Vanessa Walsh

From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

Tom Walsh, Vanessa Walsh, Sarah Vreugde et al. · Proceedings of the National Academy of Sciences · 2002 · 262 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA

Vanessa Walsh, Dorith Raviv, Amiel A. Dror et al. · Mammalian Genome · 2010 · 46 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

Lance P. Doucette, Nancy D. Merner, Sandra M. Cooke et al. · European Journal of Human Genetics · 2008 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

The Globular Domain of the Proα1(I) N-Propeptide Is Not Required for Secretion, Processing by Procollagen N-Proteinase, or Fibrillogenesis of Type I Collagen in Mice

Paul Börnstein, Vanessa Walsh, Jennifer Tullis et al. · Journal of Biological Chemistry · 2002 · 23 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +14

Analysis of the Role of the SA Gene in Blood Pressure Regulation by Gene Targeting

Vanessa Walsh, Laurence Somody, Aldo Farrell et al. · Hypertension · 2003 · 11 citations · Full text

Life Sciences, Genetics, Physiology +16