Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q36729643)
Watch
English
Understanding sex bias in autism spectrum disorder
scientific article published on 8 March 2013
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
title
Understanding sex bias in autism spectrum disorder
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
main subject
autism spectrum disorder
0 references
autism
0 references
bias
1 reference
based on heuristic
inferred from title
gender bias
1 reference
based on heuristic
inferred from title
author
Donna Werling
series ordinal
1
object named as
Donna M Werling
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
Daniel Geschwind
series ordinal
2
object named as
Daniel H Geschwind
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
language of work or name
English
0 references
publication date
8 March 2013
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
volume
110
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
issue
13
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
page(s)
4868-4869
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
cites work
Examining and interpreting the female protective effect against autistic 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=3612630
retrieved
30 September 2017
Common genetic variants, acting additively, are a major source of risk for 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=3612630
retrieved
30 September 2017
De Novo Gene Disruptions in Children on the Autistic Spectrum
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=3612630
retrieved
30 September 2017
An evaluation of the role and treatment of elevated male hormones 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=3612630
retrieved
30 September 2017
Patterns and rates of exonic de novo mutations 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=3612630
retrieved
30 September 2017
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
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=3612630
retrieved
30 September 2017
De novo mutations revealed by whole-exome sequencing are strongly 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=3612630
retrieved
30 September 2017
Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%)
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=3612630
retrieved
30 September 2017
Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium 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=3612630
retrieved
30 September 2017
Genetic Heritability and Shared Environmental Factors Among Twin 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=3612630
retrieved
30 September 2017
Rare De Novo and Transmitted Copy-Number Variation in Autistic 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=3612630
retrieved
30 September 2017
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly 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=3612630
retrieved
30 September 2017
Sibling recurrence and the genetic epidemiology 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=3612630
retrieved
30 September 2017
Lack of evidence for increased genetic loading for autism among families of affected females: a replication from family history data in two large samples
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=3612630
retrieved
30 September 2017
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=3612630
retrieved
30 September 2017
The extreme male brain theory 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=3612630
retrieved
30 September 2017
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=3612630
retrieved
30 September 2017
Sex differences in children with autism spectrum disorder identified within a high-risk infant cohort.
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=3612630
retrieved
5 September 2018
Identifiers
DOI
10.1073/PNAS.1301602110
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
ADS bibcode
2013PNAS..110.4868W
0 references
PMCID
3612630
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 2017
PubMed ID
23476067
1 reference
stated in
Europe PubMed Central
PMCID
3612630
retrieved
15 August 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