De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. (Q33398247)

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16 January 2020

title

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia (English)

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16 January 2020

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0 references

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

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16 January 2020

E Fernandez

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16 January 2020

M Ikeda

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16 January 2020

K Chambert

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16 January 2020

L Georgieva

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16 January 2020

R Wollerton

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16 January 2020

I Nikolov

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16 January 2020

L N van de Lagemaat

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P I Olason

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16 January 2020

N H Komiyama

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16 January 2020

M O Collins

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16 January 2020

S Purcell

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P Sklar

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16 January 2020

M J Owen

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16 January 2020

Y Böttcher

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16 January 2020

K Stefansson

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16 January 2020

H Stefansson

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language of work or name

English

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publication date

15 November 2011

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16 January 2020

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volume

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issue

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16 January 2020

page(s)

142-153

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De novo rates and selection of schizophrenia-associated copy number variants

16 January 2020

cites work

1 reference

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A copy number variation morbidity map of developmental delay

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

21 June 2018

1 reference

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Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

21 June 2018

1 reference

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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

21 June 2018

1 reference

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Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

21 June 2018

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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

21 June 2018

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Epigenetic regulation of learning and memory by Drosophila EHMT/G9a

21 June 2018

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Characterization of the proteome, diseases and evolution of the human postsynaptic density.

21 June 2018

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Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

21 June 2018

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A systematic review and meta-analysis of the fertility of patients with schizophrenia and their unaffected relatives.

21 June 2018

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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 June 2018

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Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

21 June 2018

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21 June 2018

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Microdeletions of 3q29 confer high risk for schizophrenia

21 June 2018

1 reference

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Suggestion of roles for both common and rare risk variants in genome-wide studies of schizophrenia

21 June 2018

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Functional impact of global rare copy number variation in autism spectrum disorders

21 June 2018

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Strong synaptic transmission impact by copy number variations in schizophrenia

21 June 2018

1 reference

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

21 June 2018

1 reference

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The role of copy number variation in schizophrenia

21 June 2018

1 reference

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Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

21 June 2018

1 reference

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Copy number variation in schizophrenia in the Japanese population

21 June 2018

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Microduplications of 16p11.2 are associated with schizophrenia

21 June 2018

1 reference

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia

21 June 2018

1 reference

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The role of DNA copy number variation in schizophrenia.

21 June 2018

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Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

21 June 2018

1 reference

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The Arc of synaptic memory

21 June 2018

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Neurexin 1 (NRXN1) deletions in schizophrenia

21 June 2018

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Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype

21 June 2018

1 reference

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

21 June 2018

1 reference

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Disruption of the neurexin 1 gene is associated with schizophrenia

21 June 2018

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The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP

21 June 2018

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Large recurrent microdeletions associated with schizophrenia

21 June 2018

1 reference

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Rare chromosomal deletions and duplications increase risk of schizophrenia

21 June 2018

1 reference

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Strong association of de novo copy number mutations with sporadic schizophrenia

21 June 2018

1 reference

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 June 2018

1 reference

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

21 June 2018

1 reference

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 June 2018

1 reference

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Strong association of de novo copy number mutations with autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3603134

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome

21 June 2018

1 reference

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Synapse proteomics of multiprotein complexes: en route from genes to nervous system diseases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3603134

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3603134

Proteomic analysis of NMDA receptor-adhesion protein signaling complexes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3603134

The NMDA antagonist model for schizophrenia: promise and pitfalls

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3603134

NMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3603134

Reproductive patterns in psychotic patients

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2011.154

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2011.154

21 January 2018

Identifiers

DOI

10.1038/MP.2011.154

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083728%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083728%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

22083728

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22083728%20AND%20SRC:MED&resulttype=core&format=json