(Q34731122)

25494366

4 August 2017

title

Transcriptome analysis reveals dysregulation of innate immune response genes and neuronal activity-dependent genes in autism (English)

1 reference

4 August 2017

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2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Andrew B. West

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

author name string

Simone Gupta

1

1 reference

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11 June 2020

Foram N Ashar

3

1 reference

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11 June 2020

Anna Moes

4

1 reference

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11 June 2020

Joel S Bader

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Jianan Zhan

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Dan E Arking

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

language of work or name

English

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publication date

10 December 2014

1 reference

25494366

4 August 2017

published in

Nature Communications

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11 June 2020

volume

5

1 reference

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11 June 2020

page(s)

5748

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

11 June 2020

copyright license

start time

1 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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7 July 2018

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7 July 2018

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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

7 July 2018

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7 July 2018

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

7 July 2018

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The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies

7 July 2018

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7 July 2018

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M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination

7 July 2018

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TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions

7 July 2018

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Microglia regulate the number of neural precursor cells in the developing cerebral cortex

7 July 2018

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Using whole-exome sequencing to identify inherited causes of autism

7 July 2018

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An integrated map of genetic variation from 1,092 human genomes

7 July 2018

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Macrophage plasticity and polarization in tissue repair and remodelling

7 July 2018

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Systematic localization of common disease-associated variation in regulatory DNA

7 July 2018

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Detecting differential usage of exons from RNA-seq data

7 July 2018

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Microglia sculpt postnatal neural circuits in an activity and complement-dependent manner

7 July 2018

1 reference

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De Novo Gene Disruptions in Children on the Autistic Spectrum

7 July 2018

1 reference

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Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

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

7 July 2018

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Wild-type microglia arrest pathology in a mouse model of Rett syndrome

7 July 2018

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

7 July 2018

1 reference

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Removing technical variability in RNA-seq data using conditional quantile normalization

7 July 2018

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GC-content normalization for RNA-Seq data

7 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=4270294

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

7 July 2018

1 reference

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Maternal infection and immune involvement in autism

7 July 2018

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7 July 2018

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Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

7 July 2018

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Divergence of human and mouse brain transcriptome highlights Alzheimer disease pathways

7 July 2018

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Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

7 July 2018

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7 July 2018

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A genome-wide linkage and association scan reveals novel loci for autism

7 July 2018

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Gene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: altered pathways in neuronal development and steroid biosynthesis

7 July 2018

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Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.

7 July 2018

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TopHat: discovering splice junctions with RNA-Seq

7 July 2018

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7 July 2018

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A systems level analysis of transcriptional changes in Alzheimer's disease and normal aging

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Mapping Early Brain Development in Autism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Utilization of lymphoblastoid cell lines as a system for the molecular modeling of autism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Gene expression profiling of lymphoblastoid cell lines from monozygotic twins discordant in severity of autism reveals differential regulation of neurologically relevant genes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Neurons produce type I interferon during viral encephalitis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

BDNF from microglia causes the shift in neuronal anion gradient underlying neuropathic pain

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

Heritable and nonheritable risk factors for autism spectrum disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4270294

GeneMerge—post-genomic analysis, data mining, and hypothesis testing

7 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=4270294

Familial recurrence of autism spectrum disorder: evaluating genetic and environmental contributions.

7 July 2018

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https://api.crossref.org/works/10.1038%2FNCOMMS6748

A common variant on chromosome 11q13 is associated with atopic dermatitis.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNCOMMS6748

Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6748

Abnormal microglial-neuronal spatial organization in the dorsolateral prefrontal cortex in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6748

Cutadapt removes adapter sequences from high-throughput sequencing reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6748

Independent surrogate variable analysis to deconvolve confounding factors in large-scale microarray profiling studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6748

Profiling of genes associated with transcriptional responses in mouse hippocampus after transient forebrain ischemia using high-density oligonucleotide DNA array.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6748

21 January 2018

Identifiers

DOI

10.1038/NCOMMS6748

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 June 2020

ADS bibcode

2014NatCo...5.5748G

0 references

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

25494366

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25494366%20AND%20SRC:MED&resulttype=core&format=json