“…The latter can manifest as either enhanced sensitivity to an odorant (specific hyperosmia) or as a strongly reduced capacity to smell particular odorants. This diminished sensitivity, also known as specific anosmia, has been reported by several investigators and in connection with a range of odorants (e.g., Amoore, Venstrom, & Davis, 1968;Bremner, Mainland, Khan, & Sobel, 2003;Hirth, Abadanian, & Goedde, 1986;Kendal-Reed, Walker, Morgan, LaMacchio, & Lutz, 1998;Lison, Blondheim, & Melmed, 1980;Lunde, Skuterud, Nilsen, & Egelandsdal, 2008;Meilgaard, 1993;Pelosi & Pisanelli, 1981;Plotto, Barnes, & Goodner, 2006;Snyder, 1931), and recently the first reports confirming a genetic basis for differences in human olfactory phenotypes have emerged (Keller et al, 2007;Menashe et al, 2007). These reports extend previous work, notably twin studies by, for example, Finkel, Pedersen, and Larsson (2001), Segal, Topolski, Wilson, Brown, and Araki (1995), and Wysocki and Beauchamp (1984), indicating heritability in olfactory functioning.…”