Funded Projects
SFARI Funded Publications
A cross-disorder dosage sensitivity map of the human genome.
Collins R.L., Glessner J.T., Porcu E., Lepamets M., Brandon R., Lauricella C., Han L., Morley T., Niestroj L.-M., Ulirsch J., Everett S., Howrigan D.P., Boone P.M., Fu J., Karczewski K.J., Kellaris G., Lowther C., Lucente D., Mohajeri K., Nõukas M., Nuttle X., Samocha K.E., Trinh M., Ullah F., Võsa U., Epi25 Consortium, Estonian Biobank Research Team, Hurles M., Aradhya S., Davis E.E., Finucane H., Gusella J., Janze A., Katsanis N., Matyakhina L., Neale B.M., Sanders D., Warren S., Hodge J.C., Lal D., Ruderfer D.M., Meck J., Mägi R., Esko T., Reymond A., Kutalik Z., Hakonarson H., Sunyaev S., Brand H., Talkowski M.
Oligogenic effects of 16p11.2 copy number variation on craniofacial development.
Qiu Y., Arbogast T., Lorenzo S.M., Li H., Tang S.C., Richardson E., Hong O., Cho S., Shanta O., Pang T., Corsello C., Deutsch C., Chevalier C., Davis E.E., Iakoucheva L., Herault Y., Katsanis N., Messer K., Sebat J.
Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus.
Männik K., Arbogast T., Lepamets M., Lepik K., Pellaz A., Ademi H., Kupchinsky Z.A., Ellegood J., Attanasio C., Messina A., Rotman S., Martin-Brevet S., Dubruc E., Chrast J., Lerch J., Qiu L.R., Laisk T., The 16p11.2 European Consortium, The Simons VIP Consortium, The eQTLGen Consortium, Henkelman R.M., Jacquemon S., Herault Y., Lindgren C.M., Peterson H., Stehle J.C., Katsanis N., Kutalik Z., Nef S., Draganski B., Davis E.E., Mägi R., Reymond A.