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Author Title [ Type(Desc)] Year
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Journal Article
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.
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.
J. I. Berman, Chudnovskaya, D., Blaskey, L., Kuschner, E., Mukherjee, P., Buckner, R., Nagarajan, S., Chung, W. K., Spiro, J. E., Sherr, E. H., and Roberts, T. P. L., Abnormal auditory and language pathways in children with 16p11.2 deletion., Neuroimage Clin, vol. 9, pp. 50-7, 2015.
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.
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.
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.
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.
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.
Y. Shin Chang, Owen, J. P., Pojman, N. J., Thieu, T., Bukshpun, P., Wakahiro, M. L. J., Berman, J. I., Roberts, T. P. L., Nagarajan, S. S., Sherr, E. H., and Mukherjee, P., White Matter Changes of Neurite Density and Fiber Orientation Dispersion during Human Brain Maturation., PLoS One, vol. 10, no. 6, p. e0123656, 2015.