Julie Muskett

Statistics

Publications

Citations

515

H-Index

Active since

2011

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

National Institutes of Health

National Institutes of Health Clinical Center

Harvard University

Boston Children's Hospital

Julie Muskett is an author at National Institute on Deafness and Other Communication Disorders specializing in genetics, human genetics, and hearing impairment.

Publications per year

2011–2020

Publications

NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy

Hiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima et al. · Proceedings of the National Academy of Sciences · 2017 · 151 citations · Full text

Life Sciences, Audiology, Immunology +16

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes

Julie M. Schultz, Rashid Bhatti, Anne C. Madeo et al. · Journal of Medical Genetics · 2011 · 105 citations

Life Sciences, Genetics, Molecular Genetics +15

Vestibular Dysfunction in Patients with Enlarged Vestibular Aqueduct

Chris Zalewski, Wade W. Chien, Kelly King et al. · Otolaryngology · 2015 · 55 citations · Full text

Medicine, Otolaryngology, Otology +14

A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct

Parna Chattaraj, Tina Munjal, Keiji Honda et al. · Journal of Medical Genetics · 2017 · 47 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4

Jane Rose, Julie Muskett, Kelly King et al. · The Laryngoscope · 2016 · 37 citations · Full text

Medicine, Genetics, Otolaryngology +17

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