SFARI | SFARI Funded Publications

An expanded sequence context model broadly explains variability in polymorphism levels across the human genome.

Aggarwala V., Voight B.F.

Is there concordance in attitudes and beliefs between parents and scientists about autism spectrum disorder?

Fischbach R.L., Harris M.J., Ballan M.S., Fischbach G., Link B.G.

Clinical phenotype of the recurrent 1q21.1 copy-number variant.

Bernier R., Steinman K.J., Reilly B., Wallace A.S., Sherr E., Pojman N., Mefford H., Gerdts J., Earl R., Hanson E., Goin-Kochel R., Berry L., Kanne S., Green Snyder L., Spence S., Ramocki M.B., Evans D.W., Spiro J., Martin C. L., Ledbetter D., Chung W.

Feedback modulation of neural network synchrony and seizure susceptibility by Mdm2-p53-Nedd4-2 signaling.

Jewett K.A., Christian C.A., Bacos J.T., Lee K. J., Zhu J., Tsai N.

Unifying views of autism spectrum disorders: A consideration of autoregulatory feedback loops.

Mullins C., Fishell G., Tsien R.

Prenatal neurogenesis in autism spectrum disorders.

Kaushik G., Zarbalis K.

Disruption of POGZ is associated with intellectual disability and autism spectrum disorders.

Stessman H., Willemsen M.H., Fenckova M., Penn O., Hoischen A., Xiong B., Wang T., Hoekzema K., Vives L., Vogel I., Brunner H.G., van der Burgt I., Ockeloen C.W., Schuurs-Hoeijmakers J.H., Klein Wassink-Ruiter J.S., Stumpel C., Stevens S.J., Vles H.S., Marcelis C.M., van Bokhoven H., Cantagrel V., Colleaux L., Nicouleau M., Lyonnet S., Bernier R., Gerdts J., Coe B.P., Romano C., Alberti A., Grillo L., Scuderi C., Nordenskjöld M., Kvarnung M., Guo H., Xia K., Piton A., Gerard B., Genevieve D., Delobel B., Lehalle D., Perrin L., Prieur F., Thevenon J., Gecz J., Shaw M., Pfundt R., Keren B., Jacquette A., Schenck A., Eichler E., Kleefstra T.

Altered functional connectivity networks in acallosal and socially impaired BTBR mice.

Sforazzini F., Bertero A., Dodero L., David G., Galbusera A., Scattoni M.L., Pasqualetti M., Gozzi A.

Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders.

Tao Y., Gao H., Ackerman B., Guo W., Saffen D., Shugart Y.Y.

Enhanced social attention in female infant siblings at risk for autism.

Chawarska K., Macari S., Powell K., DiNicola L., Shic F.