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Export 3 results:
Author Title Type [ Year(Asc)]
Filters: Author is Hunter, Jill V  [Clear All Filters]
2018
J. P. Owen, Bukshpun, P., Pojman, N., Thieu, T., Chen, Q., Lee, J., D'Angelo, D., Glenn, O. A., Hunter, J. V., Berman, J. I., Roberts, T. P., Buckner, R., Nagarajan, S. S., Mukherjee, P., and Sherr, E. H., “Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2.”, Radiology, vol. 286, no. 1, pp. 217-226, 2018.
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.