Color Blindness Latest Advances

Find the Latest Research About Color Blindness

Last Updated: 06/30/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 4635 publications

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

Journal: medRxiv : the preprint server for health sciences

Published: May 18, 2026

The genetic spectrum of achromatopsia in consanguineous families: insights from Whole exome sequencing across 15 affected individuals.

The genetic spectrum of achromatopsia in consanguineous families: insights from Whole exome sequencing across 15 affected individuals.

Journal: Ophthalmic genetics

Published: May 08, 2026

Epidemiology of Inherited Retinal Diseases in the United States: IRIS® Registry (Intelligent Research in Sight) Analysis.

Epidemiology of Inherited Retinal Diseases in the United States: IRIS® Registry (Intelligent Research in Sight) Analysis.

Journal: Ophthalmic surgery, lasers & imaging retina

Published: March 27, 2026

Crop-OCT: a Fully Integrated Imageomics Pipeline to Identify Regional and Focal Retinopathy in Murine Models.

Crop-OCT: a Fully Integrated Imageomics Pipeline to Identify Regional and Focal Retinopathy in Murine Models.

Journal: bioRxiv : the preprint server for biology

Published: March 23, 2026

Female Color Vision Deficiency is Associated with Increased Prevalence of Amblyopia, Strabismus and Ametropia.

Female Color Vision Deficiency is Associated with Increased Prevalence of Amblyopia, Strabismus and Ametropia.

Journal: Current eye research

Published: February 20, 2026

Effects of Notch Filters in Correcting Color Vision Deficiency: A Quantitative Clinical Trial.

Effects of Notch Filters in Correcting Color Vision Deficiency: A Quantitative Clinical Trial.

Journal: Diagnostics (Basel, Switzerland)

Published: February 18, 2026

Blindness to Color Vision Deficiency.

Blindness to Color Vision Deficiency.

Journal: The American journal of medicine

Published: February 16, 2026

Clinical Validation of a CRX Variant Leading to a Cone-Rod Dystrophy.

Clinical Validation of a CRX Variant Leading to a Cone-Rod Dystrophy.

Journal: Cureus

Published: February 13, 2026

DELETION INVOLVING EXON 18 OF RPGRIP1 IS a MAJOR CAUSE OF ACHROMATOPSIA.

DELETION INVOLVING EXON 18 OF RPGRIP1 IS a MAJOR CAUSE OF ACHROMATOPSIA.

Journal: Retina (Philadelphia, Pa.)

Published: February 10, 2026

Development and validation of a novel and graded colour saturation threshold test, the LSS-8.

Development and validation of a novel and graded colour saturation threshold test, the LSS-8.

Journal: BMC ophthalmology

Published: February 04, 2026

CNGA3-Related Achromatopsia: A 10-Year Follow-Up.

CNGA3-Related Achromatopsia: A 10-Year Follow-Up.

Journal: Journal of vitreoretinal diseases

Published: February 02, 2026

Correcting photoreceptor diseases at their source: CRISPR strategies for cone-rod dystrophy and achromatopsia.

Correcting photoreceptor diseases at their source: CRISPR strategies for cone-rod dystrophy and achromatopsia.

Journal: Experimental eye research

Published: February 01, 2026

Showing 1-12 of 4,635

Last Updated: 06/30/2026