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

Journal of Rheumatology

Volumn 38, Issue 5, 2011, Pages 797-801

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

^a MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

Author keywords

Association analysis; Copy number variation; Rheumatoid arthritis

Indexed keywords

MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1;

ALOX5AP GENE; ARTICLE; AUTOSOME; B2M GENE; COHORT ANALYSIS; CONTROLLED STUDY; COPY NUMBER VARIATION; GENE; GENE DELETION; GENE FREQUENCY; GENE FUNCTION; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENOTYPE; HUMAN; HUMAN GENOME; IRF1 GENE; LCP2 GENE; MAJOR CLINICAL STUDY; POPULATION GENETICS; PRIORITY JOURNAL; PRKCH GENE; PSORIASIS; RHEUMATOID ARTHRITIS; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTEMIC LUPUS ERYTHEMATOSUS; T LYMPHOCYTE; TNFAIP3 GENE; TNIP1 GENE; TRANSCRIPTION INITIATION;

ARTHRITIS, RHEUMATOID; CASE-CONTROL STUDIES; COHORT STUDIES; DNA COPY NUMBER VARIATIONS; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 79955565061     PISSN: 0315162X     EISSN: 14992752     Source Type: Journal    
DOI: 10.3899/jrheum.100758     Document Type: Article

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