Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations

por De Rubeis, Silvia, Siper, Paige M., Durkin, Allison, Weissman, Jordana, Muratet, François, Halpern, Danielle, Trelles, Maria del Pilar, Frank, Yitzchak, Lozano, Reymundo, Wang, A. Ting, Holder, J. Lloyd, Betancur, Catalina, Buxbaum, Joseph D., Kolevzon, Alexander
Publicado 2018

Assessing the utility of electronic measures as a proxy for cognitive ability

por Levy, Tess, Britvan, Bari, Grosman, Hannah, Giserman‐Kiss, Ivy, Meyering, Kristin, Weissman, Jordana, Halpern, Danielle, Zweifach, Jessica, Trelles, M. Pilar, Foss‐Feig, Jennifer H., Kolevzon, Alexander, Sanders, Stephan J., Robinson, Elise B., Buxbaum, Joseph D., Bishop, Somer, Siper, Paige M.
Publicado 2022

Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study

por Guillory, Sylvia B., Baskett, Victoria Z., Grosman, Hannah E., McLaughlin, Christopher S., Isenstein, Emily L., Wilkinson, Emma, Weissman, Jordana, Britvan, Bari, Trelles, M. Pilar, Halpern, Danielle B., Buxbaum, Joseph D., Siper, Paige M., Wang, A. Ting, Kolevzon, Alexander, Foss-Feig, Jennifer H.
Publicado 2021