David O. Zamora

1.4k total citations
35 papers, 1.2k citations indexed

About

David O. Zamora is a scholar working on Ophthalmology, Molecular Biology and Genetics. According to data from OpenAlex, David O. Zamora has authored 35 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Ophthalmology, 6 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in David O. Zamora's work include Mesenchymal stem cell research (6 papers), Ocular Diseases and Behçet’s Syndrome (6 papers) and Wound Healing and Treatments (5 papers). David O. Zamora is often cited by papers focused on Mesenchymal stem cell research (6 papers), Ocular Diseases and Behçet’s Syndrome (6 papers) and Wound Healing and Treatments (5 papers). David O. Zamora collaborates with scholars based in United States, South Korea and Vietnam. David O. Zamora's co-authors include Stephen R. Planck, James T. Rosenbaum, Robert J. Christy, Shanmugasundaram Natesan, Justine R. Smith, Yuzhen Pan, Nicole L. Wrice, Dongseok Choi, Jeffrey W. Kiel and James T. Rosenbaum and has published in prestigious journals such as Hepatology, Scientific Reports and Progress in Retinal and Eye Research.

In The Last Decade

David O. Zamora

35 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David O. Zamora United States 22 368 357 192 191 178 35 1.2k
Grenham W. Ireland United Kingdom 21 155 0.4× 558 1.6× 134 0.7× 284 1.5× 61 0.3× 34 1.6k
Kerryn L. Garrett Australia 18 289 0.8× 1.4k 4.0× 64 0.3× 108 0.6× 119 0.7× 33 2.1k
Robert D. Sampson United Kingdom 18 149 0.4× 1.0k 2.9× 234 1.2× 57 0.3× 158 0.9× 28 1.5k
Tat Fong Ng United States 19 456 1.2× 755 2.1× 281 1.5× 26 0.1× 64 0.4× 39 1.8k
Michał Machnicki United States 14 232 0.6× 501 1.4× 175 0.9× 26 0.1× 92 0.5× 22 1.4k
Audrey E. K. Hutcheon United States 29 618 1.7× 594 1.7× 87 0.5× 215 1.1× 108 0.6× 57 2.7k
Tai-ichiro Chikama Japan 28 708 1.9× 319 0.9× 82 0.4× 99 0.5× 103 0.6× 77 2.1k
Sonali Pal‐Ghosh United States 25 226 0.6× 404 1.1× 123 0.6× 158 0.8× 41 0.2× 49 1.8k
Judith A. West‐Mays Canada 31 650 1.8× 1.3k 3.7× 91 0.5× 80 0.4× 47 0.3× 60 2.7k
Claire L. Kublin United States 26 389 1.1× 363 1.0× 99 0.5× 100 0.5× 29 0.2× 43 2.1k

Countries citing papers authored by David O. Zamora

Since Specialization
Citations

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

Fields of papers citing papers by David O. Zamora

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David O. Zamora. 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 David O. Zamora. The network helps show where David O. Zamora may publish in the future.

