Kei Mizobuchi
About
In The Last Decade
Kei Mizobuchi
45 papers receiving 321 citations
Peers
Comparison fields: 5 of 35
- Molecular Biology 284
- Ophthalmology 196
- Genetics 62
- Cellular and Molecular Neuroscience 50
- Cell Biology 45
Countries citing papers authored by Kei Mizobuchi
This map shows the geographic impact of Kei Mizobuchi'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 Kei Mizobuchi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kei Mizobuchi more than expected).
Fields of papers citing papers by Kei Mizobuchi
This network shows the impact of papers produced by Kei Mizobuchi. 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 Kei Mizobuchi. The network helps show where Kei Mizobuchi may publish in the future.
Co-authorship network of co-authors of Kei Mizobuchi
This figure shows the co-authorship network connecting the top 25 collaborators of Kei Mizobuchi. A scholar is included among the top collaborators of Kei Mizobuchi 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 Kei Mizobuchi. Kei Mizobuchi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 0 | |
| 3 | 2 | |
| 4 | 1 | |
| 5 | 0 | |
| 6 | 3 | |
| 7 | 2 | |
| 8 | 1 | |
| 9 | 0 | |
| 10 | 0 | |
| 11 | 16 | |
| 12 | 2 | |
| 13 | 3 | |
| 14 | 10 | |
| 15 | 5 | |
| 16 | 4 | |
| 17 | 17 | |
| 18 | 36 | |
| 19 | Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants. | 20 |
| 20 | Mutation Analysis of Japanese Patients with Leber Congenital Amaurosis by Next Generation Sequencing | 0 |
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.