Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 19, Issue 5, Pages 588-592
Publisher
Springer Nature America, Inc
Online
2011-01-05
DOI
10.1038/ejhg.2010.221
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes
- (2010) Erin L. Heinzen 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
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
- (2010) NATURE
- 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
- Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection
- (2009) Nuala H Sykes et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- 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
- Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
- (2009) S Ben-Shachar et al. JOURNAL OF MEDICAL GENETICS
- Genome-wide association study of bipolar disorder in European American and African American individuals
- (2009) E N Smith et al. MOLECULAR PSYCHIATRY
- Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
- (2009) J Elia et al. MOLECULAR PSYCHIATRY
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- 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
- Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry
- (2009) L. J. Scott et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia
- (2009) Anna C. Need et al. PLoS Genetics
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients
- (2008) Terry Vrijenhoek et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A 15q13.3 microdeletion segregating with autism
- (2008) Alistair T Pagnamenta et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
- (2008) Anne S. Bassett et al. HUMAN MOLECULAR GENETICS
- Disruption of the neurexin 1 gene is associated with schizophrenia
- (2008) Dan Rujescu et al. HUMAN MOLECULAR GENETICS
- Singleton deletions throughout the genome increase risk of bipolar disorder
- (2008) D Zhang et al. MOLECULAR PSYCHIATRY
- Whole-genome association study of bipolar disorder
- (2008) P Sklar et al. MOLECULAR PSYCHIATRY
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
- (2008) Andrew J Sharp et al. NATURE GENETICS
- Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
- (2008) Manuel A R Ferreira et al. NATURE GENETICS
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (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
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now