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The Journal of Investigative Dermatology. Symposium Proceedings|October 28, 2005
The genetic basis of pachyonychia congenitaFrances J D Smith, Haihui Liao, Andrew J Cassidy, et al.Investigative Ophthalmology & Visual Science|May 8, 2014
siRNA silencing of the mutant keratin 12 allele in corneal limbal epithelial cells grown from patients with Meesmann's epithelial corneal dystrophyDavid G Courtney, Sarah D Atkinson, Edwin H A Allen, et al.The Journal of Allergy and Clinical Immunology|July 4, 2006
Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizationsStephan Weidinger, Thomas Illig, Hansjörg Baurecht, et al.Nature Genetics|January 31, 2006
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgarisFrances J D Smith, Alan D Irvine, Ana Terron-Kwiatkowski, et al.The Journal of Investigative Dermatology|April 6, 2007
Filaggrin null alleles are not associated with psoriasisYiwei Zhao, Ana Terron-Kwiatkowski, Haihui Liao, et al.The Journal of Allergy and Clinical Immunology|March 8, 2011
Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergySara J Brown, Yuka Asai, Heather J Cordell, et al.The Journal of Allergy and Clinical Immunology|September 9, 2008
Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema riskStephan Weidinger, Hansjörg Baurecht, Stefan Wagenpfeil, et al.Nature Genetics|April 10, 2007
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczemaAileen Sandilands, Ana Terron-Kwiatkowski, Peter R Hull, et al.Nature Genetics|March 22, 2006
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitisColin N A Palmer, Alan D Irvine, Ana Terron-Kwiatkowski, et al.Pageof 3