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Export 2 results:
Author Title Type [ Year(Asc)]
Filters: Author is Gilbert, John R  [Clear All Filters]
2011
R. - H. Chung, Ma, D., Wang, K., Hedges, D. J., Jaworski, J. M., Gilbert, J. R., Cuccaro, M. L., Wright, H. H., Abramson, R. K., Konidari, I., Whitehead, P. L., Schellenberg, G. D., Hakonarson, H., Haines, J. L., Pericak-Vance, M. A., and Martin, E. R., “An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.”, Mol Autism, vol. 2, no. 1, p. 18, 2011.
2009
K. Wang, Zhang, H., Ma, D., Bućan, M., Glessner, J. T., Abrahams, B. S., Salyakina, D., Imielinski, M., Bradfield, J. P., Sleiman, P. M. A., Kim, C. E., Hou, C., Frackelton, E., Chiavacci, R., Takahashi, N., Sakurai, T., Rappaport, E., Lajonchere, C. M., Munson, J., Estes, A., Korvatska, O., Piven, J., Sonnenblick, L. I., Retuerto, A. I. Alvarez, Herman, E. I., Dong, H., Hutman, T., Sigman, M., Ozonoff, S., Klin, A., Owley, T., Sweeney, J. A., Brune, C. W., Cantor, R. M., Bernier, R., Gilbert, J. R., Cuccaro, M. L., McMahon, W. M., Miller, J., State, M. W., Wassink, T. H., Coon, H., Levy, S. E., Schultz, R. T., Nurnberger, J. I., Haines, J. L., Sutcliffe, J. S., Cook, E. H., Minshew, N. J., Buxbaum, J. D., Dawson, G., Grant, S. F. A., Geschwind, D. H., Pericak-Vance, M. A., Schellenberg, G. D., and Hakonarson, H., “Common genetic variants on 5p14.1 associate with autism spectrum disorders.”, Nature, vol. 459, no. 7246, pp. 528-33, 2009.