Comment on

• Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. [Am J Hum Genet. 2008]
  Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, et al. Am J Hum Genet. 2008 Jan; 82(1):165-73.
• A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. [Am J Hum Genet. 2008]
  A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, et al. Am J Hum Genet. 2008 Jan; 82(1):160-4.
• Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. [Am J Hum Genet. 2008]
  Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, et al. Am J Hum Genet. 2008 Jan; 82(1):150-9.