Chang‐Seok Ki
About
In The Last Decade
Chang‐Seok Ki
552 papers receiving 10.5k citations
Peers
Comparison fields: 5 of 181
- Molecular Biology 2.9k
- Epidemiology 2.5k
- Infectious Diseases 1.8k
- Neurology 1.2k
- Genetics 1.2k
Countries citing papers authored by Chang‐Seok Ki
This map shows the geographic impact of Chang‐Seok Ki'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 Chang‐Seok Ki with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chang‐Seok Ki more than expected).
Fields of papers citing papers by Chang‐Seok Ki
This network shows the impact of papers produced by Chang‐Seok Ki. 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 Chang‐Seok Ki. The network helps show where Chang‐Seok Ki may publish in the future.
Co-authorship network of co-authors of Chang‐Seok Ki
This figure shows the co-authorship network connecting the top 25 collaborators of Chang‐Seok Ki. A scholar is included among the top collaborators of Chang‐Seok Ki 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 Chang‐Seok Ki. Chang‐Seok Ki 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 | 4 | |
| 3 | 2 | |
| 4 | 56 | |
| 5 | 4 | |
| 6 | 3 | |
| 7 | 4 | |
| 8 | 34 | |
| 9 | 1 | |
| 10 | 26 | |
| 11 | 133 | |
| 12 | 23 | |
| 13 | SLC22A5 mutations in a patient with systemic primary carnitine deficiency: the first Korean case confirmed by biochemical and molecular investigation. | 7 |
| 14 | Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma. | 25 |
| 15 | Clinical, pathological, and genetic analysis of a Korean family with thoracic aortic aneurysms and dissections carrying a novel Asp26Tyr mutation. | 12 |
| 16 | Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency. | 10 |
| 17 | 6 | |
| 18 | 24 | |
| 19 | A Case of Krabbe Disease Confirmed by Identification of Mutations in the Galactocerbroside beta-galactosidase Gene (GALC). | 1 |
| 20 | [Contribution of bronchial fibroscopy in pneumonology services in developing countries]. | 1 |
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.