Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function
Published 2010 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function
Authors
Keywords
Gene disruption, Schizophrenia, Copy number variation, Gene ontologies, Synapses, Research errors, Brain diseases, Gene expression
Journal
PLoS Genetics
Volume 6, Issue 9, Pages e1001097
Publisher
Public Library of Science (PLoS)
Online
2010-09-10
DOI
10.1371/journal.pgen.1001097
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)
- (2010) B. M. Neale et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease
- (2009) Kai Wang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Variable locus length in the human genome leads to ascertainment bias in functional inference for non-coding elements
- (2009) Leila Taher et al. BIOINFORMATICS
- Copy number variations in East-Asian population and their evolutionary and functional implications
- (2009) S.-H. Yim et al. HUMAN MOLECULAR GENETICS
- Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
- (2009) J Elia et al. MOLECULAR PSYCHIATRY
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
- (2009) Philip L De Jager et al. NATURE GENETICS
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
- (2009) Sekar Kathiresan et al. NATURE GENETICS
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN 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
- A robust statistical method for case-control association testing with copy number variation
- (2008) Chris Barnes et al. NATURE GENETICS
- Strong association of de novo copy number mutations with sporadic schizophrenia
- (2008) Bin Xu et al. NATURE GENETICS
- Integrated detection and population-genetic analysis of SNPs and copy number variation
- (2008) Steven A McCarroll et al. NATURE GENETICS
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn 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
- 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.
ExploreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search