SFARI | SFARI Funded Publications

Evaluation of data imputation strategies in complex, deeply-phenotyped data sets: The case of the EU-AIMS Longitudinal European Autism Project.

Llera A., Brammer M., Oakley B., Tillmann J., Zabihi M., Amelink J.S., Mei T., Charman T., Ecker C., Dell'Acqua F., Banaschewski T., Moessnang C., Baron-Cohen S., Holt R., Durston S., Murphy D., Loth E., Buitelaar J.K., Floris D.L., Beckmann C.F.

Convergent coexpression of autism associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies.

Liao C., Moyses-Oliveira M., de Esch C.E.F., Bhavsar R., Nuttle X., Li A., Yu A., Burt N.D., Erdin S., Fu J.M., Wang M., Morley T., Han L., CommonMind Consortium, Dion P.A., Rouleau G.A., Zhang B., Brennand K.J., Talkowski M., Ruderfer D.M.

Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functions.

Ramirez M., Badayeva Y., Yeung J., Wu J., Abdalla-Wyse A., Yang E., FANTOM 5 Consortium, Trost B., Scherer S. W., Goldowitz D.

Postmitotic accumulation of histone variant H3.3 in new cortical neurons establishes neuronal chromatin, transcriptome, and identity.

Funk O.H., Qalieh Y., Doyle D.Z., Lam M.M., Kwan K.

Digit ratio (2D:4D) and maternal testosterone-to-estradiol ratio measured in early pregnancy.

Richards G., Aydin E., Tsompanidis A., Padaigaitė E., Austin T., Allison C., Holt R., Baron-Cohen S.

Magnetoencephalography and electroencephalography can both detect differences in cortical responses to vibrotactile stimuli in individuals on the autism spectrum.

Ahlfors S.P., Graham S., Alho J., Joseph R.M., McGuiggan N.M., Nayal Z., Hämäläinen M.S., Khan S., Kenet T.

Clinical characteristics of seizures and epilepsy in individuals with recurrent deletions and duplications in the 16p11.2 region.

Moufawad El Achkar C., Rosen A., Kessler S.K., Steinman K.J., Spence S., Ramocki M., Marco E.J., Green Snyder L., Spiro J., Chung W., Annapurna P., Sherr E.

Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E mice.

Echevarria-Cooper D.M., Hawkins N.A., Misra S.N., Huffman A., Thaxton T., Thompson C.H., Ben-Shalom R., Nelson A.D., Lipkin A.M., George Jr. A. L., Bender K., Kearney J.A.

Ca2+ imaging of self and other in medial prefrontal cortex during social dominance interactions in a tube test.

Garcia-Font N., Mitchell-Heggs R., Saxena K., Gabbert C., Taylor G., Mastroberadino G., Spooner P.A., Gobbo F., Dabrowska J.K., Chattarji S., Kind P., Schultz S.R., Morris R.G.M.

D-aspartate oxidase gene duplication induces social recognition memory deficit in mice and intellectual disabilities in humans.

Lombardo B., Pagani M., De Rosa A., Nunziato M., Migliarini S., Garofalo M., Terrile M., D'Argenio V., Galbusera A., Nuzzo T., Ranieri A., Vitale A., Leggiero E., Di Maio A., Barsotti N., Borello U., Napolitano F., Mandarino A., Carotenuto M., Heresco-Levy U.,, Pasqualetti M., Malatesta P., Gozzi A., Errico F., Salvatore F., Pastore L., Usiello A.