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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study (Q28140978)

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scientific article (publication date: May 1999)

Genome-Wide Scan for Autism Susceptibility Genes

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English	Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study	scientific article (publication date: May 1999)	Genome-Wide Scan for Autism Susceptibility Genes

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4 December 2019

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

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4 December 2019

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Harald Aschauer

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M Guilloud-Bataille

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M Råstam

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E Sponheim

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M Coleman

7

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M Zappella

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L Van Maldergem

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C Penet

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4 December 2019

J Feingold

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C Gillberg

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A Brice

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publication date

1 May 1999

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22 April 2017

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4 December 2019

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Human Molecular Genetics

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22 April 2017

Europe PubMed Central

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4 December 2019

8

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22 April 2017

Europe PubMed Central

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4 December 2019

5

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22 April 2017

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4 December 2019

805-812

2 references

DOI.org query endpoint

https://doi.org/10.1093%2FHMG%2F8.5.805

22 April 2017

Europe PubMed Central

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4 December 2019

The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases

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https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

A case-control family history study of autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Linkage-Disequilibrium Mapping of Autistic Disorder, with 15q11-13 Markers

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Evidence of linkage between the serotonin transporter and autistic disorder

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

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

1 reference

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21 January 2018

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/10.1093%2FHMG%2F8.5.805

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Genomic Variation and Gene Conversion in Spinal Muscular Atrophy: Implications for Disease Process and Clinical Phenotype

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Maternal origin of inv dup(15) chromosomes in infantile autism

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

Suggestive Evidence for a Schizophrenia Susceptibility Locus on Chromosome 6q and a Confirmation in an Independent Series of Pedigrees

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.5.805

21 January 2018

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

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21 January 2018

Identifiers

10.1093/HMG/8.5.805

3 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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22 April 2017

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4 December 2019

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1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10196369%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

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