(Q50306115)

2 March 2018

title

Major contribution of dominant inheritance to autism spectrum disorders (ASDs) in population-based families. (English)

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main subject

autism spectrum disorder

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autism

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author name string

Takeshi Nishiyama

1

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Morihiro Notohara

2

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Satoshi Sumi

3

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Satoshi Takami

4

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Hirohisa Kishino

5

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publication date

6 November 2009

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Journal of Human Genetics

published in

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volume

54

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issue

12

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page(s)

721-726

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https://scigraph.springernature.com/pub.10.1038/jhg.2009.105

exact match

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cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

A broader phenotype of autism: the clinical spectrum in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Genetic influences on the broad spectrum of autism: study of proband-ascertained twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

A unified genetic theory for sporadic and inherited autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Bayesian measures of model complexity and fit

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Autistic social impairment in the siblings of children with pervasive developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Phenotypic and genetic overlap between autistic traits at the extremes of the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

Stoppage rules and genetic studies of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.105

21 January 2018

Identifiers

DOI

10.1038/JHG.2009.105

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2 March 2018

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2 March 2018