Cathryn S. Mellersh
Centre for Preventive Medicine
Animal Health Trust
Lanwades Park
Newmarket
UK
Name/email consistency: high
- Mutation in HSF4 is associated with hereditary cataract in the Australian Shepherd. Mellersh, C.S., McLaughlin, B., Ahonen, S., Pettitt, L., Lohi, H., Barnett, K.C. Vet. Ophthalmol (2009)
- Give a dog a genome. Mellersh, C. Vet. J. (2008)
- Mutation in HSF4 associated with early but not late-onset hereditary cataract in the Boston Terrier. Mellersh, C.S., Graves, K.T., McLaughlin, B., Ennis, R.B., Pettitt, L., Vaudin, M., Barnett, K.C. J. Hered. (2007)
- Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis. Mellersh, C.S., Boursnell, M.E., Pettitt, L., Ryder, E.J., Holmes, N.G., Grafham, D., Forman, O.P., Sampson, J., Barnett, K.C., Blanton, S., Binns, M.M., Vaudin, M. Genomics (2006)
- Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts. Mellersh, C.S., Pettitt, L., Forman, O.P., Vaudin, M., Barnett, K.C. Vet. Ophthalmol (2006)