Sandeepa M. Eswarappa

1.3k total citations
23 papers, 967 citations indexed

About

Sandeepa M. Eswarappa is a scholar working on Molecular Biology, Endocrinology and Food Science. According to data from OpenAlex, Sandeepa M. Eswarappa has authored 23 papers receiving a total of 967 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Endocrinology and 6 papers in Food Science. Recurrent topics in Sandeepa M. Eswarappa's work include Salmonella and Campylobacter epidemiology (6 papers), Vibrio bacteria research studies (6 papers) and Bacteriophages and microbial interactions (3 papers). Sandeepa M. Eswarappa is often cited by papers focused on Salmonella and Campylobacter epidemiology (6 papers), Vibrio bacteria research studies (6 papers) and Bacteriophages and microbial interactions (3 papers). Sandeepa M. Eswarappa collaborates with scholars based in India, United States and Norway. Sandeepa M. Eswarappa's co-authors include Paul L. Fox, Dipshikha Chakravortty, Yi Fan, Peng Yao, Alka A. Potdar, Belinda Willard, Linda M. Graham, Michael Hensel, Guruswamy Karnam and Arvindhan Nagarajan and has published in prestigious journals such as Cell, The Journal of Cell Biology and The EMBO Journal.

In The Last Decade

Sandeepa M. Eswarappa

23 papers receiving 951 citations

Peers

Sandeepa M. Eswarappa

ENDOC

Alice Lebreton France

Jon R. Armstrong United States

Françoise Porte France

Tie Chen China

Don‐Marc Franchini France

Maria Erali United States

Heinz Hoschützky Germany

E L Racoosin United States

Anne Stern Germany

Dhana G. Gorasia Australia

Alice Lebreton France

Sandeepa M. Eswarappa

1.3k ×2.4

137 ×0.8

142 ×0.9

35 ×0.3

82 ×0.8

ENDOC

Citations per year, relative to Sandeepa M. Eswarappa Sandeepa M. Eswarappa (= 1×) peers Alice Lebreton

Countries citing papers authored by Sandeepa M. Eswarappa

Since Specialization

Citations

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

Fields of papers citing papers by Sandeepa M. Eswarappa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandeepa M. Eswarappa. 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 Sandeepa M. Eswarappa. The network helps show where Sandeepa M. Eswarappa may publish in the future.

Co-authorship network of co-authors of Sandeepa M. Eswarappa

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

All Works

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20 of 20 papers shown

Eswarappa, Sandeepa M., et al.. (2017). Emerging Field of Tardigrades and their Stress Tolerance. Current Science. 112(5). 902–903. 1 indexed citations

Yao, Peng, Sandeepa M. Eswarappa, & Paul L. Fox. (2015). Translational Control Mechanisms in Angiogenesis and Vascular Biology. Current Atherosclerosis Reports. 17(5). 506–506. 5 indexed citations

Eswarappa, Sandeepa M., Alka A. Potdar, William J. Koch, et al.. (2014). Programmed Translational Readthrough Generates Antiangiogenic VEGF-Ax. Cell. 157(7). 1605–1618. 162 indexed citations

Fan, Yi, Alka A. Potdar, Yanqing Gong, et al.. (2014). Profilin-1 phosphorylation directs angiocrine expression and glioblastoma progression through HIF-1α accumulation. Nature Cell Biology. 16(5). 445–456. 74 indexed citations

Eswarappa, Sandeepa M. & Paul L. Fox. (2013). Citric acid cycle and the origin of MARS. Trends in Biochemical Sciences. 38(5). 222–228. 18 indexed citations

Yao, Peng, Alka A. Potdar, Partho Sarothi Ray, et al.. (2013). The HILDA Complex Coordinates a Conditional Switch in the 3′-Untranslated Region of the VEGFA mRNA. PLoS Biology. 11(8). e1001635–e1001635. 41 indexed citations

Fan, Yi, Abul Arif, Yanqing Gong, et al.. (2012). Stimulus-dependent phosphorylation of profilin-1 in angiogenesis. Nature Cell Biology. 14(10). 1046–1056. 62 indexed citations

