(Q30843918)

22 August 2017

Neurogenetic analysis of childhood disintegrative disorder (English)

1 reference

22 August 2017

1 reference

22

Fred R Volkmar

1 reference

22 August 2017

23

Kevin A Pelphrey

1 reference

22 August 2017

8

Brent C Vander Wyk

1 reference

22 August 2017

17

Gillian Baird

1 reference

22 August 2017

Abha R Gupta

1

1 reference

22 August 2017

Alexander Westphal

2

1 reference

22 August 2017

Daniel Y J Yang

3

1 reference

22 August 2017

Catherine A W Sullivan

4

1 reference

22 August 2017

Jeffrey Eilbott

5

1 reference

22 August 2017

Samir Zaidi

6

1 reference

22 August 2017

Avery Voos

7

1 reference

22 August 2017

Pam Ventola

9

1 reference

22 August 2017

Zainulabedin Waqar

10

1 reference

22 August 2017

Thomas V Fernandez

11

1 reference

22 August 2017

A Gulhan Ercan-Sencicek

12

1 reference

22 August 2017

Michael F Walker

13

1 reference

22 August 2017

Murim Choi

14

1 reference

22 August 2017

Allison Schneider

15

1 reference

22 August 2017

Tammy Hedderly

16

1 reference

22 August 2017

Hannah Friedman

18

1 reference

22 August 2017

Cara Cordeaux

19

1 reference

22 August 2017

Alexandra Ristow

20

1 reference

22 August 2017

Frederick Shic

21

1 reference

22 August 2017

4 April 2017

1 reference

22 August 2017

1 reference

22 August 2017

8

1 reference

22 August 2017

19

1 reference

https://scigraph.springernature.com/pub.10.1186/s13229-017-0133-0

22 August 2017

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=5379515

Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

The contribution of de novo coding mutations to autism spectrum disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Synaptic, transcriptional and chromatin genes disrupted in autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

A systematic review and meta-analysis of eye-tracking studies in children with autism spectrum disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Prioritization of neurodevelopmental disease genes by discovery of new mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Prevalence of autism spectrum disorder among children aged 8 years - autism and developmental disabilities monitoring network, 11 sites, United States, 2010

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

De novo mutations in schizophrenia implicate synaptic networks

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

The role of de novo mutations in the genetics of autism spectrum disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Attention to eyes is present but in decline in 2-6-month-old infants later diagnosed with autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

The penetrance of copy number variations for schizophrenia and developmental delay.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

De novo mutations in epileptic encephalopathies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Gaze response to dyadic bids at 2 years related to outcomes at 3 years in autism spectrum disorders: a subtyping analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

High rate of disease-related copy number variations in childhood onset schizophrenia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Prevalence and onset of regression within autism spectrum disorders: a meta-analytic review.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Revisiting regression in autism: Heller's dementia infantilis. Includes a translation of Über Dementia Infantilis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Infants deploy selective attention to the mouth of a talking face when learning speech.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Spatio-temporal transcriptome of the human brain

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

The role of the occipital face area in the cortical face perception network

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Sound before meaning: word learning in autistic disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Microdeletions of 3q29 confer high risk for schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

The NimStim set of facial expressions: judgments from untrained research participants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Epidemiology of Pervasive Developmental Disorders

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Novel isoenzyme of 2-oxoglutarate dehydrogenase is identified in brain, but not in heart

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Prevalence of childhood disintegrative disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Childhood disintegrative disorder: should it be considered a distinct diagnosis?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

The fusiform face area: a module in human extrastriate cortex specialized for face perception

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

Disintegrative disorder or "late onset" autism.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

CONSPEC and CONLERN: a two-process theory of infant face recognition

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Childhood disintegrative disorder: distinction from autistic disorder and predictors of outcome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

A comparative study of genetic and neurobiological findings in disintegrative psychosis and infantile autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Childhood disintegrative disorder: results of the DSM-IV autism field trial.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Childhood disintegrative disorder. Re-examination of the current concept.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

External validity of childhood disintegrative disorder in comparison with autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Brief report: childhood disintegrative disorder: a brief examination of eight case studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Validity of childhood disintegrative disorder apart from autistic disorder with speech loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Abnormal ventral temporal cortical activity during face discrimination among individuals with autism and Asperger syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Visual scanning of faces in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Visual fixation patterns during viewing of naturalistic social situations as predictors of social competence in individuals with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Eye-movement patterns are associated with communicative competence in autistic spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Autism: demise of the innate social orienting hypothesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Large-scale discovery of novel genetic causes of developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13229-017-0133-0

Face recognition in human extrastriate cortex.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5379515

10.1186/S13229-017-0133-0

25 November 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

22 August 2017

0 references

1 reference

22 August 2017

1 reference