Donald C. Hood

17.6k total citations · 3 hit papers
294 papers, 14.2k citations indexed

About

Donald C. Hood is a scholar working on Ophthalmology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Donald C. Hood has authored 294 papers receiving a total of 14.2k indexed citations (citations by other indexed papers that have themselves been cited), including 196 papers in Ophthalmology, 123 papers in Molecular Biology and 116 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Donald C. Hood's work include Glaucoma and retinal disorders (150 papers), Retinal Development and Disorders (123 papers) and Retinal Diseases and Treatments (102 papers). Donald C. Hood is often cited by papers focused on Glaucoma and retinal disorders (150 papers), Retinal Development and Disorders (123 papers) and Retinal Diseases and Treatments (102 papers). Donald C. Hood collaborates with scholars based in United States, Brazil and Australia. Donald C. Hood's co-authors include David G. Birch, Ali S. Raza, Jeffrey M. Liebmann, Vivienne C. Greenstein, Randy H. Kardon, Robert Ritch, Marcia A. Finkelstein, Carlos Gustavo V. De Moraes, Carlos Gustavo De Moraes and Robert Ritch and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Donald C. Hood

291 papers receiving 13.9k citations

Hit Papers

Glaucomatous damage of the macula 2007 2026 2013 2019 2012 2007 2011 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Donald C. Hood United States 69 9.7k 6.4k 5.8k 2.5k 2.3k 294 14.2k
Christine A. Curcio United States 78 16.3k 1.7× 9.0k 1.4× 10.2k 1.8× 1.7k 0.7× 2.3k 1.0× 322 22.0k
Michael F. Marmor United States 56 8.7k 0.9× 6.9k 1.1× 2.8k 0.5× 2.6k 1.1× 1.1k 0.5× 263 14.3k
Jonathan Stone Australia 71 4.1k 0.4× 9.1k 1.4× 3.2k 0.5× 5.9k 2.4× 4.0k 1.8× 204 15.5k
Graham E. Holder United Kingdom 55 7.6k 0.8× 9.8k 1.5× 2.3k 0.4× 2.6k 1.1× 1.5k 0.6× 219 13.6k
G. B. Arden United Kingdom 48 4.0k 0.4× 4.5k 0.7× 1.7k 0.3× 1.8k 0.7× 1.7k 0.7× 211 8.3k
Anne B. Fulton United States 43 2.8k 0.3× 3.9k 0.6× 2.5k 0.4× 1.2k 0.5× 815 0.4× 236 7.2k
Algis J. Vingrys Australia 49 3.6k 0.4× 2.2k 0.3× 2.2k 0.4× 720 0.3× 1.2k 0.5× 249 6.8k
Randy H. Kardon United States 51 5.4k 0.6× 1.9k 0.3× 2.2k 0.4× 714 0.3× 672 0.3× 287 9.5k
Mitchell Brigell United States 30 3.2k 0.3× 3.6k 0.6× 1.2k 0.2× 1.3k 0.5× 1.6k 0.7× 82 6.4k
Gordon T. Plant United Kingdom 56 2.4k 0.3× 2.2k 0.3× 962 0.2× 740 0.3× 1.2k 0.5× 246 9.7k

