A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding moleculesBrunella Franco, Andrea Ballabio, Silvana Guioli et al.|Nature|1991Cited by 851
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum DisordersClaire S. Leblond, Marc Délepine, Catalina Betancur et al.|PLoS Genetics|2012Cited by 443