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De novo mutation in schizophrenia
scientific article published on 26 March 2012
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
meta-analysis
0 references
title
De novo mutation in schizophrenia
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
main subject
schizophrenia
0 references
author
George Kirov
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
Michael C O'Donovan
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
Elliott Rees
object named as
Elliott Rees
series ordinal
1
0 references
author name string
Michael J Owen
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
language of work or name
English
0 references
publication date
26 March 2012
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
published in
Schizophrenia Bulletin
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
volume
38
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
page(s)
377-381
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
cites work
High frequencies of de novo CNVs in bipolar disorder and 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=3329988
retrieved
5 June 2018
Independent estimation of the frequency of rare CNVs in the UK population confirms their role in 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=3329988
retrieved
5 June 2018
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis 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=3329988
retrieved
5 June 2018
De novo rates and selection of schizophrenia-associated copy number variants
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=3329988
retrieved
5 June 2018
Exome sequencing supports a de novo mutational paradigm for 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=3329988
retrieved
5 June 2018
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=3329988
retrieved
5 June 2018
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications
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=3329988
retrieved
5 June 2018
A systematic review and meta-analysis of the fertility of patients with schizophrenia and their unaffected relatives.
1 reference
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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=3329988
retrieved
5 June 2018
Direct measure of the de novo mutation rate in autism and schizophrenia cohorts
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=3329988
retrieved
5 June 2018
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for 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=3329988
retrieved
5 June 2018
Rate, molecular spectrum, and consequences of human mutation
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=3329988
retrieved
5 June 2018
Narrowing the boundaries of the genetic architecture of schizophrenia.
1 reference
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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=3329988
retrieved
5 June 2018
Neurexin 1 (NRXN1) deletions in schizophrenia
1 reference
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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=3329988
retrieved
5 June 2018
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
1 reference
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PubMed Central
reference URL
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retrieved
5 June 2018
Rare chromosomal deletions and duplications increase risk 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=3329988
retrieved
5 June 2018
Strong association of de novo copy number mutations with sporadic 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=3329988
retrieved
5 June 2018
Genomic rearrangements and sporadic disease
1 reference
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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=3329988
retrieved
5 June 2018
Most rare missense alleles are deleterious in humans: implications for complex disease and association studies
1 reference
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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=3329988
retrieved
5 June 2018
Resolving the paradox of common, harmful, heritable mental disorders: which evolutionary genetic models work best?
1 reference
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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=3329988
retrieved
5 June 2018
Paternal age and sporadic schizophrenia: evidence for 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=3329988
retrieved
5 June 2018
A de novo paradigm for mental retardation.
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=3329988
retrieved
18 August 2018
Reproductive patterns in psychotic patients.
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=3329988
retrieved
18 August 2018
Increased exonic de novo mutation rate in individuals with schizophrenia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22451492
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/SCHBUL/SBS047
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
PMCID
3329988
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
PubMed ID
22451492
1 reference
stated in
Europe PubMed Central
PMCID
3329988
retrieved
13 October 2017
ResearchGate publication ID
221982958
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