SFARI | SFARI Funded Publications

Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells.

Prem S., Dev B., Peng C., Mehta M., Alibutud R., Connacher R.J., St. Thomas M., Zhou X., Matteson P., Xing J., Millonig J.H., DiCicco-Bloom E.

Focus on your locus with a massively parallel reporter assay.

McAfee J.C., Bell J.L., Krupa O., Matoba N., Stein J., Won H.

Autism is associated with interindividual variations of gray and white matter morphology.

Mei T., Forde N.J., Floris D.L., Dell’Acqua F., Stones R., Ilioska I., Durston S., Moessnang C., Banaschewski T., Holt R.J., Baron-Cohen S., Rausch A., Loth E., Oakley B., Charman T., Ecker C., Murphy D., EU-AIMS LEAP Group, Beckmann C.F., Llera A., Buitelaar J.K.

A capabilities approach to understanding and supporting autistic adulthood.

Pellicano E., Fatima U., Hall G., Heyworth M., Lawson W., Lilley R., Mahony J., Stears M.

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.

Antaki D., Guevara J., Maihofer A.X., Klein M., Gujral M., Grove J., Carey C.E., Hong O., Arranz M.J., Hervas A., Corsello C., Vaux K.K., Muotri A., Iakoucheva L., Courchesne E., Pierce K., Gleeson J., Robinson E., Nievergelt C.M., Sebat J.

Rare variants and the oligogenic architecture of autism.

Wang T., Zhao P.A., Eichler E.

Developmental variability in autism across 17000 autistic individuals and 4000 siblings without an autism diagnosis: Comparisons by cohort, intellectual disability, genetic etiology, and age at diagnosis.

Kuo S.S., van der Merwe C., Fu J.M., Carey C.E., Talkowski M., Bishop S., Robinson E.

Genetic correlates of phenotypic heterogeneity in autism.

Warrier V., Zhang X., Reed P., Havdahl A., Moore T.M., Cliquet F., Leblond C.S., Rolland T., Rosengren A., EU-AIMS-LEAP, iPSYCH-Autism Working Group, Spectrum 10K and APEX Consortia, Rowitch D., Hurles M., Geschwind D., Børglum A.D., Robinson E., Grove J., Martin H., Bourgeron T., Baron-Cohen S.

The impact of birth order on language development in autistic children from Simplex families.

McFayden T.C., Fok M., Ollendick T.H.

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.

Zhou X., Feliciano P., Shu C., Wang T., Astrovskaya I., Hall J., Obiajulu J.U., Wright J., Murali S., Xuming Xu S., Brueggeman L., Thomas T.R., Marchenko O., Fleisch C., Barns S.D., Green Snyder L., Han B., Chang T.S., Turner T., Harvey W.T., Nishida A., O'Roak B., Geschwind D., SPARK Consortium, Michaelson J., Volfovsky N., Eichler E., Shen Y., Chung W.