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Autism: Family connections
scientific article
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instance of
scholarly article
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title
Autism: Family connections
(English)
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main subject
autism
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author
Daniel Geschwind
series ordinal
1
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language of work or name
English
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publication date
14 August 2008
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published in
Nature
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volume
454
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issue
7206
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page(s)
838-9
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cites work
Identifying autism loci and genes by tracing recent shared ancestry
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=3645842
retrieved
7 April 2017
Signaling mechanisms linking neuronal activity to gene expression and plasticity of the nervous system
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3645842
retrieved
7 April 2017
Advances in autism genetics: on the threshold of a new neurobiology
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3645842
retrieved
7 April 2017
Structural variation of chromosomes in 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=3645842
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7 April 2017
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
1 reference
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PubMed Central
reference URL
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7 April 2017
Strong association of de novo copy number mutations with autism
1 reference
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PubMed Central
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7 April 2017
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3645842
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7 April 2017
Autism spectrum disorders: developmental disconnection syndromes
1 reference
stated in
PubMed Central
reference URL
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7 April 2017
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2
1 reference
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PubMed Central
reference URL
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7 April 2017
Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3645842
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7 April 2017
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3645842
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27 September 2017
Lessons from studying monogenic disease for common disease
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=3645842
retrieved
27 September 2017
Identifiers
DOI
10.1038/454838A
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Dimensions Publication ID
1011533564
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PMC publication ID
3645842
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PubMed publication ID
18704077
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ResearchGate publication ID
23171734
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