Umesh C. Karandikar

3.2k total citations · 2 hit papers
32 papers, 2.3k citations indexed

About

Umesh C. Karandikar is a scholar working on Molecular Biology, Infectious Diseases and Genetics. According to data from OpenAlex, Umesh C. Karandikar has authored 32 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Infectious Diseases and 10 papers in Genetics. Recurrent topics in Umesh C. Karandikar's work include Viral gastroenteritis research and epidemiology (12 papers), Developmental Biology and Gene Regulation (10 papers) and Animal Virus Infections Studies (6 papers). Umesh C. Karandikar is often cited by papers focused on Viral gastroenteritis research and epidemiology (12 papers), Developmental Biology and Gene Regulation (10 papers) and Animal Virus Infections Studies (6 papers). Umesh C. Karandikar collaborates with scholars based in United States, Japan and Sweden. Umesh C. Karandikar's co-authors include Mary K. Estes, Sue E. Crawford, Khalil Ettayebi, Sarah E. Blutt, Sasirekha Ramani, Robert L. Atmar, David Y. Graham, Xi‐Lei Zeng, James R. Broughman and Victoria R. Tenge and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Umesh C. Karandikar

32 papers receiving 2.3k citations

Hit Papers

Replication of human noroviruses in stem cell–derived hum... 2015 2026 2018 2022 2016 2015 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Umesh C. Karandikar United States 18 1.5k 617 612 522 456 32 2.3k
Xi‐Lei Zeng United States 18 1.5k 1.0× 600 1.0× 588 1.0× 352 0.7× 456 1.0× 28 2.2k
James R. Broughman United States 11 1.2k 0.8× 493 0.8× 474 0.8× 288 0.6× 399 0.9× 11 1.8k
Kosuke Murakami Japan 17 1.5k 1.0× 656 1.1× 513 0.8× 665 1.3× 570 1.3× 30 2.4k
Lin Qu China 15 1.1k 0.7× 494 0.8× 362 0.6× 409 0.8× 471 1.0× 31 2.0k
Stacy R. Finkbeiner United States 17 1.0k 0.7× 532 0.9× 687 1.1× 639 1.2× 258 0.6× 20 2.2k
Peigang Wang China 24 1.1k 0.7× 416 0.7× 136 0.2× 647 1.2× 113 0.2× 63 2.3k
Melissa K. Jones United States 19 989 0.7× 388 0.6× 493 0.8× 833 1.6× 318 0.7× 49 2.4k
Rodney Colina Uruguay 23 883 0.6× 234 0.4× 180 0.3× 525 1.0× 309 0.7× 99 2.2k
Dewen Tong China 26 532 0.3× 684 1.1× 490 0.8× 598 1.1× 203 0.4× 103 1.8k
Kozo Takase Japan 22 238 0.2× 290 0.5× 179 0.3× 785 1.5× 86 0.2× 125 2.2k

Countries citing papers authored by Umesh C. Karandikar

Since Specialization
Citations

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

Fields of papers citing papers by Umesh C. Karandikar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Umesh C. Karandikar. 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 Umesh C. Karandikar. The network helps show where Umesh C. Karandikar may publish in the future.

