Concepedia

Edward R. Wilcox

ER

Statistics

Publications

39

Citations

5.6K

H-Index

32

Active since

1984

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

National Institutes of Health

Centre of Excellence in Molecular Biology

University of the Punjab

University of California, San Francisco

Edward R. Wilcox is an author at National Institute on Deafness and Other Communication Disorders specializing in life sciences, genetics, and medical genetics.

Publications per year

1984–2023

39

Publications

39

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 557 citations · Full text

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Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

Kiyoto Kurima, Linda Peters, Yandan Yang et al. · Nature Genetics · 2002 · 476 citations · Full text

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Association of Unconventional Myosin <i>MYO15</i> Mutations with Human Nonsyndromic Deafness <i>DFNB3</i>

Aihui Wang, Yong Liang, Robert A. Fridell et al. · Science · 1998 · 441 citations

, , +15

Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

Edward R. Wilcox, Quianna Burton, Sadaf Naz et al. · Cell · 2001 · 440 citations · Full text

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Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

Zubair M. Ahmed, Saima Riazuddin, Steven L. Bernstein et al. · The American Journal of Human Genetics · 2001 · 414 citations · Full text

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