Gail E. Maconachie

Sheffield, ENG S102TS, United Kingdom

Last Updated: 09/26/2026

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Found 35 publications

Artificial intelligence-driven virtual reality eye-tracking for the objective measurement of MRD1 and MRD2 in blepharoptosis.

Artificial intelligence-driven virtual reality eye-tracking for the objective measurement of MRD1 and MRD2 in blepharoptosis.

Journal: Scientific reports

Published: December 29, 2025

Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia.

Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia.

Journal: Investigative ophthalmology & visual science

Published: September 09, 2025

Identifying biomarkers for papilledema and pseudopapilledema.

Identifying biomarkers for papilledema and pseudopapilledema.

Journal: Scientific reports

Published: February 22, 2025

Foveal Hypoplasia Grading with Optical Coherence Tomography: Agreement and Challenges Across Experience Levels.

Foveal Hypoplasia Grading with Optical Coherence Tomography: Agreement and Challenges Across Experience Levels.

Journal: Diagnostics (Basel, Switzerland)

Published: January 27, 2025

Extended optical treatment versus early patching with an intensive patching regimen in children with amblyopia in Europe (EuPatch): a multicentre, randomised controlled trial.

Extended optical treatment versus early patching with an intensive patching regimen in children with amblyopia in Europe (EuPatch): a multicentre, randomised controlled trial.

Journal: Lancet (London, England)

Published: October 13, 2023

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability.

Journal: Annals of neurology

Published: May 30, 2023

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability.

Journal: Research square

Published: March 30, 2023

Retinal Development in Infants and Young Children With Albinism: Evidence for Plasticity in Early Childhood.

Retinal Development in Infants and Young Children With Albinism: Evidence for Plasticity in Early Childhood.

Journal: American journal of ophthalmology

Published: May 26, 2022

Albinism Associated With Torsional Nystagmus Masquerading as Spasmus Nutans.

Albinism Associated With Torsional Nystagmus Masquerading as Spasmus Nutans.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: December 20, 2021

Ocular Manifestations of PNPT1-Related Neuropathy.

Ocular Manifestations of PNPT1-Related Neuropathy.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: August 20, 2021

Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.

Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study.

Journal: Ophthalmology

Published: August 10, 2021

Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles.

Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles.

Journal: International journal of molecular sciences

Published: February 06, 2021

Showing 1-12 of 35

Last Updated: 09/26/2026