Countries citing papers authored by Donald C. Hood

Since Specialization
Citations

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

Fields of papers citing papers by Donald C. Hood

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Donald C. Hood

This figure shows the co-authorship network connecting the top 25 collaborators of Donald C. Hood. A scholar is included among the top collaborators of Donald C. Hood 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 Donald C. Hood. Donald C. Hood 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.
Hood, Donald C., et al.. (2023). Toward a Real‐world Optical Coherence Tomography Reference Database: Optometric Practices as a Source of Healthy Eyes. Optometry and Vision Science. 100(8). 499–506. 3 indexed citations
2.
Thakoor, Kaveri A., Emmanouil Tsamis, Carlos Gustavo De Moraes, Paul Sajda, & Donald C. Hood. (2020). Impact of Reference Standard, Data Augmentation, and OCT Input on Glaucoma Detection Accuracy by CNNs on a New Test Set. Investigative Ophthalmology & Visual Science. 61(7). 4540–4540. 2 indexed citations
3.
Silva, Luís F.O., et al.. (2017). Retinal Ganglion Cell layer by Fourier-domain Optical Coherence Tomography and microvasculature density by Optical Coherence Tomography Angiography at the macular region in glaucoma.. Investigative Ophthalmology & Visual Science. 58(8). 712–712. 1 indexed citations
4.
Lee, Seung Min, Carlos Gustavo De Moraes, Diane Wang, et al.. (2016). A comparison of circumpapillary retinal nerve fiber layer (cpRNFL) thickness and minimum rim width at Bruch’s membrane opening (BMO-MRW) analyses in patients with mild glaucomatous damage. Investigative Ophthalmology & Visual Science. 57(12). 843–843. 1 indexed citations
5.
Hood, Donald C., Carlos Gustavo De Moraes, Rithambara Ramachandran, et al.. (2015). Improving inter-individual diagnostic agreement in early glaucoma through better use of optical coherence tomography (OCT) scans.. Investigative Ophthalmology & Visual Science. 56(7). 2060–2060. 1 indexed citations
6.
Ramachandran, Rithambara, et al.. (2015). The Thickness of the Outer Nuclear and Henle Fiber Layers in Patients with Photoreceptor Abnormalities Measured Using Optical Coherence Tomography.. Investigative Ophthalmology & Visual Science. 56(7). 5973–5973. 1 indexed citations
7.
Birch, David G., Kirsten G. Locke, Martin Klein, et al.. (2014). Annual decline in visual sensitivity at the edge of the OCT-defined ellipsoid zone (EZ) in patients with RPGR-mediated x-linked Retinitis Pigmentosa (xlRP). Investigative Ophthalmology & Visual Science. 55(13). 1398–1398. 1 indexed citations
8.
Chen, Monica F., Toco Yuen Ping Chui, Robert Ritch, et al.. (2014). Imaging Retinal Nerve Fiber Bundles in Glaucoma Patients with Deep Local Visual Field Damage of the Macular Region. Investigative Ophthalmology & Visual Science. 55(13). 4778–4778. 1 indexed citations
9.
Park, Sung Chul, Joseph L. Simonson, Daniel Su, et al.. (2012). 10-2 Versus 24-2 Visual Field Progression Analysis in Glaucomatous Eyes with Initial Parafoveal Scotomata. Investigative Ophthalmology & Visual Science. 53(14). 202–202. 1 indexed citations
10.
Xin, Daiyan, Danilo B. Fernandes, Matthew Nguyen, et al.. (2012). Hypodense Regions (Holes) Are Seen in the Retinal Nerve Fiber Layer of the Frequency-Domain OCT Scans of Eyes with Glaucoma, but not Eyes with MS or ION. Investigative Ophthalmology & Visual Science. 53(14). 3914–3914. 1 indexed citations
11.
Liebmann, Jeffrey M., Carlos Gustavo De Moraes, Danilo B. Fernandes, et al.. (2012). Glaucoma Patients with Clinically Normal Macular Appearance May Have Retinal Abnormalities. Investigative Ophthalmology & Visual Science. 53(14). 1001–1001. 1 indexed citations
12.
Raza, Ali S., Xiao Zhang, Randy H. Kardon, et al.. (2010). A Comparison of Local Retinal Ganglion Cell (RGC) Layer Thickness to Local Losses in Visual Field Sensitivity in Patients With Glaucoma. Investigative Ophthalmology & Visual Science. 51(13). 4897–4897. 1 indexed citations
13.
Raza, Ali S., Carlos Gustavo De Moraes, Jeffrey G. Odel, et al.. (2010). Small Arcuate Comma Defects Within 10 Degrees of the Fovea in Patients With Glaucoma. Investigative Ophthalmology & Visual Science. 51(13). 5514–5514. 1 indexed citations
14.
Dale, E, Donald C. Hood, Vivienne C. Greenstein, & Jeffrey G. Odel. (2009). A comparison of multifocal ERG and frequency domain OCT changes in patients with abnormalities of the retina. Documenta Ophthalmologica. 120(2). 175–186. 28 indexed citations
15.
Greenstein, Vivienne C., et al.. (2009). A Comparison of Retinal Structure and Visual Function in Foveal and Preferred Retinal Location Regions of Patients With Stargardt Disease. Investigative Ophthalmology & Visual Science. 50(13). 6269–6269. 1 indexed citations
16.
Grippo, Tomás M., et al.. (2005). Evaluation of Multifocal Visual Evoked Potential Latency in Glaucoma. Investigative Ophthalmology & Visual Science. 46(13). 3753–3753. 1 indexed citations
17.
Odel, Jeffrey G., et al.. (2005). A Quantitative Measure of Multifocal Visual Evoked Potential Latencies in Ischemic Optic Neuropathy and Optic Neuritis. Investigative Ophthalmology & Visual Science. 46(13). 642–642. 1 indexed citations
18.
Hood, Donald C., Xiao Zhang, Nitin Ohri, et al.. (2004). Possible indices for minimizing false positives on the multifocal VEP test.. Investigative Ophthalmology & Visual Science. 45(13). 3297–3297. 1 indexed citations
19.
Marmor, Michael F., Donald C. Hood, David Keating, et al.. (2003). Guidelines for basic multifocal electroretinography (mfERG). Documenta Ophthalmologica. 106(2). 105–115. 211 indexed citations
20.
Gratton, Gabriele, Monica Fabiani, Paul M. Corballis, et al.. (1997). Fast and Localized Event-Related Optical Signals (EROS) in the Human Occipital Cortex: Comparisons with the Visual Evoked Potential and fMRI. NeuroImage. 6(3). 168–180. 96 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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