Funded Projects
SFARI Funded Publications
Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p.
Weiner D.J., Ling E., Erdin S., Tai D.J.C., Yadav R., Grove J., Fu J.M., Nadig A., Carey C.E., Baya N., Bybjerg-Grauholm J., iPSCYH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta S., Macosko E.Z., Sebat J., O’Connor L.J., Hougaard D.M., Børglum A.D., Talkowski M., McCarroll S., Robinson E.
Insights into dispersed duplications and complex structural mutations from whole genome sequencing 706 families.
Whelan C.W., Handsaker R.E., Genovese G., Kashin S., Lek M., Hughes J., McElwee J., Lenardo M., MacArthur D., McCarroll S.
Single-cell RNA sequencing of microglia throughout the mouse lifespan and in the injured brain reveals complex cell-state changes.
Hammond T.R., Dufort C., Dissing-Olesen L., Giera S., Young A., Wysoker A., Walker A.J., Gergits F., Segel M., Nemesh J., Marsh S.E., Saunders A., Macosko E., Ginhoux F., Chen J., Franklin R.J.M., Piao X., McCarroll S., Stevens B.
