(Q50309794)

English

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

scientific article published in October 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

0 references

susceptibility locus

1 reference

based on heuristic

inferred from title

author name string

Trilochan Sahoo

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Aaron Theisen

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Jill A Rosenfeld

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Allen N Lamb

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

J Britt Ravnan

5

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Roger A Schultz

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Beth S Torchia

7

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Nicholas Neill

8

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Ian Casci

9

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Bassem A Bejjani

10

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Lisa G Shaffer

11

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

language of work or name

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publication date

1 October 2011

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

13

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

10

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

868-880

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Symptoms, signs, and diagnosis of schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

The genetics of schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

A genome-wide investigation of SNPs and CNVs in schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Copy-number variations associated with neuropsychiatric conditions

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Chromosomal abnormalities and mental illness.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Large recurrent microdeletions associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Schizophrenia: a common disease caused by multiple rare alleles

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

5q14.3 deletion manifesting as mitochondrial disease and autism: case report.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Psychiatric genetics: progress amid controversy

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Detection of sharing by descent, long-range phasing and haplotype imputation

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Penetrance for copy number variants associated with schizophrenia.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Population analysis of large copy number variants and hotspots of human genetic disease

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Smith-Magenis syndrome

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Neuroanatomy of comorbid schizophrenia and learning disability: a controlled study.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Voxel-based morphometry of comorbid schizophrenia and learning disability: analyses in normalized and native spaces using parametric and nonparametric statistical methods.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Phenotypic and genetic complexity of psychosis

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3182217A06

21 January 2018

Identifiers

10.1097/GIM.0B013E3182217A06

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/21792059

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