(Q50303296)

2 March 2018

title

Penetrance for copy number variants associated with schizophrenia. (English)

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2 March 2018

0 references

4

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2 March 2018

Cathryn Lewis

7

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2 March 2018

Dan Rujescu

5

Dan Rujescu

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2 March 2018

David St Clair

6

David St Clair

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2 March 2018

Evangelos Vassos

1

Evangelos Vassos

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2 March 2018

David Collier

2

David A Collier

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2 March 2018

author name string

Simon Holden

3

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2 March 2018

publication date

29 June 2010

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2 March 2018

published in

Human Molecular Genetics

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2 March 2018

volume

19

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2 March 2018

issue

17

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2 March 2018

page(s)

3477-3481

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2 March 2018

Association between microdeletion and microduplication at 16p11.2 and autism

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Large recurrent microdeletions associated with schizophrenia

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Rare chromosomal deletions and duplications increase risk of schizophrenia

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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

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High rates of schizophrenia in adults with velo-cardio-facial syndrome.

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Strong association of de novo copy number mutations with sporadic schizophrenia

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

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

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Recurrent CNVs disrupt three candidate genes in schizophrenia patients

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

Disruption of the neurexin 1 gene is associated with schizophrenia

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

Microduplications of 16p11.2 are associated with schizophrenia

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

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Phenotypic variations on the theme of CNVs

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Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

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Identification of loci associated with schizophrenia by genome-wide association and follow-up

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Advances in autism genetics: on the threshold of a new neurobiology

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Major changes in our DNA lead to major changes in our thinking

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Copy number variation and schizophrenia

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Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

21 January 2018

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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

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Structural variation of chromosomes in autism spectrum disorder

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Recurrent 16p11.2 microdeletions in autism

21 January 2018

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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

21 January 2018

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Psychiatric genetics gets a boost.

21 January 2018

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Contemplating effects of genomic structural variation

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance

21 January 2018

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Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

A systematic review of the prevalence of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ259

21 January 2018

Identifiers

DOI

10.1093/HMG/DDQ259

1 reference

2 March 2018

PubMed ID

20587603

1 reference

2 March 2018