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Susan G. Stanton

University of Western Ontario

4

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

2017 Human Genetics
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X-linked hearing loss: two gene mutation examples provide generalizable implications for clinical care.

2014 American Journal of Audiology
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Identification of a novel in-frame deletion in KCNQ4 (DFNA2A) and evidence of multiple phenocopies of unknown origin in a family with ADSNHL

2013 European Journal of Human Genetics
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On Variability and Genes: Inter-individual Differences in Auditory Brain Function

2012 Frontiers in Human Neuroscience
- Peter Sörös
- Susan G. Stanton
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