Virginia W. Norris

Identification of p.A684V missense mutation in the <i>WFS1</i> gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

Nanna Dahl Rendtorff, Marianne Lodahl, Houda Boulahbel et al. · American Journal of Medical Genetics Part A · 2011 · 124 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Does Universal Newborn Hearing Screening Identify All Children with GJB2 (Connexin 26) Deafness? Penetrance of GJB2 Deafness

Virginia W. Norris, Kathleen S. Arnos, Wendy D. Hanks et al. · Ear and Hearing · 2006 · 77 citations

Medicine, Genetics, Pediatrics +17

Patient perspectives on breast cancer treatment plan and summary documents in community oncology care

Victoria Blinder, Virginia W. Norris, N. W. Peacock et al. · Cancer · 2012 · 55 citations · Full text

Medicine, Communication, Oncology +16

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

Nele Hilgert, Matthew J. Huentelman, Ashley Q. Thorburn et al. · European Journal of Human Genetics · 2008 · 53 citations

Life Sciences, Genetics, Molecular Genetics +10

Etiology of unilateral hearing loss in a national hereditary deafness repository

Kelley M. Dodson, Alexandros Georgolios, Noelle Barr et al. · American Journal of Otolaryngology · 2012 · 40 citations

Medicine, Audiology, Otolaryngology +12