Search results

• 2012

  A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

  Casey, J. P., Magalhaes, T., Conroy, J. M., Regan, R., Shah, N., Anney, R., Shields, D. C., Abrahams, B. S., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bolton, P. F., Bourgeron, T., Brennan, S., Cali, P., Correia, C., & 106 othersCorsello, C., Coutanche, M., Dawson, G., de Jonge, M., Delorme, R., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Foley, S., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Green, J., Guter, S. J., Hakonarson, H., Holt, R., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Lamb, J. A., Leboyer, M., Le Couteur, A., Leventhal, B. L., Lord, C., Lund, S. C., Maestrini, E., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Merikangas, A., Miller, J., Minopoli, F., Mirza, G. K., Munson, J., Nelson, S. F., Nygren, G., Oliveira, G., Pagnamenta, A. T., Papanikolaou, K., Parr, J. R., Parrini, B., Pickles, A., Pinto, D., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Ragoussis, J., Roge, B., Rutter, M. L., Sequeira, A. F., Soorya, L., Sousa, I., Sykes, N., Stoppioni, V., Tancredi, R., Tauber, M., Thompson, A. P., Thomson, S., Tsiantis, J., Van Engeland, H., Vincent, J. B., Volkmar, F., Vorstman, J. A. S., Wallace, S., Wang, K., Wassink, T. H., White, K., Wing, K., Wittemeyer, K., Yaspan, B. L., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M. L., Geschwind, D. H., Haines, J. L., Hallmayer, J., Monaco, A. P., Nurnberger, J. I., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vieland, V. J., Wijsman, E. M., Green, A., Gill, M., Gallagher, L., Vicente, A. & Ennis, S., Apr 2012, In: Human Genetics. 131, 4, p. 565 - 579 15 p.

  Research output: Contribution to journal › Literature review › peer-review

  • Haplotype 100%
  • Spectrum 100%
  • Candidate Gene 100%
  • Gene 100%
  • Pervasive Developmental Disorder 100%
  157 Citations (Scopus)
• 2005

  Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review

  Veltman, M. W. M., Craig, E. E. & Bolton, P. F., Dec 2005, In: Psychiatric Genetics. 15, 4, p. 243 - 254 12 p.

  Research output: Contribution to journal › Literature review › peer-review

  • Taxonomy 100%
  • Spectrum 100%
  • Prader-Willi Syndrome 100%
  • Angelman Syndrome 100%
  • Systematic Review 100%
  167 Citations (Scopus)
• 2004

  Neuroepileptic correlates of autistic symptomatology in tuberous sclerosis

  Bolton, P. F., 2004, In: MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS. 10, 2, p. 126 - 131 6 p.

  Research output: Contribution to journal › Literature review › peer-review
  53 Citations (Scopus)