Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder
Open Access
- 13 January 2012
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 90 (1), 133-141
- https://doi.org/10.1016/j.ajhg.2011.11.025
Abstract
No abstract availableThis publication has 56 references indexed in Scilit:
- Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaHuman Genetics, 2011
- Hotspots of Large Rare Deletions in the Human GenomePLOS ONE, 2010
- Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratoriesGenetics in Medicine, 2009
- High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applicationsGenome Research, 2009
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genesNature, 2009
- Rare chromosomal deletions and duplications increase risk of schizophreniaNature, 2008
- Disruption of Neurexin 1 Associated with Autism Spectrum DisorderAmerican Journal of Human Genetics, 2008
- Strong Association of De Novo Copy Number Mutations with AutismScience, 2007
- Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genomeCytogenetic and Genome Research, 2006
- Oligonucleotide Microarray Analysis of Genomic Imbalance in Children with Mental RetardationAmerican Journal of Human Genetics, 2006