(Q28274390)

1

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A Karvouni

2

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E Zintzaras

3

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T Ylisaukko-oja

4

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L Peltonen

5

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I Järvelä

Infantile autism: a genetic study of 21 twin pairs

6

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language of work or name

English

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publication date

January 2006

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published in

Molecular Psychiatry

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volume

11

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page(s)

29-36

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issue

1

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cites work

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A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

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

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The genetics of autism.

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A case-control family history study of autism

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Autism: recent molecular genetic advances

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A genomic screen of autism: evidence for a multilocus etiology

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Genetics of austim: complex aetiology for a heterogeneous disorder

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The genetics of autism

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Autism as a paradigmatic complex genetic disorder

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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

21 January 2018

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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.

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

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Genomic screen and follow-up analysis for autistic disorder.

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A genomewide screen of 345 families for autism-susceptibility loci

21 January 2018

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Genome-wide scan for loci of Asperger syndrome

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Evidence for sex-specific risk alleles in autism spectrum disorder

21 January 2018

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Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

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Replication of autism linkage: fine-mapping peak at 17q21.

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Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

21 January 2018

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Meta-analysis of genome searches

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A note on the genome scan meta-analysis statistic.

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Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis

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Reelin is a serine protease of the extracellular matrix

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Reelin and brain development

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Reelin glycoprotein: structure, biology and roles in health and disease

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Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis.

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Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSAC Autopsy Research Report.

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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

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

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Reelin gene alleles and susceptibility to autism spectrum disorders

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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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Analysis of reelin as a candidate gene for autism

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

21 January 2018

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Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

21 January 2018

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

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Replication validity of genetic association studies

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Genetic associations in large versus small studies: an empirical assessment

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FOXP2 is not a major susceptibility gene for autism or specific language impairment

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Evaluation of FOXP2 as an autism susceptibility gene

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Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

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Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

21 January 2018

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Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein family

21 January 2018

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Three autism candidate genes: a synthesis of human genetic analysis with other disciplines

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Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

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No association between the EN2 gene and autistic disorder

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Altered serotonin synthesis in the dentatothalamocortical pathway in autistic boys.

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Impairment of dentato-thalamo-cortical pathway in autistic men: language activation data from positron emission tomography

21 January 2018

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Venlafaxine in children, adolescents, and young adults with autism spectrum disorders: an open retrospective clinical report

21 January 2018

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Use of citalopram in pervasive developmental disorders

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A functional genetic variation of the serotonin (5-HT) transporter affects 5-HT1A receptor binding in humans

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Evidence of linkage between the serotonin transporter and autistic disorder.

21 January 2018

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

21 January 2018

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

21 January 2018

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Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

21 January 2018

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The neurobiology and genetics of infantile autism

21 January 2018

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7 January 2021

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001750

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.4001750

7 January 2021

Heterogeneity testing in meta-analysis of genome searches

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001750

7 January 2021

HEGESMA: genome search meta-analysis and heterogeneity testing

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001750

7 January 2021