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Unraveling autism
scientific article
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Statements
instance of
scholarly article
0 references
title
Unraveling autism
(English)
0 references
main subject
autism
0 references
author name string
Dietrich A Stephan
series ordinal
1
author given names
Dietrich A
author last names
Stephan
1 reference
stated in
PubMed
PubMed ID
18179879
retrieved
7 February 2023
language of work or name
English
0 references
publication date
January 2008
0 references
published in
American Journal of Human Genetics
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volume
82
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issue
1
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page(s)
7-9
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cites work
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
Contribution of SHANK3 mutations to autism spectrum disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
19 March 2017
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
7 April 2017
The Autism Genome Project: goals and strategies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253980
retrieved
27 September 2017
Identifiers
DOI
10.1016/J.AJHG.2007.12.003
0 references
Fatcat ID
release_32kat6zddnhcxcz7c3t634smzq
0 references
PMCID
2253980
0 references
PubMed ID
18179879
0 references
ResearchGate publication ID
5670253
0 references
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