Funded Projects
SFARI Funded Publications
Patient brain organoids identify a link between the 16p11.2 copy number variant and the RBFOX1 gene.
Kostic M., Raymond J.J., Henry B., Tumkaya T., Khlghatyan J., Dvornik J., Hsiao J.S., Cheon S.H., Chung J., Sun Y., Dolmetsch R., Worringer K.A., Ihry R.J.
16p11.2 microdeletion imparts transcriptional alterations in human iPSC-derived models of early neural development.
Roth J.G., Muench K.L., Asokan A., Gai H., Verma Y., Weber S., Charlton C., Fowler J.L., Loh K.M., Dolmetsch R., Palmer T.
Copy number variation at 16p11.2 imparts transcriptional alterations in neural development in an hiPSC-derived model of corticogenesis.
Roth J.G., Muench K.L., Asokan A., Mallett V.M., Gai H., Verma Y., Weber S., Charlton C., Fowler J.L., Loh K.M., Dolmetsch R., Palmer T.