A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort (Q33899299)

29 July 2017

title

A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort (English)

1 reference

29 July 2017

main subject

autism spectrum disorder

0 references

author name string

Jindan Yu

1

1 reference

29 July 2017

Xue He

2

1 reference

29 July 2017

Dan Yao

3

1 reference

29 July 2017

Zhongyue Li

4

1 reference

29 July 2017

Hui Li

5

1 reference

29 July 2017

Zhengyan Zhao

6

1 reference

29 July 2017

language of work or name

English

0 references

publication date

14 May 2011

1 reference

Behavioral and Brain Functions

29 July 2017

published in

1 reference

29 July 2017

volume

7

1 reference

29 July 2017

page(s)

13

1 reference

Folding anomalies of neuroligin3 caused by a mutation in the alpha/beta-hydrolase fold domain

29 July 2017

cites work

1 reference

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Genetic factors and epigenetic factors for autism: endoplasmic reticulum stress and impaired synaptic function

5 July 2018

1 reference

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Postsynaptic scaffolding molecules modulate the localization of neuroligins

5 July 2018

1 reference

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A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export

5 July 2018

1 reference

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Finding common susceptibility variants for complex disease: past, present and future

5 July 2018

1 reference

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A synaptic trek to autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Altered synchrony and connectivity in neuronal networks expressing an autism-related mutation of neuroligin 3

5 July 2018

1 reference

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Genetics of autism spectrum disorders.

5 July 2018

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

5 July 2018

1 reference

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Familial deletion within NLGN4 associated with autism and Tourette syndrome

5 July 2018

1 reference

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Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Identification and Evaluation of Children With Autism Spectrum Disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

5 July 2018

1 reference

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The role of neuronal complexes in human X-linked brain diseases

5 July 2018

1 reference

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Recent advances in the genetics of autism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Neuroligins determine synapse maturation and function

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

The developmental neurobiology of autism spectrum disorder.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

A mutation linked with autism reveals a common mechanism of endoplasmic reticulum retention for the alpha,beta-hydrolase fold protein family

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Neuroanatomic observations of the brain in autism: a review and future directions

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Evidence for sex-specific risk alleles in autism spectrum disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Haploview: analysis and visualization of LD and haplotype maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

The structure of haplotype blocks in the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

The structure and expression of the human neuroligin-3 gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Xp deletions associated with autism in three females.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Sexual differentiation of monoaminergic neurons - genetic or epigenetic?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Analysis of four neuroligin genes as candidates for autism.

5 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1744-9081-7-13

Positive association of neuroligin-4 gene with nonspecific mental retardation in the Qinba Mountains Region of China.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1744-9081-7-13

Testing association for markers on the X chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1744-9081-7-13

The contributions of sex, genotype and age to transcriptional variance in Drosophila melanogaster

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1744-9081-7-13

Neuroscience. Autism's cause may reside in abnormalities at the synapse

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

High density SNP association study of a major autism linkage region on chromosome 17.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3120659

A multivariate test of association

29 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1744-9081-7-13

21 January 2018

Identifiers

DOI

10.1186/1744-9081-7-13

1 reference

Dimensions Publication ID

29 July 2017

1045548124

0 references

Fatcat ID

release_32qcq3b2pnhsnn6prjfaayl2d4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/32qcq3b2pnhsnn6prjfaayl2d4

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3120659

1 reference

29 July 2017

1 reference