Clinical Presentation of Atopic Dermatitis by Filaggrin Gene Mutation Status during the First 7 Years of Life in a Prospective Cohort Study

Filaggrin Genotype in Ichthyosis Vulgaris Predicts Abnormalities in Epidermal Structure and Function

(2011) Robert Gruber et al.   AMERICAN JOURNAL OF PATHOLOGY

Filaggrin loss-of-function mutation R501X and 2282del4 carrier status is associated with fissured skin on the hands: results from a cross-sectional population study

(2011) J.P. Thyssen et al.   BRITISH JOURNAL OF DERMATOLOGY

Filaggrin Null-mutations May be Associated with a Distinct Subtype of Atopic Hand Eczema

(2010) JP Thyssen et al.   ACTA DERMATO-VENEREOLOGICA

Phenotypes of atopic dermatitis

(2010) Silvia Pugliarello et al.   JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT

Raman profiles of the stratum corneum define 3 filaggrin genotype–determined atopic dermatitis endophenotypes

(2010) Gráinne M. O'Regan et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Filaggrin gene variants and atopic diseases in early childhood assessed longitudinally from birth

(2010) Klaus Bønnelykke et al.   PEDIATRIC ALLERGY AND IMMUNOLOGY

Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children

(2009) S.J. Brown et al.   BRITISH JOURNAL OF DERMATOLOGY

Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly

(2008) Ann Sergeant et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY