

Funded Projects
SFARI Funded Publications
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.
Scala M., Bradley C.A., Howe J.L., Trost B., Salazar N.B., Shum C., Mendes M., Reuter M.S., Anagnostou E., MacDonald J.R., Ko S.Y., Frankland P.W., Charlebois J., Elsabbagh M., Granger L., Anadiotis G., Pullano V., Brusco A., Keller R., Parisotto S., Pedro H.F., Lusk L., McDonnell P.P., Helbig I., Mullegama S.V., Undiagnosed Diseases Network, Douine E.D., Corona R.I., Russell B.E., Nelson S.F., Graziano C., Schwab M., Simone L., Zara F., Scherer S. W.
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Trost B., Thiruvahindrapuram B., Chan A.J.S., Engchuan W., Higginbotham E.J., Howe J.L., Loureiro L.O., Reuter M.S., Roshandel D., Whitney J., Zarrei M., Bookman M., Somerville C., Shaath R., Abdi M., Aliyev E., Patel R.V., Nalpathamkalam T., Pellecchia G., Hamdan O., Kaur G., Wang Z., MacDonald J.R., Wei J., Sung W.W.L., Lamoureux S., Hoang N., Selvanayagam T., Deflaux N., Geng M., Ghaffari S., Bates J., Young E.J., Ding Q., Shum C., D'Abate L., Bradley C.A., Rutherford A., Aguda V., Apresto B., Chen N., Desai S., Du X., Fong M.L.Y., Pullenayegum S., Samler K., Wang T., Ho K., Paton T., Pereira S.L., Herbrick J.-A., Wintle R.F., Fuerth J., Noppornpitak J., Ward H., Magee P., Al Baz A., Kajendirarajah U., Kapadia S., Vlasblom J., Valluri M., Green J., Seifer V., Quirbach M., Rennie O., Kelley E., Masjedi N., Lord C., Szego M.J., Zawati M.H., Lang M., Strug L.J., Marshall C.R., Costain G., Calli K., Iaboni A., Yusuf A., Ambrozewicz P., Gallagher L., Amaral D., Brian J., Elsabbagh M., Georgiades S., Messinger D.S., Ozonoff S., Sebat J., Sjaarda C.P., Smith I.M., Szatmari P., Zwaigenbaum L., Kushki A., Frazier T., Vorstman J.A.S., Fakhro K.A., Fernandez B.A., Lewis M.E.S., Weksberg R., Fiume M., Yuen R.K.C., Anagnostou E., Sondheimer N., Glazer D., Hartley D.M., Scherer S. W.
Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.
Tesfaye R., Huguet G., Schmilovich Z., Renne T., Loum M.A., Douard E., Saci Z., Jean-Louis M., Martineau J.L., Whelan R., Desrivieres S., Heinz A., Schumann G., Hayward C., Elsabbagh M., Jacquemont S.