SFARI

Challenges in screening for de novo noncoding variants contributing to genetically complex phenotypes.

Castro C.P., Diehl A.G., Boyle A.P.

Sharing parental genomes by siblings concordant or discordant for autism.

Wroten M., Yoon S., Andrews P., Yamrom B., Ronemus A., Buja A., Krieger A., Levy D., Ye K., Wigler M., Iossifov I.

Dimensional assessment of restricted and repetitive behaviors: Development and preliminary validation of a new measure.

Uljarević M., Frazier T., Jo B., Scahill L., Youngstrom E.A., Spackman E., Phillips J.M., Billingham W., Hardan A.

Identifying rare genetic variants in 21 highly multiplex autism families: The role of diagnosis and autistic traits.

More R.P., Warrier V., Brunel H., Buckingham C., Smith P., Allison C., Holt R., Bradshaw C.R., Baron-Cohen S.

Effect of children’s autism spectrum disorder severity on family strain and sleep quality: A cross-sectional online survey in the U.S.

Durán-Pacheco G., Silkey M., Johnson M., Liu C., Clinch S., Law K., Loss G.

Functional brain networks reflect spatial and temporal autocorrelation.

Shinn M., Hu A., Turner L., Noble S., Preller K.H., Li J.L., Mouajes F., Achard S., Scheinost D., Constable R.T., Krystal J.H., Vollenweider F.X., Lee D., Anticevic A., Bullmore E.T., Murray J. D.

Using brain cell-type-specific protein interactomes to interpret genetic data in schizophrenia.

Hsu Y.-H.H., Nacu E., Liu R., Kim A., Tsafou K., Petrossian N., Crotty W., Suh J.M., Pintacuda G., Riseman J., Martín J.M., Malolepsza E., Li T., Singh T., Ge T., Egri S.B., Tanenbaum B., Stanclift C.R., Apffel A.M., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Stanley Global Asia Initiatives, Carr S.A., Schenone M., Jaffe J., Fornelos N., Huang H., Eggan K. C., Lage K.

Funded Publications