Publications by authors named "Julie M Schultz"

13Publications

Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndrome.

Clin Genet 2020 Oct 21. Epub 2020 Oct 21.

Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1111/cge.13868DOI Listing
October 2020

A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.

J Med Genet 2015 Aug 4;52(8):548-52. Epub 2015 May 4.

School of Biological Sciences, University of the Punjab, Lahore, Pakistan.

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http://dx.doi.org/10.1136/jmedgenet-2015-103023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4529444PMC
August 2015

Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.

Invest Ophthalmol Vis Sci 2014 Nov 25;56(1):107-14. Epub 2014 Nov 25.

National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland, United States.

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http://dx.doi.org/10.1167/iovs.14-15355DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4288141PMC
November 2014

Usher syndrome type 1: genotype-phenotype relationships.

Retina 2005 Dec;25(8 Suppl):S40-S42

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD, USA.

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http://dx.doi.org/10.1097/00006982-200512001-00016DOI Listing
December 2005

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.

Dev Biol 2005 Apr;280(2):295-306

Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA.

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http://dx.doi.org/10.1016/j.ydbio.2005.01.015DOI Listing
April 2005

Modification of human hearing loss by plasma-membrane calcium pump PMCA2.

N Engl J Med 2005 Apr;352(15):1557-64

Section on Human Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Md 20850, USA.

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http://depts.washington.edu/audneuro/Griffith.pdf
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http://www.nejm.org/doi/abs/10.1056/NEJMoa043899
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http://dx.doi.org/10.1056/NEJMoa043899DOI Listing
April 2005

Recent advances in the understanding of syndromic forms of hearing loss.

Ear Hear 2003 Aug;24(4):289-302

Section on Human Genetics, National Institute on Deafness and Other Communication Disorders, NIH, Rockville, MD, USA.

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http://dx.doi.org/10.1097/01.AUD.0000079804.00047.CEDOI Listing
August 2003