Funded Projects
SFARI Funded Publications
Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome.
Taylor C.M., Finucane B.M., Moreno-De-Luca A., Walsh L.K., Martin C. L., Ledbetter D.
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.
Insufficient evidence for “autism-specific” genes.
Myers S.M., Challman T.D., Bernier R., Bourgeron T., Chung W., Constantino J., Eichler E., Jacquemont S., Miller D.T., Mitchell K.J., Zoghbi H., Martin C. L., Ledbetter D.