Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility. (Q34632596)

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Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility

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English	Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.	scientific article	Genomic Polymorphism at the Interferon-Induced Helicase (IFIH1) Locus Contributes to Graves’ Disease Susceptibility

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17535987%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6952273&resulttype=core&format=json

13 May 2020

Graves' disease

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based on heuristic

inferred from title

8

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13 May 2020

12

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13 May 2020

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Alison Sutherland

1

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13 May 2020

Jocelyn Davies

2

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13 May 2020

Catherine J Owen

3

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13 May 2020

Suresh Vaikkakara

4

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13 May 2020

Christine Walker

5

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13 May 2020

Timothy D Cheetham

6

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13 May 2020

R Andrew James

7

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13 May 2020

Peter T Donaldson

9

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13 May 2020

Heather J Cordell

10

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13 May 2020

Richard Quinton

11

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13 May 2020

language of work or name

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publication date

29 May 2007

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31 December 2019

The Journal of Clinical Endocrinology and Metabolism

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13 May 2020

92

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13 May 2020

8

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13 May 2020

3338-3341

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13 May 2020

Genetic progress towards the molecular basis of autoimmunity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intracellular pattern recognition receptors in the host response

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the TSHR gene with Graves' disease: the first disease specific locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Shared and unique functions of the DExD/H-box helicases RIG-I, MDA5, and LGP2 in antiviral innate immunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a major role of heredity in Graves' disease: a population-based study of two Danish twin cohorts

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the PD-1.3A allele of the PDCD1 gene in patients with rheumatoid arthritis negative for rheumatoid factor and the shared epitope

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Searching for the autoimmune thyroid disease susceptibility genes: from gene mapping to gene function

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human type 1 diabetes and the insulin gene: principles of mapping polygenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of PDCD1 with susceptibility to systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eighty-six cases of Addison's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enterovirus infection as a risk factor for beta-cell autoimmunity in a prospectively observed birth cohort: the Finnish Diabetes Prediction and Prevention Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17535987

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1210/JC.2007-0173

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6952273&resulttype=core&format=json

13 May 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6952273&resulttype=core&format=json

13 May 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6952273&resulttype=core&format=json

13 May 2020

ResearchGate publication ID

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