Feng Zhao
Impact in
- Rheumatology top 2%
- Moyamoya disease diagnosis and treatment
- Molecular Biology top 10%
- Congenital heart defects research
- Retinal Development and Disorders
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
Papers in
- Surgery 17
- Orthopaedic implants and arthroplasty 6
- Total Knee Arthroplasty Outcomes 6
- Knee injuries and reconstruction techniques 5
- Co-authors
- Bruce D. Gelb (4 shared papers)Masahiko Satoda (3 shared papers)Mary Ella Pierpont (2 shared papers)Yoshihide Hayashizaki (1 shared paper)Cong Han (5 shared papers)Jonathan D. Licht (1 shared paper)Xiang‐Yang Bao (4 shared papers)H. Rosemarie Davidson (1 shared paper)
- Journals
- Animal Genetics (3 papers)PLoS ONE (2 papers)Stroke (2 papers)Frontiers in Bioengineering and Biotechnology (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- ChinaUnited StatesIndonesia
In The Last Decade
Feng Zhao
89 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 133
- Rheumatology 300
- Molecular Biology 649
- Genetics 210
- Obstetrics and Gynecology 45
- Psychiatry and Mental health 86
Countries citing papers authored by Feng Zhao
This map shows the geographic impact of Feng Zhao'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 Feng Zhao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Feng Zhao more than expected).
Fields of papers citing papers by Feng Zhao
This network shows the impact of papers produced by Feng Zhao. 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 Feng Zhao. The network helps show where Feng Zhao may publish in the future.
Co-authors
The 25 scholars most cited alongside Feng Zhao, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 94 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 192 | |
| 2 | 2011 | 146 | |
| 3 | 2001 | 131 | |
| 4 | 2009 | 116 | |
| 5 | 2017 | 108 | |
| 6 | 2019 | 98 | |
| 7 | 2001 | 80 | |
| 8 | 2019 | 64 | |
| 9 | 2003 | 51 | |
| 10 | Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations. | 2007 | 39 |
| 11 | 2011 | 39 | |
| 12 | 2000 | 32 | |
| 13 | 2018 | 31 | |
| 14 | 2019 | 29 | |
| 15 | 2009 | 29 | |
| 16 | 2023 | 28 | |
| 17 | 2013 | 24 | |
| 18 | 2016 | 22 | |
| 19 | 2022 | 22 | |
| 20 | 2019 | 21 |
About Feng Zhao
Feng Zhao is a scholar working on Molecular Biology, Surgery, Rheumatology, Genetics and Epidemiology, having authored 94 papers that have together received 1.7k indexed citations. Recurring topics across this work include Orthopaedic implants and arthroplasty (6 papers), Total Knee Arthroplasty Outcomes (6 papers), Knee injuries and reconstruction techniques (5 papers), Moyamoya disease diagnosis and treatment (5 papers), Bone fractures and treatments (4 papers), Cancer-related molecular mechanisms research (4 papers), Gestational Diabetes Research and Management (4 papers) and Intracranial Aneurysms: Treatment and Complications (4 papers). The work is most often cited by research in Rheumatology (300 citations), Molecular Biology (649 citations), Genetics (210 citations), Obstetrics and Gynecology (45 citations) and Psychiatry and Mental health (86 citations). Feng Zhao has collaborated with scholars based in China, United States and Indonesia. Frequent co-authors include Bruce D. Gelb, Masahiko Satoda, Mary Ella Pierpont, Yoshihide Hayashizaki, Cong Han, Jonathan D. Licht, Xiang‐Yang Bao, H. Rosemarie Davidson, Wei-Zhong Yang and George A. Díaz. Their work appears in journals such as Animal Genetics, PLoS ONE, Stroke, Frontiers in Bioengineering and Biotechnology and The American Journal of Human Genetics.
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.