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On the twin risk in autism
scientific article
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instance of
scholarly article
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title
On the twin risk in autism
(English)
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main subject
autism
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author
Lisa A Croen
series ordinal
5
object named as
Lisa Croen
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author name string
Joachim Hallmayer
series ordinal
1
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Emma J Glasson
series ordinal
2
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Carol Bower
series ordinal
3
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Beverly Petterson
series ordinal
4
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Judith Grether
series ordinal
6
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Neil Risch
series ordinal
7
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language of work or name
English
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publication date
October 2002
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published in
American Journal of Human Genetics
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volume
71
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issue
4
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page(s)
941-6
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cites work
Excess of twins among affected sibling pairs with autism: implications for the etiology of autism
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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=378547
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7 April 2017
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions
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PubMed Central
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7 April 2017
A genomic screen of autism: evidence for a multilocus etiology
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7 April 2017
Genetics of austim: complex aetiology for a heterogeneous disorder
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7 April 2017
An autosomal genomic screen for autism. Collaborative linkage study of autism
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7 April 2017
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
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7 April 2017
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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7 April 2017
A case-control family history study of autism
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7 April 2017
Autism as a strongly genetic disorder: evidence from a British twin study
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PubMed Central
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7 April 2017
Concordance for the syndrome of autism in 40 pairs of afflicted twins
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PubMed Central
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7 April 2017
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
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PubMed Central
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7 April 2017
Infantile autism: a genetic study of 21 twin pairs
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PubMed Central
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7 April 2017
Descriptive epidemiology of autism in a California population: who is at risk?
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27 September 2017
Perinatal risk factors for infantile autism
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27 September 2017
Genetic and immunologic considerations in autism
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PubMed Central
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27 September 2017
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
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PubMed Central
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27 September 2017
A genomewide screen for autism susceptibility loci
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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=378547
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27 September 2017
Pervasive Developmental Disorders in Preschool Children
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PubMed Central
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27 September 2017
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
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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=378547
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27 September 2017
The first account of the syndrome Asperger described? Translation of a paper entitled "Die schizoiden Psychopathien im Kindesalter" by Dr. G.E. Ssucharewa; scientific assistant, which appeared in 1926 in the Monatsschrift für Psychiatrie und Neurolo
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27 September 2017
Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378547
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27 September 2017
Mapping genes in diabetes. Genetic epidemiological perspective
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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=378547
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27 September 2017
Autism and the X chromosome. Multipoint sib-pair analysis.
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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=378547
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30 May 2018
Itard's 1828 mémoire on "Mutism caused by a lesion of the intellectual functions": a historical analysis.
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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=378547
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30 May 2018
The incidence of cognitive disabilities in the siblings of autistic children.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378547
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30 May 2018
Familial heterogeneity in infantile autism.
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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=378547
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30 May 2018
The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378547
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30 May 2018
Siblings and parents of children with autism: a controlled population-based study
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378547
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30 May 2018
Increased rate of twins among affected sibling pairs 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=378547
retrieved
28 November 2018
Genomic screen and follow-up analysis for autistic 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=378547
retrieved
28 November 2018
Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex 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=378547
retrieved
28 November 2018
Genetics of autism: overview and new directions
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=378547
retrieved
28 November 2018
Lack of cognitive impairment in first-degree relatives of children with 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=378547
retrieved
28 November 2018
A population database for maternal and child health research in Western Australia using record linkage
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=378547
retrieved
28 November 2018
Implication of sex differences in the familial transmission of infantile 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=378547
retrieved
28 November 2018
Identifiers
DOI
10.1086/342990
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PMC publication ID
378547
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PubMed publication ID
12297988
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ResearchGate publication ID
11125486
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