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Author Title Type [ Year(Asc)]
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2020
J. Matsuzaki, Berman, J. I., Blaskey, L., Kuschner, E. S., Gaetz, L., Mukherjee, P., Buckner, R. L., Nagarajan, S. S., Chung, W. K., Sherr, E. H., and Roberts, T. P. L., “Abnormal Auditory Mismatch Fields in Children and Adolescents With 16p11.2 Deletion and 16p11.2 Duplication.”, Biol Psychiatry Cogn Neurosci Neuroimaging, vol. 5, no. 10, pp. 942-950, 2020.
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.
2014
J. P. Owen, Chang, Y. Shin, Pojman, N. J., 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., “Aberrant white matter microstructure in children with 16p11.2 deletions.”, J Neurosci, vol. 34, no. 18, pp. 6214-23, 2014.
A. Y. Qureshi, Mueller, S., Snyder, A. Z., Mukherjee, P., Berman, J. I., Roberts, T. P. L., Nagarajan, S. S., Spiro, J. E., Chung, W. K., Sherr, E. H., and Buckner, R. L., “Opposing brain differences in 16p11.2 deletion and duplication carriers.”, J Neurosci, vol. 34, no. 34, pp. 11199-211, 2014.
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.