SFARI | SFARI Funded Publications

The impact of birth order on language development in autistic children from Simplex families.

McFayden T.C., Fok M., Ollendick T.H.

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.

Zhou X., Feliciano P., Shu C., Wang T., Astrovskaya I., Hall J., Obiajulu J.U., Wright J., Murali S., Xuming Xu S., Brueggeman L., Thomas T.R., Marchenko O., Fleisch C., Barns S.D., Green Snyder L., Han B., Chang T.S., Turner T., Harvey W.T., Nishida A., O'Roak B., Geschwind D., SPARK Consortium, Michaelson J., Volfovsky N., Eichler E., Shen Y., Chung W.

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.

Fu J.M., Satterstrom F.K., Peng M., Brand H., Collins R.L., Dong S., Wamsley B., Klei L., Wang L., Hao S.P., Stevens C.R., Cusick C., Babadi M., Banks E., Collins B., Dodge S., Gabriel S.B., Gauthier L., Lee S.K., Liang L., Ljungdahl A., Mahjani B., Sloofman L., Smirnov A., Barbosa M., Betancur C., Brusco A., Chung B.H.Y., Cook E. H., Cuccaro M.L., Domenici E., Ferrero G.B., Gargus J.J., Herman G.E., Hertz-Picciotto I., Maciel P., Manoach D., Passos-Bueno M.R., Persico A.M., Renieri A., Sutcliffe J., Tassone F., Trabetti E., Campos G., Cardaropoli S., Carli D., Chan M.C.Y., Fallerini C., Giorgio E., Girardi A.C., Hansen-Kiss E., Lee S.L., Lintas C., Ludena Y., Nguyen R., Pavinato L., Pericak-Vance M., Pessah I.N., Schmidt R. J., Smith M., Souza C.I.S., Trajkova S., Wang J.Y.T., Yu M.H.C., Autism Sequencing Consortium (ASC), Broad Institute Center for Common Disease Genomics (Broad-CCDG), iPSYCH-BROAD Consortium, Cutler D.J., Rubeis S.D., Buxbaum J., Daly M., Devlin B., Roeder K., Sanders S., Talkowski M.

Altered theta-beta ratio in infancy associates with family history of ADHD and later ADHD-relevant temperamental traits.

Begum-Ali J., Goodwin A., Mason L., Pasco G., Charman T., Johnson M., Jones E., STAARS Team

Examining the factor structure and discriminative utility of the infant behavior questionnaire-revised in infant siblings of autistic children.

Sung S., Fenoglio A., Wolff J.J., Schultz R., Botteron K., Dager S., Estes A.M., Hazlett H., Zwaigenbaum L., Piven J., Elison J.T., IBIS Network

Measuring transcription factor binding and gene expression using barcoded self-reporting transposon calling cards and transcriptomes.

Lalli M., Yen A., Thopte U., Dong F., Moudgil A., Chen X., Milbrandt J., Dougherty J., Mitra R.

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Eising E., Mirza-Schreiber N., de Zeeuw E.L., Wang C.A., Truong D.T., Allegrini A.G., Shapland C.Y., Zhu G., Wigg K.G., Gerritse M.L., Molz B., Alagöz G., Gialluisi A., Abbondanza F., Rimfeld K., van Donkelaar M.M., Liao Z., Jansen P.R., Andlauer T.F.M., Bates T.C., Bernard M., Blokland K., Bonte M., Børglum A.D., Bourgeron T., Brandeis D., Ceroni F., Csépe V., Dale P.S., de Jong P.F., DeFries J.C., Démonet J.F., Demontis D., Feng Y., Gordon S.D., Guger S.L., Hayiou-Thomas M.E., Hernández-Cabrera J.A., Hottenga J.-J., Hulme C., Kere J., Kerr E.N., Koomar T., Landerl K., Leonard G.T., Lovett M.W., Lyytinen H., Martin N.G., Martinelli A., Maurer U., Michaelson J., Moll K., Monaco A., Morgan A.T., Nöthen M.M., Pausova Z., Pennell C.E., Pennington B., Price K.M., Rajagopal V.M., Ramus F., Richer L., Simpson N.H., Smith S.D., Snowling M.J., Stein J., Strug L.J., Talcott J.B., Tiemeier H., van der Schroeff M.P., Verhoef E., Watkins K.E., Wilkinson M., Wright M.J., Barr C.L., Boomsma D.I., Carreiras M., Franken M.-C.J., Gruen J.R., Luciano M., Müller-Myhsok B., Newbury D.F., Olson R.K., Paracchini S., Paus T., Plomin R., Reilly S., Schulte-Körne G., Tomblin J.B., van Bergen E., Whitehouse A.J.O., Willcutt E.G., St Pourcain B., Francks C., Fisher S.

Early life sleep disruption potentiates lasting sex-specific changes in behavior in genetically vulnerable Shank3 heterozygous autism model mice.

Lord J.S., Gay S.M., Harper K.M., Nikolova V.D., Smith K.M., Moy S.S., Diering G.

Isoform-level transcriptome-wide association uncovers extensive novel genetic risk mechanisms for neuropsychiatric disorders in the human brain.

Bhattacharya A., Jops C., Kim M., Wen C., Vo D.D., Hervoso J.L., Pasaniuc B., Gandal M.

Rapid specification of human pluripotent stem cells to functional astrocytes.

Lendemeijer B., Unkel M., Mossink B., Hijazi S., Sampedro S.G., Shpak G., Slump D.E., van den Hout M.C.G.N., van IJcken W.F.J., Bindels E.M.J., Hoogendijk W.J.G., Kasri N. N., de Vrij F.M.S., Kushner S.A.