SFARI | SFARI Funded Publications

The NeuroDev study: Phenotypic and genetic characterization of neurodevelopmental disorders in Kenya and South Africa.

de Menil V., Hoogenhout M., Kipkemoi P., Kamuya D., Eastman E., Galvin A., Mwangasha K., de Vries J., Kariuki S.M., Murugasen S., Mwangi P., Singh I., Stein D.J., Abubakar A., Newton C., Donald K., Robinson E.

Deregulation of synaptic plasticity in autism.

Hansel C.

The ASD living biology: From cell proliferation to clinical phenotype.

Courchesne E., Pramparo T., Gazestani V.H., Lombardo M., Pierce K., Lewis N.E.

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.

Coe B.P., Stessman H., Sulovari A., Geisheker M.R., Bakken T.E., Lake A.M., Dougherty J., Lein E.S., Hormozdiari F., Bernier R., Eichler E.

Interacting neural ensembles in orbitofrontal cortex for social and feeding behaviour.

Jennings J.H., Kim C.K., Marshel J.H., Raffiee M., Ye L., Quirin S., Pak S., Ramakrishnan C., Deisseroth K.

Early motor abilities in infants at heightened versus low risk for ASD: A Baby Siblings Research Consortium (BSRC) study.

Iverson J.M., Shic F., Wall C.A., Chawarska K., Curtin S., Estes A., Gardner J.M., Hutman T., Landa R., Levin A.R., Libertus K., Messinger D.S., Nelson C. A., Ozonoff S., Sacrey L.R., Sheperd K., Stone W.L., Tager-Flusberg H., Wolff J.J., Yirmiya N., Young G.S.

Outgroup machine learning approach identifies single nucleotide variants in noncoding DNA associated with autism spectrum disorder.

Varma M., Paskov K.M., Jung J.Y., Sierra Chrisman B., Stockham N.T., Washington P.Y., Wall D.

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.

An J.Y., Lin K., Zhu L., Werling D., Dong S., Brand H., Wang H.Z., Zhao X., Schwartz G.B., Collins R.L., Currall B.B., Dastmalchi C., Dea J., Duhn C., Gilson M.C., Klei L., Liang L., Markenscoff-Papadimitriou E., Pochareddy S., Ahituv N., Buxbaum J., Coon H., Daly M., Kim Y.S., Marth G., Neale B.M., Quinlan A., Rubenstein J., Sestan N., State M., Willsey A. J., Talkowski M., Devlin B., Roeder K., Sanders S.

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.

Gandal M., Zhang P., Hadjimichael E., Walker R.L., Chen C., Liu S., Won H., van Bakel H., Varghese M., Wang Y., Shieh A.W., Haney J., Parhami S., Belmont J., Kim M., Moran Losada P., Khan Z., Mleczko J., Xia Y., Dai R., Wang D., Yang Y.T., Xu M., Fish K., Hof P.R., Warrell J., Fitzgerald D., White K., Jaffe A.E., PsychEncode Consortium, Peters M.A., Gerstein M., Liu C., Iakoucheva L., Pinto D., Geschwind D.

Integrative functional genomic analysis of human brain development and neuropsychiatric risks.

Li M., Santpere G., Imamura Kawasawa Y., Evgrafov O.V., Gulden F.O., Pochareddy S., Sunkin S.M., Li Z., Shin Y., Zhu Y., Sousa A. M. M., Werling D., Kitchen R.R., Kang H.J., Pletikos M., Choi J., Muchnik S., Xu X., Wang D., Lorente-Galdos B., Liu S., Giusti-Rodriguez P., Won H., de Leeuw C.A., Pardinas A.F., BrainSpan Consortium, PsychEncode Consortium, PsychEncode Developmental Subgroup, Hu M., Jin F., Li Y., Owen M.J., O'Donovan M.C., Walters J.T.R., Posthuma D., Levitt P., Weinberger D.R., Hyde T.M., Kleinman J.E., Geschwind D., Hawrylycz M.J., State M., Sanders S., Sullivan P.F., Gerstein M.B., Lein E.S., Knowles J.A., Sestan N.