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Phonon triggered rhombohedral lattice distortion in vanadium at high pressure

Scientific reports, 2016-08, Vol.6 (1), p.31887-31887, Article 31887

2016

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Elasticity of hexagonal-closed-packed cobalt at high pressure and temperature: a quasiharmonic case

Physical review letters, 2008-02, Vol.100 (8), p.085501-085501, Article 085501

2008

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Gas transport across the low-permeability containment zone of an underground nuclear explosion

Scientific reports, 2020-01, Vol.10 (1), p.1437-1437, Article 1437

2020

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Delayed signatures of underground nuclear explosions

Scientific reports, 2016-03, Vol.6 (1), p.23032-23032, Article 23032

2016

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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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Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

Nature genetics, 2014-10, Vol.46 (10), p.1120-1125

2014

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Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey

Scientific reports, 2024-03, Vol.14 (1), p.5403-5403, Article 5403

2024

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Establishing risk of vision loss in Leber hereditary optic neuropathy

American journal of human genetics, 2021-11, Vol.108 (11), p.2159-2170

2021

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Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

American journal of human genetics, 2023-01, Vol.110 (1), p.170-176

2023

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X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development

American journal of human genetics, 2012-02, Vol.90 (2), p.247-259

2012

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ProxTom Lymphatic Vessel Reporter Mice Reveal Prox1 Expression in the Adrenal Medulla, Megakaryocytes, and Platelets

The American journal of pathology, 2012-04, Vol.180 (4), p.1715-1725

2012

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Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

Human molecular genetics, 2010-07, Vol.19 (13), p.2716-2724

2010

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Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations

American journal of human genetics, 2005-06, Vol.76 (6), p.1008-1022

2005

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Effect of Display Resolution on Time to Diagnosis with Virtual Pathology Slides in a Systematic Search Task

Journal of digital imaging, 2015-02, Vol.28 (1), p.68-76

2015

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

Twin research and human genetics, 2009-10, Vol.12 (5), p.441-454

2009

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Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey

BMJ open, 2021-06, Vol.11 (6), p.e048361-e048361

2021

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Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in Victoria, Australia

Clinical & experimental ophthalmology, 2013-09, Vol.41 (7), p.653-661

2013

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Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect

Investigative ophthalmology & visual science, 2018-08, Vol.59 (10), p.4054-4064

2018

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Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa

Investigative ophthalmology & visual science, 2011-09, Vol.52 (10), p.7432-7440

2011

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Associations of Birth Weight With Ocular Biometry, Refraction, and Glaucomatous Endophenotypes: The Australian Twins Eye Study

American journal of ophthalmology, 2010-12, Vol.150 (6), p.909-916.e3

2010

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Genetic Dissection of Myopia : Evidence for Linkage of Ocular Axial Length to Chromosome 5q

Ophthalmology (Rochester, Minn.), 2008-06, Vol.115 (6), p.1053-1057

2008

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Ophthalmic phenotypes and the representativeness of twin data for the general population

Investigative ophthalmology & visual science, 2011-07, Vol.52 (8), p.5565-5572

2011

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Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins

Clinical and experimental optometry, 2015-03, Vol.98 (2), p.172-176

2015

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Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study

Hypertension (Dallas, Tex. 1979), 2009-10, Vol.54 (4), p.788-795

2009

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Phonon triggered rhombohedral lattice distortion in vanadium at high pressure

Elasticity of hexagonal-closed-packed cobalt at high pressure and temperature: a quasiharmonic case

Gas transport across the low-permeability containment zone of an underground nuclear explosion

Delayed signatures of underground nuclear explosions

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

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey

Establishing risk of vision loss in Leber hereditary optic neuropathy

Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development

ProxTom Lymphatic Vessel Reporter Mice Reveal Prox1 Expression in the Adrenal Medulla, Megakaryocytes, and Platelets

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations

Effect of Display Resolution on Time to Diagnosis with Virtual Pathology Slides in a Systematic Search Task

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

Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey

Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in Victoria, Australia

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect

Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa

Associations of Birth Weight With Ocular Biometry, Refraction, and Glaucomatous Endophenotypes: The Australian Twins Eye Study

Genetic Dissection of Myopia : Evidence for Linkage of Ocular Axial Length to Chromosome 5q

Ophthalmic phenotypes and the representativeness of twin data for the general population

Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins

Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study

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