Cone Dystrophy Latest Advances
Find the Latest Research About Cone Dystrophy
Last Updated: 09/19/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 329 publications
Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.
Journal: Investigative ophthalmology & visual science
Published: August 10, 2026
Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.
Journal: Research square
Published: July 17, 2026
Therapeutic restoration of synaptic architecture, retinal and visual function, and prevention of retinal degeneration in a mouse model of retinal dystrophy.
Journal: bioRxiv : the preprint server for biology
Published: July 10, 2026
Novel mutation in a case of TTLL5-associated cone dystrophy with a characteristic 'solar flare' sign.
Journal: Ophthalmic genetics
Published: June 18, 2026
Progressive cone dystrophy in PDE6C-associated achromatopsia with a likely pathogenic variant and a VUS.
Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: May 24, 2026
The Value of Multimodal Approach in Identification of Cone Dystrophy with Supernormal Rod Response.
Journal: Klinische Monatsblatter fur Augenheilkunde
Published: March 17, 2026
Rod-Cone Dystrophy Related WDR34 Is Essential for Ciliary Integrity and Survival of Mammalian Photoreceptor Cells.
Journal: Investigative ophthalmology & visual science
Published: March 10, 2026
Double Annulus in SPATA7 Rod Cone Dystrophy.
Journal: Ophthalmology. Retina
Published: February 03, 2026
Phenotypic Manifestations in Female Carriers of RPGR ORF15 Variants Causing X-Linked Cone Dystrophy.
Phenotypic Manifestations in Female Carriers of RPGR ORF15 Variants Causing X-Linked Cone Dystrophy.
Journal: JAMA ophthalmology
Published: January 02, 2026
Progressive Cone Dystrophy and Cone-Rod Dystrophy.
Journal: Advances in experimental medicine and biology
Published: July 30, 2025
Loss-of-function variants in SAXO6, encoding a microtubule inner protein of photoreceptor cilia, cause a late-onset retinal dystrophy.
Journal: American journal of human genetics
Published: April 01, 2025
Last Updated: 09/19/2026