“…Yet another complication arises, as Camarata (2014) notes, from recent changes in nomenclature. These changes have been much debated (e.g., Huerta, Bishop, Duncan, Hus, & Lord, 2012;McPartland, Reichow, & Volkmar, 2012) and, although one of the rationales for change from DSM-IV/ICD-10 was concern about diagnosis in younger children, several studies now suggest that the new diagnostic guidelines may be overly stringent for young children as well as older and higher functioning ones (see Barton, Robins, Jashar, Brenna, & Fein, in press;Matson, Kozlowski, Hattier, Horovitz, & Sipes, 2012). As noted elsewhere, the increased awareness of genetic risk has presented issues of added urgency to screening in high risk populations, and the study of such populations, i.e., infant siblings of children with autism, has led to a substantive body of research (Szatmari, Jones, Holden, Bryson, Mahoney, Tuff, et al, 1996;Warren, Foss-Feig, Malesa, Lee, Taylor, Newsom, et al, 2012;Yirmiya, Gamliel, Pilowsky, Feldman, Baron-Cohen, & Sigman, 2006).…”