Robert S. Molday

2350 Health Sciences Mall
Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 121 publications

Clinical variability of ATP11C-related hemolytic anemia: expanding the phenotypic and diagnostic spectrum.

Clinical variability of ATP11C-related hemolytic anemia: expanding the phenotypic and diagnostic spectrum.

Journal: Blood advances

Published: November 19, 2025

Lipid nanoparticle mediated base editing of the Q344X rhodopsin mutation associated with retinitis pigmentosa.

Lipid nanoparticle mediated base editing of the Q344X rhodopsin mutation associated with retinitis pigmentosa.

Journal: Gene therapy

Published: April 28, 2025

Retinal gene therapy for Stargardt disease with dual AAV intein vectors is both safe and effective in large animal models.

Retinal gene therapy for Stargardt disease with dual AAV intein vectors is both safe and effective in large animal models.

Journal: Science advances

Published: March 26, 2025

Quantifying the Progression of Stargardt Disease in Double-Null ABCA4 Carriers Using Fundus Autofluorescence Imaging.

Quantifying the Progression of Stargardt Disease in Double-Null ABCA4 Carriers Using Fundus Autofluorescence Imaging.

Journal: Translational vision science & technology

Published: March 17, 2025

Repairing Atp10D in C57Bl/6J mice restores protein expression but does not mitigate metabolic stress from high fat diet.

Repairing Atp10D in C57Bl/6J mice restores protein expression but does not mitigate metabolic stress from high fat diet.

Journal: Scientific reports

Published: February 10, 2025

Structural and functional properties of the N- and C-terminal segments of the P4-ATPase phospholipid flippase ATP8A2.

Structural and functional properties of the N- and C-terminal segments of the P4-ATPase phospholipid flippase ATP8A2.

Journal: The Journal of biological chemistry

Published: September 19, 2024

Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies.

Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies.

Journal: Investigative ophthalmology & visual science

Published: August 01, 2024

Structural and functional characterization of the nucleotide-binding domains of ABCA4 and their role in Stargardt disease.

Structural and functional characterization of the nucleotide-binding domains of ABCA4 and their role in Stargardt disease.

Journal: The Journal of biological chemistry

Published: June 06, 2024

The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease.

The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease.

Journal: Diagnostics (Basel, Switzerland)

Published: May 31, 2024

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes.

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes.

Journal: medRxiv : the preprint server for health sciences

Published: May 27, 2024

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes.

A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes.

Journal: Neurogenetics

Published: May 03, 2024

Spatiotemporally resolved transcriptomics reveals the cellular dynamics of human retinal development.

Spatiotemporally resolved transcriptomics reveals the cellular dynamics of human retinal development.

Journal: Nature communications

Published: May 02, 2024

Showing 1-12 of 121

Last Updated: 09/26/2026