(Q35688051)

9 August 2017

title

Autism candidate genes via mouse phenomics (English)

1 reference

9 August 2017

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Jeremy J Jay

3

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Terrence F Meehan

object named as

Terrence F Meehan

1

0 references

Judith A. Blake

object named as

Judith A Blake

6

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Carol J Bult

4

object named as

Carol J Bult

1 reference

9 August 2017

Christopher J Carr

2

1 reference

9 August 2017

Elissa J Chesler

5

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9 August 2017

publication date

21 March 2011

1 reference

Journal of Biomedical Informatics

9 August 2017

published in

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9 August 2017

volume

44 Suppl 1

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9 August 2017

page(s)

S5-11

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Key role for gene dosage and synaptic homeostasis in autism spectrum disorders

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3263820

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

27 July 2018

1 reference

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Genetic heterogeneity in human disease

27 July 2018

1 reference

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Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain

27 July 2018

1 reference

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Systematic discovery of nonobvious human disease models through orthologous phenotypes

27 July 2018

1 reference

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Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006

27 July 2018

1 reference

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The Gene Ontology in 2010: extensions and refinements

27 July 2018

1 reference

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The Mouse Genome Database: enhancements and updates

27 July 2018

1 reference

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The Allen Brain Atlas: 5 years and beyond

27 July 2018

1 reference

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Ontological Discovery Environment: a system for integrating gene-phenotype associations.

27 July 2018

1 reference

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Genetics of autism spectrum disorders.

27 July 2018

1 reference

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A genomewide functional network for the laboratory mouse

27 July 2018

1 reference

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

27 July 2018

1 reference

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Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder

27 July 2018

1 reference

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27 July 2018

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Behavioral phenotyping of mouse models of neurodevelopmental disorders: relevant social behavior patterns across the life span.

27 July 2018

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27 July 2018

The genetics of autism

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27 July 2018

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The mammalian phenotype ontology: enabling robust annotation and comparative analysis

27 July 2018

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25 September 2018

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

25 September 2018

1 reference

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

25 September 2018

1 reference

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Overlapping probabilities of top ranking gene lists, hypergeometric distribution, and stringency of gene selection criterion.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3263820

Automated apparatus for quantitation of social approach behaviors in mice.

25 September 2018

1 reference

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GO::TermFinder--open source software for accessing Gene Ontology information and finding significantly enriched Gene Ontology terms associated with a list of genes

25 September 2018

1 reference

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10.1016/J.JBI.2011.03.003

25 September 2018

Identifiers

DOI

1 reference

journals/jbi/MeehanCJBCB11

9 August 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

9 August 2017

1 reference