SFARI | SFARI Funded Publications

Large-scale analyses of the relationship between sex, age and intelligence quotient heterogeneity and cortical morphometry in autism spectrum disorder.

Bedford S.A., Park M.T.M., Devenyi G.A., Tullo S., Germann J., Patel R., Anagnostou E., Baron-Cohen S., Bullmore E.T., Chura L.R., Craig M.C., Ecker C., Floris D.L., Holt R.J., Lenroot R., Lerch J., Lombardo M., Murphy D., Raznahan A., Ruigrok A.N.V., Smith E., Spencer M.D., Suckling J., Taylor M.J., Thurm A., MRC AIMS Consortium, Lai M.-C., Chakravarty M.M.

Mania- and anxiety-like behavior and impaired maternal care in female diacylglycerol kinase eta and iota double knockout mice.

Bartsch V.B., Lord J.S, Diering G., Zylka M.

Autism heterogeneity in a densely sampled U.S. population: Results from the first 1,000 participants in the RI-CART study.

McCormick C.E.B., Kavanaugh B.C., Sipsock D., Righi G., Oberman L.M., Moreno De Luca D., Gamsiz Uzun E.D., Best C.R., Jerskey B.A., Quinn J.G., Jewel S.B., Wu P.C., McLean R.L., Levine T.P., Tokadjian H., Perkins K.A., Clarke E.B., Dunn B., Gerber A.H., Tenenbaum E., Anders T.F., Rhode Island Consortium for Autism Research and Treatment (RI-CART), Sheinkopf S., Morrow E.

Natural selection influenced the genetic architecture of brain structure, behavioral and neuropsychiatric traits.

Wendt F.R., Pathak G.A., Overstreet C., Tylee D.S., Gelernter J., Atkinson E.G., Polimanti R.

Maternal experience-dependent cortical plasticity in mice is circuit- and stimulus-specific and requires MECP2.

Lau B.Y.B., Krishnan K., Huang Z.J., Shea S.

Recent ultra-rare inherited mutations identify novel autism candidate risk genes.

Wilfert A.B., Turner T.N., Murali S.C., Hsieh P., Sulovari A., Wang T., Coe B.P., Guo H., Hoekzema K., Bakken T.E., Winterkorn L.H., Evani U.S., Byrska-Bishop M., Earl R.K., Bernier R., the SPARK Consortium, Zody M.C., Eichler E.

Beliefs in vaccine as causes of autism among SPARK cohort caregivers.

Fombonne E., Goin-Kochel R., O'Roak B., SPARK Consortium.

Genome-wide molecular effects of the neuropsychiatric 16p11 CNVs in an iPSC-to-iN neuronal model.

Ward T.R., Zhang X., Leung L.C., Zhou B., Muench K., Roth J.G., Khechaduri A., Plastini M.J., Charlton C., Pattni R., Ho S., Ho M., Huang Y., Hallmayer J.F., Mourrain P., Palmer T., Urban A.E.

Exploring the familial role of social responsiveness differences between savant and non-savant children with autism.

Daniel E., Menashe I.

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism.

Satterstrom F.K., Kosmicki J.A., Wang J., Breen M.S., De Rubeis S., An J.Y., Peng M., Collins R., Grove J., Klei L., Stevens C., Reichert J., Mulhern M.S., Artomov M., Gerges S., Sheppard B., Xu X., Bhaduri A., Norman U., Brand H., Schwartz G., Nguyen R., Guerrero E.E., Dias C., Autism Sequencing Consortium, iPSYCH-Broad Consortium, Betancur C., Cook E. H., Gallagher L., Gill M., Sutcliffe J., Thurm A., Zwick M.E., Børglum A.D., State M., Çiçek A. E., Talkowski M., Cutler D.J., Devlin B., Sanders S., Roeder K., Daly M., Buxbaum J.