Autoimmune disease classification by inverse association with SNP alleles. (Q33521311): Difference between revisions

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scientific article

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Englisch	Autoimmune disease classification by inverse association with SNP alleles.	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Autoimmune disease classification by inverse association with SNP alleles. (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

object named as

Marina Sirota

1

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0 references

author name string

Marc A Schaub

2

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Serafim Batzoglou

3

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

William H Robinson

4

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Atul J Butte

5

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Europe PubMed Central

PubMed publication ID

27 July 2017

publication date

24 December 2009

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

e1000792

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Common regulatory variation impacts gene expression in a cell type-dependent manner

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

A Classifier-based approach to identify genetic similarities between diseases

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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21 June 2018

Treatment of ankylosing spondylitis and other spondyloarthritides

1 reference

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21 June 2018

Pathway and network-based analysis of genome-wide association studies in multiple sclerosis

1 reference

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21 June 2018

Identifying disease associations via genome-wide association studies

1 reference

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21 June 2018

FitSNPs: highly differentially expressed genes are more likely to have variants associated with disease

1 reference

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21 June 2018

CD226 Gly307Ser association with multiple autoimmune diseases

1 reference

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21 June 2018

Association of type 1 diabetes with two Loci on 12q13 and 16p13 and the influence coexisting thyroid autoimmunity in Japanese

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21 June 2018

Autoimmune diseases: insights from genome-wide association studies

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21 June 2018

Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms.

1 reference

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21 June 2018

Pathway analysis of seven common diseases assessed by genome-wide association

1 reference

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21 June 2018

Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives

1 reference

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21 June 2018

Rheumatoid arthritis and thyroid abnormalities.

1 reference

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21 June 2018

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

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21 June 2018

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

TNFalpha blockade in human diseases: an overview of efficacy and safety

1 reference

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TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study

1 reference

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21 June 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Risk alleles for multiple sclerosis identified by a genomewide study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Analysis of the BTNL2 truncating splice site mutation in tuberculosis, leprosy and Crohn's disease

1 reference

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21 June 2018

Co-occurrence and comorbidities in patients with immune-mediated inflammatory disorders: an exploration using US healthcare claims data, 2001-2002.

1 reference

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21 June 2018

Analysis of a functional BTNL2 polymorphism in type 1 diabetes, rheumatoid arthritis, and systemic lupus erythematosus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Co-occurrence of autoimmune thyroid disease in a multiple sclerosis cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

The BTNL2 gene and sarcoidosis susceptibility in African Americans and Whites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Sarcoidosis is associated with a truncating splice site mutation in BTNL2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

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1 reference

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IFN-beta in rheumatoid arthritis

1 reference

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21 June 2018

A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Association of TAP2 gene polymorphisms in Chinese patients with rheumatoid arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

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21 June 2018

Observations on recent studies showing increased co-occurrence of autoimmune diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Analysis of TAP2 polymorphisms in Finnish individuals with type I diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

21 June 2018

Principles for the buffering of genetic variation

1 reference

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21 June 2018

HLA association with autoimmune disease: a failure to protect?

1 reference

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Immunogenetic studies in families with rheumatoid arthritis and autoimmune thyroid disease

1 reference

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Prevalence of thyroid abnormalities in patients with rheumatoid arthritis

1 reference

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BTNL2 gene variant and sarcoidosis

1 reference

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1 reference

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2791168

31 October 2018

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10.1371/JOURNAL.PGEN.1000792

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

ResearchGate publication ID

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