Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan (Q50304368)

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scientific article published on 25 March 2006

Language	Label	Description	Also known as
English	Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan	scientific article published on 25 March 2006

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

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

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

1 reference

based on heuristic

inferred from title

pervasive developmental disorder

0 references

author name string

Satoshi Sumi

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

Hiroko Taniai

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

Taishi Miyachi

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

Mitsuyo Tanemura

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

publication date

25 March 2006

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

51

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

518-522

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

Concordance for the syndrome of autism in 40 pairs of afflicted twins

1 reference

https://api.crossref.org/works/10.1007%2FS10038-006-0392-7

21 January 2018

The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling

1 reference

https://api.crossref.org/works/10.1007%2FS10038-006-0392-7

21 January 2018

A risk-factor model of epistatic interaction, focusing on autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

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Molecular genetics of autism spectrum disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

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Genetics of common disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

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A case-control study of obstetric complications and later autistic disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

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No effect of MMR withdrawal on the incidence of autism: a total population study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

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The incidence of cognitive disabilities in the siblings of autistic children

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

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Psychiatric symptoms and disorders in adolescents with low birth weight

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pervasive Developmental Disorders in Preschool Children

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial heterogeneity in infantile autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood autism spectrum disorder in the Barwon region: a community based study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16565880

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-006-0392-7

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/16565880

ResearchGate publication ID

0 references

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