Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24535727)
Watch
English
Heterogeneity and the genetics of autism
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Heterogeneity and the genetics of autism
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
main subject
autism
0 references
heterogeneity
1 reference
based on heuristic
inferred from title
author name string
Szatmari P
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
language of work or name
English
0 references
publication date
1 March 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
published in
Journal of Psychiatry & Neuroscience
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
volume
24
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
page(s)
159-165
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
cites work
Broader autism phenotype: evidence from a family history study of multiple-incidence autism 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=1188998
retrieved
24 March 2017
A broader phenotype of autism: the clinical spectrum in twins
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=1188998
retrieved
24 March 2017
The epidemiology of Asperger syndrome. A total population study
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=1188998
retrieved
24 March 2017
A case-control family history study 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=1188998
retrieved
24 March 2017
Autism as a strongly genetic disorder: evidence from a British twin study
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=1188998
retrieved
24 March 2017
Concordance for the syndrome of autism in 40 pairs of afflicted twins
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=1188998
retrieved
24 March 2017
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
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=1188998
retrieved
24 March 2017
Infantile autism: a genetic study of 21 twin pairs
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=1188998
retrieved
24 March 2017
The future of genetic studies of complex human diseases
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=1188998
retrieved
7 April 2017
Brief report: genetic, prenatal, and immunologic factors
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=1188998
retrieved
27 September 2017
Sex differences in higher functioning people 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=1188998
retrieved
27 September 2017
Genotype relative risks: methods for design and analysis of candidate-gene association studies
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=1188998
retrieved
27 September 2017
Autism and known medical conditions: myth and substance
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=1188998
retrieved
27 September 2017
Sex differences in 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=1188998
retrieved
27 September 2017
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium.
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=1188998
retrieved
27 September 2017
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study 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=1188998
retrieved
27 September 2017
Genetic linkage and complex diseases, with special reference to psychiatric 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=1188998
retrieved
27 September 2017
Complex segregation analysis 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=1188998
retrieved
27 September 2017
Childhood disintegrative disorder: issues for DSM-IV
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=1188998
retrieved
27 September 2017
The validity of autistic spectrum disorders: a literature review
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=1188998
retrieved
27 September 2017
Is Rett syndrome a subtype of 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=1188998
retrieved
27 September 2017
The genetics, if any, of infantile autism and childhood schizophrenia
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=1188998
retrieved
27 September 2017
Genetics of manic depressive illness
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=1188998
retrieved
27 September 2017
Serotonin transporter (5-HTT) gene variants 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=1188998
retrieved
30 May 2018
Evidence of linkage between the serotonin transporter and 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=1188998
retrieved
30 May 2018
Genetics of autism: characteristics of affected and unaffected children from 37 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=1188998
retrieved
30 May 2018
The development of sex differences in 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=1188998
retrieved
30 May 2018
Differences in sex ratios in autism as a function of measured intelligence.
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=1188998
retrieved
30 May 2018
Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective 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=1188998
retrieved
30 May 2018
Obstetrical suboptimality in autistic children.
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=1188998
retrieved
30 May 2018
The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling.
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=1188998
retrieved
30 May 2018
Siblings and parents of children with autism: a controlled population-based study
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=1188998
retrieved
30 May 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=1188998
retrieved
29 November 2018
Parents and collateral relatives of children with pervasive developmental disorders: a family history study.
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=1188998
retrieved
29 November 2018
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous 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=1188998
retrieved
29 November 2018
The molecular genetics of schizophrenia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10212560
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1188998
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
PubMed ID
10212560
1 reference
stated in
Europe PubMed Central
PubMed ID
10212560
retrieved
4 July 2017
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