Co-authorship network of co-authors of David O. Zamora

This figure shows the co-authorship network connecting the top 25 collaborators of David O. Zamora. A scholar is included among the top collaborators of David O. Zamora 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 David O. Zamora. David O. Zamora 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.
Snider, Eric J., et al.. (2020). Development and Characterization of a Benchtop Corneal Puncture Injury Model. Scientific Reports. 10(1). 4218–4218. 9 indexed citations
2.
Bugay, Vladislav, Deborah Holstein, José E Cavazos, et al.. (2019). A Mouse Model of Repetitive Blast Traumatic Brain Injury Reveals Post-Trauma Seizures and Increased Neuronal Excitability. Journal of Neurotrauma. 37(2). 248–261. 43 indexed citations
3.
Natesan, Shanmugasundaram, et al.. (2019). PEGylated Platelet-Free Blood Plasma-Based Hydrogels for Full-Thickness Wound Regeneration. Advances in Wound Care. 8(7). 323–340. 11 indexed citations
4.
McDaniel, Jennifer S., et al.. (2018). Treatment of corneal chemical alkali burns with a crosslinked thiolated hyaluronic acid film. Burns. 44(5). 1179–1186. 29 indexed citations
5.
Wirostko, Barbara, et al.. (2015). Sustained Delivery of rHGH via a Novel, Biodegradable, Hyaluronic Acid (HA) Polymer Film. Investigative Ophthalmology & Visual Science. 56(7). 262–262. 1 indexed citations
6.
Natesan, Shanmugasundaram, David O. Zamora, Nicole L. Wrice, David G. Baer, & Robert J. Christy. (2013). Bilayer Hydrogel With Autologous Stem Cells Derived From Debrided Human Burn Skin for Improved Skin Regeneration. Journal of Burn Care & Research. 34(1). 18–30. 55 indexed citations
7.
Zamora, David O., Shanmugasundaram Natesan, Sandra C. Becerra, et al.. (2013). Enhanced wound vascularization using a dsASCs seeded FPEG scaffold. Angiogenesis. 16(4). 745–757. 51 indexed citations
8.
Chan, Rodney K., David O. Zamora, Nicole L. Wrice, et al.. (2012). Development of a Vascularized Skin Construct Using Adipose-Derived Stem Cells from Debrided Burned Skin. Stem Cells International. 2012. 1–11. 63 indexed citations
9.
Natesan, Shanmugasundaram, David O. Zamora, Laura J. Suggs, & Robert J. Christy. (2012). Engineering a Bilayered Hydrogel to Control ASC differentiation. Journal of Visualized Experiments. e3953–e3953. 8 indexed citations
10.
Bharadwaj, Arpita, Binoy Appukuttan, Phillip A. Wilmarth, et al.. (2012). Role of the retinal vascular endothelial cell in ocular disease. Progress in Retinal and Eye Research. 32. 102–180. 138 indexed citations
11.
Zamora, David O. & Jeffrey W. Kiel. (2010). Episcleral Venous Pressure Responses to Topical Nitroprusside andN-Nitro-l-arginine Methyl Ester. Investigative Ophthalmology & Visual Science. 51(3). 1614–1614. 24 indexed citations
12.
Zamora, David O. & Jeffrey W. Kiel. (2009). Topical Proparacaine and Episcleral Venous Pressure in the Rabbit. Investigative Ophthalmology & Visual Science. 50(6). 2949–2949. 25 indexed citations
13.
Davies, Michael H., David O. Zamora, Justine R. Smith, & Michael R. Powers. (2009). Soluble ephrin-B2 mediates apoptosis in retinal neovascularization and in endothelial cells. Microvascular Research. 77(3). 382–386. 18 indexed citations
14.
Zamora, David O., James T. Rosenbaum, & Justine R. Smith. (2008). Invasion of human retinal vascular endothelial cells by Toxoplasma gondii tachyzoites. British Journal of Ophthalmology. 92(6). 852–855. 14 indexed citations
15.
Davey, Michael P., Tammy M. Martin, Stephen R. Planck, et al.. (2006). Human endothelial cells express NOD2/CARD15 and increase IL-6 secretion in response to muramyl dipeptide. Microvascular Research. 71(2). 103–107. 52 indexed citations
16.
Zamora, David O., et al.. (2006). Human leukocytes express ephrinB2 which activates microvascular endothelial cells. Cellular Immunology. 242(2). 99–109. 22 indexed citations
17.
Zamora, David O., Michael H. Davies, Stephen R. Planck, James T. Rosenbaum, & Michael R. Powers. (2005). Soluble Forms of EphrinB2 and EphB4 Reduce Retinal Neovascularization in a Model of Proliferative Retinopathy. Investigative Ophthalmology & Visual Science. 46(6). 2175–2175. 47 indexed citations
18.
Steinle, Jena J., David O. Zamora, James T. Rosenbaum, & Harris J. Granger. (2004). β3-Adrenergic receptors mediate choroidal endothelial cell invasion, proliferation, and cell elongation. Experimental Eye Research. 80(1). 83–91. 36 indexed citations
19.
Brito, Beatriz E., et al.. (2004). Toll-like receptor 4 and CD14 expression in human ciliary body and TLR-4 in human iris endothelial cells. Experimental Eye Research. 79(2). 203–208. 45 indexed citations
20.
Brito, Beatriz E., Leslie M. O’Rourke, Xiaona Huang, et al.. (1999). Murine endotoxin-induced uveitis, but not immune complex-induced uveitis, is dependent on the IL-8 receptor homolog. Current Eye Research. 19(1). 76–85. 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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