Sung Yoon Cho
About
In The Last Decade
Sung Yoon Cho
95 papers receiving 918 citations
Peers
Comparison fields: 5 of 84
- Genetics 322
- Physiology 287
- Molecular Biology 260
- Epidemiology 178
- Rheumatology 177
Countries citing papers authored by Sung Yoon Cho
This map shows the geographic impact of Sung Yoon Cho'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 Sung Yoon Cho with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sung Yoon Cho more than expected).
Fields of papers citing papers by Sung Yoon Cho
This network shows the impact of papers produced by Sung Yoon Cho. 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 Sung Yoon Cho. The network helps show where Sung Yoon Cho may publish in the future.
Co-authorship network of co-authors of Sung Yoon Cho
This figure shows the co-authorship network connecting the top 25 collaborators of Sung Yoon Cho. A scholar is included among the top collaborators of Sung Yoon Cho 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 Sung Yoon Cho. Sung Yoon Cho 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 | 0 | |
| 5 | 4 | |
| 6 | 1 | |
| 7 | 1 | |
| 8 | 1 | |
| 9 | 5 | |
| 10 | 11 | |
| 11 | 1 | |
| 12 | 5 | |
| 13 | 2 | |
| 14 | 2 | |
| 15 | 11 | |
| 16 | 21 | |
| 17 | 7 | |
| 18 | 9 | |
| 19 | First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review. | 2 |
| 20 | Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence. | 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.