SFARI | SFARI Funded Publications

Mapping human social brain specialisation beyond the neuron using multimodal imaging in human infants.

Siddiqui M., Pinti P., Brigadoi S., Lloyd-Fox S., Elwell C.E., Johnson M., Tachtsidis I., Jones E.

Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD.

Gandal M., Haney J.R., Wamsley B., Yap C.X., Parhami S., Emani P.S., Chang N., Chen G.T., Hoftman G.D., de Alba D., Ramaswami G., Hartl C.L., Bhattacharya A., Luo C., Jin T., Wang D., Kawaguchi R., Quintero D., Ou J., Wu Y.E., Parikshak N.N., Swarup V., Belgard T.G., Gerstein M., Pasaniuc B., Geschwind D.

Behavioral responses to fevers and other medical events in children with and without ASD.

Byrne K., Zheng S., Bishop S., Boucher J., Ghods S., Kim S. H., Lord C.

Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder.

Kim I.B., Lee T., Lee J., Kim J., Lee S., Koh I.G., Kim J.H., An J.-Y., Lee H., Kim W.K., Ju Y.S., Cho Y., Yu S.J., Kim S.A., Oh M., Han D.W., Kim E., Choi J.K., Yoo H.J., Lee J.H.

Co-occurring ADHD symptoms in autistic adults are associated with less independence in daily living activities and lower subjective quality of life.

Yerys B.E., McQuaid G.A., Lee N.R., Wallace G.L.

Intact amphetamine-induced behavioral sensitization in mice with increased or decreased neuronal glutamate transporter SLC1A1/EAAT3.

Chohan M.O., Yueh H., Fein H., Kopelman J.M., Ahmari S.E., Veenstra-VanderWeele J.

Generation of DNA methylation signatures and classification of variants in rare neurodevelopmental disorders using epigencentral.

Awamleh Z., Goodman S., Kallurkar P., Wu W., Lu K., Choufani S., Turinsky A.L., Weksberg R.

Ketamine induces multiple individually distinct whole-brain functional connectivity signatures.

Moujaes F., Ji J.L., Rahmati M., Burt J., Schleifer C.H., Adkinson B., Savič A., Santamauro N., Tamayo Z., Diehl C., Kolobaric A., Flynn M., Rieser N.M., Fonteneau C., Camarro T., Xu J., Cho Y.T., Repovš G., Fineberg S.K., Morgan P., Seifritz E., Vollenweider F.X., Krystal J., Murray J. D., Preller K.H., Anticevic A.

Sensory processing in 16p11.2 deletion and 16p11.2 duplication.

Smith H., Lane C., Al-Jawahiri R., Freeth M.

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.

Weiner D.J., Ling E., Erdin S., Tai D.J.C., Yadav R., Grove J., Fu J.M., Nadig A., Carey C.E., Baya N., Bybjerg-Grauholm J., iPSCYH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta S., Macosko E.Z., Sebat J., O’Connor L.J., Hougaard D.M., Børglum A.D., Talkowski M., McCarroll S., Robinson E.