Susan Halloran Blanton

7PUBLICATIONS
32CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)AudiologyEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsDevelopmental genetics (incl. sex determination)
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Publications (7)

|Jan 10, 2026
GJB2-Related Hearing Loss: Genotype-Phenotype Correlations, Natural History, and Emerging Therapeutic Strategies.

Julia Anne Morris, Tomas Gonzalez, Susan H Blanton

|May 28, 2025
Whole-Genome DNA Methylation Analysis in Age-Related Hearing Loss.

Marie Valerie Roche, Denise Yan, Yan Guo

|Jan 10, 2025
Hypermethylation of PM20D1 Is Associated With Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families.

Nicole D Dueker, Hongyu Zhao, Hannah Gardener

|May 29, 2021
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder.

Minwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi

|Apr 30, 2021
Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy.

Evan M de Joya, Brett M Colbert, Pei-Ciao Tang

|Mar 06, 2021
Spectrum of MYO7A Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous Mutations.

Rosemary Ida Kabahuma, Wolf-Dieter Schubert, Christiaan Labuschagne

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Frequent Collaborators

3 joint publications

Xuezhong Liu

1 joint publications

Christina Kiel

1 joint publications

Tobias Strunz

1 joint publications

Bernhard H F Weber