Takeshi Iwata
About
In The Last Decade
Takeshi Iwata
160 papers receiving 3.5k citations
Peers
Comparison fields: 5 of 124
- Molecular Biology 2.4k
- Ophthalmology 1.8k
- Radiology, Nuclear Medicine and Imaging 741
- Cell Biology 394
- Genetics 353
Countries citing papers authored by Takeshi Iwata
This map shows the geographic impact of Takeshi Iwata'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 Takeshi Iwata with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Takeshi Iwata more than expected).
Fields of papers citing papers by Takeshi Iwata
This network shows the impact of papers produced by Takeshi Iwata. 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 Takeshi Iwata. The network helps show where Takeshi Iwata may publish in the future.
Co-authorship network of co-authors of Takeshi Iwata
This figure shows the co-authorship network connecting the top 25 collaborators of Takeshi Iwata. A scholar is included among the top collaborators of Takeshi Iwata 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 Takeshi Iwata. Takeshi Iwata is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | 4 | |
| 3 | 21 | |
| 4 | 24 | |
| 5 | 13 | |
| 6 | 16 | |
| 7 | 3 | |
| 8 | Investigations of Gene Pathogenicity and Establishment of a Patient Data Bank for the Hereditary Chorioretinal Dystrophy | 1 |
| 9 | 2 | |
| 10 | Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants. | 20 |
| 11 | Mutations in the X-linked gene PRPS1 cause retinal degeneration in females | 1 |
| 12 | 23 | |
| 13 | Japan Whole Exome Project for Inherited Retinal Disease | 1 |
| 14 | Human HTRA1 expression is enhanced by indel mutation in the HTRA1 regulatory element region. | 1 |
| 15 | 15 | |
| 16 | 3 | |
| 17 | Characterization of the Retina in Htra1 Deficient Mouse | 2 |
| 18 | Focal Macular Electroretinogram of Cynomolgus Monkey (Macaca fascicularis) With Early Onset Macular Degeneration | 1 |
| 19 | Comparative Proteome Analysis of Macula versus Peripheral Retina in Cynomolgus Monkey | 2 |
| 20 | Linkage and mutation analysis to identify the gene associated with macular degeneration segregating in a cynomolgus monkey (Macaca fascicularis) pedigree. | 1 |
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.