Barbara Vona
Robert Koch Str. 40
Goettingen, NI 37075, Germany
Goettingen, NI 37075, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 116 publications
International expert consensus on gene therapy for hereditary hearing loss: based on clinical trials
International expert consensus on gene therapy for hereditary hearing loss: based on clinical trials
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: September 07, 2026
Enhancer Regulation of OSR2 in Mandibular Incisor Agenesis Susceptibility.
Journal: Journal of dental research
Published: July 18, 2026
PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.
Journal: European journal of human genetics : EJHG
Published: April 17, 2026
FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.
Journal: medRxiv : the preprint server for health sciences
Published: April 10, 2026
TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing Loss.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: December 19, 2025
A comparative survey of functional evidence use in hearing and vision loss genetics.
Journal: Communications medicine
Published: December 14, 2025
Neurogenetic Disorders with Hearing Loss: Mechanisms, Classifications, and Emerging Insights.
Journal: Current neurology and neuroscience reports
Published: September 11, 2025
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 09, 2025
The TECTB-C225Y Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.
Journal: medRxiv : the preprint server for health sciences
Published: August 20, 2025
Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window.
Journal: Molecular neurobiology
Published: August 14, 2025
Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics.
Journal: Molecular medicine (Cambridge, Mass.)
Published: July 22, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trials.
Journal: Med (New York, N.Y.)
Published: July 22, 2025
Last Updated: 09/26/2026