Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism (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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Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism

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

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

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Reelin gene alleles and susceptibility to autism spectrum disorders

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Evidence supporting WNT2 as an autism susceptibility gene.

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

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

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

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Neuropsychiatric disorders in the 22q11 deletion syndrome

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Human chromosome 7: DNA sequence and biology

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Analysis of reelin as a candidate gene for autism

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

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

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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

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

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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

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

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

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

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Molecular karyotyping using an SNP array for genomewide genotyping.

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

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Detection of large-scale variation in the human genome

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Large-scale copy number polymorphism in the human genome

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Presence of large deletions in kindreds with autism

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Genetic tests of biologic systems in affective disorders.

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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.

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

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

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Finishing the euchromatic sequence of the human genome

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

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Autism in thalidomide embryopathy: a population study.

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

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

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

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Position effect in human genetic disease

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Identifiers

DOI

10.1038/SJ.MP.4001757

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13 August 2017

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