Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
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Title
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Authors
Keywords
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Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Volume 159B, Issue 7, Pages 812-822
Publisher
Wiley
Online
2012-08-22
DOI
10.1002/ajmg.b.32088
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Note: Only part of the references are listed.- Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders
- (2012) Linh Duong et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- After GWAS: Searching for Genetic Risk for Schizophrenia and Bipolar Disorder
- (2011) Elliot S. Gershon et al. AMERICAN JOURNAL OF PSYCHIATRY
- 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
- Genetics of Schizophrenia: New Findings and Challenges
- (2011) Pablo V. Gejman et al. Annual Review of Genomics and Human Genetics
- Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients
- (2011) Jacobine E. Buizer-Voskamp et al. BIOLOGICAL PSYCHIATRY
- Neurodevelopmental hypothesis of schizophrenia
- (2011) Michael J. Owen et al. BRITISH JOURNAL OF PSYCHIATRY
- Recent genomic advances in schizophrenia
- (2011) JL Doherty et al. CLINICAL GENETICS
- Neuropsychiatric Aspects of Schizophrenia
- (2011) Raquel E. Gur CNS Neuroscience & Therapeutics
- 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
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- (2011) Rachel Soemedi et al. HUMAN MOLECULAR GENETICS
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- (2011) Guiyun Xu et al. JOURNAL OF AFFECTIVE DISORDERS
- 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
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
- (2011) G Kirov et al. MOLECULAR PSYCHIATRY
- Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
- (2011) Vladimir Vacic et al. NATURE
- High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
- (2011) Dheeraj Malhotra et al. NEURON
- Early Intervention for Psychosis
- (2011) M. Marshall et al. SCHIZOPHRENIA BULLETIN
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review
- (2010) Fabiola Quintero-Rivera et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- 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
- Multiplex Amplicon Quantification (MAQ), a fast and efficient method for the simultaneous detection of copy number alterations in neuroblastoma.
- (2010) Candy Kumps et al. BMC GENOMICS
- New Copy Number Variations in Schizophrenia
- (2010) Chiara Magri et al. PLoS One
- Strong synaptic transmission impact by copy number variations in schizophrenia
- (2010) J. T. Glessner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Specific and Generalized Neuropsychological Deficits: A Comparison of Patients With Various First-Episode Psychosis Presentations
- (2009) Jolanta Zanelli et al. AMERICAN JOURNAL OF PSYCHIATRY
- 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
- Copy Number Variation in Schizophrenia in the Japanese Population
- (2009) Masashi Ikeda et al. BIOLOGICAL PSYCHIATRY
- Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
- (2009) C. G. F. de Kovel et al. BRAIN
- Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances
- (2009) Marianne Doornbos et al. European Journal of Medical Genetics
- A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease
- (2009) H. C. Mefford et al. GENOME RESEARCH
- Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance
- (2009) L. M. Dibbens et al. HUMAN MOLECULAR GENETICS
- 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
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
- (2009) Ingo Helbig et al. NATURE GENETICS
- Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
- (2009) Jonathan Sebat et al. TRENDS IN GENETICS
- A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia
- (2009) Anna C. Need et al. PLoS Genetics
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- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2008) Terry Vrijenhoek et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2008) D T Miller et al. JOURNAL OF MEDICAL 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
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- (2008) Hreinn Stefansson et al. NATURE
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- (2008) Andrew J Sharp et al. NATURE GENETICS
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
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- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
- (2008) T. Walsh et al. SCIENCE
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- (2008) Blake C Ballif et al. Molecular Cytogenetics
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