Funded Projects
SFARI Funded Publications
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.
Antaki D., Guevara J., Maihofer A.X., Klein M., Gujral M., Grove J., Carey C.E., Hong O., Arranz M.J., Hervas A., Corsello C., Vaux K.K., Muotri A., Iakoucheva L., Courchesne E., Pierce K., Gleeson J., Robinson E., Nievergelt C.M., Sebat J.
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.
Mok R.S.F., Zhang W., Sheikh T.I., Pradeepan K., Fernandes I.R., DeJong L.C., Benigno G., Hildebrandt M.R., Mufteev M., Rodrigues D.C., Wei W., Piekna A., Liu J., Muotri A., Vincent J.B., Muller L., Martinez-Trujillo J., Salter M.W., Ellis J.
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.
