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William J. Kimberling

Boys Town
University of Iowa

211

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13113

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Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

2019 Genetics in Medicine
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HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice

2015 PLOS Genetics
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Retinal Histopathology in Eyes from a Patient with Digenic Usher Syndrome Caused by Mutations in USH2A and GPR98.

2014 Investigative Ophthalmology & Visual Science
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Genetic hearing loss associated with eye disorders

2013
- William J. Kimberling
- Claes Möller
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Citations (4)
Alteration of rod and cone function in children with Usher syndrome

2011 European Journal of Ophthalmology
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Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

2011 Investigative Ophthalmology & Visual Science
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Citations (53)
Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome

2011 Ophthalmic Genetics
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Hearing Loss Disorders Associated with Renal Disease

2011 Advances in oto-rhino-laryngology
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Frequency of Usher syndrome in two pediatric populations: implications for genetic screening of deaf and hard of hearing children.

2010 Genetics in Medicine
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Citations (154)
A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.

2010 Laryngoscope
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Citations (16)