Lejin Wang
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Explore the profile of Lejin Wang including associated specialties, affiliations and a list of published articles.
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24
Citations
919
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Recent Articles
1.
Meng Q, Wang L, Zhao M, Wu X, Guo L
BMC Ophthalmol
. 2023 Jun;
23(1):290.
PMID: 37365512
Purpose: To compare the degree of myopia between the dominant and non-dominant eyes in teenagers with intermittent exotropia (IXT) in China. Methods: A total of 199 IXT patients with myopia...
2.
Zhu L, Li S, He S, Tong Q, Wang L, Li X, et al.
Eye Vis (Lond)
. 2020 Dec;
7(1):55.
PMID: 33292635
Purpose: To investigate the role of N6-methyladenosine (mA) RNA modification in the pathogenesis of Graves' ophthalmopathy (GO). Methods: Surgically excised extraocular muscles from 7 patients with GO and 5 subjects...
3.
Li Y, Jiang L, Wang L, Wang C, Liu C, Guo A, et al.
Front Cell Dev Biol
. 2020 Nov;
8:591781.
PMID: 33251218
Congenital nystagmus (CN) is an ocular movement disorder manifested as involuntary conjugated binocular oscillation and usually occurs in early infancy. The pathological mechanism underlying CN is still poorly understood. We...
4.
Yao J, Qiang W, Wei H, Xu Y, Wang B, Zheng Y, et al.
ACS Omega
. 2020 Sep;
5(36):23129-23139.
PMID: 32954163
Implantable pressure sensors enable more accurate disease diagnosis and real-time monitoring. Their widescale usage is dependent on a reliable encapsulation to protect them from corrosion of body fluids, yet not...
5.
Xia Y, Cao L, Peng X, Wang L
Strabismus
. 2020 Jul;
28(3):136-141.
PMID: 32649271
The purpose of this study is to explore the relationships between excessive near work and divergence insufficiency esotropia in young adults. A prospective study described a series of young patients...
6.
Jiang L, Li Y, Yang K, Wang Y, Wang J, Cui X, et al.
Invest Ophthalmol Vis Sci
. 2020 May;
61(5):41.
PMID: 32446246
Purpose: To identify the pathogenic gene of infantile nystagmus syndrome (INS) in three Chinese families and explore the potential pathogenic mechanism of FERM domain-containing 7 (FRMD7) mutations. Methods: Genetic testing...
7.
Miao Z, Li L, Meng X, Guo L, Cao D, Jia Y, et al.
Biomed Res Int
. 2019 Feb;
2019:5185780.
PMID: 30805365
Purpose: To investigate the safety and therapeutic effect of a modified posterior scleral reinforcement (PSR) in treating high myopia. Methods: A total of 85 highly myopic eyes in 47 children...
8.
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridia
Liu X, Wu Y, Miao Z, Zhang H, Gong B, Zhu X, et al.
Ophthalmic Genet
. 2018 Jun;
39(4):428-436.
PMID: 29902091
Purpose: Congenital aniridia, a severe bilateral panocular visual disorder, is an autosomal dominantly inherited eye anomaly. Mutations in the paired box 6 gene (PAX6) have been shown to be responsible...
9.
Liu J, Jia Y, Wang L, Bu J
Indian J Ophthalmol
. 2016 Dec;
64(11):813-817.
PMID: 27958203
Background: Congenital nystagmus (CN) is characterized by conjugated, spontaneous, and involuntary ocular oscillations. It is an inherited disease and the most common inheritance pattern is X-linked CN. In this study,...
10.
Bu J, He S, Wang L, Li J, Liu J, Zhang X
Indian J Ophthalmol
. 2016 Jul;
64(5):364-8.
PMID: 27380975
Background: Congenital cataract is a rare disorder characterized by crystallin denaturation, which becomes a major cause of childhood blindness. Although more than fifty pathogenic genes for congenital cataract have been...