SFARI

Anthony Monaco, M.D., Ph.D.

President Emeritus and Professor of Biology and Neuroscience, Tufts University

SFARI Investigator Website

Anthony Monaco is a SFARI Investigator and professor of biology and president emeritus at Tufts University.

Funded Projects

Identifying and understanding the action of autism susceptibility genes

Awarded: 2006
Award Type: Research

SFARI Funded Publications

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Eising E., Mirza-Schreiber N., de Zeeuw E.L., Wang C.A., Truong D.T., Allegrini A.G., Shapland C.Y., Zhu G., Wigg K.G., Gerritse M.L., Molz B., Alagöz G., Gialluisi A., Abbondanza F., Rimfeld K., van Donkelaar M.M., Liao Z., Jansen P.R., Andlauer T.F.M., Bates T.C., Bernard M., Blokland K., Bonte M., Børglum A.D., Bourgeron T., Brandeis D., Ceroni F., Csépe V., Dale P.S., de Jong P.F., DeFries J.C., Démonet J.F., Demontis D., Feng Y., Gordon S.D., Guger S.L., Hayiou-Thomas M.E., Hernández-Cabrera J.A., Hottenga J.-J., Hulme C., Kere J., Kerr E.N., Koomar T., Landerl K., Leonard G.T., Lovett M.W., Lyytinen H., Martin N.G., Martinelli A., Maurer U., Michaelson J., Moll K., Monaco A., Morgan A.T., Nöthen M.M., Pausova Z., Pennell C.E., Pennington B., Price K.M., Rajagopal V.M., Ramus F., Richer L., Simpson N.H., Smith S.D., Snowling M.J., Stein J., Strug L.J., Talcott J.B., Tiemeier H., van der Schroeff M.P., Verhoef E., Watkins K.E., Wilkinson M., Wright M.J., Barr C.L., Boomsma D.I., Carreiras M., Franken M.-C.J., Gruen J.R., Luciano M., Müller-Myhsok B., Newbury D.F., Olson R.K., Paracchini S., Paus T., Plomin R., Reilly S., Schulte-Körne G., Tomblin J.B., van Bergen E., Whitehouse A.J.O., Willcutt E.G., St Pourcain B., Francks C., Fisher S.

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Pagnamenta A.T., Khan H., Walker S., Gerrelli D., Wing K., Bonaglia M.C., Giorda R., Berney T., Mani E., Molteni M., Pinto D., Le Couteur A., Hallmayer J., Sutcliffe J., Szatmari P., Paterson A.D., Scherer S. W., Vieland V.J., Monaco A.

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Noor A., Whibley A., Marshall C.R., Gianakopoulos P.J., Piton A., Carson A.R., Orlic-Milacic M., Lionel A.C., Sato D., Pinto D., Drmic I., Noakes C., Senman L., Zhang X., Mo R., Gauthier J., Crosbie J., Pagnamenta A.T., Munson J., Estes A.M., Fiebig A., Franke A., Schreiber S., Stewart A.F.R., Roberts R., McPherson R., Guter S.J., Cook E. H., Dawson G., Schellenberg G.D., Battaglia A., Maestrini E., Jeng L., Hutchison T., Rajcan-Separovic E., Chudley A.E., Lewis S.M.E., Liu X., Holden J.J., Fernandez B., Zwaigenbaum L., Bryson S.E., Roberts W., Szatmari P., Gallagher L., Stratton M.R., Gecz J., Brady A.F., Schwartz C.E., Schachar R.J., Monaco A., Rouleau G., Hui C-C., Lucy Raymond F., Scherer S. W., Vincent J.B.