Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Weiner D.J., Ling E., Erdin S., Tai D.J.C., Yadav R., Grove J., Fu J.M., Nadig A., Carey C.E., Baya N., Bybjerg-Grauholm J., iPSCYH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta S., Macosko E.Z., Sebat J., O’Connor L.J., Hougaard D.M., Børglum A.D., Talkowski M., McCarroll S., Robinson E.

Repeat polymorphisms in non-coding DNA underlie top genetic risk loci for glaucoma and colorectal cancer. Mukamel R.E., Handsaker R.E., Sherman M.A., Barton A.R., Hujoel M.L.A., McCarroll S., Loh P.-R.

Insights into dispersed duplications and complex structural mutations from whole genome sequencing 706 families. Whelan C.W., Handsaker R.E., Genovese G., Kashin S., Lek M., Hughes J., McElwee J., Lenardo M., MacArthur D., McCarroll S.