SFARI | SFARI Funded Publications

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.

Maestrini E., Pagnamenta A.T., Lamb J.A., Bacchelli E., Sykes N.H., Sousa I., Toma C., Barnby G., Butler H., Winchester L., Scerri T.S., Minopoli F., Reichert J., Cai G., Buxbaum J., Korvatska O., Schellenberg G.D., Dawson G., Bildt A.D., Minderaa R.B., Mulder E.J., Morris A.P., Bailey A.J., Monaco A.

Distinct subclasses of medium spiny neurons differentially regulate striatal motor behaviors.

Bateup H., Santini E., Shen W., Birnbaum S., Valjent E., Surmeier D.J., Fisone G., Nestler E., Greengard P.

Microglial activation and increased microglial density observed in the dorsolateral prefrontal cortex in autism.

Morgan J.T., Chana G., Pardo C.A., Achim C., Semendeferi K., Buckwalter J., Courchesne E., Everall I.P.

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.

Pagnamenta A.T., Bacchelli E., de Jonge M.V., Mirza G., Scerri T.S., Minopoli F., Chiocchetti A., Ludwig K.U., Hoffmann P., Paracchini S., Lowy E., Harold D.H., Chapman J.A., Klauck S.M., Poustka F., Houben R.H., Staal W.G., Ophoff R.A., O’Donovan M.C., Williams J., Nöthen M.M., Schulte-Körne G., Deloukas P., Ragoussis J., Bailey A.J., Maestrini E., Monaco A.

Centrosome motility is essential for initial axon formation in the neocortex.

de Anda F.C., Meletis K., Ge X., Rei D., Tsai L.

Comparison of visual sensitivity to human and object motion in autism spectrum disorder.

Kaiser M.D., Delmolino L., Tanaka J.W., Shiffrar M.

MicroRNAs in psychiatric and neurodevelopmental disorders.

Xu B., Karayiorgou M., Gogos J.

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.

Ching M.S.L., Shen Y., Tan W-H., Spurling Jeste S., Morrow E., Chen X., Mukaddes N.M., Yoo S-Y., Hanson E., Hundley R., Austin C., Becker R.E., Berry G.T., Driscoll K., Engle E.C., Friedman S., Gusella J., Hisama F.M., Irons M.B., Lafiosca T., LeClair E., Miller D.T., Neessen M., Picker J.D., Rappaport L., Rooney C.M., Sarco D.P., Stoler J.M., Walsh C., Wolff R.R., Zhang T., Nasir R.H., Wu B-L.

The von Economo neurons in frontoinsular and anterior cingulate cortex in great apes and humans.

Allman J., Tetreault N.A., Hakeem A.Y., Manaye K.F., Semendeferi K., Erwin J.M., Park S., Goubert V., Hof P.R.

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

Karayiorgou M., Simon T.J., Gogos J.