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Export 3 results:
Author Title Type [ Year(Asc)]
Filters: Author is Jacquemont, Sébastien  [Clear All Filters]
2021
S. J. R. A. Chawner, Doherty, J. L., Anney, R. J. L., Antshel, K. M., Bearden, C. E., Bernier, R., Chung, W. K., Clements, C. C., Curran, S. R., Cuturilo, G., Fiksinski, A. M., Gallagher, L., Goin-Kochel, R. P., Gur, R. E., Hanson, E., Jacquemont, S., Kates, W. R., Kushan, L., Maillard, A. M., McDonald-McGinn, D. M., Mihaljevic, M., Miller, J. S., Moss, H., Pejovic-Milovancevic, M., Schultz, R. T., Green-Snyder, L. A., Vorstman, J. A., Wenger, T. L., Hall, Jand, Owen, M. J., and van den Bree, M. B. M., “A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants”, American Journal of Psychiatry, vol. 178, pp. 77-86, 2021.
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.