Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
Identification of a Gene That Causes Primary Open Angle Glaucoma
19971.1k citationsEdwin M. Stone, John H. Fingert et al.profile →
Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis
The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions
1993567 citationsVal C. Sheffield, Edwin M. Stone et al.profile →
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics
2008543 citationsArtur V. Cideciyan, Sanford L. Boye et al.Proceedings of the National Academy of Sciencesprofile →
Cloning and sequencing of a deoxyribonucleic acid copy of glyceraldehyde 3-phosphate dehydrogenase messenger ribonucleic acid isolated from chicken muscle
Countries citing papers authored by Edwin M. Stone
Since
Specialization
Citations
This map shows the geographic impact of Edwin M. Stone'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 Edwin M. Stone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edwin M. Stone more than expected).
This network shows the impact of papers produced by Edwin M. Stone. 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 Edwin M. Stone. The network helps show where Edwin M. Stone may publish in the future.
Co-authorship network of co-authors of Edwin M. Stone
This figure shows the co-authorship network connecting the top 25 collaborators of Edwin M. Stone.
A scholar is included among the top collaborators of Edwin M. Stone 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 Edwin M. Stone. Edwin M. Stone is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Choi, Michael, Ben R. Roos, Edwin M. Stone, et al.. (2015). Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos.. PubMed. 21. 1017–23.22 indexed citations
DeLuca, Adam P., Joseph C. Giacalone, Luke A. Wiley, et al.. (2014). RPGR, a common source of missed variants in exome sequencing experiments. Investigative Ophthalmology & Visual Science. 55(13). 3262–3262.1 indexed citations
10.
Braun, Terry A., Alex H. Wagner, Adam P. DeLuca, et al.. (2013). The Ocular Tissue Database. Investigative Ophthalmology & Visual Science. 54(15). 3383–3383.3 indexed citations
11.
Folk, James C., Stephen R. Russell, H. Culver Boldt, et al.. (2009). Patient Preference and Safety of Bilateral Intravitreal Injection of Anti-VEGF Therapy. Investigative Ophthalmology & Visual Science. 50(13). 247–247.1 indexed citations
12.
Goldstein, Orly, Anna V. Kukekova, Geoffrey K. Aguirre, et al.. (2008). The Mutant Gene Causing Canine Early Retinal Degeneration Identifies a Novel Pathway Critical for Photoreceptor Development. Investigative Ophthalmology & Visual Science. 49(13). 1704–1704.2 indexed citations
13.
Hayreh, Sohan Singh, John H. Fingert, Edwin M. Stone, & Daniel M. Jacobson. (2008). Familial non-arteritic anterior ischemic optic neuropathy. Graefe s Archive for Clinical and Experimental Ophthalmology. 246(9). 1295–1305.10 indexed citations
Shankar, Suma P., Valério Carelli, Terri M. King, et al.. (2005). Linkage Analysis of the X Chromosome in a Brazilian Family With Leber Hereditary Optic Neuropathy (LHON). Investigative Ophthalmology & Visual Science. 46(13). 663–663.3 indexed citations
17.
Kozma, Petra, David G. Birch, Dianna K. Hughbanks-Wheaton, et al.. (2004). Analysis of protein haplotypes in trans as factors modifying phenotypic variation of retinal dystrophies caused by a splice site mutation in the peripherin/RDS gene. Investigative Ophthalmology & Visual Science. 45(13). 3719–3719.1 indexed citations
Lotery, Andrew, F.L. Munier, Gerald A. Fishman, et al.. (2000). Allelic variation in the VMD2 gene in best disease and age-related macular degeneration.. PubMed. 41(6). 1291–6.126 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.