Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24684315)
Watch
English
A unified genetic theory for sporadic and inherited autism
scientific article
In more languages
edit
Statements
instance of
scholarly article
0 references
title
A unified genetic theory for sporadic and inherited autism
(English)
0 references
main subject
autism
0 references
author
Michael Wigler
series ordinal
12
0 references
Daniel Geschwind
series ordinal
5
0 references
Jonathan Sebat
object named as
Jonathan Sebat
series ordinal
10
0 references
Catherine Lord
series ordinal
9
object named as
Catherine Lord
0 references
author name string
Xiaoyue Zhao
series ordinal
1
0 references
Anthony Leotta
series ordinal
2
0 references
Vlad Kustanovich
series ordinal
3
0 references
Clara Lajonchere
series ordinal
4
0 references
Kiely Law
series ordinal
6
0 references
Paul Law
series ordinal
7
0 references
Shanping Qiu
series ordinal
8
0 references
Kenny Ye
series ordinal
11
0 references
language of work or name
English
0 references
publication date
31 July 2007
0 references
published in
Proceedings of the National Academy of Sciences of the United States of America
0 references
volume
104
0 references
issue
31
0 references
page(s)
12831-6
0 references
cites work
Strong association of de novo copy number mutations 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=1933261
retrieved
7 April 2017
A genomewide screen of 345 families for autism-susceptibility loci
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=1933261
retrieved
7 April 2017
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27
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=1933261
retrieved
7 April 2017
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions
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=1933261
retrieved
7 April 2017
A genomic screen of autism: evidence for a multilocus etiology
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=1933261
retrieved
7 April 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 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=1933261
retrieved
7 April 2017
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
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=1933261
retrieved
7 April 2017
Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental 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=1933261
retrieved
7 April 2017
Genomic rearrangements and gene copy-number alterations as a cause of nervous system 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=1933261
retrieved
7 April 2017
Advancing paternal age and 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=1933261
retrieved
7 April 2017
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families
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=1933261
retrieved
7 April 2017
Identification and characterization of the tuberous sclerosis gene on chromosome 16
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=1933261
retrieved
7 April 2017
Autism as a strongly genetic disorder: evidence from a British twin study
2 references
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=1933261
retrieved
7 April 2017
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073/PNAS.0705803104
retrieved
22 April 2017
Autism diagnostic observation schedule: a standardized observation of communicative and social behavior
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=1933261
retrieved
7 April 2017
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
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=1933261
retrieved
7 April 2017
Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, 14 sites, United States, 2002.
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=1933261
retrieved
28 September 2017
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic 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=1933261
retrieved
28 September 2017
Sex differences in the brain: implications for explaining 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=1933261
retrieved
28 September 2017
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities 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=1933261
retrieved
28 September 2017
X-linked genes and mental functioning
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=1933261
retrieved
28 September 2017
Molecular genetics of 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=1933261
retrieved
28 September 2017
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
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=1933261
retrieved
28 September 2017
A genomewide screen for autism susceptibility loci
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=1933261
retrieved
28 September 2017
Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism
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=1933261
retrieved
28 September 2017
Fragile X genotype characterized by an unstable region of DNA.
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=1933261
retrieved
30 May 2018
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
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=1933261
retrieved
30 May 2018
Trend analysis of the sex ratio at birth in the United States.
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=1933261
retrieved
28 November 2018
Identifiers
DOI
10.1073/PNAS.0705803104
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1041725
ADS bibcode
2007PNAS..10412831Z
0 references
OpenCitations bibliographic resource ID
1041725
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1041725
PMC publication ID
1933261
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1041725
PubMed publication ID
17652511
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1041725
ResearchGate publication ID
6185317
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
