Funded Projects
Comprehensive phenotypic characterization of 17q12 deletion syndrome
Awarded: 2012
Award Type: Research
Award Type: Research
Identifying the genes in the 17q12 region responsible for neuropsychiatric phenotypes
Awarded: 2011
Award Type: Research
Award Type: Research
Simons Variation in Individuals Project (Simons VIP)
Awarded: 2011
Award Type: Simons Searchlight
Award Type: Simons Searchlight
SFARI Funded Publications
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.
Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication.
Green Snyder L., D'Angelo D., Chen Q., Bernier R., Goin-Kochel R., Wallace A.S., Gerdts J., Kanne S., Berry L., Blaskey L., Kuschner E., Roberts T., Sherr E., Martin C. L., Ledbetter D., Spiro J., Chung W., Hanson E., Simons VIP Consortium.