Dong‐Kyu Jin
About
In The Last Decade
Dong‐Kyu Jin
254 papers receiving 3.8k citations
Peers
Comparison fields: 5 of 119
- Genetics 1.1k
- Molecular Biology 917
- Physiology 907
- Endocrinology, Diabetes and Metabolism 763
- Surgery 692
Countries citing papers authored by Dong‐Kyu Jin
This map shows the geographic impact of Dong‐Kyu Jin'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 Dong‐Kyu Jin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dong‐Kyu Jin more than expected).
Fields of papers citing papers by Dong‐Kyu Jin
This network shows the impact of papers produced by Dong‐Kyu Jin. 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 Dong‐Kyu Jin. The network helps show where Dong‐Kyu Jin may publish in the future.
Co-authorship network of co-authors of Dong‐Kyu Jin
This figure shows the co-authorship network connecting the top 25 collaborators of Dong‐Kyu Jin. A scholar is included among the top collaborators of Dong‐Kyu Jin 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 Dong‐Kyu Jin. Dong‐Kyu Jin 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 | 5 | |
| 3 | 1 | |
| 4 | 5 | |
| 5 | 2 | |
| 6 | 2 | |
| 7 | 2 | |
| 8 | 11 | |
| 9 | 21 | |
| 10 | 7 | |
| 11 | 9 | |
| 12 | 3 | |
| 13 | First Korean Case of Infantile Hypophosphatasia with Novel Mutation in ALPL and Literature Review. | 2 |
| 14 | 5 | |
| 15 | 23 | |
| 16 | 1 | |
| 17 | Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence. | 5 |
| 18 | Clinical, biochemical, and genetic analysis of korean patients with pseudohypoparathyroidism type Ia. | 3 |
| 19 | Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency. | 10 |
| 20 | 12 |
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.