

Funded Projects
SFARI Funded Publications
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.,
De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism.
Cappi C., Oliphant M.E., Péter Z., Zai G., do Rosário M.C., Sullivan C.A.W., Gupta A., Hoffman E., Virdee M., Olfson E., Abdallah S.B., Willsey A. J., Shavitt R.G., Miguel E.C., Kennedy J.L., Richter M.A., Fernandez T.
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify candidate risk genes and biological pathways.
Fernandez T., Williams Z.P., Kline T., Rajendran S., Augustine F., Wright N., Sullivan C.A.W., Olfson E., Abdallah S.B., Liu W., Hoffman E., Gupta A.