Barbara Vona

55PUBLICATIONS
292CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Medical devicesGene mapping
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Publications (55)

|May 30, 2026
A comparative survey of functional evidence use in hearing and vision loss genetics.

|Apr 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality.

|Apr 10, 2026
<i>FRMPD4</i>, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.

Daniel Liedtke, Kristen Rak, Katrina M Schrode

|Jan 09, 2026
Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window.

Daniel Owrang, Aboulfazl Rad, Masoome Alerasool

|Sep 10, 2025
Is <i>CABP2</i>-Associated Hearing Loss (DFNB93) a Gene Therapy Target? Preclinical Progress and Patient Registry.

Barbara Vona, Bernd Wollnik, Nicola Strenzke

|Aug 20, 2025
The <i>TECTB-C225Y</i> Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.

Evan B Hale, Barbara Vona, Richard J Goodyear

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Frequent Collaborators

13 joint publications

Reza Maroofian

12 joint publications

Henry Houlden

10 joint publications

Stephanie Efthymiou

7 joint publications

Aboulfazl Rad