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Title
Schizophrenia genetics: new insights from new approaches
Authors
Keywords
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Journal
BRITISH MEDICAL BULLETIN
Volume 91, Issue 1, Pages 61-74
Publisher
Oxford University Press (OUP)
Online
2009-09-03
DOI
10.1093/bmb/ldp017
References
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Related references
Note: Only part of the references are listed.- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
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- (2009) Paul Lichtenstein et al. LANCET
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- Estimation of significance thresholds for genomewide association scans
- (2008) Frank Dudbridge et al. GENETIC EPIDEMIOLOGY
- Disruption of the neurexin 1 gene is associated with schizophrenia
- (2008) Dan Rujescu et al. HUMAN MOLECULAR GENETICS
- A HapMap harvest of insights into the genetics of common disease
- (2008) Teri A. Manolio et al. JOURNAL OF CLINICAL INVESTIGATION
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- Genomewide association for schizophrenia in the CATIE study: results of stage 1
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- 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
- Strong association of de novo copy number mutations with sporadic schizophrenia
- (2008) Bin Xu et al. NATURE GENETICS
- Identification of loci associated with schizophrenia by genome-wide association and follow-up
- (2008) Michael C O'Donovan et al. NATURE GENETICS
- Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database
- (2008) Nicole C Allen 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
- Integrated detection and population-genetic analysis of SNPs and copy number variation
- (2008) Steven A McCarroll et al. NATURE GENETICS
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women
- (2008) Sagiv Shifman et al. PLoS Genetics
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
- (2008) T. Walsh et al. SCIENCE
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