SFARI | SFARI Funded Publications

Neural mechanisms of sensorimotor transformation and action selection.

Huda R., Goard M.J., Pho G.N., Sur M.

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.

Pizzo L., Jensen M., Polyak A., Rosenfeld J.A., Mannik K., Krishnan A., McCready E., Pichon O., Le Caignec C., Van Dijck A., Pope K., Voorhoeve E., Yoon J., Stankiewicz P., Wai Cheung S., Pazuchanics D., Huber E., Kumar V., Kember R., Mari F., Curró A., Castiglia L., Galesi O., Avola E., Mattina T., Fichera M., Mandarà L., Vincent M., Nizon M., Mercier S., Bénéteau C., Blesson S., Martin-Coignard D., Mosca-Boidron A-L., Caberg J.H., Bucan M., Zeesman S., Nowaczyk M.J.M., Lefebvre M., Faivre L., Callier P., Skinner C., Keren B., Perrine C., Prontera P., Marle N., Renieri A., Reymond A., Kooy F.R., Isidor B., Schwartz B., Romano C., Sistermans E., Amor D.J., Andrieux J., Girirajan S.

How effective is LENA in detecting speech vocalizations and language produced by children and adolescents with ASD in different contexts?

Jones R., Plesa Skwerer D., Pawar R., Hamo A., Carberry C., Ajodan E.L., Caulley D., Silverman M.R., McAdoo S., Meyer S., Yoder A., Clements M. A., Lord C., Tager-Flusberg H.

Altered structural brain connectivity involving the dorsal and ventral language pathways in 16p11.2 deletion syndrome.

Ahtam B., Link N., Hoff E., Grant E., Im K.

Homer1a and mGluR1/5 signaling in homeostatic sleep drive and output.

Martin S.C., Monroe S.K., Diering G.

Brain organoids as a model system for human neurodevelopment and disease.

Setia H., Muotri A.

Widespread alterations in translation elongation in the brain of juvenile Fmr1 knockout mice.

Das Sharma S., Metz J.B., Li H., Hobson B.D., Hornstein N., Sulzer D., Tang G., Sims P.

A multifaceted approach for analyzing complex phenotypic data in rodent models of autism.

Das I., Estevez M.A., Sarkar A.A., Banerjee-Basu S.

Regulatory genes and pathways disrupted in autism spectrum disorders.

Ayhan F., Konopka G.

Identification of common genetic risk variants for autism spectrum disorder.

Grove J., Ripke S., Als T.D., Mattheisen M., Walters R.K., Won H., Pallesen J., Agerbo E., Andreassen O.A., Anney R., Awashti S., Belliveau R., Bettella F., Buxbaum J., Bybjerg-Grauholm J., Bækvad-Hansen M., Cerrato F., Chambert K., Christensen J.H., Churchhouse C., Dellenvall K., Demontis D., De Rubeis S., Devlin B., Djurovic S., Dumont A.L., Goldstein J.I., Hansen C.S., Hauberg M.E., Hollegaard M.V., Hope S., Howrigan D.P., Huang H., Hultman C.M., Klei L., Maller J., Martin J., Martin A.R., Moran J.L., Nyegaard M., Nærland T., Palmer D.S., Palotie A., Pedersen C.B., Pedersen M.G., dPoterba T., Poulsen J.B., St Pourcain B., Qvist P., Rehnström K., Reichenberg A., Reichert J., Robinson E., Roeder K., Roussos P., Saemundsen E., Sandin S., Satterstrom F.K., Davey Smith G., Stefansson H., Steinberg S., Stevens C.R., Sullivan P.F., Turley P., Walters G.B., Xu X., Autism Spectrum Disorder Working Group of the Psychiatric Genomics C., BUPGEN, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 23andMe Research Team, Stefansson K., Geschwind D., Nordentoft M., Hougaard D.M., Werge T., Mors O., Mortensen P.B., Neale B.M., Daly M., Børglum A.D.