Dana J. Orten

CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

Lisa M. Astuto, Julie M. Bork, Michael D. Weston et al. · The American Journal of Human Genetics · 2002 · 230 citations · Full text

Mendelian Disorder, Genetic Disorder, Phenotype Heterogeneity +6

Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome

Bethan E. Hoskins, Carl H. Cramer, Derek Silvius et al. · The American Journal of Human Genetics · 2007 · 200 citations · Full text

Urology, Genetics, Pathology +4

<i>SIX1</i>mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR

Amit Kochhar, Dana J. Orten, Jessica L. Sorensen et al. · Human Mutation · 2008 · 94 citations

USH2A Mutation analysis in 70 Dutch families with Usher syndrome type II

Ronald J. E. Pennings, Heleen te Brinke, Michael D. Weston et al. · Human Mutation · 2004 · 62 citations · Full text

The unconventional myosin-VIIa associates with lysosomes

Lily E. Soni, Carmen M. Warren, Cecilia Bucci et al. · Cell Motility and the Cytoskeleton · 2005 · 48 citations · Full text