(Q35031003)

5 August 2017

title

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism (English)

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5 August 2017

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14

Mary-Claire King

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Diane E. Dickel

Diane E Dickel

3

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Alex S Nord

Alex S Nord

1

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Jonathan Sebat

Jonathan Sebat

11

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Tom Walsh

Tom Walsh

4

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author name string

Wendy Roeb

2

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5 August 2017

Mary Kusenda

5

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5 August 2017

Kristen Lewis O'Connor

6

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5 August 2017

Dheeraj Malhotra

7

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5 August 2017

Shane E McCarthy

8

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5 August 2017

Sunday M Stray

9

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5 August 2017

Susan M Taylor

10

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5 August 2017

STAART Psychopharmacology Network

12

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5 August 2017

Bryan King

13

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5 August 2017

Jon M McClellan

15

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5 August 2017

publication date

30 March 2011

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European Journal of Human Genetics

5 August 2017

published in

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5 August 2017

volume

19

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5 August 2017

issue

6

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5 August 2017

page(s)

727-731

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https://scigraph.springernature.com/pub.10.1038/ejhg.2011.24

5 August 2017

exact match

0 references

cites work

Functional impact of global rare copy number variation in autism spectrum disorders

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

8 July 2018

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Lack of efficacy of citalopram in children with autism spectrum disorders and high levels of repetitive behavior: citalopram ineffective in children with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Involvement of SMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Copy-number variations associated with neuropsychiatric conditions

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Identifying autism loci and genes by tracing recent shared ancestry

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Advances in autism genetics: on the threshold of a new neurobiology

8 July 2018

1 reference

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Structural variation of chromosomes in autism spectrum disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

A comparison between screened NIMH and clinically interviewed control samples on neuroticism and extraversion

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Strong association of de novo copy number mutations with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Distinct mammalian SWI/SNF chromatin remodeling complexes with opposing roles in cell-cycle control

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

PANTHER version 6: protein sequence and function evolution data with expanded representation of biological pathways

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Detection of large-scale variation in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

Autism as a strongly genetic disorder: evidence from a British twin study

8 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110052

8 July 2018

https://api.crossref.org/works/10.1038%2FEJHG.2011.24

Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.24

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.24

Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2011.24

21 January 2018

Identifiers

DOI

10.1038/EJHG.2011.24

1 reference

Dimensions Publication ID

5 August 2017

0 references

1 reference

5 August 2017

1 reference