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Prevalence and risk factors of dry eye disease in a British female cohort

British journal of ophthalmology, 2014-12, Vol.98 (12), p.1712-1717

2014

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Focusing in on the complex genetics of myopia

PLoS genetics, 2013-04, Vol.9 (4), p.e1003442-e1003442

2013

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Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated loci

Nature communications, 2018-01, Vol.9 (1), p.8-13, Article 8

2018

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A Metabolome-Wide Study of Dry Eye Disease Reveals Serum Androgens as Biomarkers

Ophthalmology (Rochester, Minn.), 2017-04, Vol.124 (4), p.505-511

2017

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Temporal trends in frequency, type and severity of myopia and associations with key environmental risk factors in the UK: Findings from the UK Biobank Study

PloS one, 2022-01, Vol.17 (1), p.e0260993

2022

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A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects

Nature communications, 2021-06, Vol.12 (1), p.3595-3595, Article 3595

2021

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Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure

Nature communications, 2018-05, Vol.9 (1), p.1684-7, Article 1684

2018

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Replication of SNP associations with keratoconus in a Czech cohort

PloS one, 2017-02, Vol.12 (2), p.e0172365-e0172365

2017

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Frequency and Distribution of Refractive Error in Adult Life: Methodology and Findings of the UK Biobank Study

PloS one, 2015-10, Vol.10 (10), p.e0139780-e0139780

2015

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Education interacts with genetic variants near GJD2, RBFOX1, LAMA2, KCNQ5 and LRRC4C to confer susceptibility to myopia

PLoS genetics, 2022-11, Vol.18 (11), p.e1010478

2022

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Genome-wide association studies of refractive error and myopia, lessons learned, and implications for the future

Investigative ophthalmology & visual science, 2014-05, Vol.55 (5), p.3344-3351

2014

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APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans

PLoS genetics, 2015-08, Vol.11 (8), p.e1005432-e1005432

2015

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The genomic loci of specific human tRNA genes exhibit ageing-related DNA hypermethylation

Nature communications, 2021-05, Vol.12 (1), p.2655-2655, Article 2655

2021

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Digital quantification of human eye color highlights genetic association of three new loci

PLoS genetics, 2010-05, Vol.6 (5), p.e1000934-e1000934

2010

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The heritability of dry eye disease in a female twin cohort

Investigative ophthalmology & visual science, 2014-11, Vol.55 (11), p.7278-7283

2014

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Effect modification by sex of genetic associations of vitamin C related metabolites in the Canadian Longitudinal study on aging

Frontiers in genetics, 2024-07, Vol.15, p.1411931

2024

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GWAS on retinal vasculometry phenotypes

PLoS genetics, 2023-02, Vol.19 (2), p.e1010583-e1010583

2023

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Genome-Wide Association Analysis of Over 170,000 Individuals from the UK Biobank Identifies Seven Loci Associated with Dietary Approaches to Stop Hypertension (DASH) Diet

Nutrients, 2022-10, Vol.14 (20), p.4431

2022

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Relationship between dry eye symptoms and pain sensitivity

JAMA ophthalmology, 2013-10, Vol.131 (10), p.1304

2013

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Genetic and Dietary Factors Influencing the Progression of Nuclear Cataract

Ophthalmology (Rochester, Minn.), 2016-06, Vol.123 (6), p.1237-1244

2016

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Ascorbic acid metabolites are involved in intraocular pressure control in the general population

Redox biology, 2019-01, Vol.20, p.349-353

2019

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Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations

Ophthalmology (Rochester, Minn.), 2017-04, Vol.124 (4), p.547-553

2017

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Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

PLoS genetics, 2010-05, Vol.6 (5), p.e1000947-e1000947

2010

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Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels

Metabolites, 2022-01, Vol.12 (1), p.61

2022

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Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study

Npj genomic medicine, 2024-06, Vol.9 (1), p.36-6, Article 36

2024

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Prevalence and risk factors of dry eye disease in a British female cohort

Focusing in on the complex genetics of myopia

Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated loci

A Metabolome-Wide Study of Dry Eye Disease Reveals Serum Androgens as Biomarkers

Temporal trends in frequency, type and severity of myopia and associations with key environmental risk factors in the UK: Findings from the UK Biobank Study

A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects

Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure

Replication of SNP associations with keratoconus in a Czech cohort

Frequency and Distribution of Refractive Error in Adult Life: Methodology and Findings of the UK Biobank Study

Education interacts with genetic variants near GJD2, RBFOX1, LAMA2, KCNQ5 and LRRC4C to confer susceptibility to myopia

Genome-wide association studies of refractive error and myopia, lessons learned, and implications for the future

APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans

The genomic loci of specific human tRNA genes exhibit ageing-related DNA hypermethylation

Digital quantification of human eye color highlights genetic association of three new loci

The heritability of dry eye disease in a female twin cohort

Effect modification by sex of genetic associations of vitamin C related metabolites in the Canadian Longitudinal study on aging

GWAS on retinal vasculometry phenotypes

Genome-Wide Association Analysis of Over 170,000 Individuals from the UK Biobank Identifies Seven Loci Associated with Dietary Approaches to Stop Hypertension (DASH) Diet

Relationship between dry eye symptoms and pain sensitivity

Genetic and Dietary Factors Influencing the Progression of Nuclear Cataract

Ascorbic acid metabolites are involved in intraocular pressure control in the general population

Evaluation of the Myocilin Mutation Gln368Stop Demonstrates Reduced Penetrance for Glaucoma in European Populations

Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels

Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study

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