

Funded Projects
SSC-ASC Whole-Genome Sequencing Consortium (project 2): Development of statistical methods
Awarded: 2018
Award Type: Research
Award Type: Research
Interactome perturbation screen to identity damaging de novo missense mutations in autism
Awarded: 2018
Award Type: Research
Award Type: Research
Spatiotemporal and cell-type convergence to reveal autism neurobiology
Awarded: 2016
Award Type: Research
Award Type: Research
SFARI Funded Publications
Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders.
Lowther C., Valkanas E., Giordano J.L., Wang H.Z., Currall B.B., O'Keefe K., Pierce-Hoffman E., Kurtas N., Whelan C.W., Hao S.P., Weisburd B., Jalili V., Fu J., Wong I., Collins R.L., Zhao X., Austin-Tse C.A., Evangelista E., Lemire G., Aggarwal V.S., Lucente D., Gauthier L.D., Tolonen C., Sahakian N., Stevens C., An J.-Y., Dong S., Norton M.E., MacKenzie T., Devlin B., Gilmore K., Powell B., Brandt A., Vetrini F., DiVito M., Sanders S., MacArthur D.G., Hodge J.C., O'Donnell-Luria A.H., Rehm H.L., Vora N.L., Levy B., Brand H., Wapner R., Talkowski M.
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Fu J.M., Satterstrom F.K., Peng M., Brand H., Collins R.L., Dong S., Wamsley B., Klei L., Wang L., Hao S.P., Stevens C.R., Cusick C., Babadi M., Banks E., Collins B., Dodge S., Gabriel S.B., Gauthier L., Lee S.K., Liang L., Ljungdahl A., Mahjani B., Sloofman L., Smirnov A., Barbosa M., Betancur C., Brusco A., Chung B.H.Y., Cook E. H., Cuccaro M.L., Domenici E., Ferrero G.B., Gargus J.J., Herman G.E., Hertz-Picciotto I., Maciel P., Manoach D., Passos-Bueno M.R., Persico A.M., Renieri A., Sutcliffe J., Tassone F., Trabetti E., Campos G., Cardaropoli S., Carli D., Chan M.C.Y., Fallerini C., Giorgio E., Girardi A.C., Hansen-Kiss E., Lee S.L., Lintas C., Ludena Y., Nguyen R., Pavinato L., Pericak-Vance M., Pessah I.N., Schmidt R., Smith M., Souza C.I.S., Trajkova S., Wang J.Y.T., Yu M.H.C., Autism Sequencing Consortium (ASC), Broad Institute Center for Common Disease Genomics (Broad-CCDG), iPSYCH-BROAD Consortium, Cutler D.J., Rubeis S.D., Buxbaum J., Daly M., Devlin B., Roeder K., Sanders S., Talkowski M.