SFARI

Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.

Chan A.J.S., Engchuan W., Reuter M.S., Wang Z., Thiruvahindrapuram B., Trost B., Nalpathamkalam T., Negrijn C., Lamoureux S., Pellecchia G., Patel R.V., Sung W.W.L., MacDonald J.R., Howe J.L., Vorstman J., Sondheimer N., Takahashi N., Miles J., Anagnostou E., Tammimies K., Zarrei M., Merico D., Stavropoulos D.J., Yuen R.K.C., Fernandez B.A., Scherer S. W.

In vivo proximity ligation reveals endogenous candidate interactors of neurexin’s intracellular domain.

Profes M.S., Tiroumalechetty A., Patel N., Lauar S.S., Sidoli S., Kurshan P.

Rhesus monkey sociality is stable across time and linked to variation in the initiation but not receipt of prosocial behavior.

Talbot C.F., Madrid J.E., Del Rosso L.A., Capitanio J.P., Garner J.P., Parker K.

Associations between executive functioning, challenging behavior, and quality of life in children and adolescents with and without neurodevelopmental conditions.

Frazier T., Crowley E., Shih A., Vasudevan V., Karpur A., Uljarevic M., Cai R.Y.

Hyperexcitable and immature-like neuronal activity in the auditory cortex of adult rats lacking the language-linked CNTNAP2 gene.

Scott K.E., Mann R.S., Schormans A.L., Schmid S., Allman B.L.

Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations.

Mok R.S.F., Zhang W., Sheikh T.I., Pradeepan K., Fernandes I.R., DeJong L.C., Benigno G., Hildebrandt M.R., Mufteev M., Rodrigues D.C., Wei W., Piekna A., Liu J., Muotri A., Vincent J.B., Muller L., Martinez-Trujillo J., Salter M.W., Ellis J.

Cerebellar atypicalities in autism?

Laidi C., Floris D.L., Tillmann J., Elandaloussi Y., Zabihi M., Charman T., Wolfers T., Durston S., Moessnang C., Dell'Acqua F., Ecker C., Loth E., Murphy D., Baron-Cohen S., Buitelaar J.K., Marquand A.F., Beckmann C.F., Frouin V., Leboyer M., Duchesnay E., Coupé P., Houenou J., EU-AIMS LEAP Group.

Funded Publications