(Q45245735)

11 December 2017

title

Lower prevalence of common filaggrin mutations in a community sample of atopic eczema: is disease severity important? (English)

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11 December 2017

2

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11 December 2017

5

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11 December 2017

Robert Gruber

1

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11 December 2017

Daniela Grabher

series ordinal

3

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11 December 2017

Elisabeth Horak

series ordinal

4

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11 December 2017

Peter Lercher

series ordinal

6

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11 December 2017

publication date

27 September 2010

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11 December 2017

published in

Vienna Clinical Weekly

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11 December 2017

volume

122

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11 December 2017

issue

19-20

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11 December 2017

page(s)

551-557

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https://scigraph.springernature.com/pub.10.1007/s00508-010-1449-3

11 December 2017

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Filaggrin mutations, atopic eczema, hay fever, and asthma in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

The burden of disease associated with filaggrin mutations: a population-based, longitudinal birth cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Filaggrin null mutations are associated with increased asthma severity in children and young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Replication validity of genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Commentary: grading the credibility of molecular evidence for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Population stratification and spurious allelic association

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Epidemiological methods for studying genes and environmental factors in complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Prevalence of respiratory and atopic disorders among children in the East and West of Germany five years after unification.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Generalized linear mixed models: a review and some extensions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Breaking the (Un)Sound Barrier: Filaggrin Is a Major Gene for Atopic Dermatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00508-010-1449-3

Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany

21 January 2018

1 reference

12 December 2020

Filaggrin mutations confer susceptibility to atopic dermatitis but not to asthma

1 reference

12 December 2020

Filaggrin mutations in children with severe atopic dermatitis

1 reference

12 December 2020

Skin barrier function and allergic risk

1 reference

12 December 2020

Meta-analysis of filaggrin polymorphisms in eczema and asthma: Robust risk factors in atopic disease

1 reference

12 December 2020

The genetics of atopic dermatitis

1 reference

12 December 2020

Two Common Loss-of-Function Mutations within the Filaggrin Gene Predispose for Early Onset of Atopic Dermatitis

1 reference

12 December 2020

Point: population stratification: a problem for case-control studies of candidate-gene associations?

1 reference

12 December 2020

Filaggrin mutations strongly predispose to early-onset and extrinsic atopic dermatitis

1 reference

12 December 2020

Population admixture may appear to mask, change or reverse genetic effects of genes underlying complex traits

1 reference

12 December 2020

10.1007/S00508-010-1449-3

Identifiers

DOI

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Dimensions Publication ID

11 December 2017

1018788996

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1 reference