Vignesh Viswanathan

600 total citations
32 papers, 344 citations indexed

About

Vignesh Viswanathan is a scholar working on Cancer Research, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Vignesh Viswanathan has authored 32 papers receiving a total of 344 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cancer Research, 7 papers in Oncology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Vignesh Viswanathan's work include Cancer Cells and Metastasis (7 papers), Cancer-related molecular mechanisms research (7 papers) and Advanced Radiotherapy Techniques (6 papers). Vignesh Viswanathan is often cited by papers focused on Cancer Cells and Metastasis (7 papers), Cancer-related molecular mechanisms research (7 papers) and Advanced Radiotherapy Techniques (6 papers). Vignesh Viswanathan collaborates with scholars based in United States, India and United Kingdom. Vignesh Viswanathan's co-authors include Bruce M. Boman, Jeremy Z. Fields, Seema Bhatlekar, Lynn M. Opdenaker, Caroline O. Facey, Quynh‐Thu Le, Dhanya K. Nambiar, Rie von Eyben, Hongbin Cao and Christina S. Kong and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and PLoS ONE.

In The Last Decade

Vignesh Viswanathan

31 papers receiving 341 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vignesh Viswanathan United States 11 159 113 94 52 49 32 344
Xiangshan Yang China 12 133 0.8× 72 0.6× 76 0.8× 70 1.3× 42 0.9× 21 295
Cornelius Maihoefer Germany 9 128 0.8× 106 0.9× 53 0.6× 62 1.2× 43 0.9× 9 297
Yae‐Eun Suh United Kingdom 9 188 1.2× 139 1.2× 117 1.2× 98 1.9× 25 0.5× 16 389
Xiaohong Jia China 8 310 1.9× 75 0.7× 66 0.7× 36 0.7× 38 0.8× 15 419
Xiaoxiao Zuo China 11 260 1.6× 158 1.4× 191 2.0× 49 0.9× 80 1.6× 23 475
Wenbo Zheng China 11 189 1.2× 196 1.7× 104 1.1× 47 0.9× 16 0.3× 21 338
Anne Tann United States 10 319 2.0× 40 0.4× 109 1.2× 71 1.4× 24 0.5× 10 495
Jessica Scarborough United States 8 77 0.5× 65 0.6× 61 0.6× 76 1.5× 13 0.3× 13 247
Blaž Grošelj Slovenia 12 296 1.9× 56 0.5× 131 1.4× 67 1.3× 23 0.5× 19 439
Mau‐Shin Chi Taiwan 9 117 0.7× 63 0.6× 62 0.7× 62 1.2× 33 0.7× 17 327

Countries citing papers authored by Vignesh Viswanathan

Since Specialization
Citations

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

Fields of papers citing papers by Vignesh Viswanathan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vignesh Viswanathan

