FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment

Por Newbury, D. F., Bonora, E., Lamb, J. A., Fisher, S. E., Lai, C. S. L., Baird, G., Jannoun, L., Slonims, V., Stott, C. M., Merricks, M. J., Bolton, P. F., Bailey, A. J., Monaco, A. P.
Publicado em 2002

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment

Por Nudel, R, Simpson, N H, Baird, G, O’Hare, A, Conti-Ramsden, G, Bolton, P F, Hennessy, E R, Ring, S M, Davey Smith, G, Francks, C, Paracchini, S, Monaco, A P, Fisher, S E, Newbury, D F
Publicado em 2014

Intrinsic gray-matter connectivity of the brain in adults with autism spectrum disorder

Por Ecker, Christine, Ronan, Lisa, Feng, Yue, Daly, Eileen, Murphy, Clodagh, Ginestet, Cedric E., Brammer, Michael, Fletcher, Paul C., Bullmore, Edward T., Suckling, John, Baron-Cohen, Simon, Williams, Steve, Loth, Eva, Murphy, Declan G. M., Bailey, A. J., Baron-Cohen, S., Bolton, P. F., Bullmore, E. T., Carrington, S., Chakrabarti, B., Daly, E. M., Deoni, S. C., Ecker, C., Happe, F., Henty, J., Jezzard, P., Johnston, P., Jones, D. K., Lai, M. C., Lombardo, M. V., Madden, A., Mullins, D., Murphy, C. M., Murphy, D. G., Pasco, G., Sadek, S., Spain, D., Steward, R., Suckling, J., Wheelwright, S., Williams, S. C.
Publicado em 2013