Rare SHANK2 variants in schizophrenia

por Peykov, S, Berkel, S, Degenhardt, F, Rietschel, M, Nöthen, M M, Rappold, G A
Publicado 2015

Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

por Bacon, C, Schneider, M, Le Magueresse, C, Froehlich, H, Sticht, C, Gluch, C, Monyer, H, Rappold, G A
Publicado 2015

Identification and functional characterization of rare SHANK2 variants in schizophrenia

por Peykov, S, Berkel, S, Schoen, M, Weiss, K, Degenhardt, F, Strohmaier, J, Weiss, B, Proepper, C, Schratt, G, Nöthen, M M, Boeckers, T M, Rietschel, M, Rappold, G A
Publicado 2015