Nancy Aychoua

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 13 publications

Lens Opacity in ABCA4-Associated Stargardt Disease Patients in the ProgStar Study.

Lens Opacity in ABCA4-Associated Stargardt Disease Patients in the ProgStar Study.

Journal: Investigative ophthalmology & visual science

Published: July 22, 2026

MERTK-associated retinal dystrophy: clinical course and imaging.

MERTK-associated retinal dystrophy: clinical course and imaging.

Journal: Ophthalmic genetics

Published: May 04, 2026

CDH23-associated Usher syndrome: genotype-phenotype correlations.

CDH23-associated Usher syndrome: genotype-phenotype correlations.

Journal: Ophthalmic genetics

Published: February 19, 2026

Clinical Findings and Molecular Genetics of USH1C-Associated Usher Syndrome.

Clinical Findings and Molecular Genetics of USH1C-Associated Usher Syndrome.

Journal: JAMA ophthalmology

Published: November 26, 2025

Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophy.

Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophy.

Journal: Molecular therapy. Nucleic acids

Published: August 15, 2025

Assessing Agreement between Blue-Light and Green-Light Autofluorescence of Macular Hyperautofluorescent Rings in Inherited Retinal Diseases.

Assessing Agreement between Blue-Light and Green-Light Autofluorescence of Macular Hyperautofluorescent Rings in Inherited Retinal Diseases.

Journal: Ophthalmology science

Published: May 28, 2025

Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome.

Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome.

Journal: Investigative ophthalmology & visual science

Published: April 21, 2025

Multimorbidity Through the Lens of the Eye: Pathogenic Variants for Multiple Systemic Disorders Found in an Autosomal Dominant Congenital Cataract Cohort.

Multimorbidity Through the Lens of the Eye: Pathogenic Variants for Multiple Systemic Disorders Found in an Autosomal Dominant Congenital Cataract Cohort.

Journal: Genes

Published: April 17, 2025

CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History.

CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History.

Journal: Investigative ophthalmology & visual science

Published: July 17, 2024

Cone-driven strong flash electroretinograms in healthy adults: Prevalence of negative waveforms.

Cone-driven strong flash electroretinograms in healthy adults: Prevalence of negative waveforms.

Journal: Documenta ophthalmologica. Advances in ophthalmology

Published: December 05, 2022

Prospective study of pediatric patients presenting with idiopathic infantile nystagmus-Management and molecular diagnostics.

Prospective study of pediatric patients presenting with idiopathic infantile nystagmus-Management and molecular diagnostics.

Journal: Frontiers in genetics

Published: June 24, 2022

Variability of retinopathy consequent upon novel mutations in LAMA1.

Variability of retinopathy consequent upon novel mutations in LAMA1.

Journal: Ophthalmic genetics

Published: May 26, 2022

Showing 1-12 of 13

Last Updated: 09/26/2026