SHANK1 Deletions in Males with Autism Spectrum Disorder
Open Access
- 4 May 2012
- journal article
- research article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 90 (5), 879-887
- https://doi.org/10.1016/j.ajhg.2012.03.017
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Rare Deletions at the Neurexin 3 Locus in Autism Spectrum DisorderAmerican Journal of Human Genetics, 2012
- SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanismMolecular Psychiatry, 2011
- Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual DisabilityAmerican Journal of Human Genetics, 2011
- Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturationThe EMBO Journal, 2011
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsNature, 2010
- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic DiseaseAmerican Journal of Human Genetics, 2009
- Defining key features of the broad autism phenotype: A comparison across parents of multiple‐ and single‐incidence autism familiesAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2008
- Structural Variation of Chromosomes in Autism Spectrum DisorderAmerican Journal of Human Genetics, 2008
- Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersNature Genetics, 2006
- Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autismNature Genetics, 2003