Schizophrenia genetics: new insights from new approaches (Q37483078)

20 August 2017

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title

Schizophrenia genetics: new insights from new approaches (English)

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20 August 2017

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3

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20 August 2017

Hywel J Williams

1

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PubMed ID

19443537

20 August 2017

Michael J Owen

series ordinal

2

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20 August 2017

14 May 2009

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20 August 2017

British Medical Bulletin

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20 August 2017

91

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20 August 2017

61-74

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The surprisingly rich contours of schizophrenia epidemiology

20 August 2017

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https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

The neuropathology of schizophrenia. A critical review of the data and their interpretation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genome-wide association studies: theoretical and practical concerns

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Schizophrenia: genes at last?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

A HapMap harvest of insights into the genetics of common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Schizophrenia: a common disease caused by multiple rare alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Estimation of significance thresholds for genomewide association scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Clustering of metabolic comorbidity in schizophrenia: a genetic contribution?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genomewide association for schizophrenia in the CATIE study: results of stage 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Strong association of de novo copy number mutations with autism

21 January 2018

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https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Neuroligins and neurexins link synaptic function to cognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Disruption of the neurexin 1 gene is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Association within a family of a balanced autosomal translocation with major mental illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBMB%2FLDP017

21 January 2018

Identifiers

DOI

10.1093/BMB/LDP017

1 reference

20 August 2017

1 reference

PubMed ID

19443537