Funded Projects
SFARI Funded Publications
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.
Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome.
Panagiotakos G., Haveles C., Arjun A., Petrova R., Rana A., Portmann T., Pașca S.P., Palmer T., Dolmetsch R.