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Author Title Type [ Year(Asc)]
Filters: Keyword is Chromosome Deletion  [Clear All Filters]
J. Jenkins, Chow, V., Blaskey, L., Kuschner, E., Qasmieh, S., Gaetz, L., J Edgar, C., Mukherjee, P., Buckner, R., Nagarajan, S. S., Chung, W. K., Spiro, J. E., Sherr, E. H., Berman, J. I., and Roberts, T. P. L., Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication., Cereb Cortex, vol. 26, no. 5, pp. 1957-64, 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.
Y. Shin Chang, Owen, J. P., Pojman, N. J., Thieu, T., Bukshpun, P., Wakahiro, M. L. J., Marco, E. J., Berman, J. I., Spiro, J. E., Chung, W. K., Buckner, R. L., Roberts, T. P. L., Nagarajan, S. S., Sherr, E. H., and Mukherjee, P., Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications., Hum Brain Mapp, vol. 37, no. 8, pp. 2833-48, 2016.
J. I. Berman, Chudnovskaya, D., Blaskey, L., Kuschner, E., Mukherjee, P., Buckner, R., Nagarajan, S., Chung, W. K., Sherr, E. H., and Roberts, T. P. L., Relationship between M100 Auditory Evoked Response and Auditory Radiation Microstructure in 16p11.2 Deletion and Duplication Carriers., AJNR Am J Neuroradiol, vol. 37, no. 6, pp. 1178-84, 2016.
T. L. Wenger, Kao, C., McDonald-McGinn, D. M., Zackai, E. H., Bailey, A., Schultz, R. T., Morrow, B. E., Emanuel, B. S., and Hakonarson, H., The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder., Sci Rep, vol. 6, p. 19372, 2016.