Funded Projects
SFARI Funded Publications
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
Fernandez T., Williams Z., Kline T., Rajendran S., Augustine F., Wright N., Sullivan C.A.W., Olfson E., Abdallah S.B., Liu W., Hoffman E., Gupta A., Singer H.S.
High-throughput functional analysis of autism genes in zebrafish identifies convergence in dopaminergic and neuroimmune pathways.
Weinschutz Mendes H., Neelakantan U., Liu Y., Fitzpatrick S.E., Chen T., Wu W., Pruitt A., Jin D.S., Jamadagni P., Carlson M., Lacadie C.M., Enriquez K.D., Li N., Zhao D., Ijaz S., Sakai C., Szi C., Rooney B., Ghosh M., Nwabudike I., Gorodezky A., Chowdhury S., Zaheer M., McLaughlin S., Fernandez J.M., Wu J., Eilbott J.A., Vander Wyk B., Rihel J., Papademetris X., Wang Z., Hoffman E.
PTEN mutations in autism spectrum disorder and congenital hydrocephalus: Developmental pleiotropy and therapeutic targets.
DeSpenza T. Jr., Carlson M., Panchagnula S., Robert S., Duy P.Q., Mermin-Bunnell N., Reeves B.C., Kundishora A., Elsamadicy A.A., Smith H., Ocken J., Alper S.L., Jin S.C., Hoffman E., Kahle K., Valdivia Espino J.