Eswarappa, Sandeepa M., Sylvie Estrela, & Sam P. Brown. (2012). Within-Host Dynamics of Multi-Species Infections: Facilitation, Competition and Virulence. PLoS ONE. 7(6). e38730–e38730. 44 indexed citations

Eswarappa, Sandeepa M., Jessin Janice, Sudhagar V. Balasundaram, & Dipshikha Chakravortty. (2012). Non-neutral evolution in non-LEE-encoded type III effectors of attaching and effacing Escherichia coli. Microbes and Infection. 15(2). 147–151. 3 indexed citations

10.

Yao, Peng, et al.. (2011). Repression of VEGFA by CA‐rich element‐binding microRNAs is modulated by hnRNP L. The EMBO Journal. 30(7). 1324–1334. 97 indexed citations

11.

Jagadeesh, G., et al.. (2011). Needleless Vaccine Delivery Using Micro-Shock Waves. Clinical and Vaccine Immunology. 18(4). 539–545. 45 indexed citations

12.

Lahiri, Amit, Sandeepa M. Eswarappa, Priyanka Das, & Dipshikha Chakravortty. (2010). Altering the balance between pathogen containing vacuoles and lysosomes: A lesson from Salmonella. Virulence. 1(4). 325–329. 9 indexed citations

13.

Eswarappa, Sandeepa M., Vidya Devi Negi, Sangeeta Chakraborty, B. K. Chandrasekhar Sagar, & Dipshikha Chakravortty. (2009). Division of the Salmonella -Containing Vacuole and Depletion of Acidic Lysosomes in Salmonella -Infected Host Cells Are Novel Strategies of Salmonella enterica To Avoid Lysosomes. Infection and Immunity. 78(1). 68–79. 45 indexed citations

14.

Eswarappa, Sandeepa M., Guruswamy Karnam, Arvindhan Nagarajan, Sangeeta Chakraborty, & Dipshikha Chakravortty. (2009). lac Repressor Is an Antivirulence Factor of Salmonella enterica: Its Role in the Evolution of Virulence in Salmonella. PLoS ONE. 4(6). e5789–e5789. 29 indexed citations

15.

Nagarajan, Arvindhan, Sudhagar V. Balasundaram, Jessin Janice, et al.. (2009). sopB of Salmonella enterica serovar Typhimurium is a potential DNA vaccine candidate in conjugation with live attenuated bacteria. Vaccine. 27(21). 2804–2811. 24 indexed citations

16.

Eswarappa, Sandeepa M.. (2009). Location of Pathogenic Bacteria during Persistent Infections: Insights from an Analysis Using Game Theory. PLoS ONE. 4(4). e5383–e5383. 23 indexed citations

17.

Eswarappa, Sandeepa M., Jessin Janice, Sudhagar V. Balasundaram, Narendra M. Dixit, & Dipshikha Chakravortty. (2009). Host-specificity of Salmonella enterica serovar Gallinarum: Insights from comparative genomics. Infection Genetics and Evolution. 9(4). 468–473. 20 indexed citations

18.

Eswarappa, Sandeepa M., Jessin Janice, Arvindhan Nagarajan, et al.. (2008). Differentially Evolved Genes of Salmonella Pathogenicity Islands: Insights into the Mechanism of Host Specificity in Salmonella. PLoS ONE. 3(12). e3829–e3829. 47 indexed citations

19.

Eswarappa, Sandeepa M., Nirmalya Basu, Omana Joy, & Dipshikha Chakravortty. (2008). Folimycin (concanamycin A) inhibits LPS-induced nitric oxide production and reduces surface localization of TLR4 in murine macrophages. Innate Immunity. 14(1). 13–24. 15 indexed citations

20.

Eswarappa, Sandeepa M., et al.. (2008). The yejABEF operon of Salmonella confers resistance to antimicrobial peptides and contributes to its virulence. Microbiology. 154(2). 666–678. 81 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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