Co-authorship network of co-authors of Umesh C. Karandikar

This figure shows the co-authorship network connecting the top 25 collaborators of Umesh C. Karandikar. A scholar is included among the top collaborators of Umesh C. Karandikar 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 Umesh C. Karandikar. Umesh C. Karandikar 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.
Fofanova, Tatiana, Umesh C. Karandikar, Jennifer M. Auchtung, et al.. (2024). A novel system to culture human intestinal organoids under physiological oxygen content to study microbial-host interaction. PLoS ONE. 19(7). e0300666–e0300666. 12 indexed citations
2.
Ayyar, B. Vijayalakshmi, Khalil Ettayebi, Umesh C. Karandikar, et al.. (2023). CLIC and membrane wound repair pathways enable pandemic norovirus entry and infection. Nature Communications. 14(1). 1148–1148. 26 indexed citations
3.
Swaminathan, Ganesh, Nabiollah Kamyabi, Hannah Carter, et al.. (2021). Effect of substrate stiffness on human intestinal enteroids’ infectivity by enteroaggregative Escherichia coli. Acta Biomaterialia. 132. 245–259. 12 indexed citations
4.
Murakami, Kosuke, Victoria R. Tenge, Umesh C. Karandikar, et al.. (2020). Bile acids and ceramide overcome the entry restriction for GII.3 human norovirus replication in human intestinal enteroids. Proceedings of the National Academy of Sciences. 117(3). 1700–1710. 80 indexed citations
6.
Lin, Shih‐Ching, Lin Qu, Khalil Ettayebi, et al.. (2020). Human norovirus exhibits strain-specific sensitivity to host interferon pathways in human intestinal enteroids. Proceedings of the National Academy of Sciences. 117(38). 23782–23793. 70 indexed citations
7.
Bhalchandra, Seema, Ying Chen, Xi‐Lei Zeng, et al.. (2019). Two- and Three-Dimensional Bioengineered Human Intestinal Tissue Models for Cryptosporidium. Methods in molecular biology. 2052. 373–402. 22 indexed citations
8.
Tapia, Rocío, et al.. (2019). Sperm Flagellar 1 Binds Actin in Intestinal Epithelial Cells and Contributes to Formation of Filopodia and Lamellipodia. Gastroenterology. 157(6). 1544–1555.e3. 5 indexed citations
9.
Chang‐Graham, Alexandra L., Heather A. Danhof, Melinda A. Engevik, et al.. (2019). Human Intestinal Enteroids With Inducible Neurogenin-3 Expression as a Novel Model of Gut Hormone Secretion. Cellular and Molecular Gastroenterology and Hepatology. 8(2). 209–229. 58 indexed citations
10.
Zou, Winnie Y., Sarah E. Blutt, Sue E. Crawford, et al.. (2017). Human Intestinal Enteroids: New Models to Study Gastrointestinal Virus Infections. Methods in molecular biology. 1576. 229–247. 106 indexed citations
11.
Ettayebi, Khalil, Sue E. Crawford, Kosuke Murakami, et al.. (2016). Replication of human noroviruses in stem cell–derived human enteroids. Science. 353(6306). 1387–1393. 1028 indexed citations breakdown →
12.
Karandikar, Umesh C., Sue E. Crawford, Nadim J. Ajami, et al.. (2016). Detection of human norovirus in intestinal biopsies from immunocompromised transplant patients. Journal of General Virology. 97(9). 2291–2300. 83 indexed citations
13.
Karandikar, Umesh C., Meng Jin, Barbara Jusiak, et al.. (2014). Drosophila Eyes Absent Is Required for Normal Cone and Pigment Cell Development. PLoS ONE. 9(7). e102143–e102143. 16 indexed citations
14.
Jusiak, Barbara, Umesh C. Karandikar, Su‐Jin Kwak, et al.. (2014). Regulation of Drosophila Eye Development by the Transcription Factor Sine oculis. PLoS ONE. 9(2). e89695–e89695. 25 indexed citations
15.
Li, Yumei, Yuwei Jiang, Yiyun Chen, et al.. (2013). optix functions as a link between the retinal determination network and the dpp pathway to control morphogenetic furrow progression in Drosophila. Developmental Biology. 381(1). 50–61. 16 indexed citations
16.
Kim, Jee‐Eun, et al.. (2009). Evidence that the C‐terminal domain (CtD) autoinhibits neural repression by Drosophila E(spl)M8. genesis. 48(1). 44–55. 7 indexed citations
17.
Karandikar, Umesh C., et al.. (2009). On the mechanism underlying the divergent retinal and bristle defects of M8* (E(spl)D) in Drosophila. genesis. 47(7). 456–468. 8 indexed citations
18.
Zhang, Sophia, et al.. (2006). Drosophila CK2 regulates lateral-inhibition during eye and bristle development. Mechanisms of Development. 123(9). 649–664. 18 indexed citations
19.
Karandikar, Umesh C., Jonathan M. Shaffer, Clifton P. Bishop, & Ashok P. Bidwai. (2005). Drosophila CK2 phosphorylates Deadpan, a member of the HES family of basic-helix-loop-helix (bHLH) repressors. Molecular and Cellular Biochemistry. 274(1-2). 133–139. 4 indexed citations
20.
Karandikar, Umesh C., et al.. (2004). Drosophila CK2 regulates eye morphogenesis via phosphorylation of E(spl)M8. Mechanisms of Development. 121(3). 273–286. 21 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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