Colin S. Munro
Publications by Year
Research Areas
Skin and Cellular Biology Research, Genetic and rare skin diseases., Hair Growth and Disorders, Plant Reproductive Biology, Wnt/β-catenin signaling in development and cancer
Most-Cited Works
- → Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis(2006)2,920 cited
- → Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris(2006)1,026 cited
- → Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease(1999)729 cited
- → Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema(2007)661 cited
- → Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis(2009)212 cited
- → Clinical and Pathological Features of Pachyonychia Congenita(2005)207 cited
- → An immunohistochemical analysis of human aortic fatty streaks(1987)178 cited
- → trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation(2001)177 cited
- → Missense Mutations in Keratin 17 Cause Either Pachyonychia Congenita Type 2 or a Phenotype Resembling Steatocystoma Multiplex(1997)167 cited
- → Epidermal mosaicism producing localised acne: somatic mutation in FGFR2(1998)156 cited