Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

Molecular Psychiatry

Volumn 17, Issue 4, 2012, Pages 421-432

  Priebe, L ^a   Degenhardt, F A ^a   Herms, S ^a   Haenisch, B ^a   Mattheisen, M ^a   Nieratschker, V ^b   Weingarten, M ^a   Witt, S ^b   Breuer, R ^b   Paul, T ^b   Alblas, M ^a   Moebus, S ^c   Lathrop, M ^d   Leboyer, M ^e,f,g   Schreiber, S ^h   Grigoroiu Serbanescu, M ⁱ   Maier, W ^a   Propping, P ^a   Rietschel, M ^b   Nothen M M ^a   Cichon, S ^a,j   Muhleisen T W ^a   more..

^a UNIVERSITY OF BONN   (Germany)

^b CENTRAL INSTITUTE OF MENTAL HEALTH   (Germany)

^c UNIVERSITY HOSPITAL ESSEN   (Germany)

^d CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^e INSERM   (France)

^f FACULTÉ DE MÉDECINE   (France)

^g HENRI MONDOR HOSPITAL   (France)

^h UNIVERSITY OF KIEL   (Germany)

ⁱ Psychiatric Hospital Bucharest   (Romania)

^j FORSCHUNGSZENTRUM JÜLICH   (Germany)

more..

Author keywords

association; bipolar disorder; copy number variant; early age at onset; genome wide burden

Indexed keywords

ADULT; ARTICLE; BIPOLAR DISORDER; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; GENE DELETION; GENE DUPLICATION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGE FACTORS; AGE OF ONSET; BIPOLAR DISORDER; CASE-CONTROL STUDIES; DATABASES, GENETIC; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GERMANY; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84859003845     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/mp.2011.8     Document Type: Article

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