Funded Projects
SFARI Funded Publications
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models.
Tai D.J.C., Razaz P., Erdin S., Gao D., Wang J., Nuttle X., de Esch C.E., Collins R.L., Currall B.B., O'Keefe K., Burt N.D., Yadav R., Wang L., Mohajeri K., Aneichyk T., Ragavendran A., Stortchevoi A., Morini E., Ma W., Lucente D., Hastie A., Kelleher R., Perlis R.H., Talkowski M., Gusella J.
A cross-disorder dosage sensitivity map of the human genome.
Collins R.L., Glessner J.T., Porcu E., Lepamets M., Brandon R., Lauricella C., Han L., Morley T., Niestroj L.-M., Ulirsch J., Everett S., Howrigan D.P., Boone P.M., Fu J., Karczewski K.J., Kellaris G., Lowther C., Lucente D., Mohajeri K., Nõukas M., Nuttle X., Samocha K.E., Trinh M., Ullah F., Võsa U., Epi25 Consortium, Estonian Biobank Research Team, Hurles M.E., Aradhya S., Davis E.E., Finucane H., Gusella J., Janze A., Katsanis N., Matyakhina L., Neale B.M., Sanders D., Warren S., Hodge J.C., Lal D., Ruderfer D.M., Meck J., Mägi R., Esko T., Reymond A., Kutalik Z., Hakonarson H., Sunyaev S., Brand H., Talkowski M.
Human iPSC-derived neuron of 16p11.2 deletion reveals haplotype-specific expression of MAPK3 and its contribution to variable NDD phenotypes.
Liu F., Liang C., Li Z., Zhao S., Shangguan S., Yuan H., Yao R., Qin Z., Zhang S., Zou L., Gao Z., Chen Q., Wen S., Peng J., Yin F., Chen F., Qiu X., Luo J., Xie Y., Lu D., Zhang Y., Xie H., Wang H., Cui X., Wang J., Huang H., Liu R., Sun X., Chen C., Wu N., Liu C., Shen Y., Gusella J., Chen X.
