Additional support for the association of SLITRK1 var321 and Tourette syndrome

Por O’Roak, BJ, Morgan, TM, Fishman, DO, Saus, E, Alonso, P, Gratacòs, M, Estivill, X, Teltsh, O, Kohn, Y, Kidd, KK, Cho, J, Lifton, RP, State, MW
Publicado em 2010

High rate of disease-related copy number variations in childhood onset schizophrenia

Por Ahn, K, Gotay, N, Andersen, TM, Anvari, AA, Gochman, P, Lee, Y, Sanders, S, Guha, S, Darvasi, A, Glessner, JT, Hakonarson, H, Lencz, T, State, MW, Shugart, YY, Rapoport, JL
Publicado no Mol Psychiatry (2013)

Using whole exome sequencing to identify inherited causes of autism

Por Yu, T.W., Chahrour, M.H., Coulter, M.E., Jiralerspong, S., Okamura-Ikeda, K., Ataman, B., Schmitz-Abe, K., Harmin, D.A., Adli, M., Malik, A.N., D’Gama, A.M., Lim, E.T., Sanders, S.J., Mochida, G.H., Partlow, J.N., Sunu, C.M., Felie, J.M., Rodriguez, J., Nasir, R.H., Ware, J., Joseph, R.M., Hill, R.S., Kwan, B.Y., Al-Saffar, M., Mukaddes, N.M., Hashmi, A., Balkhy, S., Gascon, G.G., Hisama, F.M., LeClair, E., Poduri, A., Oner, O., Al-Saad, S., Al-Awadi, S.A., Bastaki, L., Ben-Omran, T., Teebi, A., Al-Gazali, L., Eapen, V., Stevens, C.R., Rappaport, L., Gabriel, S.B., Markianos, K., State, M.W., Greenberg, M.E., Taniguchi, H., Braverman, N.E., Morrow, E.M., Walsh, C.A.
Publicado em 2013