A.F. Wright
About
In The Last Decade
A.F. Wright
8 papers receiving 169 citations
Peers
Comparison fields: 5 of 54
- Molecular Biology 72
- Nephrology 71
- Ophthalmology 53
- Pathology and Forensic Medicine 30
- Epidemiology 25
Countries citing papers authored by A.F. Wright
This map shows the geographic impact of A.F. Wright'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 A.F. Wright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.F. Wright more than expected).
Fields of papers citing papers by A.F. Wright
This network shows the impact of papers produced by A.F. Wright. 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 A.F. Wright. The network helps show where A.F. Wright may publish in the future.
Co-authorship network of co-authors of A.F. Wright
This figure shows the co-authorship network connecting the top 25 collaborators of A.F. Wright. A scholar is included among the top collaborators of A.F. Wright 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 A.F. Wright. A.F. Wright is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 15 | |
| 3 | 91 | |
| 4 | 43 | |
| 5 | Effects of MitoQ and Sod2 on Rates of Retinal Degeneration in Rd1, Atrd1, Rho–/– and Rds Mutant Mice | 0 |
| 6 | Phenotype of Heterozygotes with Mutations in the ORF 15 (Open Reading Frame 15) of RPGR | 1 |
| 7 | Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online. | 3 |
| 8 | 16 | |
| 9 | Genetic linkage analysis in 26 families with Bardet-Biedl syndrome | 4 |
| 10 | 3 |
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.