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English
Parental origin, DNA structure, and the schizophrenia spectrum
scientific article published on April 2011
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
editorial
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title
Parental origin, DNA structure, and the schizophrenia spectrum
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
main subject
schizophrenia
1 reference
based on heuristic
inferred from title
author name string
Anne S Bassett
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
language of work or name
English
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publication date
1 April 2011
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stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
number of pages
4
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based on heuristic
inferred from page(s)
published in
American Journal of Psychiatry
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
volume
168
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
page(s)
350-353
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
cites work
Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic 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=3276592
retrieved
27 May 2018
Rethinking 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=3276592
retrieved
27 May 2018
Clinically detectable copy number variations in a Canadian catchment population of 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=3276592
retrieved
27 May 2018
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
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=3276592
retrieved
27 May 2018
Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and 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=3276592
retrieved
27 May 2018
Maternal transmission of a rare GABRB3 signal peptide variant is 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=3276592
retrieved
27 May 2018
The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
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=3276592
retrieved
27 May 2018
Schizophrenia and 22q11.2 deletion 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=3276592
retrieved
27 May 2018
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation 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=3276592
retrieved
27 May 2018
Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes
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=3276592
retrieved
27 May 2018
Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism 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=3276592
retrieved
27 May 2018
The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment.
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=3276592
retrieved
16 August 2018
Identifiers
DOI
10.1176/APPI.AJP.2011.11010173
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
PMCID
3276592
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
PubMed ID
21474594
1 reference
stated in
Europe PubMed Central
PMCID
3276592
retrieved
4 November 2017
ResearchGate publication ID
51033871
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