Pao Lin Kuo
About
In The Last Decade
Pao Lin Kuo
17 papers receiving 249 citations
Peers
Comparison fields: 5 of 50
- Genetics 183
- Molecular Biology 127
- Reproductive Medicine 101
- Biomedical Engineering 45
- Pediatrics, Perinatology and Child Health 39
Countries citing papers authored by Pao Lin Kuo
This map shows the geographic impact of Pao Lin Kuo'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 Pao Lin Kuo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pao Lin Kuo more than expected).
Fields of papers citing papers by Pao Lin Kuo
This network shows the impact of papers produced by Pao Lin Kuo. 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 Pao Lin Kuo. The network helps show where Pao Lin Kuo may publish in the future.
Co-authorship network of co-authors of Pao Lin Kuo
This figure shows the co-authorship network connecting the top 25 collaborators of Pao Lin Kuo. A scholar is included among the top collaborators of Pao Lin Kuo 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 Pao Lin Kuo. Pao Lin Kuo 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 | 49 | |
| 3 | 16 | |
| 4 | 25 | |
| 5 | 4 | |
| 6 | 27 | |
| 7 | Six cases of deletion 9p24 and trisomy 19q13.4 inherited from a familial balanced translocation. | 5 |
| 8 | 42 | |
| 9 | 28 | |
| 10 | Cytogenetic surveillance of mentally-retarded school children in southern Taiwan. | 7 |
| 11 | Partial trisomy 1 with congenital hydrocephalus and hypogammaglobulinemia: report of one case. | 1 |
| 12 | 30 | |
| 13 | Diagnosis of Prader-Willi syndrome in the neonatal period | 1 |
| 14 | AZFa candidate gene deletions in Taiwanese patients with spermatogenic failure. | 6 |
| 15 | 40 | |
| 16 | EEG--a valuable tool in early diagnosis of Angelman syndrome. | 1 |
| 17 | Doppler velocimetry of intraplacental fetal arteries. | 13 |
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.