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Author Title Type [ Year(Asc)]
Filters: Author is Goin-Kochel, Robin P  [Clear All Filters]
2016
L. A. Green Snyder, D'Angelo, D., Chen, Q., Bernier, R., Goin-Kochel, R. P., Wallace, A. Stevens, Gerdts, J., Kanne, S., Berry, L., Blaskey, L., Kuschner, E., Roberts, T., Sherr, E., Martin, C. L., Ledbetter, D. H., Spiro, J. E., Chung, W. K., and Hanson, E., “Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.”, J Autism Dev Disord, vol. 46, no. 8, pp. 2734-2748, 2016.
D. D'Angelo, Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. A. Green, Hippolyte, L., Hanson, E., Maillard, A. M., W Faucett, A., Macé, A., Pain, A., Bernier, R., Chawner, S. J. R. A., David, A., Andrieux, J., Aylward, E., Baujat, G., Caldeira, I., Conus, P., Ferrari, C., Forzano, F., Gérard, M., Goin-Kochel, R. P., Grant, E., Hunter, J. V., Isidor, B., Jacquette, A., Jønch, A. E., Keren, B., Lacombe, D., Le Caignec, C., Martin, C. Lese, Männik, K., Metspalu, A., Mignot, C., Mukherjee, P., Owen, M. J., Passeggeri, M., Rooryck-Thambo, C., Rosenfeld, J. A., Spence, S. J., Steinman, K. J., Tjernagel, J., Van Haelst, M., Shen, Y., Draganski, B., Sherr, E. H., Ledbetter, D. H., van den Bree, M. B. M., Beckmann, J. S., Spiro, J. E., Reymond, A., Jacquemont, S., and Chung, W. K., “Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.”, JAMA Psychiatry, vol. 73, no. 1, pp. 20-30, 2016.
2012
F. Zufferey, Sherr, E. H., Beckmann, N. D., Hanson, E., Maillard, A. M., Hippolyte, L., Macé, A., Ferrari, C., Kutalik, Z., Andrieux, J., Aylward, E., Barker, M., Bernier, R., Bouquillon, S., Conus, P., Delobel, B., W Faucett, A., Goin-Kochel, R. P., Grant, E., Harewood, L., Hunter, J. V., Lebon, S., Ledbetter, D. H., Martin, C. Lese, Männik, K., Martinet, D., Mukherjee, P., Ramocki, M. B., Spence, S. J., Steinman, K. J., Tjernagel, J., Spiro, J. E., Reymond, A., Beckmann, J. S., Chung, W. K., and Jacquemont, S., “A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.”, J Med Genet, vol. 49, no. 10, pp. 660-8, 2012.
C. Lord, Petkova, E., Hus, V., Gan, W., Lu, F., Martin, D. M., Ousley, O., Guy, L., Bernier, R., Gerdts, J., Algermissen, M., Whitaker, A., Sutcliffe, J. S., Warren, Z., Klin, A., Saulnier, C., Hanson, E., Hundley, R., Piggot, J., Fombonne, E., Steiman, M., Miles, J., Kanne, S. M., Goin-Kochel, R. P., Peters, S. U., Cook, E. H., Guter, S., Tjernagel, J., Green-Snyder, L. Anne, Bishop, S., Esler, A., Gotham, K., Luyster, R., Miller, F., Olson, J., Richler, J., and Risi, S., “A multisite study of the clinical diagnosis of different autism spectrum disorders.”, Arch Gen Psychiatry, vol. 69, no. 3, pp. 306-13, 2012.