Reduced burden of very large and rare CNVs in bipolar affective disorder
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Title
Reduced burden of very large and rare CNVs in bipolar affective disorder
Authors
Keywords
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Journal
BIPOLAR DISORDERS
Volume 15, Issue 8, Pages 893-898
Publisher
Wiley
Online
2013-10-16
DOI
10.1111/bdi.12125
References
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Related references
Note: Only part of the references are listed.- Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
- (2012) Maarten J. Van Den Bossche et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
- (2012) Dheeraj Malhotra et al. CELL
- Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
- (2012) Santhosh Girirajan et al. NEW ENGLAND JOURNAL OF MEDICINE
- 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
- De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants
- (2011) Elliott Rees et al. BIOLOGICAL PSYCHIATRY
- 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
- An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
- (2011) Erin B. Kaminsky et al. GENETICS IN MEDICINE
- 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
- High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
- (2011) Dheeraj Malhotra et al. NEURON
- 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
- 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
- Excellent school performance at age 16 and risk of adult bipolar disorder: national cohort study
- (2010) James H. MacCabe et al. BRITISH JOURNAL OF PSYCHIATRY
- Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
- (2010) Nigel M Williams et al. LANCET
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
- (2010) NATURE
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
- (2009) Audrey Guilmatre et al. ARCHIVES OF GENERAL 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
- Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
- (2009) Paul Lichtenstein et al. LANCET
- 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
- Psychosis Genetics: Modeling the Relationship Between Schizophrenia, Bipolar Disorder, and Mixed (or "Schizoaffective") Psychoses
- (2009) N. Craddock et al. SCHIZOPHRENIA BULLETIN
- Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
- (2009) Jonathan Sebat et al. TRENDS IN GENETICS
- Singleton deletions throughout the genome increase risk of bipolar disorder
- (2008) D Zhang et al. MOLECULAR PSYCHIATRY
- 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
- Phenotypic variations on the theme of CNVs
- (2008) Michael C O'Donovan et al. NATURE GENETICS
- A robust statistical method for case-control association testing with copy number variation
- (2008) Chris Barnes et al. NATURE GENETICS
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