(Q34294530)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

review article

3 references

PubMed publication ID

30 April 2021

25 October 2022

Animal models of psychiatric disorders that reflect human copy number variation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

14 September 2019

DNA copy number variations

2 references

14 September 2019

30 April 2021

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

author name string

Toru Takumi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

publication date

30 July 2012

6 references

19 June 2019

30 June 2019

14 September 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

30 April 2021

25 October 2022

6 references

19 June 2019

30 June 2019

14 September 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

30 April 2021

25 October 2022

2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

page(s)

589524

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 3.0 Unported

11 February 2020

copyright license

5 references

19 June 2019

30 June 2019

14 September 2019

30 April 2021

on focus list of Wikimedia project

25 October 2022

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

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6 July 2018

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6 July 2018

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Large-scale analysis of the regulatory architecture of the mouse genome with a transposon-associated sensor

6 July 2018

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Mouse mutagenesis and disease models for neuropsychiatric disorders

6 July 2018

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Modeling autistic features in animals

6 July 2018

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Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis

6 July 2018

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Mouse models of autism: testing hypotheses about molecular mechanisms

6 July 2018

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Decreased exploratory activity in a mouse model of 15q duplication syndrome; implications for disturbance of serotonin signaling

6 July 2018

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Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother.

6 July 2018

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The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders

6 July 2018

1 reference

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Ultrasonic vocalizations in mouse models for speech and socio-cognitive disorders: insights into the evolution of vocal communication

6 July 2018

1 reference

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Behavioural phenotyping assays for mouse models of autism

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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Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia

6 July 2018

1 reference

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Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

6 July 2018

1 reference

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Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.

6 July 2018

1 reference

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

6 July 2018

1 reference

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Copy-number variants in neurodevelopmental disorders: promises and challenges

6 July 2018

1 reference

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Microduplications of 16p11.2 are associated with schizophrenia

6 July 2018

1 reference

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Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome).

6 July 2018

1 reference

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Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome

6 July 2018

1 reference

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Review of the evidence for treatment of children with autism with selective serotonin reuptake inhibitors

6 July 2018

1 reference

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Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

6 July 2018

1 reference

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DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

6 July 2018

1 reference

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Association and mutation analyses of 16p11.2 autism candidate genes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

6 July 2018

1 reference

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Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion.

6 July 2018

1 reference

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Trends in large-scale mouse mutagenesis: from genetics to functional genomics

6 July 2018

1 reference

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

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=3414062

Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Structural variation of chromosomes in autism spectrum disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

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=3414062

Methods and strategies for analyzing copy number variation using DNA microarrays

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Global variation in copy number in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Mapping cortical thickness in children with 22q11.2 deletions

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Neurochemistry in the pathophysiology of autism.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum 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=3414062

Detection of large-scale variation in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Large-scale copy number polymorphism in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Mutagenic insertion and chromosome engineering resource (MICER).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Radiation-induced genomic instability and its implications for radiation carcinogenesis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum 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=3414062

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Characteristics of two cases with dup(15)(q11.2-q12): one of maternal and one of paternal origin

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Prader-Willi and Angelman syndromes: sister imprinted 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=3414062

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

The 22q11 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=3414062

Embryonic lethality and tumorigenesis caused by segmental aneuploidy on mouse chromosome 11.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Autism in Angelman syndrome: a population-based study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Autism associated with marker chromosome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Target frequency and integration pattern for insertion and replacement vectors in embryonic stem 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=3414062

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

A genetic screen for novel behavioral mutations in mice.

6 July 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Angelman syndrome 2005: updated consensus for diagnostic criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Autism in Angelman syndrome: implications for autism research.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Autism and maternally derived aberrations of chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Children and adolescents with velocardiofacial syndrome: a volumetric MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F589524

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3414062

Engineering a mouse balancer chromosome

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22900207

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Two new balancer chromosomes on mouse chromosome 4 to facilitate functional annotation of human chromosome 1p

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22900207

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22900207

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1155/2012/589524

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

PubMed publication ID

22900207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22900207%20AND%20SRC:MED&resulttype=core&format=json