA in disease regulation (33 papers). N. Selvamurugan collaborates with scholars based in India, United States and Japan. N. Selvamurugan's co-authors include Saravanan Sekaran, Nicola C. Partridge, K. Balagangadharan, Shantikumar V. Nair, A. Moorthi, R. Jayakumar, Hiroshi Tamura, Selvaraj Vimalraj, S. Dhivya and S. Viji Chandran 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

N. Selvamurugan

192 papers receiving 12.4k citations

Hit Papers

A review of chitosan and ... 2016 2026 2019 2022 2016 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N. Selvamurugan India 62 5.9k 4.7k 3.6k 1.4k 1.4k 197 12.6k
Lianfu Deng China 58 4.5k 0.8× 3.1k 0.7× 2.8k 0.8× 636 0.5× 2.0k 1.5× 217 11.3k
Jiacan Su China 58 4.3k 0.7× 2.0k 0.4× 3.9k 1.1× 1.0k 0.7× 1.7k 1.2× 333 11.2k
Hasan Uludağ Canada 53 3.3k 0.6× 2.3k 0.5× 4.4k 1.2× 542 0.4× 1.4k 1.0× 237 9.5k
Joaquím M. Oliveira Portugal 64 7.9k 1.3× 5.6k 1.2× 1.9k 0.5× 328 0.2× 3.1k 2.3× 360 15.3k
Bo Lei China 52 4.4k 0.7× 2.8k 0.6× 2.2k 0.6× 637 0.5× 1.3k 0.9× 235 10.2k
Xiaojun Zhou China 49 3.8k 0.6× 2.3k 0.5× 2.2k 0.6× 943 0.7× 973 0.7× 239 8.4k
Changsheng Liu China 66 9.0k 1.5× 6.1k 1.3× 2.5k 0.7× 263 0.2× 3.0k 2.2× 449 16.7k
Kaili Lin China 67 9.5k 1.6× 4.0k 0.8× 2.0k 0.5× 407 0.3× 2.6k 1.9× 256 14.0k
Xinquan Jiang China 53 5.3k 0.9× 2.2k 0.5× 1.7k 0.5× 573 0.4× 1.9k 1.3× 152 8.4k
Jérôme Guicheux France 62 3.5k 0.6× 1.6k 0.3× 2.5k 0.7× 449 0.3× 2.4k 1.7× 261 10.5k

Countries citing papers authored by N. Selvamurugan

Since Specialization
Citations

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

Fields of papers citing papers by N. Selvamurugan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Selvamurugan

This figure shows the co-authorship network connecting the top 25 collaborators of N. Selvamurugan. A scholar is included among the top collaborators of N. Selvamurugan 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 N. Selvamurugan. N. Selvamurugan 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.
2.
Selvamurugan, N., et al.. (2024). RUNX2 regulation in osteoblast differentiation: A possible therapeutic function of the lncRNA and miRNA-mediated network. Differentiation. 140. 100803–100803. 4 indexed citations
3.
Akshaya, R.L., et al.. (2024). Regulatory and therapeutic implications of competing endogenous RNA network in breast cancer progression and metastasis: A review. International Journal of Biological Macromolecules. 266(Pt 2). 131075–131075. 9 indexed citations
4.
Siram, Karthik, et al.. (2024). Chitosan nanocarriers for non-coding RNA therapeutics: A review. International Journal of Biological Macromolecules. 263(Pt 1). 130361–130361. 12 indexed citations
5.
Akshaya, R.L., et al.. (2024). In vivo validation of the functional role of MicroRNA-4638-3p in breast cancer bone metastasis. Journal of Cancer Research and Clinical Oncology. 150(2). 63–63. 1 indexed citations
6.
Selvamurugan, N., et al.. (2024). Role of crosslinkers in advancing chitosan-based biocomposite scaffolds for bone tissue engineering: A comprehensive review. International Journal of Biological Macromolecules. 283(Pt 1). 137625–137625. 4 indexed citations
8.
Selvamurugan, N., et al.. (2024). A potential function for MicroRNA-124 in normal and pathological bone conditions. Non-coding RNA Research. 9(3). 687–694. 2 indexed citations
9.
Lavanya, K., K. Balagangadharan, S. Viji Chandran, & N. Selvamurugan. (2023). Chitosan-coated and thymol-loaded polymeric semi-interpenetrating hydrogels: An effective platform for bioactive molecule delivery and bone regeneration in vivo. Biomaterials Advances. 146. 213305–213305. 28 indexed citations
10.
Selvamurugan, N., et al.. (2023). Role and architectural significance of porous chitosan-based scaffolds in bone tissue engineering. International Journal of Biological Macromolecules. 251. 126238–126238. 34 indexed citations
11.
Akshaya, R.L., et al.. (2023). Transforming Growth Factor-β1-mediated Regulation of circ_DISP3 and ATF3 in Human Triple-negative Breast Cancer Cells. Gene Expression. 22(4). 297–305. 3 indexed citations
12.
Selvamurugan, N., et al.. (2023). Nanoceramics-reinforced chitosan scaffolds in bone tissue engineering. Materials Advances. 4(18). 3907–3928. 14 indexed citations
13.
Lavanya, K., et al.. (2023). Recent Advancements in Electrospun Chitin and Chitosan Nanofibers for Bone Tissue Engineering Applications. Journal of Functional Biomaterials. 14(5). 288–288. 21 indexed citations
14.
Krishnan, R., et al.. (2022). Role of p300, a histone acetyltransferase enzyme, in osteoblast differentiation. Differentiation. 124. 43–51. 14 indexed citations
15.
Akshaya, R.L., et al.. (2020). A computational study of non-coding RNAs on the regulation of activating transcription factor 3 in human breast cancer cells. Computational Biology and Chemistry. 89. 107386–107386. 9 indexed citations
16.
Balagangadharan, K., Ritu Trivedi, M. Vairamani, & N. Selvamurugan. (2019). Sinapic acid-loaded chitosan nanoparticles in polycaprolactone electrospun fibers for bone regeneration in vitro and in vivo. Carbohydrate Polymers. 216. 1–16. 78 indexed citations
17.
Soundarya, S., et al.. (2018). Sustained release of chrysin from chitosan-based scaffolds promotes mesenchymal stem cell proliferation and osteoblast differentiation. Carbohydrate Polymers. 195. 356–367. 58 indexed citations
18.
Mohanakrishnan, Vishal, et al.. (2016). MicroRNA‐590‐5p Stabilizes Runx2 by Targeting Smad7 During Osteoblast Differentiation. Journal of Cellular Physiology. 232(2). 371–380. 83 indexed citations
19.
Vimalraj, Selvaraj & N. Selvamurugan. (2013). MicroRNAs: Synthesis, Gene Regulation and Osteoblast Differentiation. Current Issues in Molecular Biology. 15. 7–18. 85 indexed citations
20.
Sathy, Binulal N., N. Selvamurugan, K.T. Shalumon, et al.. (2009). Role of Nanofibrous Poly(Caprolactone) Scaffolds in Human Mesenchymal Stem Cell Attachment and Spreading for In Vitro Bone Tissue Engineering—Response to Osteogenic Regulators. Tissue Engineering Part A. 16(2). 393–404. 110 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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