(Q34323019)

1 August 2017

0 references

Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes (English)

1 reference

1 August 2017

0 references

1 reference

Leng Han

3

0 references

author name string

Xiongjian Luo

1

1 reference

1 August 2017

Liang Huang

2

1 reference

1 August 2017

Zhenwu Luo

4

1 reference

1 August 2017

Fang Hu

5

1 reference

1 August 2017

Roger Tieu

6

1 reference

1 August 2017

Lin Gan

7

1 reference

1 August 2017

language of work or name

English

0 references

publication date

24 March 2014

1 reference

1 August 2017

published in

Schizophrenia Bulletin

1 reference

1 August 2017

volume

40

1 reference

1 August 2017

issue

6

1 reference

1 August 2017

page(s)

1285-1299

1 reference

describes a project that uses

1 August 2017

Cytoscape

1 reference

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

inferred from PubMed Central ID database lookup

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Protein-protein interaction and pathway analyses of top schizophrenia genes reveal schizophrenia susceptibility genes converge on common molecular networks and enrichment of nucleosome (chromatin) assembly genes in schizophrenia susceptibility loci

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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

6 July 2018

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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

6 July 2018

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Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2

6 July 2018

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Genome-wide association study identifies five new schizophrenia loci

6 July 2018

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Common variants at VRK2 and TCF4 conferring risk of schizophrenia

6 July 2018

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A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population

6 July 2018

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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

6 July 2018

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Common variants in the BCL9 gene conferring risk of schizophrenia

6 July 2018

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

6 July 2018

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After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

6 July 2018

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

6 July 2018

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Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

6 July 2018

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Support for the involvement of the ERBB4 gene in schizophrenia: a genetic association analysis.

6 July 2018

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A versatile gene-based test for genome-wide association studies

6 July 2018

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Strong synaptic transmission impact by copy number variations in schizophrenia

6 July 2018

1 reference

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22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

6 July 2018

1 reference

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Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

6 July 2018

1 reference

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6 July 2018

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Gene enrichment profiles reveal T-cell development, differentiation, and lineage-specific transcription factors including ZBTB25 as a novel NF-AT repressor

6 July 2018

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Copy number variation in schizophrenia in the Japanese population

6 July 2018

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Microduplications of 16p11.2 are associated with schizophrenia

6 July 2018

1 reference

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Neurexin 1 (NRXN1) deletions in schizophrenia

6 July 2018

1 reference

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A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case

6 July 2018

1 reference

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

6 July 2018

1 reference

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Common variants conferring risk of schizophrenia

6 July 2018

1 reference

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

6 July 2018

1 reference

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Integrating computational biology and forward genetics in Drosophila

6 July 2018

1 reference

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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

A large-scale analysis of tissue-specific pathology and gene expression of human disease genes and complexes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Neuroligins and neurexins link synaptic function to cognitive disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Large recurrent microdeletions associated with schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Rare chromosomal deletions and duplications increase risk of schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

The function of BCL9 in Wnt/beta-catenin signaling and colorectal cancer cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Strong association of de novo copy number mutations with sporadic schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

ENDEAVOUR update: a web resource for gene prioritization in multiple species

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

A human phenome-interactome network of protein complexes implicated in genetic disorders

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Schizophrenia: a common disease caused by multiple rare alleles

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Neurexin-neuroligin signaling in synapse development

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

The modular nature of genetic diseases.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Altered neuregulin 1-erbB4 signaling contributes to NMDA receptor hypofunction in schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Gene prioritization through genomic data fusion

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

The involvement of ErbB4 with schizophrenia: association and expression studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

A systematic review of the prevalence of schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Neuroligins mediate excitatory and inhibitory synapse formation: involvement of PSD-95 and neurexin-1beta in neuroligin-induced synaptic specificity.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Cytoscape: a software environment for integrated models of biomolecular interaction networks

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

A highly significant association between a COMT haplotype and schizophrenia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

The allelic architecture of human disease genes: common disease-common variant... or not?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the alpha7-nicotinic acetylcholine receptor subunit gene (CHRNA7)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Disruption of two novel genes by a translocation co-segregating with schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

The genetics of schizophrenia: a current, genetic-epidemiologic perspective

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4193716

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.

6 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

'The missing genes: what happened to the heritability of psychiatric disorders?'.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Protein-protein interaction analysis reveals common molecular processes/pathways that contribute to risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Predicting disease genes using protein-protein interactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Haplotype transmission disequilibrium and evidence for linkage of the CHRNA7 gene region to schizophrenia in Southern African Bantu families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Evidence for linkage disequilibrium between the alpha 7-nicotinic receptor gene (CHRNA7) locus and schizophrenia in Azorean families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Association study of IL10, IL1beta, and IL1RN and schizophrenia using tag SNPs from a comprehensive database: suggestive association with rs16944 at IL1beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Increased inflammatory markers identified in the dorsolateral prefrontal cortex of individuals with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Association between polymorphism of the SNAP29 gene promoter region and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Haplotypes in the expression quantitative trait locus of interleukin-1β gene are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBU045

Polymorphism in SNAP29 gene promoter region associated with schizophrenia

21 January 2018

1 reference

12 December 2020

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

12 December 2020

Family-based association studies of COMT gene polymorphisms and schizophrenia in the Chinese population

1 reference

12 December 2020

Further evidence for association between ErbB4 and schizophrenia and influence on cognitive intermediate phenotypes in healthy controls

1 reference

12 December 2020

Convergent evidence shows a positive association of interleukin-1 gene complex locus with susceptibility to schizophrenia in the Caucasian population

1 reference

12 December 2020

Identifiers

DOI

10.1093/SCHBUL/SBU045

1 reference

1 August 2017

1 reference

1 August 2017

1 reference