E. DelBono

975 total citations
20 papers, 334 citations indexed

About

E. DelBono is a scholar working on Ophthalmology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, E. DelBono has authored 20 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Ophthalmology, 8 papers in Molecular Biology and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in E. DelBono's work include Glaucoma and retinal disorders (11 papers), melanin and skin pigmentation (3 papers) and Retinopathy of Prematurity Studies (3 papers). E. DelBono is often cited by papers focused on Glaucoma and retinal disorders (11 papers), melanin and skin pigmentation (3 papers) and Retinopathy of Prematurity Studies (3 papers). E. DelBono collaborates with scholars based in United States and Brazil. E. DelBono's co-authors include Janey L. Wiggs, Jonathan L. Haines, Robert L. Murphy, Louis R. Pasquale, Daniel B. Mirel, Stephanie Loomis, Brian L. Yaspan, Wael Abdrabou, Wendy Brodeur and Lana M. Olson and has published in prestigious journals such as CHEST Journal, Human Molecular Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

E. DelBono

20 papers receiving 327 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. DelBono United States 8 193 125 70 63 49 20 334
Simon Dulz Germany 11 84 0.4× 87 0.7× 51 0.7× 27 0.4× 34 0.7× 34 234
Elizabeth A. Del Bono United States 10 459 2.4× 206 1.6× 237 3.4× 109 1.7× 83 1.7× 16 651
Anna Turno‐Kręcicka Poland 11 208 1.1× 70 0.6× 62 0.9× 21 0.3× 11 0.2× 44 299
Jane S. Myung United States 8 189 1.0× 103 0.8× 139 2.0× 28 0.4× 16 0.3× 14 312
Joseph W. Berkow United States 13 183 0.9× 107 0.9× 107 1.5× 18 0.3× 22 0.4× 24 348
Jacinthe Rouleau United States 7 231 1.2× 349 2.8× 44 0.6× 18 0.3× 11 0.2× 13 562
Svein Ove Semb Norway 11 159 0.8× 145 1.2× 97 1.4× 114 1.8× 13 0.3× 14 470
Manzo Taguchi Japan 11 308 1.6× 57 0.5× 76 1.1× 24 0.4× 7 0.1× 18 357
P Amalric France 8 203 1.1× 96 0.8× 80 1.1× 20 0.3× 22 0.4× 64 271
Birgit Kjer Denmark 11 126 0.7× 359 2.9× 77 1.1× 28 0.4× 35 0.7× 14 483

Countries citing papers authored by E. DelBono

Since Specialization
Citations

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

Fields of papers citing papers by E. DelBono

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. DelBono

This figure shows the co-authorship network connecting the top 25 collaborators of E. DelBono. A scholar is included among the top collaborators of E. DelBono 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 E. DelBono. E. DelBono 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.
Gaier, Eric D., Isao Nakata, Philip Skidd, et al.. (2017). Diagnostic genetic testing for patients with bilateral optic neuropathy and comparison of clinical features according to OPA1 mutation status.. PubMed. 23. 548–560. 9 indexed citations
2.
Nakata, Isao, et al.. (2016). Inherited optic atrophy gene discovery using whole exome sequencing.. Investigative Ophthalmology & Visual Science. 57(12). 5063–5063. 1 indexed citations
3.
Wiggs, Janey L., Jae H. Kang, Brian L. Yaspan, et al.. (2011). Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA. Human Molecular Genetics. 20(23). 4707–4713. 121 indexed citations
4.
DelBono, E., et al.. (2010). A Novel Pax6 In-Frame Insertion in the Paired Domain is Associated With a Severe Ocular Phenotype. Investigative Ophthalmology & Visual Science. 51(13). 3071–3071. 1 indexed citations
5.
Fan, Baojian, Dayse F Sena, Louis R. Pasquale, et al.. (2010). Lack of Association of Polymorphisms in Elastin With Pseudoexfoliation Syndrome and Glaucoma. Journal of Glaucoma. 19(7). 432–436. 4 indexed citations
6.
Fan, Baojian, Cynthia L. Grosskreutz, Louis R. Pasquale, et al.. (2008). Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma.. PubMed. 14. 2484–91. 25 indexed citations
7.
Hauser, Michael A., Dayse F Sena, E. DelBono, et al.. (2006). Distribution of WDR36 DNA Sequence Variants in Primary Open Angle Glaucoma Patients. Investigative Ophthalmology & Visual Science. 47(13). 177–177. 1 indexed citations
8.
Hauser, Michael A., Dayse F Sena, Karen LaRocque-Abramson, et al.. (2006). Distribution of Optineurin Sequence Variations in an Ethnically Diverse Population of Low-tension Glaucoma Patients From the United States. Journal of Glaucoma. 15(5). 358–363. 64 indexed citations
9.
Wyatt, David W., et al.. (2006). Distribution of DNA Sequence Variants in COL8A1 and COL8A2 in Glaucoma Patients With Thin CCT. 47(13). 2826–2826. 4 indexed citations
10.
DelBono, E., Dayse F Sena, Simone Finzi, & Janey L. Wiggs. (2005). Phenotype of CYP1B1 Gene Mutations in U.S. and Brazilian Patients With Primary Congenital Glaucoma. Investigative Ophthalmology & Visual Science. 46(13). 38–38. 1 indexed citations
11.
Wagner, Sören, et al.. (2005). A Second Locus for Pigment Dispersion Syndrome Maps to Chromosome 18q21. Investigative Ophthalmology & Visual Science. 46(13). 29–29. 5 indexed citations
12.
Clarke, L., Kelly Rogers, Sören Wagner, et al.. (2004). Evaluation of small leucine–rich proteoglycans located on chromosome 12q21 in families with juvenile–onset myopia.. Investigative Ophthalmology & Visual Science. 45(13). 1245–1245. 3 indexed citations
13.
Sena, Dayse F, Louis R. Pasquale, R. Rand Allingham, et al.. (2004). Evaluation of NOS3 polymorphisms in patients with primary open angle glaucoma. Investigative Ophthalmology & Visual Science. 45(13). 4391–4391. 2 indexed citations
14.
Azar, Nathalie F., et al.. (2004). The SLRP gene cluster on chromosome 12 is deleted in a patient with a chromosome 12q21–q22 deletion and clinical features of cornea plana.. Investigative Ophthalmology & Visual Science. 45(13). 1523–1523. 1 indexed citations
15.
Lynch, Sean, et al.. (2002). DNA sequence variants in the tyrosinase-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma.. PubMed. 8. 127–9. 23 indexed citations
16.
Wiggs, Janey L., J. S. Andersen, E. DelBono, et al.. (1997). A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-36. 38(4). 1 indexed citations
17.
Wiggs, Janey L., R. Rand Allingham, E. DelBono, et al.. (1996). The juvenile glaucoma gene on 1q21-q31 is not associated with Primary Open Angle Glaucoma (POAG). eCommons - AKU (Aga Khan University). 37(3). 1 indexed citations
18.
Wilkins, Robert L., et al.. (1990). Lung Sound Nomenclature Survey. CHEST Journal. 98(4). 886–889. 30 indexed citations
19.
DelBono, E., et al.. (1986). Observer Agreement, Chest Auscultation, and Crackles in Asbestos-Exposed Workers. CHEST Journal. 89(1). 27–29. 14 indexed citations
20.
DelBono, E., et al.. (1982). The prevalence and character of crackles (rales) in young women without significant lung disease.. PubMed. 126(5). 921–3. 23 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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