(Q30358026)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

title

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

main subject

autism spectrum disorder

0 references

author

Marco Bellinzoni

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Thomas Bourgeron

36

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Thomas Rolland

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Julien Buratti

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Ryan Yuen

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Yasushi Shimoda

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Dominique Bonneau

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Marion Leboyer

31

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Stephen W. Scherer

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

Richard Delorme

34

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

author name string

O Mercati

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

G Huguet

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

A Danckaert

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

G André-Leroux

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

A Maruani

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

L Gouder

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

A Mathieu

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

F Amsellem

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

M Benabou

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

J Van-Gils

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

A Beggiato

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

M Konyukh

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

J-P Bourgeois

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

M J Gazzellone

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

S Walker

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

M Delépine

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

A Boland

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

B Régnault

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

M Francois

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

T Van Den Abbeele

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

A L Mosca-Boidron

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

L Faivre

26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

K Watanabe

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

I Cloëz-Tayarani

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

M Rastam

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

C Gillberg

33

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

language of work or name

English

0 references

publication date

10 May 2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

page(s)

625-633

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 4.0 International

4 April 2020

copyright license

start time

10 May 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

From the genetic architecture to synaptic plasticity in autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Whole-genome sequencing of quartet families with autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

T-Brain-1--A Potential Master Regulator in Autism Spectrum Disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Heterozygous deletion of CHL1 gene: detailed array-CGH and clinical characterization of a new case and review of the literature

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

A candidate gene association study further corroborates involvement of contactin genes in autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Copy number variation in Han Chinese individuals with autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Adropin is a brain membrane-bound protein regulating physical activity via the NB-3/Notch signaling pathway in mice

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Most genetic risk for autism resides with common variation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Disentangling the heterogeneity of autism spectrum disorder through genetic findings

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Severe multisensory speech integration deficits in high-functioning school-aged children with Autism Spectrum Disorder (ASD) and their resolution during early adolescence

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

The genetic landscapes of autism spectrum disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Contactins in the neurobiology of autism.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Structure of the Repulsive Guidance Molecule (RGM)-Neogenin Signaling Hub

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Shining a light on CNTNAP2: complex functions to complex disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Contactin 4, -5 and -6 differentially regulate neuritogenesis while they display identical PTPRG binding sites.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Activity-dependent neuronal signalling and autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Expanding the Ig superfamily code for laminar specificity in retina: expression and role of contactins

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

An anatomically comprehensive atlas of the adult human brain transcriptome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Contactins: structural aspects in relation to developmental functions in brain disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Contactin 4 as an autism susceptibility locus

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Sensory processing in autism: a review of neurophysiologic findings.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

The Simons Simplex Collection: a resource for identification of autism genetic risk factors

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Neural circuit formation in the cerebellum is controlled by cell adhesion molecules of the Contactin family

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Contribution of the neural cell recognition molecule NB-3 to synapse formation between parallel fibers and Purkinje cells in mouse.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

CHARMM: the biomolecular simulation program

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Contactins: emerging key roles in the development and function of the nervous system

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Comparative protein structure modeling using Modeller

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Disruption of contactin 4 in three subjects with autism spectrum disorder

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Neural recognition molecules CHL1 and NB-3 regulate apical dendrite orientation in the neocortex via PTP alpha

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Prevalence of motor impairment in autism spectrum disorders.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Cross-talk between F3/contactin and Notch at axoglial interface: a role in oligodendrocyte development.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Annotation: What do we know about sensory dysfunction in autism? A critical review of the empirical evidence

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Speech-sound-selective auditory impairment in children with autism: they can perceive but do not attend

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Aberrant responses to acoustic stimuli in mice deficient for neural recognition molecule NB-2

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

Neurobiological findings in 20 relatively gifted children with Kanner-type autism or Asperger syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

The "autistic psychopaths" in childhood

3 June 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Peripheral auditory asymmetry in infantile autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Perception of complex sounds: abnormal pattern of cortical activation in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Autism and auditory brain stem responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Perception of complex sounds in autism: abnormal auditory cortical processing in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Auditory spatial localization and attention deficits in autistic adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Brain hyper-reactivity to auditory novel targets in children with high-functioning autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Shared and Divergent Auditory and Tactile Processing in Children with Autism and Children with Sensory Processing Dysfunction Relative to Typically Developing Peers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Impaired motor coordination in mice lacking neural recognition molecule NB-3 of the contactin/F3 subgroup

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Deficiency of neural recognition molecule NB-2 affects the development of glutamatergic auditory pathways from the ventral cochlear nucleus to the superior olivary complex in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Loss of NB-3 aggravates cerebral ischemia by impairing neuron survival and neurite growth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

NB-3/Notch1 pathway via Deltex1 promotes neural progenitor cell differentiation into oligodendrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

All humans, great or small, short or tall

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Disruption of Contactin 4 in two subjects with autism in Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

The Diagnostic Interview for Social and Communication Disorders: background, inter-rater reliability and clinical use.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Reliability and validity of a parent questionnaire on childhood motor skills.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Preferential localization of neural cell recognition molecule NB-2 in developing glutamatergic neurons in the rat auditory brainstem

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Association of Duchenne muscular dystrophy with autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

Ig superfamily cell adhesion molecules in the brain

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5378808

26 November 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

inferred from DOI database lookup

7 January 2021

based on heuristic

2-year-old boy who has been diagnosed with autism

1 reference

https://api.crossref.org/works/10.1038%2FMP.2016.61

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/MP.2016.61

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27166760%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

PubMed publication ID

27166760

1 reference