Clinical presentation of atopic dermatitis by filaggrin gene mutation status during the first 7 years of life in a prospective cohort study (Q34481975)

2 August 2017

title

Clinical presentation of atopic dermatitis by filaggrin gene mutation status during the first 7 years of life in a prospective cohort study (English)

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2 August 2017

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4

Torkil Menné

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2 August 2017

Morten Arendt Rasmussen

object named as

Morten Arendt Rasmussen

Jacob Pontoppidan Thyssen

2

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object named as

Jacob P Thyssen

3

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Hans Bisgaard

object named as

Hans Bisgaard

5

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author name string

Charlotte Giwercman Carson

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2 August 2017

language of work or name

English

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publication date

15 November 2012

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2 August 2017

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2 August 2017

volume

7

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2 August 2017

issue

11

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2 August 2017

page(s)

e48678

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Creative Commons Attribution 4.0 International

2 August 2017

copyright license

start time

15 November 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity.

6 July 2018

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

6 July 2018

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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.

6 July 2018

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Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

6 July 2018

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Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

6 July 2018

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Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

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Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march.

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

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Childhood asthma after bacterial colonization of the airway in neonates

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The U.K. Working Party's Diagnostic Criteria for Atopic Dermatitis. II. Observer variation of clinical diagnosis and signs of atopic dermatitis.

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21 January 2018

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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

27 October 2018

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Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood

21 January 2018

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

21 January 2018

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Intermittent Inhaled Corticosteroids in Infants with Episodic Wheezing

21 January 2018

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Individuals who are homozygous for the 2282del4 and R501X filaggrin null mutations do not always develop dermatitis and complete long-term remission is possible

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3499508

Filaggrin null-mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study

9 December 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3499508

Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic Eczema

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3499508

Prevalence and morphology of hand eczema in patients with atopic dermatitis

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23166590

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fleshing out filaggrin phenotypes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23166590

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23166590

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0048678

1 reference

2 August 2017

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1 reference

2 August 2017

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