Lejin Wang
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- Photoreceptor and optogenetics research 2
- Molecular Biology top 10%
- Retinal Development and Disorders 5
- Connexins and lens biology 3
- Ion channel regulation and function 2
- Ophthalmology top 5%
- Retinal Diseases and Treatments 4
- Glaucoma and retinal disorders 2
- Sensory Systems top 10%
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- Epilepsy research and treatment 2
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- Vestibular and auditory disorders 2
- Co-authors
- Qing K. WangQing WangSarah E. TopolEric J. TopolChun‐Po Steve FanWei DuJingyi ShiJianmin Cui
- Partner nations
- ChinaUnited States
In The Last Decade
Lejin Wang
17 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 78
- Cellular and Molecular Neuroscience 315
- Cardiology and Cardiovascular Medicine 354
- Molecular Biology 808
- Ophthalmology 84
- Sensory Systems 40
Countries citing papers authored by Lejin Wang
This map shows the geographic impact of Lejin Wang'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 Lejin Wang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lejin Wang more than expected).
Fields of papers citing papers by Lejin Wang
This network shows the impact of papers produced by Lejin Wang. 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 Lejin Wang. The network helps show where Lejin Wang may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Lejin Wang, 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 | 2023 | 13 | |
| 2 | 2016 | 4 | |
| 3 | 2016 | 13 | |
| 4 | A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family. | 2012 | 21 |
| 5 | A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family. | 2011 | 13 |
| 6 | 2009 | 0 | |
| 7 | 2008 | 27 | |
| 8 | 2008 | 210 | |
| 9 | Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family. | 2008 | 5 |
| 10 | 2007 | 45 | |
| 11 | [Analysis of mutation in KRT12 gene in a Chinese family with Meesmann's corneal dystrophy]. | 2007 | 8 |
| 12 | 2005 | 435 | |
| 13 | Du, W., Bautista, J. F., Yang, H., Diez-Sampedro, A., You, S. A, Wang, L. et al. Calcium-sensitive potassiumchannelopathy in human epilepsy and paroxysmal movement disorder. Nat. Genet. 37, 733-738 | 2005 | 1 |
| 14 | 2003 | 283 | |
| 15 | 2003 | 31 | |
| 16 | 2001 | 78 | |
| 17 | 2001 | 10 | |
| 18 | 2001 | 9 |
About Lejin Wang
Lejin Wang is a scholar working on Ophthalmology, Neurology and Sensory Systems, having authored 18 papers that have together received 1.2k indexed citations. Recurring topics across this work include Retinal Development and Disorders (5 papers), Retinal Diseases and Treatments (4 papers), Connexins and lens biology (3 papers), Photoreceptor and optogenetics research (2 papers), Glaucoma and retinal disorders (2 papers), Ion channel regulation and function (2 papers), Epilepsy research and treatment (2 papers) and Vestibular and auditory disorders (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (315 citations), Cardiology and Cardiovascular Medicine (354 citations) and Molecular Biology (808 citations). Lejin Wang has collaborated with scholars based in China and United States. Frequent co-authors include Qing K. Wang, Qing Wang, Sarah E. Topol, Eric J. Topol, Chun‐Po Steve Fan, Wei Du, Jingyi Shi, Jianmin Cui, Prakash Kotagal and Jocelyn F. Bautista. Their work appears in journals such as Ophthalmic Genetics, Nature Genetics, Science, Mitochondrion and Cell.
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.