(Q37235652)

19 August 2017

1 reference

title

Copy-number variations associated with autism spectrum disorder (English)

1 reference

19 August 2017

main subject

autism spectrum disorder

0 references

autism

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author name string

Hiroaki Kakinuma

series ordinal

1

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19 August 2017

Hitoshi Sato

series ordinal

2

1 reference

19 August 2017

language of work or name

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1 August 2008

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19 August 2017

1 reference

19 August 2017

volume

9

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19 August 2017

issue

8

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19 August 2017

page(s)

1143-1154

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Pharmacological Treatment Options for Autism Spectrum Disorders in Children and Adolescents

19 August 2017

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21 January 2018

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Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism.

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21 January 2018

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Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism

21 January 2018

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High frequency of neurexin 1beta signal peptide structural variants in patients with autism

21 January 2018

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Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual

21 January 2018

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Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Common deletion polymorphisms in the human genome.

21 January 2018

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

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15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

21 January 2018

1 reference

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A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.

21 January 2018

1 reference

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Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

1 reference

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Deletion of chromosome 2q37 and autism: a distinct subtype?

21 January 2018

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Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum

21 January 2018

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21 January 2018

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Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

21 January 2018

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Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

21 January 2018

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Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism

21 January 2018

1 reference

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Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

21 January 2018

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Molecular mechanisms for genomic disorders

21 January 2018

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Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.

21 January 2018

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Recurrent 16p11.2 microdeletions in autism

21 January 2018

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Xp deletions associated with autism in three females.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

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21 January 2018

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Oxytocin increases trust in humans

21 January 2018

1 reference

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The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

Disruption of neurexin 1 associated with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory

21 January 2018

1 reference

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DOC2A and DOC2B are sensors for neuronal activity with unique calcium-dependent and kinetic properties

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

Autism: highly heritable but not inherited

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

Genetic counseling in autism and pervasive developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

Recent development in pharmacogenomics: from candidate genes to genome-wide association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.2217%2F14622416.9.8.1143

10.2217/14622416.9.8.1143

21 January 2018

Identifiers

DOI

1 reference

19 August 2017

1 reference