This figure shows the co-authorship network connecting the top 25 collaborators of Vignesh Viswanathan. A scholar is included among the top collaborators of Vignesh Viswanathan 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 Vignesh Viswanathan. Vignesh Viswanathan 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.
Melemenidis, Stavros, Vignesh Viswanathan, Suparna Dutt, et al.. (2025). Effectiveness of FLASH vs. Conventional Dose Rate Radiotherapy in a Model of Orthotopic, Murine Breast Cancer. Cancers. 17(7). 1095–1095. 1 indexed citations
2.
Guan, Li, Vignesh Viswanathan, Yuyan Jiang, et al.. (2024). Tert-expressing cells contribute to salivary gland homeostasis and tissue regeneration after radiation therapy. Genes & Development. 38(11-12). 569–582. 1 indexed citations
3.
Wang, Jinghui, Stavros Melemenidis, Rakesh Manjappa, et al.. (2024). Dosimetric calibration of anatomy‐specific ultra‐high dose rate electron irradiation platform for preclinical FLASH radiobiology experiments. Medical Physics. 51(12). 9166–9178. 3 indexed citations
4.
Viswanathan, Vignesh, et al.. (2024). Axiomatic Aggregations of Abductive Explanations. Proceedings of the AAAI Conference on Artificial Intelligence. 38(10). 11096–11104. 1 indexed citations
5.
Fu, Jie, Zi Yang, Stavros Melemenidis, et al.. (2024). Exploring Deep Learning for Estimating the Isoeffective Dose of FLASH Irradiation From Mouse Intestinal Histological Images. International Journal of Radiation Oncology*Biology*Physics. 119(3). 1001–1010. 4 indexed citations
6.
Melemenidis, Stavros, Vignesh Viswanathan, Rakesh Manjappa, et al.. (2023). Human enteroids as a tool to study conventional and ultra-high dose rate radiation. Integrative Biology. 15. 3 indexed citations
7.
Boman, Bruce M., Vignesh Viswanathan, Caroline O. Facey, Jeremy Z. Fields, & James W. Stave. (2023). The v8-10 variant isoform of CD44 is selectively expressed in the normal human colonic stem cell niche and frequently is overexpressed in colon carcinomas during tumor development. Cancer Biology & Therapy. 24(1). 2195363–2195363. 10 indexed citations
8.
Guan, Li, Dhanya K. Nambiar, Hongbin Cao, et al.. (2023). NFE2L2 Mutations Enhance Radioresistance in Head and Neck Cancer by Modulating Intratumoral Myeloid Cells. Cancer Research. 83(6). 861–874. 36 indexed citations
9.
Nambiar, Dhanya K., Vignesh Viswanathan, Hongbin Cao, et al.. (2023). Galectin-1 Mediates Chronic STING Activation in Tumors to Promote Metastasis through MDSC Recruitment. Cancer Research. 83(19). 3205–3219. 26 indexed citations
10.
Wu, Yufan, Rakesh Manjappa, Lawrie Skinner, et al.. (2023). Clinical Linear Accelerator-Based Electron FLASH: Pathway for Practical Translation to FLASH Clinical Trials. International Journal of Radiation Oncology*Biology*Physics. 117(2). 482–492. 14 indexed citations
11.
Sodji, Quaovi H., Dhanya K. Nambiar, Vignesh Viswanathan, et al.. (2022). The Combination of Radiotherapy and Complement C3a Inhibition Potentiates Natural Killer cell Functions Against Pancreatic Cancer. Cancer Research Communications. 2(7). 725–738. 16 indexed citations
12.
Hartfield, Cheryl, et al.. (2022). Emerging Technologies for Advanced 3D Package Characterization to Enable the More-Than-Moore Era. ECS Transactions. 109(2). 15–29. 2 indexed citations
13.
Hartfield, Cheryl, et al.. (2022). Emerging Technologies for Advanced 3D Package Characterization to Enable the More-Than-Moore Era. ECS Meeting Abstracts. MA2022-02(17). 855–855. 1 indexed citations
14.
Ha, Byung Hang, Cheng Liu, Stavros Melemenidis, et al.. (2022). Real-time optical oximetry during FLASH radiotherapy using a phosphorescent nanoprobe. Radiotherapy and Oncology. 176. 239–243. 5 indexed citations
15.
Facey, Caroline O., et al.. (2021). The Role of miRNAs, miRNA Clusters, and isomiRs in Development of Cancer Stem Cell Populations in Colorectal Cancer. International Journal of Molecular Sciences. 22(3). 1424–1424. 19 indexed citations
16.
Cao, Hongbin, Qian He, Rie von Eyben, et al.. (2020). The role of Glial cell derived neurotrophic factor in head and neck cancer. PLoS ONE. 15(2). e0229311–e0229311. 4 indexed citations
17.
Viswanathan, Vignesh, Shirish Damle, Tao Zhang, et al.. (2017). An miRNA Expression Signature for the Human Colonic Stem Cell Niche Distinguishes Malignant from Normal Epithelia. Cancer Research. 77(14). 3778–3790. 16 indexed citations
18.
Opdenaker, Lynn M., et al.. (2016). Somatostatin signaling via SSTR1 contributes to the quiescence of colon cancer stem cells. BMC Cancer. 16(1). 941–941. 26 indexed citations
19.
Viswanathan, Vignesh, Jeremy Z. Fields, & Bruce M. Boman. (2014). The miRNA23b-regulated signaling network as a key to cancer development—implications for translational research and therapeutics. Journal of Molecular Medicine. 92(11). 1129–1138. 9 indexed citations
20.
Bhatlekar, Seema, et al.. (2012). Abstract LB-102: Role of HOX genes in regulation of stem cell populations in normal and malignant colon tissue. Cancer Research. 72(8_Supplement). LB–102. 1 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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