Yong-Wha Lee
About
In The Last Decade
Yong-Wha Lee
57 papers receiving 605 citations
Peers
Comparison fields: 5 of 96
- Molecular Biology 226
- Clinical Biochemistry 134
- Physiology 91
- Pathology and Forensic Medicine 78
- Endocrinology, Diabetes and Metabolism 69
Countries citing papers authored by Yong-Wha Lee
This map shows the geographic impact of Yong-Wha Lee'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 Yong-Wha Lee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yong-Wha Lee more than expected).
Fields of papers citing papers by Yong-Wha Lee
This network shows the impact of papers produced by Yong-Wha Lee. 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 Yong-Wha Lee. The network helps show where Yong-Wha Lee may publish in the future.
Co-authorship network of co-authors of Yong-Wha Lee
This figure shows the co-authorship network connecting the top 25 collaborators of Yong-Wha Lee. A scholar is included among the top collaborators of Yong-Wha Lee 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 Yong-Wha Lee. Yong-Wha Lee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 0 | |
| 3 | 1 | |
| 4 | 4 | |
| 5 | 14 | |
| 6 | 4 | |
| 7 | 7 | |
| 8 | 5 | |
| 9 | 28 | |
| 10 | 21 | |
| 11 | 3 | |
| 12 | 24 | |
| 13 | 8 | |
| 14 | 17 | |
| 15 | SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation. | 7 |
| 16 | 8 | |
| 17 | A novel KRIT1 gene mutation in a patient with cerebral and multiple spinal cavernous malformations. | 7 |
| 18 | 51 | |
| 19 | 26 | |
| 20 | 27 |
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.