SFARI | SFARI Funded Publications

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism.

Satterstrom F.K., Kosmicki J.A., Wang J., Breen M.S., De Rubeis S., An J.Y., Peng M., Collins R., Grove J., Klei L., Stevens C., Reichert J., Mulhern M.S., Artomov M., Gerges S., Sheppard B., Xu X., Bhaduri A., Norman U., Brand H., Schwartz G., Nguyen R., Guerrero E.E., Dias C., Autism Sequencing Consortium, iPSYCH-Broad Consortium, Betancur C., Cook E. H., Gallagher L., Gill M., Sutcliffe J., Thurm A., Zwick M.E., Børglum A.D., State M., Çiçek A. E., Talkowski M., Cutler D.J., Devlin B., Sanders S., Roeder K., Daly M., Buxbaum J.

Usp9X controls ankyrin-repeat domain protein homeostasis during dendritic spine development.

Yoon S., Parnell E., Kasherman M., Forrest M.P., Myczek K., Premarathne S., Sanchez Vega M.C., Piper M., Burne T.H.J., Jolly L.A., Wood S.A., Penzes P.

Psychotic symptoms in 16p11.2 copy-number variant carriers.

Jutla A., Turner J.B., Green Snyder L., Chung W., Veenstra-VanderWeele J.

Mechanisms underlying gain modulation in the cortex.

Ferguson K.A., Cardin J.

Using multiple measurements of tissue to estimate cell-type-specific gene expression via deconvolution.

Wang J., Devlin B., Roeder K.

Animal functional magnetic resonance imaging: Trends and path toward standardization.

Mandino F., Cerri D.H., Garin C.M., Straathof M., van Tilborg G.A.F., Chakravarty M.M., Dhenain M., Dijkhuizen R.M., Gozzi A., Hess A., Keilholz S.D., Lerch J.P., Shih Y.I., Grandjean J.

Autism spectrum disorder.

Lord C., Brugha T.S., Charman T., Cusack J., Dumas G., Frazier T., Jones E., Jones R., Pickles A., State M., Taylor J.L., Veenstra-VanderWeele J.

Common functional networks in the mouse brain revealed by multi-centre resting-state fMRI analysis.

Grandjean J., Canella C., Anckaerts C., Ayrancı G., Bougacha S., Bienert T., Buehlmann D., Coletta L., Gallino D., Gass N., Garin C.M., Nadkarni NA., Hübner N., Karatas M., Komaki Y., Kreitz S., Mandino F., Mechling A.E., Sato C., Sauer K., Shah D., Strobelt S., Takata N., Wank I., Wu T., Yahata N., Yeow L.Y., Yee Y., Aoki I., Chakravarty M.M., Chang W-T., Dhenain M., von Elverfeldt D., Harsan L-A., Hess A., Jiang T., Keliris G.A., Lerch J., Meyer-Lindenberg A., Okano H., Rudin M., Sartorius A., Van der Linden A., Verhoye M., Weber-Fahr W., Wenderoth N., Zerbi V., Gozzi A.

Synaptic dysfunction in human neurons with autism-associated deletions in PTCHD1-AS.

Ross P.J., Zhang W., Mok R.S.F., Zaslavsky K., Deneault E., D’Abate L., Rodrigues D.C., Yuen R.K.C., Faheem M., Mufteev M., Piekna A., Wei W., Pasceri P., Landa R., Nagy A., Varga B., Salter M.W., Scherer S. W., Ellis J.

A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency.

Mastro T.L., Preza A., Basu S., Chattarji S., Till S.M., Kind P., Kennedy M.B.