Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease (Q35665929)

9 August 2017

Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease (English)

1 reference

9 August 2017

2

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9 June 2020

Sara Pulit

3

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9 June 2020

Gosia Trynka

4

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9 June 2020

Soumya Raychaudhuri

7

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9 June 2020

David A van Heel

8

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9 June 2020

Paul I W de Bakker

10

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9 June 2020

9

Cisca Wijmenga

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9 June 2020

author name string

Javier Gutierrez-Achury

1

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9 June 2020

Karen A Hunt

5

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9 June 2020

Jihane Romanos

6

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9 June 2020

language of work or name

English

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publication date

20 April 2015

1 reference

9 August 2017

1 reference

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9 June 2020

volume

47

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9 June 2020

issue

6

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9 June 2020

page(s)

577-578

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https://scigraph.springernature.com/pub.10.1038/ng.3268

9 June 2020

exact match

0 references

cites work

The contribution of genetic variants to disease depends on the ruler

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Risk of pediatric celiac disease according to HLA haplotype and country

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Systematic identification of trans eQTLs as putative drivers of known disease associations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Negligible impact of rare autoimmune-locus coding-region variants on missing heritability

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Improved heritability estimation from genome-wide SNPs

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Synthetic associations created by rare variants do not explain most GWAS results

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

GCTA: a tool for genome-wide complex trait analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Recent insights in the epidemiology of autoimmune diseases: improved prevalence estimates and understanding of clustering of diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Concordance, disease progression, and heritability of coeliac disease in Italian twins

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Imputing amino acid polymorphisms in human leukocyte antigens

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

A better coefficient of determination for genetic profile analysis.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Intraepithelial lymphocytes in celiac disease immunopathology

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449296

Cohort profile: 1958 British birth cohort (National Child Development Study).

25 September 2018

1 reference

Fine mapping seronegative and seropositive rheumatoid arthritis to shared and distinct HLA alleles by adjusting for the effects of heterogeneity.

21 January 2018

1 reference

Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects

21 January 2018

1 reference

Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes

21 January 2018

1 reference

New HLA haplotype frequency reference standards: high-resolution and large sample typing of HLA DR-DQ haplotypes in a sample of European Americans

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/NG.3268

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25894500%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

9 June 2020

0 references

1 reference

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9 June 2020

1 reference

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