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.

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.