Concepedia

Julie M. Schultz

JM

11

Publications

957

Citations

11

H-Index

2001

Active since

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

National Institutes of Health

University of the Punjab

Centre of Excellence in Molecular Biology

National Eye Institute

Julie M. Schultz is an author at National Institute on Deafness and Other Communication Disorders specializing in medicine, genetics, and auditory research.

Top concepts

Publications per year

2001–2020

11

Publications

11

Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh et al. · The American Journal of Human Genetics · 2013 · 238 citations · Full text

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Modification of Human Hearing Loss by Plasma-Membrane Calcium Pump PMCA2

Julie M. Schultz, Yandan Yang, Ariel J. Caride et al. · New England Journal of Medicine · 2005 · 175 citations · Full text

, , +14

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

Ayala Lagziel, Zubair M. Ahmed, Julie M. Schultz et al. · Developmental Biology · 2005 · 152 citations

, , +12

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed et al. · The American Journal of Human Genetics · 2009 · 120 citations · Full text

, , +9

Allelic hierarchy of <i>CDH23</i> 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 · 103 citations

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