(Q35049391)

6 August 2017

title

The discovery of integrated gene networks for autism and related disorders (English)

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6 August 2017

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3

Elhanan Borenstein

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6 August 2017

4

Evan E Eichler

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6 August 2017

Fereydoun Hormozdiari

series ordinal

1

object named as

Fereydoun Hormozdiari

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6 August 2017

2

Osnat Penn

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6 August 2017

publication date

5 November 2014

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6 August 2017

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6 August 2017

volume

25

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6 August 2017

issue

1

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6 August 2017

page(s)

142-154

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Refining analyses of copy number variation identifies specific genes associated with developmental delay

6 August 2017

cites work

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De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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De novo mutations in schizophrenia implicate synaptic networks

8 July 2018

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A de novo convergence of autism genetics and molecular neuroscience

8 July 2018

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Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism

8 July 2018

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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism

8 July 2018

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8 July 2018

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Transmission disequilibrium of small CNVs in simplex autism

8 July 2018

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Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Diverse types of genetic variation converge on functional gene networks involved in schizophrenia

8 July 2018

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

8 July 2018

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Rate of de novo mutations and the importance of father's age to disease risk

8 July 2018

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Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability

8 July 2018

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8 July 2018

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8 July 2018

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

8 July 2018

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

8 July 2018

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

8 July 2018

1 reference

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Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

8 July 2018

1 reference

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Networks of neuronal genes affected by common and rare variants in autism spectrum disorders

8 July 2018

1 reference

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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

8 July 2018

1 reference

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Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

8 July 2018

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Protein interactome reveals converging molecular pathways among autism disorders

8 July 2018

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Transcriptomic analysis of autistic brain reveals convergent molecular pathology

8 July 2018

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Subnetwork state functions define dysregulated subnetworks in cancer

8 July 2018

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8 July 2018

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8 July 2018

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Dynamic functional modules in co-expressed protein interaction networks of dilated cardiomyopathy

8 July 2018

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Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

8 July 2018

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8 July 2018

1 reference

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Identification of functional modules using network topology and high-throughput data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

How complete are current yeast and human protein-interaction networks?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

The ups and downs of Wnt signaling in prevalent neurological disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular target

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

Wnt signaling: multiple functions in neural development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

Cytoscape: a software environment for integrated models of biomolecular interaction networks

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

Discovering regulatory and signalling circuits in molecular interaction networks

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4317170

8 July 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.178855.114

Epilepsy in autism is associated with intellectual disability and gender: evidence from a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.178855.114

Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.178855.114

Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.178855.114

Protein-protein interaction networks and biology--what's the connection?

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.178855.114

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1101%2FGR.178855.114

21 January 2018

Identifiers

DOI

10.1101/GR.178855.114

1 reference

6 August 2017

1 reference

6 August 2017

1 reference