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Mosaic copy number variation in schizophrenia
scientific article
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instance of
scholarly article
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title
Mosaic copy number variation in schizophrenia
(English)
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main subject
schizophrenia
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author
George Kirov
series ordinal
12
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Michael E. Talkowski
object named as
Michael Talkowski
series ordinal
4
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Elizabeth Suchi Chen
object named as
Elizabeth S Chen
series ordinal
5
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Douglas M. Ruderfer
object named as
Douglas M Ruderfer
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1
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Jennifer L. Moran
object named as
Jennifer Moran
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3
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Aiden Corvin
object named as
Aiden Corvin
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9
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Michael C O'Donovan
object named as
Michael C O'Donovan
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14
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Christina M. Hultman
series ordinal
11
object named as
Christina M Hultman
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James F. Gusella
series ordinal
7
object named as
James F Gusella
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Patrick F. Sullivan
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18
object named as
Patrick F Sullivan
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Pamela Sklar
series ordinal
20
object named as
Pamela Sklar
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Douglas Blackwood
series ordinal
8
object named as
Douglas H Blackwood
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David St Clair
series ordinal
17
object named as
David St Clair
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Shaun Purcell
series ordinal
19
object named as
Shaun M Purcell
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Carolina Gigek
series ordinal
6
object named as
Carolina Gigek
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Hugh Gurling
series ordinal
10
object named as
Hugh M Gurling
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Carlos N Pato
series ordinal
16
object named as
Carlos Pato
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author name string
Kim Chambert
series ordinal
2
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Patrick Magnusson
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13
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Michael J Owen
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15
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Carl Ernst
series ordinal
21
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language of work or name
English
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publication date
September 2013
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published in
European Journal of Human Genetics
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volume
21
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issue
9
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page(s)
1007-11
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cites work
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BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1
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20 March 2017
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
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Common variants on chromosome 6p22.1 are associated with schizophrenia
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20 March 2017
Rare chromosomal deletions and duplications increase risk of schizophrenia
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Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder
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20 March 2017
Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders
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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
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PubMed Central
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Microdeletions of 3q29 confer high risk for schizophrenia
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29 September 2017
Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome
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29 September 2017
Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease
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29 September 2017
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
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29 September 2017
Lifetime prevalence, demographic risk factors, and diagnostic validity of nonaffective psychosis as assessed in a US community sample. The National Comorbidity Survey
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29 September 2017
The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study
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2 June 2018
DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEJHG.2012.287
retrieved
21 January 2018
Identifiers
DOI
10.1038/EJHG.2012.287
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3999278
OpenCitations bibliographic resource ID
3999278
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3999278
PMC publication ID
3746263
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3999278
PubMed publication ID
23321615
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3999278
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