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Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

Human molecular genetics, 2013-11, Vol.22 (22), p.4579-4590

2013

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Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration: Same or different disease?

Progress in retinal and eye research, 2010, Vol.29 (1), p.19-29

2010

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Ion transport function of SLC4A11 in corneal endothelium

Investigative ophthalmology & visual science, 2013-06, Vol.54 (6), p.4330-4340

2013

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Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese

Ophthalmology (Rochester, Minn.), 2011-02, Vol.118 (2), p.368-375

2011

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Association of peripheral anterior synechiae with anterior segment parameters in eyes with primary angle closure glaucoma

Scientific reports, 2021-07, Vol.11 (1), p.13906-13906, Article 13906

2021

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Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma

Nature genetics, 2014-10, Vol.46 (10), p.1115-1119

2014

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Trinucleotide repeat expansion length as a predictor of the clinical progression of Fuchs' Endothelial Corneal Dystrophy

PloS one, 2019-01, Vol.14 (1), p.e0210996-e0210996

2019

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Comparison of machine learning approaches for structure–function modeling in glaucoma

Annals of the New York Academy of Sciences, 2022-09, Vol.1515 (1), p.237-248

2022

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Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci for Estimating Angle Closure Disease Severity

Ophthalmology (Rochester, Minn.), 2021-03, Vol.128 (3), p.403-409

2021

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Clinical and Genetic Aspects of the TGFBI -associated Corneal Dystrophies

The ocular surface, 2014-10, Vol.12 (4), p.234-251

2014

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SLC4A11 is an EIPA-sensitive Na(+) permeable pHi regulator

American Journal of Physiology: Cell Physiology, 2013-10, Vol.305 (7), p.C716-C727

2013

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Relationship of Smoking and Cardiovascular Risk Factors with Polypoidal Choroidal Vasculopathy and Age-related Macular Degeneration in Chinese Persons

Ophthalmology (Rochester, Minn.), 2011-05, Vol.118 (5), p.846-852

2011

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Missense mutations in the sodium borate cotransporter SLC4A11 cause late‐onset Fuchs corneal dystrophya

Human mutation, 2010-11, Vol.31 (11), p.1261-1268

2010

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Primary angle closure glaucoma genomic associations and disease mechanism

Current opinion in ophthalmology, 2020-03, Vol.31 (2), p.101

2020

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Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant

Investigative ophthalmology & visual science, 2014-10, Vol.55 (11), p.7073-7078

2014

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The Heritability and Sibling Risk of Angle Closure in Asians

Ophthalmology (Rochester, Minn.), 2011-03, Vol.118 (3), p.480-485

2011

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Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus

Human molecular genetics, 2015-11, Vol.24 (22), p.6552-6563

2015

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SPARC deficiency results in improved surgical survival in a novel mouse model of glaucoma filtration surgery

PloS one, 2010-02, Vol.5 (2), p.e9415-e9415

2010

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Aggregate Effects of Intraocular Pressure and Cup-to-Disc Ratio Genetic Variants on Glaucoma in a Multiethnic Asian Population

Ophthalmology (Rochester, Minn.), 2015-06, Vol.122 (6), p.1149-1157

2015

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Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma

American journal of ophthalmology, 2019-12, Vol.208, p.160-165

2019

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Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

Human molecular genetics, 2013-12, Vol.22 (25), p.5288-5294

2013

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In-utero epigenetic factors are associated with early-onset myopia in young children

PloS one, 2019-05, Vol.14 (5), p.e0214791-e0214791

2019

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Collagen-related genes influence the glaucoma risk factor, central corneal thickness

Human molecular genetics, 2011-02, Vol.20 (4), p.649-658

2011

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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

Nature genetics, 2006-07, Vol.38 (7), p.755-757

2006

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Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration: Same or different disease?

Ion transport function of SLC4A11 in corneal endothelium

Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese

Association of peripheral anterior synechiae with anterior segment parameters in eyes with primary angle closure glaucoma

Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma

Trinucleotide repeat expansion length as a predictor of the clinical progression of Fuchs' Endothelial Corneal Dystrophy

Comparison of machine learning approaches for structure–function modeling in glaucoma

Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci for Estimating Angle Closure Disease Severity

Genome-wide association study of Parkinson's disease in East Asians

Clinical and Genetic Aspects of the TGFBI -associated Corneal Dystrophies

SLC4A11 is an EIPA-sensitive Na(+) permeable pHi regulator

Relationship of Smoking and Cardiovascular Risk Factors with Polypoidal Choroidal Vasculopathy and Age-related Macular Degeneration in Chinese Persons

Missense mutations in the sodium borate cotransporter SLC4A11 cause late‐onset Fuchs corneal dystrophya

Primary angle closure glaucoma genomic associations and disease mechanism

Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant

The Heritability and Sibling Risk of Angle Closure in Asians

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus

SPARC deficiency results in improved surgical survival in a novel mouse model of glaucoma filtration surgery

Aggregate Effects of Intraocular Pressure and Cup-to-Disc Ratio Genetic Variants on Glaucoma in a Multiethnic Asian Population

Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

In-utero epigenetic factors are associated with early-onset myopia in young children

Collagen-related genes influence the glaucoma risk factor, central corneal thickness

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

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