Associated Papers
Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry.
Qu HQ et al.
Journal of Molecular Medicine (berlin, Germany), 2025
39730912 (PubMed )
Supplement: 109_2024_2510_MOESM2_ESM.xlsx › Sheet1
Using a Machine Learning Approach to Identify Low-Frequency and Rare FLG Alleles Associated with Remission of Atopic Dermatitis.
Berna R et al.
Jid Innovations : Skin Science From Molecules to Population Health, 2021
Association of FLG single nucleotide variations with clinical phenotypes of atopic dermatitis.
Kim M et al.
Plos One, 2017
29281699 (PubMed )
Supplement: pone.0190077.s002.xlsx › Sheet1
An Analysis of the Filaggrin Gene Polymorphism in Korean Atopic Dermatitis Patients.
Park KY et al.
Journal of Korean Medical Science, 2016
27366014 (PubMed )
Supplement: jkms-31-1136-s001.pdf
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
Ichthyosis vulgaris: the filaggrin mutation disease.
Thyssen JP et al.
The British Journal of Dermatology, 2013
Genetic Polymorphism of FLG in Korean Ichthyosis Vulgaris Patients.
Kim EJ et al.
Annals of Dermatology, 2011
Filaggrin polymorphism P478S, IgE level, and atopic phenotypes.
Wang IJ et al.
The British Journal of Dermatology, 2011
Prevalence of filaggrin gene polymorphisms (exon-3) in patients with atopic dermatitis in a multiracial Brazilian population.
Laczynski CMM et al.
Anais Brasileiros De Dermatologia, 0
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