Identifying crossovers and shared genetic material in whole genome sequencing data from families. Paskov K., Chrisman B., Stockham N., Washington P.Y., Dunlap K., Jung J.-Y., Wall D.

The contributions of rare inherited and polygenic risk to ASD in multiplex families. Cirnigliaro M., Chang T.S., Arteaga A.S., Pérez-Cano L., Ruzzo E.K., Gordon A., Bicks L.K., Jung J.-Y., Lowe J.K., Wall D., Geschwind D.

Multi-omic analysis along the gut-brain axis points to a functional architecture of autism. Morton J.T., Jin D.-m., Mills R., Shao Y., Rahman G., McDonald D., Zhu Q., Balaban M., Jiang Y., Cantrell K., Gonzalez A., Carmel J., Frankiensztajn L.M., Martin-Brevet S., Harold-Berding K., Needham B.D., Zurita M.F., David M., Averina O., Kovtun A., Noto A., Mussap M., Wang M., Frank D.N., Li E., Zhou W., Fanos V., Danilenko V., Wall D., Cárdenas P., Baldeón M.E., Jacquemont S., Koren O., Elliott E., Xavier R.J., Mazmanian S., Knight R., Gilbert J.A., Donovan S.M., Lawley T.D., Carpenter B., Bonneau R., Taroncher-Oldenburg G.