Tamiko Nishimura
About
In The Last Decade
Tamiko Nishimura
22 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 91
- Molecular Biology 890
- Clinical Biochemistry 145
- Cancer Research 105
- Genetics 104
- Nutrition and Dietetics 87
Countries citing papers authored by Tamiko Nishimura
This map shows the geographic impact of Tamiko Nishimura'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 Tamiko Nishimura with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tamiko Nishimura more than expected).
Fields of papers citing papers by Tamiko Nishimura
This network shows the impact of papers produced by Tamiko Nishimura. 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 Tamiko Nishimura. The network helps show where Tamiko Nishimura may publish in the future.
Co-authorship network of co-authors of Tamiko Nishimura
This figure shows the co-authorship network connecting the top 25 collaborators of Tamiko Nishimura. A scholar is included among the top collaborators of Tamiko Nishimura 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 Tamiko Nishimura. Tamiko Nishimura is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 0 | |
| 3 | 16 | |
| 4 | 3 | |
| 5 | 9 | |
| 6 | 21 | |
| 7 | 68 | |
| 8 | 178 | |
| 9 | 55 | |
| 10 | 78 | |
| 11 | 46 | |
| 12 | 41 | |
| 13 | 55 | |
| 14 | 30 | |
| 15 | 135 | |
| 16 | 77 | |
| 17 | 169 | |
| 18 | [Molecular pathology of Charcot-Marie-Tooth disease type 1A: abnormal expression of PMP-22]. | 0 |
| 19 | [A case of variant Gerstmann-Sträussler-Scheinker disease with the mutation of codon P105L]. | 9 |
| 20 | New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1. | 41 |
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.