Anna Sarosiak
Warsaw, MZ, Poland
Last Updated: 09/26/2026
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Found 8 publications
Zebrafish in-vivo study reveals deleterious activity of human TBC1D24 genetic variants linked with autosomal dominant hearing loss.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: May 23, 2024
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss.
Journal: Human genetics
Published: December 14, 2021
TBC1D24 emerges as an important contributor to progressive postlingual dominant hearing loss.
Journal: Scientific reports
Published: March 15, 2021
Complex Phenotypic Presentation of Syndromic Hearing Loss Deciphered as Three Separate Clinical Entities: How Genetic Testing Guides Final Diagnosis.
Journal: Audiology & neuro-otology
Published: June 17, 2020
High expression of Matrix Gla Protein in Schnyder corneal dystrophy patients points to an active role of vitamin K in corneal health.
Journal: Acta ophthalmologica
Published: March 21, 2020
First confirmatory study on PTPRQ as an autosomal dominant non-syndromic hearing loss gene.
Journal: Journal of translational medicine
Published: July 16, 2019
Clinical diversity in patients with Schnyder corneal dystrophy-a novel and known UBIAD1 pathogenic variants.
Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
Published: December 06, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026