SFARI

The Relationships, Employment, Autonomy, and Life Satisfaction (REALS) measures for autistic adults and adults with other intellectual and developmental disabilities: Psychometric testing of the self-report and proxy versions.

Conner C.M., Yu L., MacKenzie K.T., Zeglen K.N., Rutenberg E.L., Pilkonis P.A., Eack S.M., Mazefsky C.A.

Chromosome X-wide common variant association study in autism spectrum disorder.

Mendes M., Chen D.Z., Engchuan W., Leal T.P., Thiruvahindrapuram B., Trost B., Howe J.L., Pellecchia G., Nalpathamkalam T., Alexandrova R., Salazar N.B., McKee E.A., Rivera-Alfaro N., Lai M.-C., Bandres-Ciga S., Roshandel D., Bradley C.A., Anagnostou E., Sun L., Scherer S. W.

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.

Scala M., Bradley C.A., Howe J.L., Trost B., Salazar N.B., Shum C., Mendes M., Reuter M.S., Anagnostou E., MacDonald J.R., Ko S.Y., Frankland P.W., Charlebois J., Elsabbagh M., Granger L., Anadiotis G., Pullano V., Brusco A., Keller R., Parisotto S., Pedro H.F., Lusk L., McDonnell P.P., Helbig I., Mullegama S.V., Undiagnosed Diseases Network, Douine E.D., Corona R.I., Russell B.E., Nelson S.F., Graziano C., Schwab M., Simone L., Zara F., Scherer S. W.

Using deep learning to classify developmental differences in reaching and placing movements in children with and without autism spectrum disorder.

Su W.-C., Mutersbaugh J., Huang W.-L., Bhat A., Gandjbakhche A.

Parental experiences and perspectives of healthcare providers’ genetic testing recommendations for their children diagnosed with autism spectrum disorder in the United States.

Zhao S., Li M., Chen W.-J., Rennie B.J., Hsiao Y.-Y., Guan Y.

Funded Publications

The Relationships, Employment, Autonomy, and Life Satisfaction (REALS) measures for autistic adults and adults with other intellectual and developmental disabilities: Psychometric testing of the self-report and proxy versions.

Chromosome X-wide common variant association study in autism spectrum disorder.

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.

Using deep learning to classify developmental differences in reaching and placing movements in children with and without autism spectrum disorder.

Parental experiences and perspectives of healthcare providers’ genetic testing recommendations for their children diagnosed with autism spectrum disorder in the United States.

Prematurity and genetic liability for autism spectrum disorder.

A deep learning model for prediction of autism status using whole-exome sequencing data.

Enrichment of a subset of Neanderthal polymorphisms in autistic probands and siblings.

Copy-number variants differ in frequency across genetic ancestry groups.

Delayed milestones and demographic factors relate to the accuracy of autism screening in females using spoken language.

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