Filaggrin gene defects are independent risk factors for atopic asthma in a Polish population: a study in ECAP cohort (Q33834147)

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24 January 2020

title

Filaggrin gene defects are independent risk factors for atopic asthma in a Polish population: a study in ECAP cohort (English)

1 reference

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24 January 2020

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3

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24 January 2020

Piotr Samel-Kowalik

5

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24 January 2020

Agnieszka Lipiec

7

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24 January 2020

Edyta Krzych-Fałta

10

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24 January 2020

Rafał Płoski

15

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24 January 2020

14

Sławomir Majewski

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24 January 2020

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Joanna Ponińska

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24 January 2020

2

Bolesław Samoliński

1 reference

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24 January 2020

4

Filip Raciborski

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24 January 2020

author name string

Artur Walkiewicz

6

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24 January 2020

Barbara Piekarska

8

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24 January 2020

Jarosław Komorowski

9

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24 January 2020

Andrzej Namysłowski

11

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24 January 2020

Jacek Borowicz

12

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24 January 2020

Grażyna Kostrzewa

13

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24 January 2020

language of work or name

English

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publication date

18 February 2011

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24 January 2020

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24 January 2020

volume

6

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24 January 2020

issue

2

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24 January 2020

page(s)

e16933

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Creative Commons Attribution 4.0 International

24 January 2020

copyright license

start time

18 February 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

A large-scale, consortium-based genomewide association study of asthma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

Filaggrin gene defects and risk of developing allergic sensitisation and allergic disorders: systematic review and meta-analysis

28 July 2018

1 reference

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

World Health Organization; GA(2)LEN; AllerGen. Allergic Rhinitis and its Impact on Asthma (ARIA) 2008 update (in collaboration with the World Health Organization, GA(2)LEN and AllerGen)

28 July 2018

1 reference

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

Allergic rhinitis and its impact on asthma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041817

Filaggrin in atopic dermatitis.

28 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0016933

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0016933

Does allergy in parents depend on allergy in their children? Recall bias in parental questioning of atopic diseases. Multicenter Allergy Study Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0016933

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0016933

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/10.1371%2FJOURNAL.PONE.0016933

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0016933

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/10.1371%2FJOURNAL.PONE.0016933

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21365004

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21365004

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21365004

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0016933

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21365004%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

0 references

1 reference

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24 January 2020

PubMed publication ID

21365004

1 reference