(Q35054670)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

Gene expression analysis in lymphoblasts derived from patients with autism spectrum disorder (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

main subject

autism spectrum disorder

0 references

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Kazutaka Ohi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

author name string

Yuka Yasuda

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Hidenaga Yamamori

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Motoyuki Fukumoto

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Satomi Umeda-Yano

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Ikuko Mohri

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Akira Ito

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Masako Taniike

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Masatoshi Takeda

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

publication date

26 May 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1186/2040-2392-2-9

2 February 2020

exact match

0 references

cites work

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Conserved role of intragenic DNA methylation in regulating alternative promoters

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific Pten knock-out mice

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Autism and brain development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Identifying autism loci and genes by tracing recent shared ancestry

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Neurexin 1alpha structural variants associated with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Familial deletion within NLGN4 associated with autism and Tourette syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Disruption of neurexin 1 associated with autism spectrum disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Contribution of SHANK3 mutations to autism spectrum disorder

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

The story of Rett syndrome: from clinic to neurobiology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

More than just synaptic building blocks: scaffolding proteins of the post-synaptic density regulate dendritic patterning

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Neurexin-neuroligin signaling in synapse development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Neuroligins and neurexins: linking cell adhesion, synapse formation and cognitive function

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

The Autism-Spectrum Quotient (AQ) Japanese version: evidence from high-functioning clinical group and normal adults

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Four Na+/H+ exchanger isoforms are distributed to Golgi and post-Golgi compartments and are involved in organelle pH regulation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Molecular characterization of bipolar disorder by comparing gene expression profiles of postmortem brains of major mental disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Rett syndrome: the complex nature of a monogenic disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

X chromosome inactivation and X-linked mental retardation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

Integrative analysis of the cancer transcriptome

8 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

Emotional distress and its correlates among parents of children with pervasive developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

Association study of KIBRA gene with memory performance in a Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

The impact of a genome-wide supported psychosis variant in the ZNF804A gene on memory function in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

Expression analysis of neuregulin-1 in the dorsolateral prefrontal cortex in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

Effect of antipsychotic drugs on DISC1 and dysbindin expression in mouse frontal cortex and hippocampus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

DNA methylation regulates tissue-specific expression of Shank3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

Heterogeneous dysregulation of microRNAs across the autism spectrum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F2040-2392-2-9

BDNF-Akt-Bcl2 antiapoptotic signaling pathway is compromised in the brain of autistic subjects.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3118341

25 October 2018

Identifiers

DOI

10.1186/2040-2392-2-9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

2 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21615902%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference