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Genetics of glaucoma

Human molecular genetics, 2017-08, Vol.26 (R1), p.R21-R27

2017

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DNAJC30 biallelic mutations extend mitochondrial complex I-deficient phenotypes to include recessive Leber's hereditary optic neuropathy

The Journal of clinical investigation, 2021-03, Vol.131 (6)

Wiggs, Janey L

2021

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CPAMD8, a New Gene for Anterior Segment Dysgenesis and Childhood Glaucoma

Ophthalmology (Rochester, Minn.), 2020-06, Vol.127 (6), p.767-768

Wiggs, Janey L

2020

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Glaucoma Genes and Mechanisms

Progress in molecular biology and translational science, 2015, Vol.134, p.315-342

Wiggs, Janey L

2015

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Interaction of background genetic risk, psychotropic medications, and primary angle closure glaucoma in the UK Biobank

PloS one, 2022-06, Vol.17 (6), p.e0270530

2022

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Juvenile-onset open-angle glaucoma – A clinical and genetic update

Survey of ophthalmology, 2022-07, Vol.67 (4), p.1099-1117

2022

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Clinical implications of recent advances in primary open-angle glaucoma genetics

Eye (London), 2020-01, Vol.34 (1), p.29-39

2020

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The genetic basis for adult onset glaucoma: Recent advances and future directions

Progress in retinal and eye research, 2022-09, Vol.90, p.101066-101066, Article 101066

2022

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Glaucoma: genes, phenotypes, and new directions for therapy

The Journal of clinical investigation, 2010-09, Vol.120 (9), p.3064-3072

2010

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The Genetic Influence on Corticosteroid-Induced Ocular Hypertension: A Field Positioned for Discovery

American journal of ophthalmology, 2019-06, Vol.202, p.1-5

2019

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The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities‐A review

Clinical & experimental ophthalmology, 2022-03, Vol.50 (2), p.143-162

2022

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Progress in Diagnostic Genetic Testing for Inherited Eye Disease

JAMA ophthalmology, 2017-12, Vol.135 (12), p.1385

Wiggs, Janey L

2017

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The cell and molecular biology of complex forms of glaucoma: updates on genetic, environmental, and epigenetic risk factors

Investigative ophthalmology & visual science, 2012-05, Vol.53 (5), p.2467-2469

Wiggs, Janey L

2012

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Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss

Experimental eye research, 2020-01, Vol.190, p.107893-107893, Article 107893

2020

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Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma

Nature genetics, 2018-06, Vol.50 (6), p.778-782

2018

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Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data

Ophthalmology (Rochester, Minn.), 2022-06, Vol.129 (6), p.694-707

2022

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The Association of Physical Activity with Glaucoma and Related Traits in the UK Biobank

Ophthalmology (Rochester, Minn.), 2023-10, Vol.130 (10), p.1024-1036

2023

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Is Estrogen a Therapeutic Target for Glaucoma?

Seminars in ophthalmology, 2016-03, Vol.31 (1-2), p.140-146

2016

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Statin Use in Relation to Intraocular Pressure, Glaucoma, and Ocular Coherence Tomography Parameters in the UK Biobank

Investigative ophthalmology & visual science, 2022-05, Vol.63 (5), p.31

2022

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Genetic Basis of Pigment Dispersion Syndrome and Pigmentary Glaucoma: An Update and Functional Insights

Genes, 2024-01, Vol.15 (2), p.142

2024

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Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma

PLoS genetics, 2014-05, Vol.10 (5), p.e1004372-e1004372

2014

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Intraocular Pressure, Glaucoma, and Dietary Caffeine Consumption: A Gene-Diet Interaction Study from the UK Biobank

Ophthalmology (Rochester, Minn.), 2021-06, Vol.128 (6), p.866-876

2021

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Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature

Circulation (New York, N.Y.), 2022-01, Vol.145 (2), p.134-150

2022

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POU6F2, a risk factor for glaucoma, myopia and dyslexia, labels specific populations of retinal ganglion cells

Scientific reports, 2024-05, Vol.14 (1), p.10096-10096, Article 10096

2024

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Genetics of glaucoma

DNAJC30 biallelic mutations extend mitochondrial complex I-deficient phenotypes to include recessive Leber's hereditary optic neuropathy

CPAMD8, a New Gene for Anterior Segment Dysgenesis and Childhood Glaucoma

Glaucoma Genes and Mechanisms

Interaction of background genetic risk, psychotropic medications, and primary angle closure glaucoma in the UK Biobank

Juvenile-onset open-angle glaucoma – A clinical and genetic update

Clinical implications of recent advances in primary open-angle glaucoma genetics

The genetic basis for adult onset glaucoma: Recent advances and future directions

Glaucoma: genes, phenotypes, and new directions for therapy

The Genetic Influence on Corticosteroid-Induced Ocular Hypertension: A Field Positioned for Discovery

The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities‐A review

Progress in Diagnostic Genetic Testing for Inherited Eye Disease

The cell and molecular biology of complex forms of glaucoma: updates on genetic, environmental, and epigenetic risk factors

Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss

Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma

Photoreceptor Layer Thinning Is an Early Biomarker for Age-Related Macular Degeneration: Epidemiologic and Genetic Evidence from UK Biobank OCT Data

The Association of Physical Activity with Glaucoma and Related Traits in the UK Biobank

Is Estrogen a Therapeutic Target for Glaucoma?

Statin Use in Relation to Intraocular Pressure, Glaucoma, and Ocular Coherence Tomography Parameters in the UK Biobank

Genetic Basis of Pigment Dispersion Syndrome and Pigmentary Glaucoma: An Update and Functional Insights

A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts

Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma

Intraocular Pressure, Glaucoma, and Dietary Caffeine Consumption: A Gene-Diet Interaction Study from the UK Biobank

Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature

POU6F2, a risk factor for glaucoma, myopia and dyslexia, labels specific populations of retinal ganglion cells

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