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Fang Lu

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.
2008 · Ying Lin, Ting Liu, et al. · PubMed Central · 38
A novel mutation in BBS7 gene causes Bardet-Biedl syndrome in a Chinese family.
2008 · Zhenglin Yang, Yang Yang, et al. · PubMed Central · 17
Malattia Leventinese/doyne Honeycomb Retinal Dystrophy in a Chinese Family With Mutation of the Efemp1 Gene
2014 · Ting Zhang, Xuelu Xie, et al. · Retina · 16
[Mutation analysis of the PAX6 gene in a family with congenital aniridia and cataract].
2009 · Ying Lin, Jing Li, et al. · PubMed · 4
ABCB6 Mutations Cause Ocular Coloboma
2012 · Lejin Wang, Fei He, et al. · The American Journal of Human Genetics · 3
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[Two Novel Mutations at the CD36 Gene Splicing Sites and Their Molecular Basis for the CD36 Deficiency].
2020 · Li-Lan Li, Jie-Run Chen, et al. · PubMed · 2
[A novel CD36 mutation T538C (Trp180Arg) results in CD36 deficiency and establishment of a genotyping method for the novel mutation based on sequence-specific primer PCR].
2016 · Lilan Li, Baoren He, et al. · PubMed · 2
[Genetic and phenotypic analysis of a patient with phosphogylcerate dehydrogenase deficiency].
2021 · Zhiyan Tao, Fang Lu · PubMed · 1
[Disease gene screening of known loci in a Chinese family with autosomal dominant retinitis pigmentosa].
2009 · Wei Liu, Fang Lu, et al. · PubMed · 1
Active Iris in Retinopathy of Prematurity and Regression Following Intravitreal Ranibizumab Injection
2018 · Fang Lu · Ophthalmic surgery, lasers & imaging retina
[Molecular genetic analysis and clinical phenotype of a pedigree with familial dominant drusen].
2015 · Ting Zhang, Xuelu Xie, et al. · PubMed
Works count: 12
Citation count: 84
H-index: 4
I10-index: 3
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