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Title
Copy Number Variants in German Patients with Schizophrenia
Authors
Keywords
Schizophrenia, Law and legal sciences, Quality control, Copy number variation, Schools, Genetic predisposition, Heredity, Human genetics
Journal
PLoS One
Volume 8, Issue 7, Pages e64035
Publisher
Public Library of Science (PLoS)
Online
2013-07-03
DOI
10.1371/journal.pone.0064035
References
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Related references
Note: Only part of the references are listed.- Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample
- (2012) Franziska Degenhardt et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- 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 survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder
- (2011) L Priebe et al. MOLECULAR PSYCHIATRY
- Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
- (2011) Vladimir Vacic et al. NATURE
- Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia
- (2011) Detelina Grozeva et al. SCHIZOPHRENIA RESEARCH
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- (2010) Daniel Moreno-De-Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- New Copy Number Variations in Schizophrenia
- (2010) Chiara Magri et al. PLoS One
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- Copy number variations of chromosome 16p13.1 region associated with schizophrenia
- (2009) A Ingason et al. MOLECULAR PSYCHIATRY
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- 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
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