(Q35215915)

English

Autism-associated gene expression in peripheral leucocytes commonly observed between subjects with autism and healthy women having autistic children

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

7 August 2017

Autism-associated gene expression in peripheral leucocytes commonly observed between subjects with autism and healthy women having autistic children (English)

1 reference

Europe PubMed Central

7 August 2017

0 references

1 reference

based on heuristic

inferred from title

object named as

Tomoko Kawai

3

0 references

author name string

Yuki Kuwano

1

1 reference

Europe PubMed Central

7 August 2017

Yoko Kamio

2

1 reference

Europe PubMed Central

7 August 2017

Sakurako Katsuura

4

1 reference

Europe PubMed Central

7 August 2017

Naoko Inada

5

1 reference

Europe PubMed Central

7 August 2017

Akiko Takaki

6

1 reference

Europe PubMed Central

7 August 2017

Kazuhito Rokutan

7

1 reference

Europe PubMed Central

7 August 2017

language of work or name

0 references

publication date

15 September 2011

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

6

1 reference

Europe PubMed Central

7 August 2017

9

1 reference

Europe PubMed Central

7 August 2017

e24723

1 reference

Europe PubMed Central

7 August 2017

copyright license

Creative Commons Attribution 4.0 International

15 September 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Autism and increased paternal age related changes in global levels of gene expression regulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

The role of MeCP2 in brain development and neurodevelopmental disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Genetic advances in autism: heterogeneity and convergence on shared pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Synthesis and function of ribosomal proteins--fading models and new perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Ribosomes in axons--scrounging from the neighbors?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Whole genome microarray analysis of gene expression in subjects with fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

A genetic variant that disrupts MET transcription is associated with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Autism as a disorder of neural information processing: directions for research and targets for therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Identification of MeCP2 mutations in a series of females with autistic disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Linkage and association of the glutamate receptor 6 gene with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

The autism-spectrum quotient (AQ): evidence from Asperger syndrome/high-functioning autism, males and females, scientists and mathematicians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

The genetics of autism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

A case-control family history study of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Autism as a strongly genetic disorder: evidence from a British twin study

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Physical linkage of the genes for platelet membrane glycoproteins IIb and IIIa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Genetic influences and infantile autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

13 July 2018

Autism: the phenotype in relatives.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Evidence supporting WNT2 as an autism susceptibility gene.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Automatic processing of emotional faces in high-functioning pervasive developmental disorders: An affective priming study.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Autism-Spectrum Quotient-Japanese version and its short forms for screening normally intelligent persons with pervasive developmental disorders.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Genetics. Insights into the pathogenesis of autism.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

ITGB3 shows genetic and expression interaction with SLC6A4.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Study of MECP2 gene in Rett syndrome variants and autistic girls.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Identifying blood biomarkers for mood disorders using convergent functional genomics.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024723

21 January 2018

Identification of blood biomarkers for psychosis using convergent functional genomics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3174190

26 September 2018

Identifiers

10.1371/JOURNAL.PONE.0024723

1 reference

Europe PubMed Central

7 August 2017

2011PLoSO...624723K

0 references

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

ResearchGate publication ID

0 references

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=Q35215915&oldid=1868841897"