A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 165, Issue 8, 2014, Pages 619-626

  Rudd, Danielle S ^a,b   Axelsen, Michael ^b   Epping, Eric A ^b   Andreasen, Nancy C ^b   Wassink, Thomas H ^b  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

Author keywords

15q11.2; Pleiotropy; Polygenic; Recurrent CNV; Schizophrenia

Indexed keywords

ADOLESCENT; ADULT; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETICS; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; METHODS; MIDDLE AGED; MODELS, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA; SEQUENCE DELETION; YOUNG ADULT;

ADOLESCENT; ADULT; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MALE; MIDDLE AGED; MODELS, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA; SEQUENCE DELETION; YOUNG ADULT;

EID: 84922946316     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32266     Document Type: Article

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