Robyn V. Jamieson

Sydney, NSW, Australia

Last Updated: 09/26/2026

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Found 76 publications

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings.

ABCA4 Versus PRPH2-Associated Retinopathy: Clinical and Electrophysiological Findings.

Journal: Investigative ophthalmology & visual science

Published: April 14, 2026

NRL-associated autosomal recessive retinopathy: novel variants expanding the phenotype, natural history and a comprehensive literature search.

NRL-associated autosomal recessive retinopathy: novel variants expanding the phenotype, natural history and a comprehensive literature search.

Journal: Ophthalmic genetics

Published: October 16, 2025

Australian research priorities for inherited retinal diseases: a James Lind Alliance priority setting partnership.

Australian research priorities for inherited retinal diseases: a James Lind Alliance priority setting partnership.

Journal: BMJ open

Published: September 30, 2025

The quality-of-life impacts and economic burden of X-linked retinitis pigmentosa caused by variants in RPGR.

The quality-of-life impacts and economic burden of X-linked retinitis pigmentosa caused by variants in RPGR.

Journal: Eye (London, England)

Published: July 15, 2025

Longitudinal study in autosomal recessive PROM1 inherited retinal disease.

Longitudinal study in autosomal recessive PROM1 inherited retinal disease.

Journal: Ophthalmic genetics

Published: June 10, 2025

A Practical Guide to Genetic Eye Conditions for Paediatricians.

A Practical Guide to Genetic Eye Conditions for Paediatricians.

Journal: Journal of paediatrics and child health

Published: April 02, 2025

Phototransduction in the Genomic Era: Mechanisms, Genetics and Therapeutic Advances.

Phototransduction in the Genomic Era: Mechanisms, Genetics and Therapeutic Advances.

Journal: Clinical & experimental ophthalmology

Published: February 24, 2025

Connecting cilium, stress response, and proteostasis abnormalities inform variant and therapy assessment in RPGRIP1 retinal organoids.

Connecting cilium, stress response, and proteostasis abnormalities inform variant and therapy assessment in RPGRIP1 retinal organoids.

Journal: Stem cell reports

Published: February 19, 2025

Understanding the phenotype of genetically associated electronegative ERG retinopathies: comparing the full-field ERG b:a ratio.

Understanding the phenotype of genetically associated electronegative ERG retinopathies: comparing the full-field ERG b:a ratio.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: January 21, 2025

THE FIGHT INHERITED RETINAL BLINDNESS! PROJECT: A New Treatment Outcome and Natural History Registry for Inherited Retinal Disease.

THE FIGHT INHERITED RETINAL BLINDNESS! PROJECT: A New Treatment Outcome and Natural History Registry for Inherited Retinal Disease.

Journal: Retina (Philadelphia, Pa.)

Published: October 17, 2024

Dismantling barriers to research and clinical care for individuals with a vision impairment.

Dismantling barriers to research and clinical care for individuals with a vision impairment.

Journal: The Medical journal of Australia

Published: July 15, 2024

Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measures.

Hardy-Rand-Rittler colour vision testing in cone and cone-rod dystrophies: correlation with structural and functional outcome measures.

Journal: Eye (London, England)

Published: June 17, 2024

Showing 1-12 of 76

Last Updated: 09/26/2026