Robert J. Morell

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

Life Sciences, Genetics, Molecular Genetics +8

Mutations in the Connexin 26 Gene (<i>GJB2</i>) among Ashkenazi Jews with Nonsyndromic Recessive Deafness

Robert J. Morell, Hung Jeff Kim, Linda J. Hood et al. · New England Journal of Medicine · 1998 · 545 citations

Life Sciences, Genetics, Molecular Genetics +11

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

Life Sciences, Genetics, Molecular Genetics +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

Life Sciences, Genetics, Molecular Genetics +7

Correction of Deafness in <i>shaker-2</i> Mice by an Unconventional Myosin in a BAC Transgene

Frank J. Probst, Robert A. Fridell, Yehoash Raphael et al. · Science · 1998 · 421 citations

Life Sciences, Genetics, Molecular Genetics +17