Genome-wide association analysis of copy number variation in recurrent depressive disorder
Published 2011 View Full Article
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Title
Genome-wide association analysis of copy number variation in recurrent depressive disorder
Authors
Keywords
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Journal
MOLECULAR PSYCHIATRY
Volume 18, Issue 2, Pages 183-189
Publisher
Springer Nature
Online
2011-11-01
DOI
10.1038/mp.2011.144
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Related references
Note: Only part of the references are listed.- Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample
- (2011) Andrew McQuillin et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genome-Wide Association Study of Major Recurrent Depression in the U.K. Population
- (2010) Cathryn M. Lewis et al. AMERICAN JOURNAL OF PSYCHIATRY
- Rare Copy Number VariantsA Point of Rarity in Genetic Risk for Bipolar Disorder and SchizophreniaRare Copy Number Variants
- (2010) Detelina Grozeva ARCHIVES OF GENERAL PSYCHIATRY
- Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
- (2010) Nigel M Williams et al. LANCET
- Poor replication of candidate genes for major depressive disorder using genome-wide association data
- (2010) F J Bosker et al. MOLECULAR PSYCHIATRY
- Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
- (2010) Joseph T. Glessner et al. PLoS One
- Differential efficacy of escitalopram and nortriptyline on dimensional measures of depression
- (2009) Rudolf Uher et al. BRITISH JOURNAL OF PSYCHIATRY
- The role of copy number variation in schizophrenia
- (2009) George Kirov Expert Review of Neurotherapeutics
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- The role of genetic variation in the causation of mental illness: an evolution-informed framework
- (2009) R Uher MOLECULAR PSYCHIATRY
- A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
- (2009) Marwan Shinawi et al. NATURE GENETICS
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Erratum: Common disorders are quantitative traits
- (2009) Robert Plomin et al. NATURE REVIEWS GENETICS
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- Copy-number variations associated with neuropsychiatric conditions
- (2008) Edwin H. Cook Jr et al. NATURE
- 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
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
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