(Q28282047)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Strong association of de novo copy number mutations with sporadic schizophrenia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Joseph A Gogos

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Bin Xu

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

E J van Rensburg

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Maria Karayiorgou

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

language of work or name

English

0 references

publication date

30 May 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

volume

1 reference

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8 January 2020

issue

1 reference

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8 January 2020

page(s)

880-885

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

A polygenic theory of schizophrenia

8 January 2020

cites work

1 reference

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

21 April 2017

1 reference

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

21 April 2017

1 reference

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

21 April 2017

1 reference

Strong association of de novo copy number mutations with autism

21 April 2017

1 reference

Structural variation of chromosomes in autism spectrum disorder

21 April 2017

1 reference

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 April 2017

1 reference

Global variation in copy number in the human genome

21 April 2017

1 reference

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

21 April 2017

1 reference

Haplotypes spanning SPEC2, PDZ-GEF2 and ACSL6 genes are associated with schizophrenia

21 April 2017

1 reference

Characterisation of PDZ-GEFs, a family of guanine nucleotide exchange factors specific for Rap1 and Rap2

21 April 2017

1 reference

Defective neurogenesis in citron kinase knockout mice by altered cytokinesis and massive apoptosis

21 April 2017

1 reference

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 April 2017

1 reference

Schizophrenia genetics: uncovering positional candidate genes

21 April 2017

1 reference

7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

7 January 2021

Chromosomal abnormalities and mental illness.

1 reference

7 January 2021

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1

1 reference

7 January 2021

Assessment of the frequency of the 22q11 deletion in Afrikaner schizophrenic patients

1 reference

7 January 2021

Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1.

1 reference

7 January 2021

Intracellular and trans-synaptic regulation of glutamatergic synaptogenesis by EphB receptors.

1 reference

7 January 2021

Specification of distinct dopaminergic neural pathways: roles of the Eph family receptor EphB1 and ligand ephrin-B2.

1 reference

7 January 2021

Evidence of association between bipolar disorder and Citron on chromosome 12q24.

1 reference

7 January 2021

miRNAs on the move: miRNA biogenesis and the RNAi machinery

1 reference

7 January 2021

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

1 reference

7 January 2021

Genomic rearrangements and sporadic disease

1 reference

7 January 2021

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

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG.162

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18511947%20AND%20SRC:MED&resulttype=core&format=json