Rutai Hui
About
In The Last Decade
Rutai Hui
322 papers receiving 8.7k citations
Hit Papers
Peers
Comparison fields: 5 of 165
- Cardiology and Cardiovascular Medicine 3.2k
- Molecular Biology 2.2k
- Pulmonary and Respiratory Medicine 1.3k
- Surgery 1.1k
- Endocrinology, Diabetes and Metabolism 1.1k
Countries citing papers authored by Rutai Hui
This map shows the geographic impact of Rutai Hui'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 Rutai Hui with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rutai Hui more than expected).
Fields of papers citing papers by Rutai Hui
This network shows the impact of papers produced by Rutai Hui. 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 Rutai Hui. The network helps show where Rutai Hui may publish in the future.
Co-authorship network of co-authors of Rutai Hui
This figure shows the co-authorship network connecting the top 25 collaborators of Rutai Hui. A scholar is included among the top collaborators of Rutai Hui 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 Rutai Hui. Rutai Hui is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 5 | |
| 2 | 11 | |
| 3 | 10 | |
| 4 | 5 | |
| 5 | 3 | |
| 6 | 20 | |
| 7 | 12 | |
| 8 | 2 | |
| 9 | 4 | |
| 10 | 16 | |
| 11 | 6 | |
| 12 | 52 | |
| 13 | Molecular analysis for diagnosis of Marfan syndrome and Marfan-associated disorders. | 4 |
| 14 | Identification of a novel lethal fibrillin-1 gene mutation in a Chinese Marfan family and correlation of 3' fibrillin-1 gene mutations with phenotype. | 7 |
| 15 | [A novel hot-spot mutation S236G in the cardiac myosin binding protein C gene in Chinese patient with hypertrophic cardiomyopathy]. | 2 |
| 16 | [The genotype-phenotype correlation of MYH7 gene G15391A mutation and MYBPC3 gene G12101A mutation in familial hypertrophic cardiomyopathy]. | 1 |
| 17 | [Clinical features of dilated cardiomyopathy-like hypertrophic cardiomyopathy caused by a 13261 G > A mutation in cardiac myosin-binding protein C gene]. | 1 |
| 18 | [Association of alpha-adducin gene and G-protein beta3-subunit gene with essential hypertension in Chinese]. | 5 |
| 19 | [Metabolic syndrome strongly linked to stroke in Chinese]. | 9 |
| 20 | [Alpha-adducin gene G/W460 polymorphism is associated with intracerebral hemorrhage in Chinese]. | 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.