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Copy number variation in schizophrenia
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Copy number variation in schizophrenia
(English)
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
main subject
schizophrenia
0 references
author name string
Suleyman Gulsuner
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
Jon M McClellan
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
language of work or name
English
0 references
publication date
1 January 2015
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
published in
Neuropsychopharmacology
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
volume
40
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
page(s)
252-254
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
exact match
https://scigraph.springernature.com/pub.10.1038/npp.2014.216
0 references
cites work
CNVs conferring risk of autism or schizophrenia affect cognition in controls
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=4262903
retrieved
6 September 2017
Formation of chimeric genes by copy-number variation as a mutational mechanism 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=4262903
retrieved
6 September 2017
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=4262903
retrieved
6 September 2017
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=4262903
retrieved
6 September 2017
Genetic heterogeneity in human 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=4262903
retrieved
6 September 2017
Rare structural variants disrupt multiple genes in neurodevelopmental pathways 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=4262903
retrieved
6 September 2017
Identifiers
DOI
10.1038/NPP.2014.216
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
Dimensions Publication ID
1011059381
0 references
PMCID
4262903
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
PubMed ID
25482180
1 reference
stated in
Europe PubMed Central
PMCID
4262903
retrieved
1 September 2017
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