Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Autosome-wide copy number variation association analysis for rheumatoid arthritis using the WTCCC high-density SNP genotype data.

The Journal of rheumatology - 1 May 2011

Uddin Mohammed, Sturge Mitch, Rahman Proton, Woods Michael O

Abstract excerpt

OBJECTIVE: Rheumatoid arthritis (RA) is a complex autoimmune rheumatic disease that is strongly influenced by genetic factors. Numerous genes are convincingly associated with RA, including genes in tumor necrosis factor signaling (TNF) and the nuclear factor-κB pathway. To date, except for genes within the HLA region, no data exist regarding potential copy number variations (CNV) involving RA-associated genes. We...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arthritis, Rheumatoid
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cohort Studies

Share to DNA Copy Number Variations

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Genotype

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 21362769
DOI: 10.3899/jrheum.100758

Genes

LCP2
PRKCH
TNF
TNFAIP3
TNIP1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Autosome-wide copy number variation association analysis for rheumatoid arthritis using the WTCCC high-density SNP genotype data.PMID 21362769Read ↗

Association of VPREB1 Gene Copy Number Variation and Rheumatoid Arthritis Susceptibility.Semantic proximity Read ↗

Synovial transcriptome-wide association study implicates novel genes underlying rheumatoid arthritis risk.Semantic proximity Read ↗

Synovial transcriptome-wide association study implicates novel genes underlying rheumatoid arthritis riskSemantic proximity Read ↗

Clinical implications of copy number variations in autoimmune disorders.Semantic proximity Read ↗

From the era of genome analysis to the era of genomic drug discovery: a pioneering example of rheumatoid arthritis.Semantic proximity Read ↗

Gene-regulatory network study of rheumatoid arthritis in single-cell chromatin landscapes of peripheral blood mononuclear cellsSemantic proximity Read ↗

Characterization of Rheumatoid Arthritis Risk-Associated SNPs and Identification of Novel Therapeutic Sites Using an In-Silico ApproachSemantic proximity Read ↗

Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locus.Semantic proximity Read ↗

Copy number variation in the human genome and its implication in autoimmunity.Semantic proximity Read ↗

Differentially Methylated DNA Regions in Monozygotic Twin Pairs Discordant for Rheumatoid Arthritis: An Epigenome-Wide StudySemantic proximity Read ↗

Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes.Semantic proximity Read ↗

Epigenome-wide association study of rheumatoid arthritis identifies differentially methylated loci in B cellsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.