Cheryl Y. Evans-Gregory

Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 52 publications

The crossroads of ocular inflammation and inherited retinal degenerations: a report of two cases.

The crossroads of ocular inflammation and inherited retinal degenerations: a report of two cases.

Journal: Digital journal of ophthalmology : DJO

Published: June 30, 2026

Two novel genetic associations with sector retinitis pigmentosa: USH2A and PRPF31.

Two novel genetic associations with sector retinitis pigmentosa: USH2A and PRPF31.

Journal: Ophthalmic genetics

Published: March 05, 2026

Identification of novel pathogenic variants in the PHYH gene and extending the phenotypic range in Refsum disease.

Identification of novel pathogenic variants in the PHYH gene and extending the phenotypic range in Refsum disease.

Journal: Ophthalmic genetics

Published: November 25, 2025

Expanding the Genotypic Landscape of Congenital Stationary Night Blindness in an Ethnically Diverse Canadian Population.

Expanding the Genotypic Landscape of Congenital Stationary Night Blindness in an Ethnically Diverse Canadian Population.

Journal: Human mutation

Published: September 26, 2025

RPE65 Variant p.(E519K) Causes a Novel Dominant Adult-Onset Maculopathy in 83 Affected Individuals.

RPE65 Variant p.(E519K) Causes a Novel Dominant Adult-Onset Maculopathy in 83 Affected Individuals.

Journal: Investigative ophthalmology & visual science

Published: September 23, 2025

Genotypic and phenotypic landscape of novel RPGR variants in patients from Western Canada.

Genotypic and phenotypic landscape of novel RPGR variants in patients from Western Canada.

Journal: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie

Published: July 17, 2025

Quantitative Choroidal Analysis of Molecularly Characterized Retinitis Pigmentosa.

Quantitative Choroidal Analysis of Molecularly Characterized Retinitis Pigmentosa.

Journal: Investigative ophthalmology & visual science

Published: July 03, 2025

Molecular insights into foveal hypoplasia: development, genetics, mechanisms, and models.

Molecular insights into foveal hypoplasia: development, genetics, mechanisms, and models.

Journal: Molecular vision

Published: May 26, 2025

RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals.

RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals.

Journal: Research square

Published: May 19, 2025

The effect of oral belzutifan on retinal hemangioblastomas in von Hippel-Lindau syndrome.

The effect of oral belzutifan on retinal hemangioblastomas in von Hippel-Lindau syndrome.

Journal: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie

Published: May 07, 2025

Ethnic disparities in inherited retinal degenerations.

Ethnic disparities in inherited retinal degenerations.

Journal: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie

Published: December 13, 2024

Mutation of beta-tubulin 4B gene (TUBB4B) causes autosomal dominant retinitis pigmentosa with sensorineural hearing loss in a multigenerational family.

Mutation of beta-tubulin 4B gene (TUBB4B) causes autosomal dominant retinitis pigmentosa with sensorineural hearing loss in a multigenerational family.

Journal: Molecular vision

Published: December 07, 2024

Showing 1-12 of 52

Last Updated: 09/26/2026