Howard P. Stevens

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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

Life Sciences, Genetics, Molecular Genetics +13

RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome

Diana C. Blaydon, Sarah Etheridge, Janet M. Risk et al. · The American Journal of Human Genetics · 2012 · 208 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Characterization of Paraneoplastic Pemphigus Autoantigens by Immunoblot Analysis

Takashi Hashimoto, Masayuki Amagai, Kyoko Watanabe et al. · Journal of Investigative Dermatology · 1995 · 186 citations · Full text

Life Sciences, Immunology, Pathology +11

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

Hermelita Winter, Mike A. Rogers, Lutz Langbein et al. · Nature Genetics · 1997 · 176 citations

Medicine, Dermatology, Genetics +14

Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas

Howard P. Stevens · Archives of Dermatology · 1996 · 145 citations

Medicine, Dermatology, Genetics +9