Venkatesh Govindarajan

1.1k total citations
27 papers, 881 citations indexed

About

Venkatesh Govindarajan is a scholar working on Molecular Biology, Surgery and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Venkatesh Govindarajan has authored 27 papers receiving a total of 881 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Surgery and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Venkatesh Govindarajan's work include Fibroblast Growth Factor Research (5 papers), Intraperitoneal and Appendiceal Malignancies (5 papers) and Connexins and lens biology (4 papers). Venkatesh Govindarajan is often cited by papers focused on Fibroblast Growth Factor Research (5 papers), Intraperitoneal and Appendiceal Malignancies (5 papers) and Connexins and lens biology (4 papers). Venkatesh Govindarajan collaborates with scholars based in United States and China. Venkatesh Govindarajan's co-authors include Paul A. Overbeek, Brian W. Loggie, Masataka Ito, Richard A. Lang, Helen P. Makarenkova, Peter Thomas, Poonam Sharma, Sonya C. Faber, Li Sun and Gerald McMahon and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Development.

In The Last Decade

Venkatesh Govindarajan

27 papers receiving 869 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Venkatesh Govindarajan United States 17 491 210 143 139 131 27 881
Roger A. Fleischman United States 17 558 1.1× 92 0.4× 31 0.2× 172 1.2× 33 0.3× 29 1.2k
Hiroyuki Hatanaka Japan 23 756 1.5× 394 1.9× 55 0.4× 51 0.4× 43 0.3× 66 1.6k
Elizabeth M. Jablonski United States 11 505 1.0× 60 0.3× 26 0.2× 42 0.3× 57 0.4× 11 1.1k
C McKeown United Kingdom 13 735 1.5× 168 0.8× 58 0.4× 139 1.0× 9 0.1× 25 1.3k
Federica Mangili Italy 16 159 0.3× 204 1.0× 45 0.3× 107 0.8× 53 0.4× 64 875
Rocio Moran United States 16 324 0.7× 128 0.6× 31 0.2× 52 0.4× 7 0.1× 27 854
Ferrell R. Campbell United States 12 475 1.0× 236 1.1× 36 0.3× 85 0.6× 13 0.1× 19 1.0k
David Wilkes United States 15 501 1.0× 216 1.0× 30 0.2× 57 0.4× 12 0.1× 27 915
Leah DiMascio United States 7 504 1.0× 55 0.3× 25 0.2× 75 0.5× 13 0.1× 11 896
René Silye Austria 13 465 0.9× 96 0.5× 26 0.2× 72 0.5× 509 3.9× 27 1.1k

Countries citing papers authored by Venkatesh Govindarajan

Since Specialization
Citations

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

Fields of papers citing papers by Venkatesh Govindarajan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Venkatesh Govindarajan

