Funded Projects
SFARI Funded Publications
Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.
Urresti J., Zhang P., Moran-Losada P., Yu N.-K., Negraes P.D., Trujillo C.A., Antaki D., Amar M., Chau K., Pramod A.B., Diedrich J., Tejwani L., Romero S., Sebat J., Yates J.R. III, Muotri A., Iakoucheva L.
Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling.
Amar M., Pramod A.B., Yu N.-K., Herrera V.M., Qiu L.R., Moran-Losada P., Zhang P., Trujillo C.A., Ellegood J., Urresti J., Chau K., Diedrich J., Chen J., Gutierrez J., Sebat J., Ramanathan D., Lerch J., Yates J.R. 3rd, Muotri A., Iakoucheva L.
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.
Antaki D., Maihofer A., Klein M., Guevara J., Grove J., Carey C., Hong O., Arranz M., Hervas A., Corsello C., Muotri A., Iakoucheva L., Courchesne E., Pierce K., Gleeson J., Robinson E., Nievergelt C., Sebat J.
