Madhusudhan Budatha

1.6k total citations · 1 hit paper
17 papers, 1.3k citations indexed

About

Madhusudhan Budatha is a scholar working on Molecular Biology, Insect Science and Plant Science. According to data from OpenAlex, Madhusudhan Budatha has authored 17 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Insect Science and 4 papers in Plant Science. Recurrent topics in Madhusudhan Budatha's work include Insect Resistance and Genetics (5 papers), Angiogenesis and VEGF in Cancer (4 papers) and Insect Pest Control Strategies (3 papers). Madhusudhan Budatha is often cited by papers focused on Insect Resistance and Genetics (5 papers), Angiogenesis and VEGF in Cancer (4 papers) and Insect Pest Control Strategies (3 papers). Madhusudhan Budatha collaborates with scholars based in United States, India and United Kingdom. Madhusudhan Budatha's co-authors include Martin A. Schwartz, Nicolas Baeyens, George Tellides, Guangxin Li, Pei‐Yu Chen, Lingfeng Qin, Michael Simons, Brian G. Coon, Sanguk Yun and Hiromi Yanagisawa and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Cell Biology and PLoS ONE.

In The Last Decade

Madhusudhan Budatha

17 papers receiving 1.2k citations

Hit Papers

Endothelial-to-mesenchymal transition drives atherosclero... 2015 2026 2018 2022 2015 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
Madhusudhan Budatha United States 15 624 220 203 198 197 17 1.3k
Yumei Lai China 27 959 1.5× 239 1.1× 137 0.7× 165 0.8× 246 1.2× 57 1.8k
Davy Vanhoutte United States 23 946 1.5× 237 1.1× 297 1.5× 375 1.9× 114 0.6× 33 2.1k
Yoshino Yoshitake Japan 22 735 1.2× 243 1.1× 97 0.5× 150 0.8× 139 0.7× 55 1.4k
Éva Korpos Germany 19 458 0.7× 166 0.8× 341 1.7× 257 1.3× 56 0.3× 35 1.4k
Naoki Maehara Japan 23 780 1.3× 222 1.0× 164 0.8× 340 1.7× 174 0.9× 85 1.8k
Audrey M. Bernstein United States 20 504 0.8× 392 1.8× 133 0.7× 95 0.5× 119 0.6× 42 1.3k
Toshi Komurasaki Japan 19 646 1.0× 130 0.6× 165 0.8× 126 0.6× 128 0.6× 36 1.4k
Yoshinao Soma Japan 24 420 0.7× 283 1.3× 223 1.1× 145 0.7× 351 1.8× 79 1.8k
Kazuhiro Kobuke Japan 18 503 0.8× 145 0.7× 75 0.4× 272 1.4× 210 1.1× 52 1.3k
Mark Lauer United States 25 643 1.0× 781 3.5× 274 1.3× 132 0.7× 237 1.2× 43 1.5k

Countries citing papers authored by Madhusudhan Budatha

Since Specialization
Citations

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

Fields of papers citing papers by Madhusudhan Budatha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Madhusudhan Budatha

