Tsuyoshi Yoshihara
About
In The Last Decade
Tsuyoshi Yoshihara
15 papers receiving 976 citations
Peers
Comparison fields: 5 of 59
- Neurology 609
- Cellular and Molecular Neuroscience 439
- Molecular Biology 391
- Genetics 259
- Neurology 252
Countries citing papers authored by Tsuyoshi Yoshihara
This map shows the geographic impact of Tsuyoshi Yoshihara'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 Tsuyoshi Yoshihara with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tsuyoshi Yoshihara more than expected).
Fields of papers citing papers by Tsuyoshi Yoshihara
This network shows the impact of papers produced by Tsuyoshi Yoshihara. 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 Tsuyoshi Yoshihara. The network helps show where Tsuyoshi Yoshihara may publish in the future.
Co-authorship network of co-authors of Tsuyoshi Yoshihara
This figure shows the co-authorship network connecting the top 25 collaborators of Tsuyoshi Yoshihara. A scholar is included among the top collaborators of Tsuyoshi Yoshihara 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 Tsuyoshi Yoshihara. Tsuyoshi Yoshihara 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 | 19 | |
| 3 | 203 | |
| 4 | 85 | |
| 5 | 73 | |
| 6 | 167 | |
| 7 | 42 | |
| 8 | 72 | |
| 9 | 229 | |
| 10 | 29 | |
| 11 | 21 | |
| 12 | 12 | |
| 13 | [X-Linked Charcot-Marie-Tooth disease with a new mutation (Thr191Ala) in the connexin32]. | 1 |
| 14 | [Two families of Charcot-Marie-Tooth disease with Adie's pupil, axonal neuropahy and the Thr124Met mutation in the peripheral myelin protein zero gene]. | 3 |
| 15 | 38 |
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.