Eyal Banin

Jerusalem, JM 91120, Israel

Last Updated: 09/26/2026

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Found 146 publications

Smarcc1 drives optic stalk patterning and optic nerve head astrocyte differentiation.

Smarcc1 drives optic stalk patterning and optic nerve head astrocyte differentiation.

Journal: Development (Cambridge, England)

Published: April 28, 2026

The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population.

The Genetic Landscape of Inherited Retinal Diseases in the Israeli Population.

Journal: Investigative ophthalmology & visual science

Published: April 13, 2026

Temporal vision adaptation and restoration in achromatopsia.

Temporal vision adaptation and restoration in achromatopsia.

Journal: iScience

Published: December 03, 2025

PRCD-associated retinitis pigmentosa in dogs and humans.

PRCD-associated retinitis pigmentosa in dogs and humans.

Journal: Experimental eye research

Published: December 01, 2025

Measuring Rod- and Cone-Photoreceptor-Specific Vision in Inherited Retinal Diseases Using a Commercial Perimeter.

Measuring Rod- and Cone-Photoreceptor-Specific Vision in Inherited Retinal Diseases Using a Commercial Perimeter.

Journal: Investigative ophthalmology & visual science

Published: October 17, 2025

Addressing Challenges in Developing Treatments for Inherited Retinal Diseases: Recommendations From the Third Monaciano Symposium.

Addressing Challenges in Developing Treatments for Inherited Retinal Diseases: Recommendations From the Third Monaciano Symposium.

Journal: Translational vision science & technology

Published: August 27, 2025

Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration.

Founder Homozygous Nonsense CREB3 Variant and Variable-Onset Retinal Degeneration.

Journal: JAMA ophthalmology

Published: July 17, 2025

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics

Published: June 02, 2025

Bilateral Idiopathic Multifocal Pigment Epithelial Detachments: A Case Series and Review of Literature.

Bilateral Idiopathic Multifocal Pigment Epithelial Detachments: A Case Series and Review of Literature.

Journal: Retina (Philadelphia, Pa.)

Published: May 13, 2025

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity.

Journal: NPJ genomic medicine

Published: April 22, 2025

Visual Tract Integrity Before and After Gene Therapy in Congenital Achromatopsia.

Visual Tract Integrity Before and After Gene Therapy in Congenital Achromatopsia.

Journal: Translational vision science & technology

Published: February 05, 2025

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Journal: medRxiv : the preprint server for health sciences

Published: January 20, 2025

Showing 1-12 of 146

Last Updated: 09/26/2026