Xiaowu Gai
About
In The Last Decade
Xiaowu Gai
84 papers receiving 4.1k citations
Hit Papers
Peers
Comparison fields: 5 of 128
- Molecular Biology 2.2k
- Epidemiology 1.4k
- Rheumatology 704
- Urology 579
- Genetics 574
Countries citing papers authored by Xiaowu Gai
This map shows the geographic impact of Xiaowu Gai'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 Xiaowu Gai with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xiaowu Gai more than expected).
Fields of papers citing papers by Xiaowu Gai
This network shows the impact of papers produced by Xiaowu Gai. 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 Xiaowu Gai. The network helps show where Xiaowu Gai may publish in the future.
Co-authorship network of co-authors of Xiaowu Gai
This figure shows the co-authorship network connecting the top 25 collaborators of Xiaowu Gai. A scholar is included among the top collaborators of Xiaowu Gai 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 Xiaowu Gai. Xiaowu Gai 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 | 5 | |
| 3 | 3 | |
| 4 | 23 | |
| 5 | 2 | |
| 6 | 2 | |
| 7 | 42 | |
| 8 | 7 | |
| 9 | 14 | |
| 10 | 29 | |
| 11 | 36 | |
| 12 | Improved understanding of the disease mechanism of steroid induced glaucoma using gene editing techniques | 0 |
| 13 | 32 | |
| 14 | 10 | |
| 15 | 179 | |
| 16 | Adaptive Optics Scanning Laser Ophthalmoscopy and High Resolution Imaging in Autosomal Dominant Retinitis Pigmentosa Caused by a Novel PRPF31 Nonsense Mutation | 1 |
| 17 | 113 | |
| 18 | 142 | |
| 19 | 41 | |
| 20 | 46 |
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.