Salvatore A. D’Anna

1.5k total citations
24 papers, 1.1k citations indexed

About

Salvatore A. D’Anna is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Molecular Biology. According to data from OpenAlex, Salvatore A. D’Anna has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Ophthalmology, 8 papers in Radiology, Nuclear Medicine and Imaging and 4 papers in Molecular Biology. Recurrent topics in Salvatore A. D’Anna's work include Retinal Diseases and Treatments (5 papers), Glaucoma and retinal disorders (5 papers) and Retinal Imaging and Analysis (4 papers). Salvatore A. D’Anna is often cited by papers focused on Retinal Diseases and Treatments (5 papers), Glaucoma and retinal disorders (5 papers) and Retinal Imaging and Analysis (4 papers). Salvatore A. D’Anna collaborates with scholars based in United States, Japan and Thailand. Salvatore A. D’Anna's co-authors include B. F. Hochheimer, Henry A. Kues, Gerard A. Lutty, James D. Weiland, Mark S. Humayun, Harry A. Quigley, Eugene de Juan, Mohammed A. Aziz, Henry Newland and Bruce M. Greene and has published in prestigious journals such as New England Journal of Medicine, The Journal of Infectious Diseases and Ophthalmology.

In The Last Decade

Salvatore A. D’Anna

22 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Salvatore A. D’Anna United States 18 396 246 240 230 208 24 1.1k
Serge G. Rosolen France 16 297 0.8× 216 0.9× 171 0.7× 152 0.7× 381 1.8× 49 906
Sabine Chahory France 15 282 0.7× 84 0.3× 160 0.7× 17 0.1× 305 1.5× 46 845
Carl L. Scholtz United Kingdom 21 121 0.3× 173 0.7× 82 0.3× 57 0.2× 175 0.8× 43 1.1k
Thomas A. Eskin United States 25 92 0.2× 364 1.5× 144 0.6× 67 0.3× 436 2.1× 64 1.7k
Melanie Murphy Australia 13 76 0.2× 44 0.2× 77 0.3× 20 0.1× 179 0.9× 46 521
Masaaki Suzuki Japan 23 14 0.0× 64 0.3× 30 0.1× 99 0.4× 323 1.6× 90 1.6k
Melvin L. Rubin United States 16 413 1.0× 106 0.4× 177 0.7× 10 0.0× 390 1.9× 57 919
Karen Chen United States 11 41 0.1× 237 1.0× 110 0.5× 19 0.1× 257 1.2× 24 987
Antonio Bergua Germany 17 416 1.1× 33 0.1× 260 1.1× 27 0.1× 115 0.6× 57 709
Hiroshi Ishikawa Japan 17 10 0.0× 124 0.5× 27 0.1× 64 0.3× 292 1.4× 75 1.2k

Countries citing papers authored by Salvatore A. D’Anna

Since Specialization
Citations

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

Fields of papers citing papers by Salvatore A. D’Anna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Salvatore A. D’Anna. 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 Salvatore A. D’Anna. The network helps show where Salvatore A. D’Anna may publish in the future.

