Lejin Wang

1.6k citations
18 papers · 1.2k · h-index 11

Impact in

Papers in

    • Retinal Development and Disorders 4
    • Connexins and lens biology 3
    • Ion channel regulation and function 2
    • Retinal Diseases and Treatments 2

Lejin Wang

17 papers receiving 1.2k citations

Peers

Lejin Wang
Comparison fields: 5 of 73
  • Cardiology and Cardiovascular Medicine 304
  • Cellular and Molecular Neuroscience 271
  • Molecular Biology 739
  • Genetics 193
  • Sensory Systems 31
Replace Ana María Cobo with:
Ana María Cobo Spain
Kenzo Hamano Japan
Iain Fenton United Kingdom
M L Savontaus Finland
M. Spadaro Italy
Majid Fardaei Iran
Yi Chu Australia
Daisuke Furutama Japan
J. L. Haines United States
Lynsie Morris United States
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Citations per field
00.5×3.9×
Ana María Cobo · 1×
Citations per year

Countries citing papers authored by Lejin Wang

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authors

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.

Border = papers with Lejin Wang Line = papers co-authored together Lejin Wang links everyone, so they are left out of the graph.

All Works

18 of 18 papers shown
#Work
1 2005438
2 2003281
3 2008210
4 200177
5 200745
6 200331
7 200827
8
A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family.
201221
9 202317
10 201613
11
A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family.
201113
12 200110
13 20019
14
[Analysis of mutation in KRT12 gene in a Chinese family with Meesmann's corneal dystrophy].
20078
15
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family.
20085
16 20164
17
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
20051
18 20090

About Lejin Wang

Lejin Wang is a scholar working on Molecular Biology, Ophthalmology, Cardiology and Cardiovascular Medicine, Psychiatry and Mental health and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 1.2k indexed citations. Recurring topics across this work include Retinal Development and Disorders (4 papers), Connexins and lens biology (3 papers), Retinal Diseases and Treatments (2 papers), Epilepsy research and treatment (2 papers), Ion channel regulation and function (2 papers), Ophthalmology and Visual Impairment Studies (1 paper), Cardiac electrophysiology and arrhythmias (1 paper) and Galectins and Cancer Biology (1 paper). The work is most often cited by research in Cardiology and Cardiovascular Medicine (304 citations), Cellular and Molecular Neuroscience (271 citations), Molecular Biology (739 citations), Genetics (193 citations) and Sensory Systems (31 citations). Lejin Wang has collaborated with scholars based in China, United States and India. Frequent co-authors include Qing K. Wang, Eric J. Topol, Sarah E. Topol, Qing Wang, Ana Dı́ez-Sampedro, Jianmin Cui, Huanghe Yang, Hans O. Lüders, Wei Du and George B. Richerson. Their work appears in journals such as Ophthalmic Genetics, Cell, Mitochondrion, Science and Nature 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.

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