Genlin Li
Impact in
- Ophthalmology top 5%
- Retinal Diseases and Treatments
- Retinal and Optic Conditions
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- Retinal Development and Disorders
- CRISPR and Genetic Engineering
- RNA regulation and disease
Papers in
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- Retinal Development and Disorders 12
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- Glaucoma and retinal disorders 3
- Retinal Diseases and Treatments 2
- Co-authors
- Liping Yang (10 shared papers)Zhizhong Ma (6 shared papers)Ningning Chen (4 shared papers)Lin Zhao (3 shared papers)Xiaozhen Liu (2 shared papers)Minghua Shan (1 shared paper)Bing Dong (1 shared paper)Likun Wang (1 shared paper)
- Journals
- BMC Ophthalmology (2 papers)PLoS ONE (2 papers)Human Genetics (1 paper)Clinical and Experimental Ophthalmology (1 paper)Genes (1 paper)
- Partner nations
- China
In The Last Decade
Genlin Li
17 papers receiving 301 citations
Peers
Comparison fields: 5 of 37
- Ophthalmology 69
- Molecular Biology 217
- Genetics 56
- Pharmacology 12
- Cellular and Molecular Neuroscience 20
Countries citing papers authored by Genlin Li
This map shows the geographic impact of Genlin Li'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 Genlin Li with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Genlin Li more than expected).
Fields of papers citing papers by Genlin Li
This network shows the impact of papers produced by Genlin Li. 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 Genlin Li. The network helps show where Genlin Li may publish in the future.
Co-authors
The 25 scholars most cited alongside Genlin Li, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 58 | |
| 2 | Novel mutations in the CYP4V2 gene associated with Bietti crystalline corneoretinal dystrophy. | 2005 | 46 |
| 3 | 2020 | 46 | |
| 4 | 2014 | 33 | |
| 5 | 2016 | 24 | |
| 6 | 2015 | 18 | |
| 7 | Novel mutations of CRB1 in Chinese families presenting with retinal dystrophies. | 2014 | 16 |
| 8 | 2013 | 11 | |
| 9 | 2020 | 10 | |
| 10 | 2020 | 9 | |
| 11 | 2022 | 7 | |
| 12 | 2021 | 7 | |
| 13 | 2019 | 6 | |
| 14 | 2020 | 6 | |
| 15 | 2018 | 3 | |
| 16 | 2024 | 2 | |
| 17 | [Progress in studies on effects of extracellular matrix in occurrence of proliferative vitreoretinopathy]. | 2008 | 2 |
| 18 | 2015 | 1 |
About Genlin Li
Genlin Li is a scholar working on Molecular Biology, Ophthalmology, Cardiology and Cardiovascular Medicine, Genetics and Neurology, having authored 18 papers that have together received 305 indexed citations. Recurring topics across this work include Retinal Development and Disorders (12 papers), Glaucoma and retinal disorders (3 papers), Retinal Diseases and Treatments (2 papers), Ocular Disorders and Treatments (2 papers), Cardiac electrophysiology and arrhythmias (1 paper), Moringa oleifera research and applications (1 paper), Genetic and Kidney Cyst Diseases (1 paper) and Botanical Research and Applications (1 paper). The work is most often cited by research in Ophthalmology (69 citations), Molecular Biology (217 citations), Genetics (56 citations), Pharmacology (12 citations) and Cellular and Molecular Neuroscience (20 citations). Genlin Li has collaborated with scholars based in China. Frequent co-authors include Liping Yang, Zhizhong Ma, Ningning Chen, Lin Zhao, Xiaozhen Liu, Minghua Shan, Bing Dong, Likun Wang, Yongsheng Yang and Yang Li. Their work appears in journals such as BMC Ophthalmology, PLoS ONE, Human Genetics, Clinical and Experimental Ophthalmology and Genes.
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.