A statistical framework for mapping risk genes from de novo mutations in whole-genome-sequencing studies. Liu Y., Liang Y., Çiçek A. E., Li Z., Li J., Muhle R., Krenzer M., Mei Y., Wang Y., Knoblauch N., Morrison J., Zhao S., Jiang Y., Geller E., Ionita-Laza I., Wu J., Xia K., Noonan J., Sun Z.S., He X.

Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci. Sanders S., He X., Willsey A. J., Ercan-Sencicek A.G., Samocha K.E., Çiçek A. E., Murtha M.T., Bal V.H., Bishop S., Dong S., Goldberg A.P., Jinlu C., Keaney J.F. 3rd, Klei L., Mandell J.D., Moreno-De-Luca D., Poultney C.S., Robinson E., Smith L., Solli-Nowlan T., Su M.Y., Teran N.A., Walker M.F., Werling D., Beaudet A., Cantor R.M., Fombonne E., Geschwind D., Grice D.E., Lord C., Lowe J.K., Mane S.M., Martin D.M., Morrow E., Talkowski M., Sutcliffe J., Walsh C., Yu T., Autism Sequencing Consortium, Ledbetter D., Martin C. L., Cook E. H., Buxbaum J., Daly M., Devlin B., Roeder K., State M.

DAWN: A framework to identify autism genes and subnetworks using gene expression and genetics. Liu L., Lei J., Sanders S., Willsey A. J., Kou Y., Çiçek A. E., Klei L., Lu C., He X., Li M., Muhle R., Ma'ayan A., Noonan J., Sestan N., McFadden K.A., State M., Buxbaum J., Devlin B., Roeder K.