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Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry

Ophthalmology (Rochester, Minn.), 2021-11, Vol.128 (11), p.1549-1560

2021

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Delayed melatonin circadian timing, lower melatonin output, and sleep disruptions in myopic, or short-sighted, children

Sleep (New York, N.Y.), 2024-01, Vol.47 (1), p.1

2024

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Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma

Ophthalmology (Rochester, Minn.), 2020-06, Vol.127 (6), p.758-766

2020

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Anterior segment biometry with the Pentacam: Comprehensive assessment of repeatability of automated measurements

Journal of cataract and refractive surgery, 2008, Vol.34 (1), p.103-113

2008

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The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literature

Molecular vision, 2022-09, Vol.28, p.257-268

2022

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Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract

European journal of human genetics : EJHG, 2017-06, Vol.25 (6), p.711-718

2017

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Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia

PloS one, 2013-08, Vol.8 (8), p.e72518-e72518

2013

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A comparison between the amblyopic eye and normal fellow eye ocular architecture in children with hyperopic anisometropic amblyopia

Journal of AAPOS, 2012-10, Vol.16 (5), p.428-430

2012

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Pathogenic genetic variants identified in Australian families with paediatric cataract

BMJ open ophthalmology, 2022-08, Vol.7 (1), p.e001064

2022

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High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia

G3 : genes - genomes - genetics, 2017-10, Vol.7 (10), p.3257-3268

2017

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Repeatability of corneal first-surface wavefront aberrations measured with Pentacam corneal topography

Journal of cataract and refractive surgery, 2008-05, Vol.34 (5), p.727-734

2008

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Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality

American journal of perinatology reports, 2017-04, Vol.7 (2), p.e138-e143

2017

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Adequacy of published screening criteria for retinopathy of prematurity

Clinical & experimental ophthalmology, 2016-03, Vol.44 (2), p.121-127

2016

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Creating a digital retinoscope by combining a mobile smartphone camera and a retinoscope

Journal of AAPOS, 2014-08, Vol.18 (4), p.387-388

2014

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Ocular malformation in a newborn secondary to maternal hypovitaminosis A

Journal of AAPOS, 2010-06, Vol.14 (3), p.274-276

2010

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Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome

Journal of AAPOS, 2009-08, Vol.13 (4), p.374-378

2009

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Multisegment coloboma in a case of Marfan syndrome: another possible effect of increased TGFβ signaling

Journal of AAPOS, 2014-02, Vol.18 (1), p.90-92

2014

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Real‐world outcomes of low‐dose atropine therapy on myopia progression in an Australian cohort during the COVID ‐19 pandemic

Clinical & experimental ophthalmology, 2023-11, Vol.51 (8), p.775-780

2023

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Case report: North Carolina macular dystrophy misdiagnosed as congenital ocular toxoplasmosis

Molecular vision, 2019, Vol.25, p.731-733

2019

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Complications of Limbal Stay Sutures in Strabismus Surgery

Strabismus, 2021-07, Vol.29 (3), p.139-143

2021

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Fundus fluorescein angiography imaging of retinopathy of prematurity in infants: A review

Survey of ophthalmology, 2023-09, Vol.68 (5), p.849-860

2023

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Macular Hypoplasia in Congenital Disorder of Glycosylation Type Ia

Case reports in ophthalmology, 2012-04, Vol.3 (1), p.142-144

2012

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An international comparison of retinopathy of prematurity grading performance within the Benefits of Oxygen Saturation Targeting II trials

Eye (London), 2018-01, Vol.32 (1), p.74-80

2018

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Objective monitoring of papilloedema using confocal scanning laser ophthalmoscopy

Clinical & experimental ophthalmology, 2007-12, Vol.35 (9), p.863-865

2007

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Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants

Cornea, 2022-08, Vol.41 (8), p.1009

2022

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Childhood and Early Onset Glaucoma Classification and Genetic Profile in a Large Australasian Disease Registry

Delayed melatonin circadian timing, lower melatonin output, and sleep disruptions in myopic, or short-sighted, children

Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma

Anterior segment biometry with the Pentacam: Comprehensive assessment of repeatability of automated measurements

The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literature

Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract

Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia

A comparison between the amblyopic eye and normal fellow eye ocular architecture in children with hyperopic anisometropic amblyopia

Pathogenic genetic variants identified in Australian families with paediatric cataract

High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia

Repeatability of corneal first-surface wavefront aberrations measured with Pentacam corneal topography

Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality

Adequacy of published screening criteria for retinopathy of prematurity

Creating a digital retinoscope by combining a mobile smartphone camera and a retinoscope

Ocular malformation in a newborn secondary to maternal hypovitaminosis A

Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome

Multisegment coloboma in a case of Marfan syndrome: another possible effect of increased TGFβ signaling

Real‐world outcomes of low‐dose atropine therapy on myopia progression in an Australian cohort during the COVID ‐19 pandemic

Case report: North Carolina macular dystrophy misdiagnosed as congenital ocular toxoplasmosis

Complications of Limbal Stay Sutures in Strabismus Surgery

Fundus fluorescein angiography imaging of retinopathy of prematurity in infants: A review

Macular Hypoplasia in Congenital Disorder of Glycosylation Type Ia

An international comparison of retinopathy of prematurity grading performance within the Benefits of Oxygen Saturation Targeting II trials

Objective monitoring of papilloedema using confocal scanning laser ophthalmoscopy

Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants

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