(Q38436462)

English

RNA sequencing of transformed lymphoblastoid cells from siblings discordant for autism spectrum disorders reveals transcriptomic and functional alterations: Evidence for sex-specific effects

scientific article published on 16 August 2016

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

RNA sequencing of transformed lymphoblastoid cells from siblings discordant for autism spectrum disorders reveals transcriptomic and functional alterations: Evidence for sex-specific effects (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

autism spectrum disorder

0 references

0 references

1 reference

based on heuristic

inferred from title

author name string

Daniel S Tylee

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Alfred J Espinoza

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Jonathan L Hess

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Muhammad A Tahir

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Sarah Y McCoy

5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Joshua K Rim

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Totadri Dhimal

7

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Ori S Cohen

8

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Stephen J Glatt

9

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

16 August 2016

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Autism Research

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

439-455

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Behavioral Problems and Competencies Reported by Parents of Normal and Disturbed Children Aged Four Through Sixteen

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Maternal Infection Requiring Hospitalization During Pregnancy and Autism Spectrum Disorders

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Mutations causing syndromic autism define an axis of synaptic pathophysiology

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Why are autism spectrum conditions more prevalent in males?

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The Vineland Adaptive Behavior Scales: supplementary norms for individuals with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Increased gene expression of FOXP1 in patients with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Immunological findings in autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Validation of a brief quantitative measure of autistic traits: comparison of the social responsiveness scale with the autism diagnostic interview-revised

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Altered gene expression and function of peripheral blood natural killer cells in children with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Gene and miRNA expression profiles in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Autism-related deficits via dysregulated eIF4E-dependent translational control

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Blood-based gene expression signatures of infants and toddlers with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The Autism Diagnostic Observation Schedule: revised algorithms for improved diagnostic validity

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Gene expression changes in children with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

mTOR signaling: at the crossroads of plasticity, memory and disease

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The Repetitive Behavior Scale-Revised: Independent Validation in Individuals with Autism Spectrum Disorders

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Is my network module preserved and reproducible?

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

voom: Precision weights unlock linear model analysis tools for RNA-seq read counts

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Genome-scale neurogenetics: methodology and meaning

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The Epidemiology of Autism Spectrum Disorders *

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Exome arrays capture polygenic rare variant contributions to schizophrenia.

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Analysis of whole genome biomarker expression in blood and brain

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The familial risk of autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Exaggerated translation causes synaptic and behavioural aberrations associated with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Molecular correlates of social dominance: a novel role for ependymin in aggression

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Evidence for sex-specific risk alleles in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The positive false discovery rate: a Bayesian interpretation and the q -value

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

The association and linkage of the HLA-A2 class I allele with autism

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

On the outside, looking in: a review and evaluation of the comparability of blood and brain "-omes".

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Enriching the gene set analysis of genome-wide data by incorporating directionality of gene expression and combining statistical hypotheses and methods

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

1 reference

https://api.crossref.org/works/10.1002%2FAUR.1679

21 January 2018

Identifiers

10.1002/AUR.1679

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38436462&oldid=1759668158"