The 3q29 deletion confers >40-fold increase in risk for schizophrenia
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Title
The 3q29 deletion confers >40-fold increase in risk for schizophrenia
Authors
Keywords
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Journal
MOLECULAR PSYCHIATRY
Volume 20, Issue 9, Pages 1028-1029
Publisher
Springer Nature
Online
2015-06-09
DOI
10.1038/mp.2015.76
References
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Related references
Note: Only part of the references are listed.- A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model
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- A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability
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- Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia
- (2013) Jennifer Gladys Mulle et al. BIOLOGICAL PSYCHIATRY
- Analysis of copy number variations at 15 schizophrenia-associated loci
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- CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
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- Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays
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- Schizophrenia genetics: progress, at last
- (2012) Jennifer Gladys Mulle CURRENT OPINION IN GENETICS & DEVELOPMENT
- Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
- (2011) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients
- (2011) Jacobine E. Buizer-Voskamp et al. BIOLOGICAL PSYCHIATRY
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle et al. AMERICAN JOURNAL OF HUMAN GENETICS
- New Copy Number Variations in Schizophrenia
- (2010) Chiara Magri et al. PLoS One
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Strong association of de novo copy number mutations with sporadic schizophrenia
- (2008) Bin Xu et al. NATURE GENETICS
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
- (2008) T. Walsh et al. SCIENCE
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