The Autism Sequencing Consortium: Large scale, high throughput sequencing in autism spectrum disorders

por Buxbaum, J. D., Daly, M. J., Devlin, B., Lehner, T., Roeder, K., State, M. W.
Publicado 2012

Mental disorders of known aetiology and precision medicine in psychiatry: a promising but neglected alliance

por Fraguas, D., Díaz-Caneja, C. M., State, M. W., O’Donovan, M. C., Gur, R. E., Arango, C.
Publicado en Psychol Med (2016)

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts

por Moreno-De-Luca, D, Sanders, S J, Willsey, A J, Mulle, J G, Lowe, J K, Geschwind, D H, State, M W, Martin, C L, Ledbetter, D H
Publicado 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 2013