This figure shows the co-authorship network connecting the top 25 collaborators of Venkatesh Govindarajan. A scholar is included among the top collaborators of Venkatesh Govindarajan 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 Venkatesh Govindarajan. Venkatesh Govindarajan 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.
Govindarajan, Venkatesh, et al.. (2023). Pictilisib-Induced Resistance Is Mediated through FOXO1-Dependent Activation of Receptor Tyrosine Kinases in Mucinous Colorectal Adenocarcinoma Cells. International Journal of Molecular Sciences. 24(15). 12331–12331. 4 indexed citations
2.
3.
Thomas, Peter, et al.. (2016). Patient‐derived xenograft mouse models of pseudomyxoma peritonei recapitulate the human inflammatory tumor microenvironment. Cancer Medicine. 5(4). 711–719. 16 indexed citations
4.
Judge, Sean J., Peter Thomas, Venkatesh Govindarajan, Poonam Sharma, & Brian W. Loggie. (2015). Malignant Peritoneal Mesothelioma: Characterization of the Inflammatory Response in the Tumor Microenvironment. Annals of Surgical Oncology. 23(5). 1496–1500. 13 indexed citations
5.
Wolf, Louise, Wilbur R. Harrison, Jie Huang, et al.. (2013). Histone posttranslational modifications and cell fate determination: lens induction requires the lysine acetyltransferases CBP and p300. Nucleic Acids Research. 41(22). 10199–10214. 54 indexed citations
6.
Licht, Jonathan D., et al.. (2013). Spry1 and Spry2 are necessary for eyelid closure. Developmental Biology. 383(2). 227–238. 17 indexed citations
7.
Thomas, Peter, et al.. (2012). Kras mutations and p53 overexpression in pseudomyxoma peritonei: association with phenotype and prognosis. Journal of Surgical Research. 180(1). 97–103. 41 indexed citations
8.
Licht, Jonathan D., et al.. (2011). Spry1andSpry2Are Necessary for Lens Vesicle Separation and Corneal Differentiation. Investigative Ophthalmology & Visual Science. 52(9). 6887–6887. 32 indexed citations
9.
Foster, Jason M., Uppala Radhakrishna, Venkatesh Govindarajan, et al.. (2010). Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma. World Journal of Surgical Oncology. 8(1). 88–88. 30 indexed citations
10.
Zhang, Yan, et al.. (2010). Activated Ras alters lens and corneal development through induction of distinct downstream targets. BMC Developmental Biology. 10(1). 13–13. 19 indexed citations
11.
Rainey, Mark A., Manju George, Guoguang Ying, et al.. (2010). The endocytic recycling regulator EHD1 is essential for spermatogenesis and male fertility in mice. BMC Developmental Biology. 10(1). 37–37. 48 indexed citations
12.
Zhang, Yan, et al.. (2008). Dominant inhibition of lens placode formation in mice. Developmental Biology. 323(1). 53–63. 7 indexed citations
13.
Zhao, Min, Christopher J. Destache, G. Zhan, et al.. (2008). Regulation of retinal morphology and posterior segment amino acidsby 8-isoprostaglandin E2 in bovine eyes ex vivo. Methods and Findings in Experimental and Clinical Pharmacology. 30(8). 615–615. 2 indexed citations
14.
Zhang, Yan, Paul A. Overbeek, & Venkatesh Govindarajan. (2007). Perinatal ablation of the mouse lens causes multiple anterior chamber defects.. PubMed. 13. 2289–300. 20 indexed citations
15.
Govindarajan, Venkatesh & Paul A. Overbeek. (2006). FGF9 can induce endochondral ossification in cranial mesenchyme. BMC Developmental Biology. 6(1). 7–7. 52 indexed citations
16.
Overbeek, Paul A., et al.. (2004). Reversible Regulation of Ocular Transgene Expression. Investigative Ophthalmology & Visual Science. 45(13). 3424–3424. 1 indexed citations
17.
Reneker, Lixing W., Leike Xie, Li Xu, Venkatesh Govindarajan, & Paul A. Overbeek. (2004). Activated Ras induces lens epithelial cell hyperplasia but not premature differentiation. The International Journal of Developmental Biology. 48(8-9). 879–888. 12 indexed citations
18.
Govindarajan, Venkatesh, Masataka Ito, Helen P. Makarenkova, Richard A. Lang, & Paul A. Overbeek. (2000). Endogenous and Ectopic Gland Induction by FGF-10. Developmental Biology. 225(1). 188–200. 73 indexed citations
19.
Makarenkova, Helen P., Masataka Ito, Venkatesh Govindarajan, et al.. (2000). FGF10 is an inducer and Pax6 a competence factor for lacrimal gland development. Development. 127(12). 2563–2572. 174 indexed citations
20.
Govindarajan, Venkatesh, et al.. (1995). An ECM-Bound, PDGF-like Growth Factor and a TGF-α-like Growth Factor Are Required for Gastrulation and Spiculogenesis in theLytechinusEmbryo. Developmental Biology. 172(2). 541–551. 29 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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