Somer Bishop, Ph.D.

Assistant Professor, University of California, San Francisco

SFARI Investigator, SFARI Scientific Review Board Website

Funded Projects

SFARI Funded Publications

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk. Satterstrom F.K., Kosmicki, J.A., Wang J., Breen M.S., Rubeis S.D., An J-Y., Peng M., Collins R.L., Grove J., Lambertus K., Stevens C., Reichart J., Mulhern M., Artomov M., Gerges S., Sheppard B., Xu X., Bhaduri A., Norman U., Brand H., Schwartz G., Nguyen R., Guerrero E., Dias C., Aleksic B., Anney R.J.L., Barbosa M., Bishop S., Brusco A., Bybjerg-Grauholm J., Carracedo A., Chan M.C.Y., Chiocchetti A., Chung B., Coon H., Cuccaro M., Curró A., Bernardina B.D., Doan R., Domenici E., Dong S., Fallerini C., Fernández-Prieto M., Ferrero G.B., Freitag C.M., Fromer M., Gargus J.J., Geschwind D., Giorgio E., González-Peñas J., Guter S., Halpern D., Hassen-Kiss E., He X., Herman G., Hertz-Picciotto I., Hougaard D.M., Hultman C.M., Ionita-Laza I., Jacob S., Jamison J., Jugessur A., Kaartinen M., Knudsen G.P., Kolevzon A., Kushima I., Lee S.L., Lehtimäki T., Lim E.T., Lintas C., Lipkin W. I., Lopergolo D.L., Lopes F., Ludena Y., Maciel P., Magnus P. , Mahjani B., Maltman N., Manoach D.S., Meiri G., Menashe I., Miller J., Minshew N., de Souza E.M.M., Moreira D., Morrow E., Mors O., Mortensen P.B., Mosconi M., Muglia P., Neale B., Nordentoft M., Ozaki N., Palotie A., Parellada M., Passos-Bueno M.R., Pericak-Vance M., Persico A., Pessah I., Puura K., Reichenberg A., Renieri A., Riberi E., Robinson E., Samocha K.E., Sandin S., Santangelo S.L., Schellenberg G., Scherer S. W., Sabine S., Schmidt R., Schmitt L., Silva I.M.W., Singh T., Siper P., Smith M., Soares G., Stoltenberg C., Suren P., Susser E., Sweeney J., Szatmari P., Tang L., Tassone F., Teufel K., Trabetti E., del Pilar Trelles M., Walsh C., Weiss L., Werge T., Werling D., Wigdor E.M., Wilkinson E., Willsey A. J., Yu T., Yu M.H.C., Yuen R., Zachi E., Betancur C., Cook E. H., Gallagher L., Gill M., Lehner T., Senthil G., Sutcliffe J., Thurm A., Zwick M.E., Børglum A.D., State M., Cicek A. E., Talkowski M., Cutler D.J., Devlin B., Sanders S., Roeder K., Buxbaum J., Daly M.
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Weiner D.J., Wigdor E.M., Ripke S., Walters R.K., Kosmicki J.A., Grove J., Samocha K.E., Goldstein J.I., Okbay A., Bybjerg-Grauholm J., Werge T., Hougaard D.M., Taylor J., iPSYCH-Board Autism Group, Psychiatric Genomics Consortium Autism Group, Skuse D., Devlin B., Anney R., Sanders S., Bishop S., Mortensen P.B., Borglum A.D., Smith G.D., Daly M., Robinson E.
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