SFARI | SFARI Funded Publications

What are you looking at? Gaze following with and without target objects in asd and typical development.

Thorup E., Nyström P., Bölte S., Falck-Ytter T.

Social attention in anorexia nervosa and autism spectrum disorder: Role of social motivation.

Kerr-Gaffney J., Jones E., Mason L., Hayward H., Murphy D., Loth E., Tchanturia K.

Reexamining empathy in autism: Empathic disequilibrium as a novel predictor of autism diagnosis and autistic traits.

Shalev I., Warrier V., Greenberg D.M., Smith P., Allison C., Baron-Cohen S., Eran A., Uzefovsky F.

Combinations of genes at the 16p11.2 and 22q11.2 CNVs contribute to neurobehavioral traits.

Vysotskiy M., Autism Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Weiss L.

Prioritizing de novo autism risk variants with calibrated gene- and variant-scoring models.

Jiang Y., Urresti J., Pagel K.A., Pramod A.B., Iakoucheva L., Radivojac P.

Genome-wide by environment interaction study of stressful life events and hospital-treated depression in the iPSYCH2012 sample.

Suppli N.P., Andersen K.K., Agerbo E., Rajagopal V.M., Appadurai V., Coleman J.R.I., Breen G., Bybjerg-Grauholm J., Bækvad-Hansen M., Pedersen C.B., Pedersen M.G., Thompson W.K., Munk-Olsen T., Benros M.E., Als T.D., Grove J., Werge T., Børglum A.D., Hougaard D.M., Mors O., Nordentoft M., Mortensen P.B., Musliner K.L.

High body mass polygenic risk in mothers enhances de novo functional mutations in epigenetic and microtubule gene pathways in their offspring with autism spectrum disorder.

Lohman B., Shabalin A.A., Farrell A., Marth G., Docherty A., Coon H.

Atypical gaze patterns in autistic adults are heterogeneous across but reliable within individuals.

Keles U., Kliemann D., Byrge L., Saarimäki H., Paul L.K., Kennedy D.P., Adolphs R.

Cell-type specific transcriptomic signatures of neocortical circuit organization and their relevance to autism.

Moussa A.J., Wester J.

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders.

Lowther C., Valkanas E., Giordano J.L., Wang H.Z., Currall B.B., O'Keefe K., Pierce-Hoffman E., Kurtas N., Whelan C.W., Hao S.P., Weisburd B., Jalili V., Fu J., Wong I., Collins R.L., Zhao X., Austin-Tse C.A., Evangelista E., Lemire G., Aggarwal V.S., Lucente D., Gauthier L.D., Tolonen C., Sahakian N., Stevens C., An J.-Y., Dong S., Norton M.E., MacKenzie T., Devlin B., Gilmore K., Powell B., Brandt A., Vetrini F., DiVito M., Sanders S., MacArthur D.G., Hodge J.C., O'Donnell-Luria A.H., Rehm H.L., Vora N.L., Levy B., Brand H., Wapner R., Talkowski M.