K. Narisawa
About
In The Last Decade
K. Narisawa
66 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 66
- Molecular Biology 743
- Clinical Biochemistry 734
- Biochemistry 213
- Rheumatology 170
- Pediatrics, Perinatology and Child Health 121
Countries citing papers authored by K. Narisawa
This map shows the geographic impact of K. Narisawa'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 K. Narisawa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Narisawa more than expected).
Fields of papers citing papers by K. Narisawa
This network shows the impact of papers produced by K. Narisawa. 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 K. Narisawa. The network helps show where K. Narisawa may publish in the future.
Co-authorship network of co-authors of K. Narisawa
This figure shows the co-authorship network connecting the top 25 collaborators of K. Narisawa. A scholar is included among the top collaborators of K. Narisawa 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 K. Narisawa. K. Narisawa 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 | 35 | |
| 3 | 10 | |
| 4 | 9 | |
| 5 | 5 | |
| 6 | [Identification of missense mutations and haplotyping of carnitine palmitoyltransferase II gene]. | 1 |
| 7 | 21 | |
| 8 | Association between a polymorphism of the 65K-glutamate decarboxylase gene and insulin-dependent diabetes mellitus | 1 |
| 9 | Molecular analysis of methylmalonic acidemia: Identification of novel mutations in the methylmalonyl-CoA mutase gene with decreased level of mutant mRNA | 1 |
| 10 | 4 | |
| 11 | 6 | |
| 12 | 71 | |
| 13 | 27 | |
| 14 | 48 | |
| 15 | 24 | |
| 16 | 40 | |
| 17 | 7 | |
| 18 | 3 | |
| 19 | 21 | |
| 20 | 5 |
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.