A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

[1]  Katarzyna Chawarska,et al.  Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. , 2008, American journal of human genetics.

[2]  J. Sebat,et al.  Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. , 2008, American journal of human genetics.

[3]  C. Corsello,et al.  Combining information from multiple sources in the diagnosis of autism spectrum disorders. , 2006, Journal of the American Academy of Child and Adolescent Psychiatry.

[4]  D. Stephan,et al.  Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. , 2006, The New England journal of medicine.

[5]  David I. Smith,et al.  Common fragile sites, extremely large genes, neural development and cancer. , 2006, Cancer letters.

[6]  D. Geschwind,et al.  Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs , 2005, Molecular Psychiatry.

[7]  Eric Fombonne,et al.  Pervasive developmental disorders in preschool children: confirmation of high prevalence. , 2005, The American journal of psychiatry.

[8]  E. Grice,et al.  A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk , 2005, Nature.

[9]  Aravinda Chakravarti,et al.  Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies , 2004, Nature Genetics.

[10]  Colin L. Stewart,et al.  Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1 , 2003, The Journal of cell biology.

[11]  P. Heutink,et al.  CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. , 2003, Genomics.

[12]  Aravinda Chakravarti,et al.  Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. , 2003, American journal of human genetics.

[13]  G. Abecasis,et al.  Merlin—rapid analysis of dense genetic maps using sparse gene flow trees , 2002, Nature Genetics.

[14]  S. Folstein,et al.  Genetics of austim: complex aetiology for a heterogeneous disorder , 2001, Nature Reviews Genetics.

[15]  Peter Shrager,et al.  Caspr2, a New Member of the Neurexin Superfamily, Is Localized at the Juxtaparanodes of Myelinated Axons and Associates with K+ Channels , 1999, Neuron.

[16]  N E Morton,et al.  Analysis of family resemblance. 3. Complex segregation of quantitative traits. , 1974, American journal of human genetics.

[17]  Morton Ne.  Analysis of family resemblance. I. Introduction. , 1974 .

[18]  L. Kanner.  Autistic disturbances of affective contact. , 1968, Acta paedopsychiatrica.

[19]  D. Falconer.  The inheritance of liability to certain diseases, estimated from the incidence among relatives , 1965 .