(Q36277199)

13 August 2017

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title

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

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13 August 2017

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Vorstman JA

1

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13 August 2017

Staal WG

2

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13 August 2017

van Daalen E

3

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13 August 2017

van Engeland H

4

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13 August 2017

Hochstenbach PF

5

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13 August 2017

Franke L

6

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13 August 2017

language of work or name

English

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publication date

1 January 2006

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13 August 2017

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13 August 2017

11

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13 August 2017

1, 18-28

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13 August 2017

1

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001757

13 August 2017

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Autism as a strongly genetic disorder: evidence from a British twin study

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A broader phenotype of autism: the clinical spectrum in twins

21 January 2018

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RETRACTED: Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children

21 January 2018

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The epidemiology of autism: a review.

21 January 2018

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A population-based study of measles, mumps, and rubella vaccination and autism

21 January 2018

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Measles, mumps, and rubella vaccination and bowel problems or developmental regression in children with autism: population study

21 January 2018

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The role of mercury in the pathogenesis of autism

21 January 2018

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Prenatal, perinatal, and neonatal factors in autism, pervasive developmental disorder-not otherwise specified, and the general population

21 January 2018

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Pregnancy and birth complications in autism and liability to the broader autism phenotype.

21 January 2018

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

21 January 2018

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A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

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Role of the serotonin transporter gene in the behavioral expression of autism

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Evidence of linkage between the serotonin transporter and autistic disorder.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Serotonin transporter (5-HTT) gene variants associated with autism?

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Evidence for an association with the serotonin transporter promoter region polymorphism and autism

21 January 2018

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Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder

21 January 2018

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Association between a GABRB3 polymorphism and autism.

21 January 2018

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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

21 January 2018

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Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

21 January 2018

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Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism

21 January 2018

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Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Analysis of the RELN gene as a genetic risk factor for autism

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Reelin gene alleles and susceptibility to autism spectrum disorders

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

21 January 2018

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Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

21 January 2018

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Evidence supporting WNT2 as an autism susceptibility gene.

21 January 2018

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Association between the FOXP2 gene and autistic disorder in Chinese population.

21 January 2018

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Neurogenomics: at the intersection of neurobiology and genome sciences

21 January 2018

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The future of genetic studies of complex human diseases

21 January 2018

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Genetic analysis of genome-wide variation in human gene expression

21 January 2018

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Chromosomal disorders and autism.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Autism as a paradigmatic complex genetic disorder

21 January 2018

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

21 January 2018

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Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

21 January 2018

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

21 January 2018

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Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Structure of chromosomal duplicons and their role in mediating human genomic disorders

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Segmental duplications: an 'expanding' role in genomic instability and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Phenotype of adults with the 22q11 deletion syndrome: A review

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Neuropsychiatric disorders in the 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Human chromosome 7: DNA sequence and biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Analysis of reelin as a candidate gene for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Molecular karyotyping using an SNP array for genomewide genotyping.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Presence of large deletions in kindreds with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Genetic tests of biologic systems in affective disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Finishing the euchromatic sequence of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Prevalence of pervasive developmental disorders in children and adolescents with mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

Autism in thalidomide embryopathy: a population study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

7 January 2021

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

7 January 2021

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

7 January 2021

Position effect in human genetic disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

7 January 2021

Autism spectrum disorders in children with physical or mental disability or both. II: Screening aspects.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001757

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001757

1 reference

13 August 2017

1 reference