Karen Pierce, Ph.D.

The ASD living biology: From cell proliferation to clinical phenotype. Courchesne E., Pramparo T., Gazestani V.H., Lombardo M.V., Pierce K., Lewis N.E.

Paternally inherited cis-regulatory structural variants are associated with autism. Brandler W.M., Antaki D., Gujral M., Kleiber M.L., Whitney J., Maile M.S., Hong O., Chapman T.R., Tan S., Tandon P., Pang T., Tang S.C., Vaux K.K., Yang Y., Harrington E., Juul S., Turner D.J., Thiruvahindrapuram B., Kaur G., Wang Z., Kingsmore S.F., Gleeson J., Bisson D., Kakaradov B., Telenti A., Venter J.C., Corominas R., Toma C., Cormand B., Rueda I., Guijarro S., Messer K.S., Nievergelt C.M., Arranz M.J., Courchesne E., Pierce K., Muotri A., Iakoucheva L., Hervas A., Scherer S. W., Corsello C., Sebat J.

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Geisheker M.R., Heymann G., Wang T., Coe B.P., Turner T.N., Stessman H., Hoekzema K., Kvarnung M., Shaw M., Friend K., Liebelt J., Barnett C., Thompson E.M., Haan E., Guo H., Anderlid B.M., Nordgren A., Lindstrand A., Vandeweyer G., Alberti A., Avola E., Vinci M., Giusto S., Pramparo T., Pierce K., Nalabolu S., Michaelson J., Sedlacek Z., Santen G.W.E., Peeters H., Hakonarson H., Courchesne E., Romano C., Kooy R.F., Bernier R., Nordenskjöld M., Gecz J., Xia K., Zweifel L.S., Eichler E.