(Q50308058)

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Allelic expression analysis in the brain suggests a role for heterogeneous insults affecting epigenetic processes in autism spectrum disorders.

scientific article published on 21 March 2014

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

Allelic expression analysis in the brain suggests a role for heterogeneous insults affecting epigenetic processes in autism spectrum disorders. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

autism spectrum disorder

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3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

object named as

Eyal Ben-David

1

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author name string

Shahar Shohat

2

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

publication date

21 March 2014

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

Human Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

23

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

15

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

4111-4124

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

De Novo Gene Disruptions in Children on the Autistic Spectrum

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Neuroanatomy of autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

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

1 reference

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21 January 2018

High-resolution analysis of parent-of-origin allelic expression in the mouse brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Sex-specific parent-of-origin allelic expression in the mouse brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Physiological functions of imprinted genes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

X-inactivation and human disease: X-linked dominant male-lethal disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Brief report: non-random X chromosome inactivation in females with autism.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Analysis of X chromosome inactivation in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Epigenetics: monoallelic expression in the immune system.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Allelic inactivation regulates olfactory receptor gene expression

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Monoallelic yet combinatorial expression of variable exons of the protocadherin-alpha gene cluster in single neurons.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Widespread monoallelic expression on human autosomes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Stochastic choice of allelic expression in human neural stem cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Effects of cis-regulatory variation differ across regions of the adult human brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

A genotype resource for postmortem brain samples from the Autism Tissue Program

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Autosomal monoallelic expression in the mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

The pseudoautosomal regions, SHOX and disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

A novel variant of Inpp5f is imprinted in brain, and its expression is correlated with differential methylation of an internal CpG island

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

A genome-wide approach to identifying novel-imprinted genes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Angelman Syndrome, a Genomic Imprinting Disorder of the Brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

The new neurobiology of autism: cortex, connectivity, and neuronal organization

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Intrinsic gray-matter connectivity of the brain in adults with autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

ggbio: an R package for extending the grammar of graphics for genomic data

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Survey of allelic expression using EST mining

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

SHRiMP2: sensitive yet practical SHort Read Mapping

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https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

lumi: a pipeline for processing Illumina microarray

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

GO-Elite: a flexible solution for pathway and ontology over-representation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Patterns of X chromosome inactivation in the Rett syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU128

21 January 2018

Identifiers

10.1093/HMG/DDU128

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/24659497

ResearchGate publication ID

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