Whole-genome detection of disease-associated deletions or excess homozygosity in a case-control study of rheumatoid arthritis

Human Molecular Genetics

Volumn 22, Issue 6, 2013, Pages 1249-1261

  Wu, Chih Chieh ^a   Shete, Sanjay ^a   Jo, Eun Ji ^c   Xu, Yaji ^d   Lu, Emily Y ^b   Chen, Wei V ^b   Amos, Christopher I ^b,e  

^a Department of Epidemiology ^*  (United States)

^b UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d YALE UNIVERSITY   (United States)

^e DARTMOUTH MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 10P; CHROMOSOME 13Q; CHROMOSOME 14; CONTROLLED STUDY; COPY NUMBER VARIATION; DISEASE ASSOCIATION; GENE CLUSTER; GENE DELETION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MAJOR HISTOCOMPATIBILITY COMPLEX; POLYMORPHIC LOCUS; PRIORITY JOURNAL; RHEUMATOID ARTHRITIS; SINGLE NUCLEOTIDE POLYMORPHISM;

ARTHRITIS, RHEUMATOID; CASE-CONTROL STUDIES; DNA COPY NUMBER VARIATIONS; FEMALE; GENOME-WIDE ASSOCIATION STUDY; HOMOZYGOTE; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE DELETION;

EID: 84874545024     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/dds512     Document Type: Article

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