Emily Wilcox

Statistics

Publications

Citations

168

H-Index

Active since

1994

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

Centre of Excellence in Molecular Biology

National Institutes of Health

Emily Wilcox is an author at National Institute on Deafness and Other Communication Disorders specializing in life sciences, genetic disorders, and human genetics.

Publications per year

1994–2002

Publications

A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Anil K. Lalwani, J. Rodney Brister, Fex J et al. · PubMed · 1994 · 60 citations

Medicine, Audiology, Hearing Science +4

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

Kikuro Fukushima, A. Ramesh, C. R. Srikumari Srisailapathy et al. · Genome Research · 1995 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

<i>DFNB3</i>, Spectrum of <i>MYO15A</i> Recessive Mutant Alleles and an Emerging Genotype-Phenotype Correlation

Thomas B. Friedman, John T. Hinnant, Manju Ghosh et al. · Advances in oto-rhino-laryngology · 2002 · 19 citations

Life Sciences, Genetics, Molecular Genetics +14

Clinical Presentation of DFNB12 and Usher Syndrome Type 1D

Julie M. Bork, Robert J. Morell, Shaheen Khan et al. · Advances in oto-rhino-laryngology · 2002 · 19 citations

Life Sciences, Pathology, Human Genetics +4

A locus for Waardenburg syndrome type II maps to chromosome 1p13.3-2.1

Anil K. Lalwani, Theresa B. San Agustin, Emily Wilcox · The American Journal of Human Genetics · 1994 · 14 citations

Life Sciences, Genetics, Molecular Genetics +11

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