Lejin Wang

1.6k total citations
18 papers, 1.2k citations indexed

About

Lejin Wang is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lejin Wang has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Ophthalmology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lejin Wang's work include Retinal Development and Disorders (5 papers), Retinal Diseases and Treatments (4 papers) and Connexins and lens biology (3 papers). Lejin Wang is often cited by papers focused on Retinal Development and Disorders (5 papers), Retinal Diseases and Treatments (4 papers) and Connexins and lens biology (3 papers). Lejin Wang collaborates with scholars based in China and United States. Lejin Wang's co-authors include Qing K. Wang, Qing Wang, Sarah E. Topol, Eric J. Topol, Chun‐Po Steve Fan, Prakash Kotagal, Huanghe Yang, Jingyi Shi, Hans O. Lüders and Jianmin Cui and has published in prestigious journals such as Science, Cell and Nature Genetics.

In The Last Decade

Lejin Wang

17 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Lejin Wang China 11 808 354 315 221 88 18 1.2k
J. L. Haines United States 18 590 0.7× 63 0.2× 121 0.4× 295 1.3× 71 0.8× 45 1.3k
Kazutoshi Nishiyama Japan 14 820 1.0× 103 0.3× 351 1.1× 91 0.4× 24 0.3× 20 1.1k
Ana María Cobo Spain 14 703 0.9× 193 0.5× 393 1.2× 252 1.1× 93 1.1× 28 979
Velina Guergueltcheva Bulgaria 23 899 1.1× 114 0.3× 561 1.8× 176 0.8× 61 0.7× 52 1.6k
Arifumi Kosakai Japan 17 422 0.5× 73 0.2× 329 1.0× 65 0.3× 93 1.1× 25 1.0k
Nobuyoshi Fukuhara Japan 17 693 0.9× 126 0.4× 205 0.7× 63 0.3× 25 0.3× 35 1.1k
Simon Hammans United Kingdom 25 1.4k 1.7× 59 0.2× 425 1.3× 142 0.6× 43 0.5× 45 1.7k
Daisuke Furutama Japan 18 743 0.9× 133 0.4× 520 1.7× 47 0.2× 14 0.2× 36 1.2k
Fumi Urano Japan 12 653 0.8× 43 0.1× 417 1.3× 204 0.9× 20 0.2× 21 1.1k
M L Savontaus Finland 15 1.2k 1.5× 41 0.1× 218 0.7× 158 0.7× 32 0.4× 18 1.4k

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-authorship network of co-authors of Lejin Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Lejin Wang. A scholar is included among the top collaborators of Lejin Wang based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lejin Wang. Lejin Wang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Meng, Qingyu, Shuting Liang, Xi Wu, et al.. (2023). Choroidal thickness, myopia, and myopia control interventions in children: a Meta-analysis and systemic review. International Journal of Ophthalmology. 16(3). 453–464. 13 indexed citations
2.
Liu, Jing, et al.. (2016). A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese family. Indian Journal of Ophthalmology. 64(11). 813–813. 4 indexed citations
3.
Wang, Lejin, et al.. (2016). A novel splice donor site mutation in EPHA2 caused congenital cataract in a Chinese family. Indian Journal of Ophthalmology. 64(5). 364–368. 13 indexed citations
4.
Dong, Jiamei, Wei Du, Yuan Li, et al.. (2012). A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese family.. PubMed. 18. 81–6. 21 indexed citations
5.
Du, Wei, et al.. (2011). A novel frame-shift mutation in FRMD7 causes X-linked idiopathic congenital nystagmus in a Chinese family.. PubMed. 17. 2765–8. 13 indexed citations
6.
7.
Zhang, Shirong, Mugen Liu, Pengyun Wang, et al.. (2008). Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family.. PubMed. 14. 1893–7. 5 indexed citations
8.
Zhang, Shirong, Lejin Wang, Yansheng Hao, et al.. (2008). T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber’s hereditary optic neuropathy in a Chinese family. Mitochondrion. 8(3). 205–210. 27 indexed citations
9.
Zhang, Xianqin, Shenghan Chen, Shin Yoo, et al.. (2008). Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death. Cell. 135(6). 1017–1027. 210 indexed citations
10.
Wang, Lejin, Xin Tian, Qingsheng Zhang, & Liang Liu. (2007). [Analysis of mutation in KRT12 gene in a Chinese family with Meesmann's corneal dystrophy].. PubMed. 43(10). 885–9. 8 indexed citations
11.
Liu, Jing Yu, Xiang Ren, Xiufeng Yang, et al.. (2007). Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation. Journal of Human Genetics. 52(6). 565–570. 45 indexed citations
12.
Du, Wei, Jocelyn F. Bautista, Huanghe Yang, et al.. (2005). Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder. Nature Genetics. 37(7). 733–738. 435 indexed citations
13.
Du, Wei, Jocelyn F. Bautista, Huanghe Yang, et al.. (2005). 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. 1 indexed citations
14.
Wang, Lejin, Chun‐Po Steve Fan, Sarah E. Topol, Eric J. Topol, & Qing Wang. (2003). Mutation of MEF2A in an Inherited Disorder with Features of Coronary Artery Disease. Science. 302(5650). 1578–1581. 283 indexed citations
15.
Wang, Lejin, et al.. (2003). Novel deletion in the pre‐mRNA splicing gene PRPF31 causes autosomal dominant retinitis pigmentosa in a large Chinese family. American Journal of Medical Genetics Part A. 121A(3). 235–239. 31 indexed citations
16.
Wang, Qing, Qiuyun Chen, Kanxing Zhao, et al.. (2001). Update on the molecular genetics of retinitis pigmentosa. Ophthalmic Genetics. 22(3). 133–154. 78 indexed citations
17.
Zhao, Kanxing, et al.. (2001). Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa. Ophthalmic Genetics. 22(3). 155–162. 10 indexed citations
18.
Zhao, Kanxing, et al.. (2001). Novel deletion of the RPGR gene in a Chinese family with X-linked retinitis pigmentosa. Ophthalmic Genetics. 22(3). 187–194. 9 indexed citations

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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