Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage

Journal of Human Genetics

Volumn 55, Issue 11, 2010, Pages 726-730

  Bae, Joon Seol ^a   Cheong, Hyun Sub ^b   Park, Byung Lae ^b   Kim, Lyoung Hyo ^b   Park, Tae Joon ^a   Kim, Jason Yongha ^a   Pasaje, Charisse Flerida A ^a   Lee, Jin Sol ^a   Cui, Tailin ^c   Inoue, Ituro ^c   Shin, Hyoung Doo ^a,b  

^a Sogang University   (South Korea)

^b SNP Genetics Inc   (South Korea)

^c TOKAI UNIVERSITY   (Japan)

Author keywords

copy number variation; genetic epidemiology; genome wide CNV association study; genomics; subarachnoid aneurysmal hemorrhage

Indexed keywords

ADULT; AGE; AGED; ARTICLE; BRAIN ARTERY ANEURYSM RUPTURE; BRAIN HEMORRHAGE; CONTROLLED STUDY; COPY NUMBER VARIATION; DATA BASE; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; FEMALE; GENDER; GENE DELETION; GENE DUPLICATION; GENETIC ASSOCIATION; GENOTYPE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MORTALITY; MULTIVARIATE LOGISTIC REGRESSION ANALYSIS; POLYMERASE CHAIN REACTION; RISK; SUBARACHNOID ANEURYSMAL HEMORRHAGE;

ADULT; AGED; AGED, 80 AND OVER; ASIAN CONTINENTAL ANCESTRY GROUP; DATABASES, GENETIC; DNA COPY NUMBER VARIATIONS; GENE DOSAGE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; JAPAN; MIDDLE AGED; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; SUBARACHNOID HEMORRHAGE;

EID: 78649518025     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1038/jhg.2010.97     Document Type: Article

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