Saoud Khuzaei-Al

Headley Way
Oxford, ENG OX39DU, United Kingdom

Last Updated: 09/26/2026

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Found 22 publications

Genotypic and Phenotypic Insights on 11 Novel Variants in the ABCA4 Gene.

Genotypic and Phenotypic Insights on 11 Novel Variants in the ABCA4 Gene.

Journal: Genes

Published: April 24, 2026

OCT and Autofluorescence Phenotypic Features in Autosomal Dominant RHO-Associated Retinitis Pigmentosa Variants.

OCT and Autofluorescence Phenotypic Features in Autosomal Dominant RHO-Associated Retinitis Pigmentosa Variants.

Journal: Vision (Basel, Switzerland)

Published: February 14, 2026

Expanding the Genetic Spectrum in IMPG1 and IMPG2 Retinopathy.

Expanding the Genetic Spectrum in IMPG1 and IMPG2 Retinopathy.

Journal: Genes

Published: October 31, 2025

Stargardt's Connected Research Network Inaugural Meeting: Landscape Review and Horizon Scanning of Stargardt Disease.

Stargardt's Connected Research Network Inaugural Meeting: Landscape Review and Horizon Scanning of Stargardt Disease.

Journal: Translational vision science & technology

Published: September 17, 2025

Genotype-Phenotype Correlations in PRPH2 Retinopathies: A Comprehensive Analysis of 36 Patients from the Oxford Eye Hospital, UK.

Genotype-Phenotype Correlations in PRPH2 Retinopathies: A Comprehensive Analysis of 36 Patients from the Oxford Eye Hospital, UK.

Journal: Genes

Published: July 31, 2025

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

Journal: medRxiv : the preprint server for health sciences

Published: July 09, 2025

Inherited retinal disease pathway in the UK: a patient perspective and the potential of AI.

Inherited retinal disease pathway in the UK: a patient perspective and the potential of AI.

Journal: The British journal of ophthalmology

Published: January 03, 2025

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene.

Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene.

Journal: Nature machine intelligence

Published: September 09, 2024

Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases.

Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases.

Journal: Ophthalmology science

Published: August 07, 2024

Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases.

Retinograd-AI: An Open-Source Automated Fundus Autofluorescence Retinal Image Gradability Assessment for Inherited Retinal Diseases.

Journal: Ophthalmology science

Published: August 07, 2024

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom.

Journal: Ophthalmology science

Published: August 02, 2024

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom.

Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom.

Journal: medRxiv : the preprint server for health sciences

Published: April 08, 2024

Showing 1-12 of 22

Last Updated: 09/26/2026