Director and Vice President of Research, Bloorview Research Institute
WebsiteSFARI Funded Publications
Chromosome X-wide common variant association study in autism spectrum disorder.
Mendes M., Chen D.Z., Engchuan W., Leal T.P., Thiruvahindrapuram B., Trost B., Howe J.L., Pellecchia G., Nalpathamkalam T., Alexandrova R., Salazar N.B., McKee E.A., Rivera-Alfaro N., Lai M.-C., Bandres-Ciga S., Roshandel D., Bradley C.A., Anagnostou E., Sun L., Scherer S. W.
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.
Specific EEG resting state biomarkers in FXS and ASD.
Proteau-Lemieux M., Knoth I.S., Davoudi S., Martin C.-O., Bélanger A.-M., Fontaine V., Côté V., Agbogba K., Vachon K., Whitlock K., Biag H.M.B., Thurman A.J., Rosenfelt C., Tassone F., Frei J., Capano L., Abbeduto L., Jacquemont S., Hessl D., Hagerman R., Schneider A., Bolduc F., Anagnostou E., Lippé S.