Jessica Squires

A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect

S. Stanton, T. Young, D. O’Rielly, 2016, Human Genetics.

Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss

B. Fernandez, T. Young, D. O’Rielly, 2019, BMC Medical Genetics.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

Daniel Vincent, F. Glaser, S. Stanton, 2022, Human Genetics.

Autosomal Dominant Non-Syndromic Hearing Loss Maps to DFNA33 (13q34) and Co-Segregates with Splice Site Variants in ATP11A, A Phospholipid Flippase Gene

Daniel Vincent, S. Stanton, O. Barel, 2021 .

Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses

Daniel Vincent, S. Stanton, T. Young, 2023, European Journal of Human Genetics.