Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease (Q30426720)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22057235%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22057235%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

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1 reference

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16 January 2020

Graham Heap

21

1 reference

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16 January 2020

Chris Wallace

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1 reference

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16 January 2020

Jeffrey C Barrett

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1 reference

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16 January 2020

Gosia Trynka

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1 reference

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16 January 2020

Nicholas A Bockett

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1 reference

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16 January 2020

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16 January 2020

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16 January 2020

Charles Mein

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1 reference

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16 January 2020

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16 January 2020

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16 January 2020

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1 reference

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16 January 2020

Hania Szajewska

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16 January 2020

Jezabel Varade

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16 January 2020

Alexandra Zhernakova

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16 January 2020

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16 January 2020

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16 January 2020

Elena Urcelay

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

David A van Heel

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16 January 2020

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Leo A B Joosten

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

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1 reference

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16 January 2020

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16 January 2020

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Cordelia Langford

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16 January 2020

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Karin Fransen

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16 January 2020

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Patrick C A Dubois

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16 January 2020

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Karen A Hunt

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16 January 2020

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Jihane Romanos

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16 January 2020

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16 January 2020

Maria Cristina Mazzilli

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16 January 2020

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16 January 2020

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Vanisha Mistry

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16 January 2020

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Concepción Núñez

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16 January 2020

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Isabel Polanco

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16 January 2020

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Mathieu Platteel

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16 January 2020

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Anna Rybak

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16 January 2020

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Victorien M Wolters

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16 January 2020

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Cleo C van Diemen

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16 January 2020

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16 January 2020

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Ajit Sood

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

Rodrigo Coutinho de Almeida

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16 January 2020

Javier Gutierrez

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16 January 2020

Leticia Plaza Izurieta

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16 January 2020

Valentina Izzo

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16 January 2020

Vandana Midah

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16 January 2020

Barbara Mora

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16 January 2020

Marinita Morelli

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16 January 2020

Carmen Ribes-Koninckx

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16 January 2020

José Luis Santiago

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16 January 2020

Riccardo Troncone

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16 January 2020

Spanish Consortium on the Genetics of Coeliac Disease (CEGEC)

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16 January 2020

PreventCD Study Group

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16 January 2020

Maria Teresa Bardella

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16 January 2020

language of work or name

English

0 references

publication date

6 November 2011

1 reference

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16 January 2020

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16 January 2020

volume

43

1 reference

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16 January 2020

page(s)

1193-1201

1 reference

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16 January 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22057235%20AND%20SRC:MED&resulttype=core&format=json

Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction

16 January 2020

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Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

14 July 2018

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A rare variant in MYH6 is associated with high risk of sick sinus syndrome

14 July 2018

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Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

14 July 2018

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Promise and pitfalls of the Immunochip

14 July 2018

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Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

14 July 2018

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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

14 July 2018

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation

14 July 2018

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14 July 2018

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14 July 2018

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Hundreds of variants clustered in genomic loci and biological pathways affect human height

14 July 2018

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From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

14 July 2018

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Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia

14 July 2018

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Association of trypanolytic ApoL1 variants with kidney disease in African Americans

14 July 2018

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14 July 2018

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Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection

14 July 2018

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Multiple common variants for celiac disease influencing immune gene expression

14 July 2018

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Rare variants create synthetic genome-wide associations

14 July 2018

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Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling

14 July 2018

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Detecting shared pathogenesis from the shared genetics of immune-related diseases

14 July 2018

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Progress and challenges in genome-wide association studies in humans

14 July 2018

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Shared and distinct genetic variants in type 1 diabetes and celiac disease

14 July 2018

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14 July 2018

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Newly identified genetic risk variants for celiac disease related to the immune response

14 July 2018

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A deletion mutation of the protein tyrosine phosphatase kappa (Ptprk) gene is responsible for T-helper immunodeficiency (thid) in the LEC rat.

14 July 2018

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14 July 2018

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

14 July 2018

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14 July 2018

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Population structure, differential bias and genomic control in a large-scale, case-control association study

14 July 2018

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14 July 2018

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14 July 2018

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Seroprevalence, correlates, and characteristics of undetected coeliac disease in England

14 July 2018

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14 July 2018

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14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242065

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.

14 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.998

Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.998

HLA-DQ and risk gradient for celiac disease.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.998

Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22057235

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Revisiting genome wide association studies (GWAS) in coeliac disease: replication study in Spanish population and expression analysis of candidate genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22057235

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22057235

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22057235%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22057235%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22057235%20AND%20SRC:MED&resulttype=core&format=json