David P. Kelsell

Identification of the breast cancer susceptibility gene BRCA2

Richard Wooster, Graham R. Bignell, Jonathan Lancaster et al. · Nature · 1995 · 3.6K citations

Breast Oncology, Cancer Genomics, Breast Cancer +3

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

David P. Kelsell, John Dunlop, Howard P. Stevens et al. · Nature · 1997 · 1.5K citations

Mendelian Disorder, Developmental Biology, Genetic Disorder +2

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Frances J.D. Smith, Robin A.J. Eady, I.M. Leigh et al. · Nature Genetics · 1996 · 391 citations

Pathology, Degenerative Disease, General Pathology +4

Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis

David P. Kelsell, Elizabeth E. Norgett, H Unsworth et al. · The American Journal of Human Genetics · 2005 · 351 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +6

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

Susan L. Neuhausen, Sylvie Mazoyer, Lori S. Friedman et al. · PubMed · 1996 · 338 citations

Brca1 Mutations, Brca1 Mutation, Genetics +17