Nkecha Brown

Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

Gabriele Richard, Fatima Rouan, Colin E. Willoughby et al. · The American Journal of Human Genetics · 2002 · 369 citations · Full text

Missense Mutations, Genetic Disorder, Pathogenesis +4

trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation

Fatima Rouan, Thomas W. White, Nkecha Brown et al. · Journal of Cell Science · 2001 · 177 citations

Genetic Heterogeneity in Erythrokeratodermia Variabilis: Novel Mutations in the Connexin Gene GJB4 (Cx30.3) and Genotype-Phenotype Correlations

Gabriele Richard, Nkecha Brown, Fatima Rouan et al. · Journal of Investigative Dermatology · 2003 · 129 citations · Full text

Biology, Genotype-phenotype Correlations, Allelic Variant +9

Expanding The Phenotypic Spectrum of Cx26 Disorders: Bart–Pumphrey Syndrome is Caused by a Novel Missense Mutation in GJB2

Gabriele Richard, Nkecha Brown, Akemi Ishida‐Yamamoto et al. · Journal of Investigative Dermatology · 2004 · 114 citations · Full text

Disease Mechanism, Genetic Disorder, Bart–pumphrey Syndrome +8

The spectrum of mutations in erythrokeratodermias - novel and de novo mutations in GJB3

Gabriele Richard, Nkecha Brown, Leslie E. Smith et al. · Human Genetics · 2000 · 90 citations

Somatic Variant, Genetic Disorder, Novo Mutations +7