Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder (Q46504843)

22 December 2017

title

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

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22 December 2017

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Manuel Mattheisen

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Maria Grigoroiu-Serbanescu

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Markus M Nöthen

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Sven Cichon

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S Cichon

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Mark Lathrop

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M Lathrop

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M Leboyer

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M Rietschel

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W Maier

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F A Degenhardt

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author name string

L Priebe

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B Haenisch

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V Nieratschker

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M Weingarten

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S Witt

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R Breuer

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T Paul

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M Alblas

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S Moebus

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S Schreiber

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P Propping

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T W Mühleisen

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language of work or name

English

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publication date

1 March 2011

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published in

Molecular Psychiatry

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volume

17

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issue

4

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page(s)

421-432

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https://scigraph.springernature.com/pub.10.1038/mp.2011.8

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cites work

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Rare chromosomal deletions and duplications increase risk of schizophrenia

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

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Singleton deletions throughout the genome increase risk of bipolar disorder

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Genomic landscape of a three-generation pedigree segregating affective disorder

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Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

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The breakpoint cluster region gene on chromosome 22q11 is associated with bipolar disorder.

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7 January 2021

Increase inGSK3β gene copy number variation in bipolar disorder

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7 January 2021

Age at onset in bipolar-related major affective illness: clinical and genetic implications

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7 January 2021

Heterozygous deletion of mitotic arrest-deficient protein 1 (MAD1) increases the incidence of tumors in mice

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7 January 2021

Disruption of the neurexin 1 gene is associated with schizophrenia

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7 January 2021

Identifiers

DOI

10.1038/MP.2011.8

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22 December 2017

PubMed ID

21358712

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22 December 2017