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Last Updated: 01/07/2026

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Found 1537 publications

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 08, 2025

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

Epidemiological and genetic insights of Usher syndrome in Turkish population: A cross-sectional preliminary study from University of Health Sciences, Turkey.

Epidemiological and genetic insights of Usher syndrome in Turkish population: A cross-sectional preliminary study from University of Health Sciences, Turkey.

Journal: The Journal of international medical research
Published: November 07, 2025

Compound heterozygous variants in PCDH15 non-coding regions in an Usher Syndrome Type 1F patient: minigene assay reveals pathogenicity of c.3123-1G>C.

Compound heterozygous variants in PCDH15 non-coding regions in an Usher Syndrome Type 1F patient: minigene assay reveals pathogenicity of c.3123-1G>C.

Journal: Ophthalmic genetics
Published: October 24, 2025

A sound vision: MYO7A gene therapy reaches the inner ear.

A sound vision: MYO7A gene therapy reaches the inner ear.

Journal: The Journal of physiology
Published: September 22, 2025

Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal Degeneration.

Exon Skipping Therapy Restores Ciliary Function in USH2A-Related Retinal Degeneration.

Journal: Investigative ophthalmology & visual science
Published: September 19, 2025

Cloud-Based Personalized sEMG Classification Using Lightweight CNNs for Long-Term Haptic Communication in Deaf-Blind Individuals.

Cloud-Based Personalized sEMG Classification Using Lightweight CNNs for Long-Term Haptic Communication in Deaf-Blind Individuals.

Journal: Bioengineering (Basel, Switzerland)
Published: September 15, 2025

Computational study of deleterious missense SNPs in the USH1G gene implicated in Usher syndrome.

Computational study of deleterious missense SNPs in the USH1G gene implicated in Usher syndrome.

Journal: Journal of biomolecular structure & dynamics
Published: September 02, 2025

Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Author Correction: Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.

Journal: Nature genetics
Published: August 26, 2025

Structural Abnormalities of the Brain Detected by 7 Tesla MRI in Patients with Usher Syndrome.

Structural Abnormalities of the Brain Detected by 7 Tesla MRI in Patients with Usher Syndrome.

Journal: Journal of clinical medicine
Published: August 14, 2025

Progression of Dark-Adapted Visual Fields Over 3 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) Study.

Progression of Dark-Adapted Visual Fields Over 3 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) Study.

Journal: Investigative ophthalmology & visual science
Published: August 12, 2025

Ciliopathy: Usher Syndrome.

Ciliopathy: Usher Syndrome.

Journal: Advances in experimental medicine and biology
Published: July 30, 2025
Showing 1-12 of 1,537

Last Updated: 01/07/2026