This figure shows the co-authorship network connecting the top 25 collaborators of Madhusudhan Budatha. A scholar is included among the top collaborators of Madhusudhan Budatha 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 Madhusudhan Budatha. Madhusudhan Budatha is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Budatha, Madhusudhan, Jiasheng Zhang, & Martin A. Schwartz. (2021). Fibronectin‐Mediated Inflammatory Signaling Through Integrin α5 in Vascular Remodeling. Journal of the American Heart Association. 10(17). e021160–e021160. 28 indexed citations
2.
Wang, Wei Wei, Yamei Wang, Raghu Tadagavadi, et al.. (2020). IL-10 from dendritic cells but not from T regulatory cells protects against cisplatin-induced nephrotoxicity. PLoS ONE. 15(9). e0238816–e0238816. 17 indexed citations
3.
Budatha, Madhusudhan, Jiasheng Zhang, Zhen W. Zhuang, et al.. (2018). Inhibiting Integrin α5 Cytoplasmic Domain Signaling Reduces Atherosclerosis and Promotes Arteriogenesis. Journal of the American Heart Association. 7(3). 27 indexed citations
4.
Conway, Daniel E., Brian G. Coon, Madhusudhan Budatha, et al.. (2017). VE-Cadherin Phosphorylation Regulates Endothelial Fluid Shear Stress Responses through the Polarity Protein LGN. Current Biology. 27(14). 2219–2225.e5. 64 indexed citations
5.
Yun, Sanguk, Madhusudhan Budatha, James E. Dahlman, et al.. (2016). Interaction between integrin α5 and PDE4D regulates endothelial inflammatory signalling. Nature Cell Biology. 18(10). 1043–1053. 78 indexed citations
6.
Coon, Brian G., Nicolas Baeyens, Jinah Han, et al.. (2015). Intramembrane binding of VE-cadherin to VEGFR2 and VEGFR3 assembles the endothelial mechanosensory complex. The Journal of Cell Biology. 208(7). 975–986. 232 indexed citations
7.
Chen, Pei‐Yu, Lingfeng Qin, Nicolas Baeyens, et al.. (2015). Endothelial-to-mesenchymal transition drives atherosclerosis progression. Journal of Clinical Investigation. 125(12). 4514–4528. 417 indexed citations breakdown →
8.
Coon, Brian G., Nicolas Baeyens, Jinah Han, et al.. (2015). Intramembrane binding of VE-cadherin to VEGFR2 and VEGFR3 assembles the endothelial mechanosensory complex. The Journal of General Physiology. 145(4). 1454OIA13–1454OIA13. 3 indexed citations
9.
Budatha, Madhusudhan, T. Ignacio Montoya, Ayako Suzuki, et al.. (2013). Dysregulation of Protease and Protease Inhibitors in a Mouse Model of Human Pelvic Organ Prolapse. PLoS ONE. 8(2). e56376–e56376. 26 indexed citations
10.
Budatha, Madhusudhan, Shayzreen M. Roshanravan, Qian Zheng, et al.. (2011). Extracellular matrix proteases contribute to progression of pelvic organ prolapse in mice and humans. Journal of Clinical Investigation. 121(5). 2048–2059. 117 indexed citations
11.
Budatha, Madhusudhan, et al.. (2011). Is hexamerin receptor a GPI-anchored protein in Achaea janata (Lepidoptera: Noctuidae)?. Journal of Biosciences. 36(3). 545–553. 3 indexed citations
12.
Huang, Jianbin, Elaine C. Davis, Shelby L. Chapman, et al.. (2009). Fibulin-4 Deficiency Results in Ascending Aortic Aneurysms. Circulation Research. 106(3). 583–592. 135 indexed citations
13.
Meur, Gargi, et al.. (2008). Constitutive expression of Arabidopsis NPR1 confers enhanced resistance to the early instars of Spodoptera litura in transgenic tobacco. Physiologia Plantarum. 133(4). 765–775. 35 indexed citations
14.
Budatha, Madhusudhan, Gargi Meur, & Aparna Dutta‐Gupta. (2007). Identification and characterization of midgut proteases in Achaea janata and their implications. Biotechnology Letters. 30(2). 305–310. 21 indexed citations
15.
Budatha, Madhusudhan, et al.. (2007). Characterization of Bacillus thuringiensis Cry toxin binding novel GPI anchored aminopeptidase from fat body of the moth Spodoptera litura. Biotechnology Letters. 29(11). 1651–1657. 15 indexed citations
16.
Budatha, Madhusudhan, Gargi Meur, & Aparna Dutta‐Gupta. (2007). A novel aminopeptidase in the fat body of the moth Achaea janata as a receptor for Bacillus thuringiensis Cry toxins and its comparison with midgut aminopeptidase. Biochemical Journal. 405(2). 287–297. 24 indexed citations
17.
Meur, Gargi, et al.. (2006). Differential induction of NPR1 during defense responses in Brassica juncea. Physiological and Molecular Plant Pathology. 68(4-6). 128–137. 20 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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