Feng Zhang
Impact in
- Cancer Research top 0.5%
- Cancer-related molecular mechanisms research
- Genetics top 0.1%
- Genomic variations and chromosomal abnormalities
Papers in
-
- RNA Research and Splicing 25
- RNA modifications and cancer 21
- Genetics 113
- Genomic variations and chromosomal abnormalities 35
- Co-authors
- James R. Lupski (21 shared papers)Wenli Gu (2 shared papers)Shizhong Zheng (46 shared papers)Matthew E. Hurles (1 shared paper)Zili Zhang (31 shared papers)Jiangjuan Shao (35 shared papers)Jin Li (51 shared papers)Claudia M.B. Carvalho (6 shared papers)
- Journals
- PLoS ONE (14 papers)Human Molecular Genetics (13 papers)Annals of Plastic Surgery (9 papers)The American Journal of Human Genetics (9 papers)Frontiers in Oncology (8 papers)
- Partner nations
- ChinaUnited StatesUnited Kingdom
In The Last Decade
Feng Zhang
706 papers receiving 20.2k citations
Feng Zhang's Hit Papers
Peers
Comparison fields: 5 of 194
- Cancer Research 2.5k
- Genetics 4.4k
- Hepatology 955
- Molecular Biology 8.5k
- Reproductive Medicine 877
Countries citing papers authored by Feng Zhang
This map shows the geographic impact of Feng Zhang'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 Zhang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Feng Zhang more than expected).
Fields of papers citing papers by Feng Zhang
This network shows the impact of papers produced by Feng Zhang. 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 Zhang. The network helps show where Feng Zhang may publish in the future.
Co-authors
The 25 scholars most cited alongside Feng Zhang, 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 736 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Copy Number Variation in Human Health, Disease, and Evolution Hit paper breakdown → | 2009 | 879 |
| 2 | 2008 | 448 | |
| 3 | 2009 | 422 | |
| 4 | Activation of ferritinophagy is required for the RNA-binding protein ELAVL1/HuR to regulate ferroptosis in hepatic stellate cells Hit paper breakdown → | 2018 | 383 |
| 5 | Non-coding genetic variants in human disease: Figure 1. Hit paper breakdown → | 2015 | 383 |
| 6 | 2009 | 360 | |
| 7 | 2007 | 345 | |
| 8 | 2009 | 337 | |
| 9 | 2004 | 319 | |
| 10 | 2019 | 231 | |
| 11 | 2009 | 225 | |
| 12 | 2005 | 215 | |
| 13 | 2017 | 212 | |
| 14 | 2009 | 204 | |
| 15 | 2015 | 190 | |
| 16 | 2018 | 188 | |
| 17 | 2012 | 186 | |
| 18 | 2020 | 159 | |
| 19 | 2013 | 157 | |
| 20 | 2014 | 156 |
About Feng Zhang
Feng Zhang is a scholar working on Molecular Biology, Genetics, Cancer Research, Surgery and Epidemiology, having authored 736 papers that have together received 20.4k indexed citations. Recurring topics across this work include Cancer-related molecular mechanisms research (41 papers), Genomic variations and chromosomal abnormalities (35 papers), Chromosomal and Genetic Variations (29 papers), Liver physiology and pathology (27 papers), RNA Research and Splicing (25 papers), MicroRNA in disease regulation (24 papers), Liver Disease Diagnosis and Treatment (24 papers) and RNA modifications and cancer (21 papers). The work is most often cited by research in Cancer Research (2.5k citations), Genetics (4.4k citations), Hepatology (955 citations), Molecular Biology (8.5k citations) and Reproductive Medicine (877 citations). Feng Zhang has collaborated with scholars based in China, United States and United Kingdom. Frequent co-authors include James R. Lupski, Wenli Gu, Shizhong Zheng, Matthew E. Hurles, Zili Zhang, Jiangjuan Shao, Jin Li, Claudia M.B. Carvalho, Xiaochun Yu and Anping Chen. Their work appears in journals such as PLoS ONE, Human Molecular Genetics, Annals of Plastic Surgery, The American Journal of Human Genetics and Frontiers in Oncology.
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.