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The penetrance of copy number variations for schizophrenia and developmental delay.
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
title
The penetrance of copy number variations for schizophrenia and developmental delay
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
main subject
schizophrenia
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author
George Kirov
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Michael C O'Donovan
series ordinal
12
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Elliott Rees
series ordinal
2
1 reference
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Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
James Walters
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Valentina Escott-Price
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Sophie E Legge
series ordinal
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Jennifer L. Moran
series ordinal
10
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
author name string
Lyudmila Georgieva
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Alexander L Richards
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Kimberly D Chambert
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Gerwyn Davies
series ordinal
8
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Steven A McCarroll
series ordinal
11
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
Michael J Owen
series ordinal
13
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
language of work or name
English
0 references
publication date
28 August 2013
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
published in
Biological Psychiatry
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
volume
75
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
issue
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
page(s)
378-385
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
cites work
Estimates of penetrance for recurrent pathogenic copy-number variations
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=4229045
retrieved
7 July 2018
Phenotypic heterogeneity of genomic disorders and rare 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=4229045
retrieved
7 July 2018
CNVs: harbingers of a rare variant revolution in psychiatric genetics
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=4229045
retrieved
7 July 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=4229045
retrieved
7 July 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=4229045
retrieved
7 July 2018
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
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=4229045
retrieved
7 July 2018
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
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=4229045
retrieved
7 July 2018
Neurexin 1 (NRXN1) deletions 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=4229045
retrieved
7 July 2018
Prevalence of autism-spectrum conditions: UK school-based population study
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=4229045
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7 July 2018
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
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=4229045
retrieved
7 July 2018
Disruption of the neurexin 1 gene is associated with 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=4229045
retrieved
7 July 2018
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
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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=4229045
retrieved
7 July 2018
Large recurrent microdeletions associated with schizophrenia
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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=4229045
retrieved
7 July 2018
Rare chromosomal deletions and duplications increase risk 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=4229045
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7 July 2018
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
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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=4229045
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7 July 2018
Comparative genome hybridization suggests a role for NRXN1 and APBA2 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=4229045
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7 July 2018
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)
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=4229045
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7 July 2018
The genetic basis for mental retardation
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=4229045
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7 July 2018
Genetic disorders in children and young adults: a population study
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=4229045
retrieved
7 July 2018
Penetrance for copy number variants associated with 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=4229045
retrieved
27 October 2018
Identifiers
DOI
10.1016/J.BIOPSYCH.2013.07.022
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
PMC publication ID
4229045
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
PubMed publication ID
23992924
1 reference
stated in
Europe PubMed Central
PMC publication ID
4229045
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23992924%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
ResearchGate publication ID
256329655
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