Usher Syndrome Latest Advances

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.

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.

Journal: The Journal of international medical research

Published: November 07, 2025

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: October 30, 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.

Journal: Ophthalmic genetics

Published: October 24, 2025

Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health.

Journal: Cellular and molecular life sciences : CMLS

Published: October 08, 2025

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.

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.

Journal: Bioengineering (Basel, Switzerland)

Published: September 15, 2025

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.

Journal: Nature genetics

Published: August 26, 2025

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

Journal: Journal of clinical medicine

Published: August 14, 2025

Usher Syndrome Latest Advances

Find the Latest Research About Usher Syndrome

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.

Clinical Findings and Molecular Genetics of USH1C-Associated Usher Syndrome.

Clinical Findings and Molecular Genetics of USH1C-Associated Usher Syndrome.

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.

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

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.

Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health.

Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health.

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

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

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

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

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.

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.

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.

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.