Jonathan B. Ruddle

Cellular Inclusion Bodies of Mutant Huntingtin Exon 1 Obscure Small Fibrillar Aggregate Species

The interactions of genes, age, and environment in glaucoma pathogenesis

Investigation of associations between Piezo1 mechanoreceptor gain-of-function variants and glaucoma-related phenotypes in humans and mice

Myopia

Adverse events and complications associated with intravitreal injection of anti-VEGF agents: a review of literature

The molecular basis of human retinal and vitreoretinal diseases

Myopia genetics: a review of current research and emerging trends

Retinitis Pigmentosa: Genes and Disease Mechanisms

Clinical safety of ranibizumab in age-related macular degeneration

TFOS DEWS II Epidemiology Report

Functional analysis of human mutations in homeodomain transcription factor PITX3

Retinal Vascular Caliber Measurements: Clinical Significance, Current Knowledge and Future Perspectives

Anterior segment uses of bevacizumab

The Association between Time Spent Outdoors and Myopia in Children and Adolescents

The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age‐Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults

The GEnes in Myopia (GEM) study in understanding the aetiology of refractive errors

Distribution of conjunctival ultraviolet autoflourescence in a population-based study: the Norfolk Island Eye Study

Hypoxia-Inducible Factor-Dependent Expression of Angiopoietin-Like 4 by Conjunctival Epithelial Cells Promotes the Angiogenic Phenotype of Pterygia.

Genetics of glaucoma

The Heritability of Ocular Traits

The Heritability of Dry Eye Disease in a Female Twin Cohort

A fine-grained social network recommender system

The p Factor

Insights into keratoconus from a genetic perspective

A Survey of Recommendation Systems: Recommendation Models, Techniques, and Application Fields

Genes and mutations causing retinitis pigmentosa

Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk Individuals

Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma

Higher Prevalence of Myocilin Mutations in Advanced Glaucoma in Comparison with Less Advanced Disease in an Australasian Disease Registry

Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness

RPGR ORF15 genotype and clinical variability of retinal degeneration in an Australian population

Genetic Dissection of Myopia

Vascular Changes After Intra-bleb Injection of Bevacizumab

Genetic Isolates in Ophthalmic Diseases

Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins

The PITX3 gene in posterior polar congenital cataract in Australia.

Effect of Birth Parameters on Retinal Vascular Caliber

Ophthalmic Phenotypes and the Representativeness of Twin Data for the General Population