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Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Research Abstract Details 

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  • Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Abstract Text:

    george kirovGeorge Kirov,dilihan gumusDilihan Gumus,wei chenWei Chen,nadine nortonNadine Norton,lyudmila georgievaLyudmila Georgieva,murat sariMurat Sari,michael c o'donovanMichael C O'Donovan,fikret erdoganFikret Erdogan,michael j owenMichael J Owen,hans-hilger ropersHans-Hilger Ropers,reinhard ullmannReinhard Ullmann,george kirovGeorge Kirov,dilihan gumusDilihan Gumus,wei chenWei Chen,nadine nortonNadine Norton,lyudmila georgievaLyudmila Georgieva,murat sariMurat Sari,michael c o'donovanMichael C O'Donovan,fikret erdoganFikret Erdogan,michael j owenMichael J Owen,hans-hilger ropersHans-Hilger Ropers,reinhard ullmannReinhard Ullmann,

    Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders. We sought to determine the relevance of CNVs to the aetiology of schizophrenia (SZ). Whole-genome, high-resolution, tiling path BAC array comparative genomic hybridization (array CGH) was employed to test DNA from 93 individuals with DSM-IV SZ. Common DNA copy number changes that are unlikely to be directly pathogenic in SZ were filtered out by comparison to a reference dataset of 372 control individuals analyzed in our laboratory, and a screen against the Database of Genomic Variants. The remaining aberrations were validated with Affymetrix 250K SNP arrays or 244K Agilent oligo-arrays and tested for inheritance from the parents. A total of 13 aberrations satisfied our criteria. Two of them are very likely to be pathogenic. The first one is a deletion at 2p16.3 that was present in an affected sibling and disrupts NRXN1. The second one is a de novo duplication at 15q13.1 spanning APBA2. The proteins of these two genes interact directly and play a role in synaptic development and function. Both genes have been affected by CNVs in patients with autism and mental retardation, but neither has been previously implicated in SZ.

    Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Publishing Authors By Initials

    g kirovG Kirov,d gumusD Gumus,w chenW Chen,n nortonN Norton,l georgievaL Georgieva,m sariM Sari,mc o'donovanMC O'Donovan,f erdoganF Erdogan,mj owenMJ Owen,hh ropersHH Ropers,r ullmannR Ullmann,g kirovG Kirov,d gumusD Gumus,w chenW Chen,n nortonN Norton,l georgievaL Georgieva,m sariM Sari,mc o'donovanMC O'Donovan,f erdoganF Erdogan,mj owenMJ Owen,hh ropersHH Ropers,r ullmannR Ullmann,

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    Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Human molecular genetics

    VOLUME: 17

    Page Numbers: 458-65

    Journal Abbreviation: Hum. Mol. Genet.

    ISSN: 0964-6906

    DAY: 6

    MONTH: 11

    YEAR: 2007

    Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Information

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    LANGUAGE: eng

    NlmUniqueID: 9208958

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    AFFILIATION: The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Hum Mol Genet

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