Director, Neurodevelopmental Disorders Phenotyping Program, Boston Children’s Hospital
WebsiteFunded Projects
SFARI Funded Publications
A genetics-first approach to dissecting the heterogeneity of autism: Phenotypic comparison of autism risk copy number variants.
Chawner S.J.R.A., Doherty J.L., Anney R., Antshel K.M., Bearden C., Bernier R., Chung W., Clements C.C., Curran S.R., Cuturilo G., Fiksinski A.M., Gallagher L., Goin-Kochel R., Gur R.E., Hanson E., Jacquemont S., Kates W.R., Kushan L., Maillard A.M., McDonald-McGinn D.M., Mihaljevic M., Miller J.S., Moss H., Pejovic-Milovancevic M., Schultz R., Green Snyder L., Vorstman J.A., Wenger T.L., IMAGINE-ID Consortium, Hall J., Owen M.J., van den Bree M.B.M.
Evaluating heterogeneity in ASD symptomatology, cognitive ability, and adaptive functioning among 16p11.2 CNV carriers.
Hudac C.M., Bove J., Barber S., Duyzend M., Wallace A., Martin C. L., Ledbetter D., Hanson E., Goin-Kochel R., Green Snyder L., Chung W., Eichler E., Bernier R.