(Q34974394)

5 August 2017

1 reference

title

Genetics of autism spectrum disorders. (English)

1 reference

5 August 2017

main subject

autism spectrum disorder

0 references

autism

0 references

author name string

Ravinesh A Kumar

series ordinal

1

1 reference

5 August 2017

Susan L Christian

series ordinal

2

1 reference

5 August 2017

publication date

1 May 2009

1 reference

Current Neurology and Neuroscience Reports

5 August 2017

published in

1 reference

5 August 2017

volume

9

1 reference

5 August 2017

issue

3

1 reference

5 August 2017

page(s)

188-197

1 reference

https://scigraph.springernature.com/pub.10.1007/s11910-009-0029-2

5 August 2017

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-009-0029-2

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

12 December 2020

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

1 reference

12 December 2020

Disruption of neurexin 1 associated with autism spectrum disorder

1 reference

12 December 2020

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

1 reference

12 December 2020

Autism as a paradigmatic complex genetic disorder

1 reference

12 December 2020

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

12 December 2020

Strong association of de novo copy number mutations with autism

1 reference

12 December 2020

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

Autism and Metabolic Diseases

1 reference

12 December 2020

The genetics of autistic disorders and its clinical relevance: a review of the literature

1 reference

12 December 2020

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

12 December 2020

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

1 reference

12 December 2020

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene

1 reference

12 December 2020

Epidemiology of autistic disorder and other pervasive developmental disorders

1 reference

12 December 2020

Structural variation of chromosomes in autism spectrum disorder

1 reference

12 December 2020

Chromosome 2q37 deletion: clinical and molecular aspects

1 reference

12 December 2020

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

1 reference

12 December 2020

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

12 December 2020

The neurobiology of autism

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

1 reference

12 December 2020

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

1 reference

12 December 2020

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

1 reference

12 December 2020

Reelin signaling is impaired in autism

1 reference

12 December 2020

Xp deletions associated with autism in three females.

1 reference

12 December 2020

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Autism spectrum disorders: developmental disconnection syndromes

1 reference

12 December 2020

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.

1 reference

12 December 2020

Contribution of SHANK3 mutations to autism spectrum disorder

1 reference

12 December 2020

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

1 reference

12 December 2020

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

1 reference

12 December 2020

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

1 reference

12 December 2020

A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence

1 reference

12 December 2020

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

12 December 2020

Childhood autism and associated comorbidities

1 reference

12 December 2020

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

1 reference

12 December 2020

MeCP2 dysfunction in Rett syndrome and related disorders

1 reference

12 December 2020

Recurrent 16p11.2 microdeletions in autism

1 reference

12 December 2020

Deletion 22q11: spectrum of associated disorders

1 reference

12 December 2020

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

12 December 2020

10.1007/S11910-009-0029-2

Identifiers

DOI

1 reference

Dimensions Publication ID

5 August 2017

1033404346

0 references

1 reference