Co-authorship network of co-authors of Salvatore A. D’Anna

This figure shows the co-authorship network connecting the top 25 collaborators of Salvatore A. D’Anna. A scholar is included among the top collaborators of Salvatore A. D’Anna 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 Salvatore A. D’Anna. Salvatore A. D’Anna 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.
Ramella‐Roman, Jessica C., Scott A. Mathews, Donald D. Duncan, et al.. (2008). Measurement of oxygen saturation in the retina with a spectroscopic sensitive multi aperture camera. Optics Express. 16(9). 6170–6170. 37 indexed citations
2.
Margalit, E., James D. Weiland, R. E. Clatterbuck, et al.. (2003). Visual and electrical evoked response recorded from subdural electrodes implanted above the visual cortex in normal dogs under two methods of anesthesia. Journal of Neuroscience Methods. 123(2). 129–137. 67 indexed citations
3.
Piyathaisere, Duke V, Eyal Margalit, Shih‐Jen Chen, et al.. (2003). Heat Effects on the Retina. Ophthalmic surgery, lasers & imaging retina. 34(2). 114–120. 31 indexed citations
4.
Nishiwaki, Hirokazu, R. Zeimer, Morton F. Goldberg, et al.. (2002). Laser Targeted Photo-occlusion of Rat Choroidal Neovascularization Without Collateral Damage †¶. Photochemistry and Photobiology. 75(2). 149–149. 8 indexed citations
5.
Levkovitch-Verbin, Hana, et al.. (2001). Optic nerve transection in monkeys may result in secondary degeneration of retinal ganglion cells.. PubMed. 42(5). 975–82. 122 indexed citations
6.
Kues, Henry A., Salvatore A. D’Anna, Robert Osiander, William R. Green, & John C. Monahan. (1999). Absence of ocular effects after either single or repeated exposure to 10 mW/cm2 from a 60 GHz CW source. Bioelectromagnetics. 20(8). 463–473. 39 indexed citations
7.
Majji, Ajit B, Mark S. Humayun, James D. Weiland, et al.. (1999). Long-term histological and electrophysiological results of an inactive epiretinal electrode array implantation in dogs.. PubMed. 40(9). 2073–81. 132 indexed citations
8.
McLeod, D. Scott, Salvatore A. D’Anna, & Gerard A. Lutty. (1998). Clinical and histopathologic features of canine oxygen-induced proliferative retinopathy.. PubMed. 39(10). 1918–32. 54 indexed citations
9.
Kues, Henry A., et al.. (1992). Increased sensitivity of the non‐human primate eye to microwave radiation following ophthalmic drug pretreatment. Bioelectromagnetics. 13(5). 379–393. 25 indexed citations
10.
Repka, Michael X., et al.. (1991). A Primate Model of Macular Cyst. Ophthalmology. 98(4). 535–540. 1 indexed citations
11.
Repka, Michael X., et al.. (1990). A Primate Model of Anterior Segment ischemia after Strabismus Surgery. Ophthalmology. 97(4). 456–461. 32 indexed citations
12.
Newland, Henry, A T White, Bruce M. Greene, et al.. (1988). Effect of single-dose ivermectin therapy on human Onchocerca volvulus infection with onchocercal ocular involvement.. British Journal of Ophthalmology. 72(8). 561–569. 41 indexed citations
13.
White, A T, Henry Newland, Hugh R. Taylor, et al.. (1987). Controlled Trial and Dose-Finding Study of Ivermectin for Treatment of Onchocerciasis. The Journal of Infectious Diseases. 156(3). 463–470. 62 indexed citations
14.
Hochheimer, B. F., Gerard A. Lutty, & Salvatore A. D’Anna. (1987). Ocular fluorescein phototoxicity. Applied Optics. 26(8). 1473–1473. 5 indexed citations
15.
Kues, Henry A., Lawrence W. Hirst, Gerard A. Lutty, Salvatore A. D’Anna, & G R Dunkelberger. (1985). Effects of 2.45‐GHz microwaves on primate corneal endothelium. Bioelectromagnetics. 6(2). 177–188. 40 indexed citations
16.
Greene, Bruce M., Hugh R. Taylor, Eddie W. Cupp, et al.. (1985). Comparison of Ivermectin and Diethylcarbamazine in the Treatment of Onchocerciasis. New England Journal of Medicine. 313(3). 133–138. 179 indexed citations
17.
D’Anna, Salvatore A. & Terry W. George. (1984). Retinal Fundus Cameras. Ophthalmology. 91(1). 94–119. 1 indexed citations
18.
George, Terry W. & Salvatore A. D’Anna. (1983). A Comparison of Retinal, Fundus Cameras. Ophthalmology. 90(9). 80–98. 2 indexed citations
19.
Hochheimer, B. F., et al.. (1980). Potential hazards from specific ophthalmic devices. Vision Research. 20(12). 1039–1053. 53 indexed citations
20.
Hochheimer, B. F. & Salvatore A. D’Anna. (1978). Angiography with new dyes. Experimental Eye Research. 27(1). 1–16. 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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