(Q53102540)

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Association analysis of the CCL3L1 copy number locus by paralogue ratio test in Norwegian rheumatoid arthritis patients and healthy controls.

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scholarly article

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

Association analysis of the CCL3L1 copy number locus by paralogue ratio test in Norwegian rheumatoid arthritis patients and healthy controls. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

rheumatoid arthritis

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based on heuristic

inferred from title

4

object named as

T K Kvien

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Europe PubMed Central

PubMed publication ID

11 May 2018

author name string

G B N Nordang

1

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

D Carpenter

2

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

M K Viken

3

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

J A L Armour

5

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

B A Lie

6

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

publication date

12 July 2012

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

Genes and Immunity

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

13

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

7

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

579-582

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Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

https://scigraph.springernature.com/pub.10.1038/gene.2012.30

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A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

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STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus

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

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

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Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci

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Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins

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Common variants at CD40 and other loci confer risk of rheumatoid arthritis

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Global variation in copy number in the human genome

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https://api.crossref.org/works/10.1038%2FGENE.2012.30

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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

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Integrated detection and population-genetic analysis of SNPs and copy number variation

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The fine-scale and complex architecture of human copy-number variation

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Towards a comprehensive structural variation map of an individual human genome

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

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Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

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Inhibition of the development of collagen-induced arthritis in rhesus monkeys by a small molecular weight antagonist of CCR5.

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Negative association between the chemokine receptor CCR5-Delta32 polymorphism and rheumatoid arthritis: a meta-analysis

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Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis

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Immunity to citrullinated proteins in rheumatoid arthritis

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A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis

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https://api.crossref.org/works/10.1038%2FGENE.2012.30

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Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis

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https://api.crossref.org/works/10.1038%2FGENE.2012.30

21 January 2018

Accuracy and differential bias in copy number measurement of CCL3L1 in association studies with three auto-immune disorders

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CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus

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21 January 2018

Experimental aspects of copy number variant assays at CCL3L1

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21 January 2018

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

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21 January 2018

Reply to: "Experimental aspects of copy number variant assays at CCL3L1".

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A robust statistical method for case-control association testing with copy number variation

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21 January 2018

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.

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Determination of beta-defensin genomic copy number in different populations: A comparison of three methods

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Gene copy number: learning to count past two.

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21 January 2018

CCL3L1 and HIV/AIDS susceptibility

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21 January 2018

CCL3L1 and HIV/AIDS susceptibility

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21 January 2018

The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritis

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21 January 2018

Differences in synovial tissue infiltrates between anti–cyclic citrullinated peptide–positive rheumatoid arthritis and anti–cyclic citrullinated peptide–negative rheumatoid arthritis

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Selective accumulation of CCR5+ T lymphocytes into inflamed joints of rheumatoid arthritis

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7 January 2021

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A non-peptide CCR5 antagonist inhibits collagen-induced arthritis by modulating T cell migration without affecting anti-collagen T cell responses

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7 January 2021

based on heuristic

inferred from DOI database lookup

Multiplex Paralogue Ratio Tests for accurate measurement of multiallelic CNVs

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/GENE.2012.30

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 May 2018

http://europepmc.org/abstract/MED/22785612

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