Associated Papers
A comprehensive approach for identifying filaggrin mutations and copy number variants by long-read sequencing.
Yuda A et al.
Genomics, 2025
Trajectories of egg sensitization in childhood: Two birth cohorts in Asia and Europe.
Nakamura T et al.
Allergy, 2025
Gene variants associated with skin barrier dysfunction in atopic dermatitis: a systematic review and meta-analysis.
Cordeiro PL et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo, 2025
Association between filaggrin gene mutations and the clinical features of molluscum contagiosum: The Yamanashi Adjunct Study of the Japan Environment and Children's Study.
Kojima R et al.
The Journal of Dermatology, 2024
Filaggrin gene variants among Saudi patients with ichthyosis vulgaris.
Alakloby OM et al.
Bmc Medical Genomics, 2023
In silico analysis of the profilaggrin sequence indicates alterations in the stability, degradation route, and intracellular protein fate in filaggrin null mutation carriers.
Paul AA et al.
Frontiers in Molecular Biosciences, 2023
Prevalence of filaggrin loss-of-function variants in Chilean population with and without atopic dermatitis.
Cárdenas GV et al.
International Journal of Dermatology, 2022
Filaggrin-gene mutation has minimal effect on the disease severity in the lesions of atopic dermatitis.
Ota M et al.
The Journal of Dermatology, 2021
Filaggrin Loss-of-Function Mutations Are Risk Factors for Severe Food Allergy in Children with Atopic Dermatitis.
Astolfi A et al.
Journal of Clinical Medicine, 2021
Missense, silent, non-sense and frame-shift mutations in exon 3 of the filaggrin gene in patients with bronchial asthma, atopic dermatitis, allergic rhinitis and mixed atopy.
Salama RH et al.
Nucleosides, Nucleotides & Nucleic Acids, 2021
Filaggrin gene mutations with special reference to atopic dermatitis.
Gupta J et al.
Current Treatment Options in Allergy, 2020
Correlation of age-of-onset of Atopic Dermatitis with Filaggrin loss-of-function variant status.
Smieszek SP et al.
Scientific Reports, 2020
Multifaceted Analyses of Epidermal Serine Protease Activity in Patients with Atopic Dermatitis.
Nomura H et al.
International Journal of Molecular Sciences, 2020
Atopic dermatitis without serum immunoglobulin E elevation or loss-of-function filaggrin gene mutation in a patient with X-linked agammaglobulinemia.
Yamazaki E et al.
The Journal of Dermatology, 2020
Dysbiotic Lesional Microbiome With Filaggrin Missense Variants Associate With Atopic Dermatitis in India.
Nath S et al.
Frontiers in Cellular and Infection Microbiology, 2020
Effect of filaggrin loss-of-function mutations on atopic dermatitis in young age: a longitudinal birth cohort study.
Koseki R et al.
Journal of Human Genetics, 2019
3D-Organotypic Cultures to Unravel Molecular and Cellular Abnormalities in Atopic Dermatitis and Ichthyosis Vulgaris.
Leman G et al.
Cells, 2019
Palmar hyperlinearity in early childhood atopic dermatitis is associated with filaggrin mutation and sensitization to egg.
Fukuie T et al.
Pediatric Dermatology, 2019
Filaggrin gene polymorphisms in Iranian ichthyosis vulgaris and atopic dermatitis patients.
Hassani B et al.
International Journal of Dermatology, 2018
Peptide nucleic acid (PNA) probe-based analysis to detect filaggrin mutations in atopic dermatitis patients.
Hwang J et al.
Experimental Dermatology, 2018
New insights into the phenotypes of atopic dermatitis linked with allergies and asthma in children: An overview.
Amat F et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology, 2018
Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report.
Wang X et al.
Bmc Medical Genetics, 2018
Prevalence of filaggrin gene mutations in patients with atopic dermatitis and ichthyosis vulgaris in Kyushu area of Japan and South Korea.
Teye K et al.
Journal of Dermatological Science, 2017
Filaggrin Mutation in Korean Patients with Atopic Dermatitis.
On HR et al.
Yonsei Medical Journal, 2017
Compound heterozygotes for filaggrin gene mutations do not always show severe atopic dermatitis.
Sekiya A et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2017
The study of filaggrin gene mutations and copy number variation in atopic dermatitis patients from Volga-Ural region of Russia.
Gimalova GF et al.
Gene, 2016
FLG mutations in the East Asian atopic dermatitis patients: genetic and clinical implication.
Li K et al.
Experimental Dermatology, 2016
A rare variant in CYP27A1 and its association with atopic dermatitis with high serum total IgE.
Suzuki H et al.
Allergy, 2016
A novel filaggrin gene mutation 7487delC in an Indonesian (Javanese) patient with atopic dermatitis.
Trisnowati N et al.
International Journal of Dermatology, 2016
Novel FLG null mutations in Korean patients with atopic dermatitis and comparison of the mutational spectra in Asian populations.
Park J et al.
The Journal of Dermatology, 2015
Genetic susceptibility for cow's milk allergy in Dutch children: the start of the allergic march?
Henneman P et al.
Clinical and Translational Allergy, 2015
Filaggrin loss-of-function mutations are not a predisposing factor for atopic dermatitis in an Ishigaki Island under subtropical climate.
Sasaki T et al.
Journal of Dermatological Science, 2014
Evidence That Loss-of-Function Filaggrin Gene Mutations Evolved in Northern Europeans to Favor Intracutaneous Vitamin D3 Production.
Thyssen JP et al.
Evolutionary Biology, 2014
Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations.
Kono M et al.
Allergy, 2014
Atopic dermatitis presenting as generalized poikiloderma with filaggrin gene mutation.
Nakazawa S et al.
The Journal of Dermatology, 2014
Association between P478S polymorphism of the filaggrin gene & atopic dermatitis.
Kim SY et al.
The Indian Journal of Medical Research, 2013
Mutations in the Filaggrin are Predisposing Factor in Korean Children With Atopic Dermatitis.
Yu HS et al.
Allergy, Asthma & Immunology Research, 2013
Ichthyosis vulgaris: the filaggrin mutation disease.
Thyssen JP et al.
The British Journal of Dermatology, 2013
Food sensitization in Japanese infants is associated with a common Filaggrin variant.
Nomura T et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology, 2013
Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis.
Li M et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2013
Filaggrin mutations associated with skin and allergic diseases.
Irvine AD et al.
The New England Journal of Medicine, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.
Chen H et al.
The British Journal of Dermatology, 2011
Combined occurrence of filaggrin mutations and IL-10 or IL-13 polymorphisms predisposes to atopic dermatitis.
Lesiak A et al.
Experimental Dermatology, 2011
Filaggrin polymorphism P478S, IgE level, and atopic phenotypes.
Wang IJ et al.
The British Journal of Dermatology, 2011
Distinct barrier integrity phenotypes in filaggrin-related atopic eczema following sequential tape stripping and lipid profiling.
Angelova-Fischer I et al.
Experimental Dermatology, 2011
Filaggrin gene defects and the risk of developing allergic disorders.
Osawa R et al.
Allergology International : Official Journal of the Japanese Society of Allergology, 2011
Loss-of-function mutations within the filaggrin gene and atopic dermatitis.
Kawasaki H et al.
Current Problems in Dermatology, 2011
Japanese-specific filaggrin gene mutations in Japanese patients suffering from atopic eczema and asthma.
Osawa R et al.
The Journal of Investigative Dermatology, 2010
Chromosome 11q13.5 variant: No association with atopic eczema in the Japanese population.
Nomura Y et al.
Journal of Dermatological Science, 2010