Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. Chan A.J.S., Engchuan W., Reuter M.S., Wang Z., Thiruvahindrapuram B., Trost B., Nalpathamkalam T., Negrijn C., Lamoureux S., Pellecchia G., Patel R.V., Sung W.W.L., MacDonald J.R., Howe J.L., Vorstman J., Sondheimer N., Takahashi N., Miles J., Anagnostou E., Tammimies K., Zarrei M., Merico D., Stavropoulos D.J., Yuen R.K.C., Fernandez B.A., Scherer S. W.

CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. Sugathan A., Biagioli M., Golzio C., Erdin S., Blumenthal I., Manavalan P., Ragavendran A., Brand H., Lucente D., Miles J., Sheridan S.D., Stortchevoi A., Kellis M., Haggarty S.J., Katsanis N., Gusella J., Talkowski M.

A multisite study of the clinical diagnosis of different autism spectrum disorders. Lord C., Petkova E., Hus V., Gan W., Lu F., Martin D.M., Ousley O., Guy L., Bernier R., Gerdts J., Algermissen M., Whitaker A., Sutcliffe J., Warren Z., Klin A., Saulnier C., Hanson E., Hundley R., Piggot J., Fombonne E., Steiman M., Miles J., Kanne S., Goin-Kochel R., Peters S.U., Cook E. H., Guter S., Tjernagel J., Green Snyder L., Bishop S., Esler A., Gotham K., Luyster R., Miller F., Olson J., Richler J., Risi S.