A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
Top Cited Papers
Open Access
- 1 January 2008
- journal article
- other
- Published by Elsevier in American Journal of Human Genetics
- Vol. 82 (1) , 160-164
- https://doi.org/10.1016/j.ajhg.2007.09.015
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility GenePublished by Elsevier ,2008
- Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum DisordersAmerican Journal of Human Genetics, 2008
- Common fragile sites, extremely large genes, neural development and cancerCancer Letters, 2006
- Pervasive Developmental Disorders in Preschool Children: Confirmation of High PrevalenceAmerican Journal of Psychiatry, 2005
- A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease riskNature, 2005
- Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLsMolecular Psychiatry, 2005
- Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studiesNature Genetics, 2004
- Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1The Journal of cell biology, 2003
- Merlin—rapid analysis of dense genetic maps using sparse gene flow treesNature Genetics, 2001
- The inheritance of liability to certain diseases, estimated from the incidence among relativesAnnals of Human Genetics, 1965