King's College London

• Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness

  Ching, C. R. K., Gutman, B. A., Sun, D., Villalon Reina, J., Ragothaman, A., Isaev, D., Zavaliangos-petropulu, A., Lin, A., Jonas, R. K., Kushan, L., Pacheco-hansen, L., Vajdi, A., Forsyth, J. K., Jalbrzikowski, M., Bakker, G., Van Amelsvoort, T., Antshel, K. M., Fremont, W., Kates, W. R., Campbell, L. E., & 35 othersMccabe, K. L., Craig, M. C., Daly, E., Gudbrandsen, M., Murphy, C. M., Murphy, D. G., Murphy, K. C., Fiksinski, A., Koops, S., Vorstman, J., Crowley, T. B., Emanuel, B. S., Gur, R. E., Mcdonald-mcginn, D. M., Roalf, D. R., Ruparel, K., Schmitt, J. E., Zackai, E. H., Durdle, C. A., Goodrich-hunsaker, N. J., Simon, T. J., Bassett, A. S., Butcher, N. J., Chow, E. W. C., Vila-rodriguez, F., Cunningham, A., Doherty, J., Linden, D. E., Moss, H., Owen, M. J., Van Den Bree, M., Crossley, N. A., Repetto, G. M., Thompson, P. M. & Bearden, C. E., 1 Jul 2020, In: American Journal of Psychiatry. 177, 7, p. 589-600 12 p.

  Research output: Contribution to journal › Article › peer-review

• Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

  Zhao, Y., Diacou, A., Johnston, H. R., Musfee, F. I., McDonald-McGinn, D. M., McGinn, D., Crowley, T. B., Repetto, G. M., Swillen, A., Breckpot, J., Vermeesch, J. R., Kates, W. R., Digilio, M. C., Unolt, M., Marino, B., Pontillo, M., Armando, M., Di Fabio, F., Vicari, S., van den Bree, M., & 30 othersMoss, H., Owen, M. J., Murphy, K. C., Murphy, C. M., Murphy, D., Schoch, K., Shashi, V., Tassone, F., Simon, T. J., Shprintzen, R. J., Campbell, L., Philip, N., Heine-Suñer, D., García-Miñaúr, S., Fernández, L., Antonarakis, S. E., Biondi, M., Boot, E., Breetvelt, E., Busa, T., Butcher, N., Buzzanca, A., Carmel, M., Cleynen, I., Cutler, D., Dallapiccola, B., de la Fuente Sanches, M. A., Epstein, M. P., Evers, R. & Lattanzi, G., 2 Jan 2020, In: American Journal of Human Genetics. 106, 1, p. 26-40 15 p.

  Research output: Contribution to journal › Article › peer-review

• Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

  the International 22q11.2 Brain and Behavior Consortium, 5 Oct 2018, (E-pub ahead of print) In: American Journal of Medical Genetics, Part A. 176, 10, p. 2172-2181 10 p.

  Research output: Contribution to journal › Article › peer-review

• Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

  Bassett, A. S., Lowther, C., Merico, D., Costain, G., Chow, E. W. C., van Amelsvoort, T., McDonald-McGinn, D., Gur, R. E., Swillen, A., Van den Bree, M., Murphy, K., Gothelf, D., Bearden, C. E., Eliez, S., Kates, W., Philip, N., Sashi, V., Campbell, L., Vorstman, J., Cubells, J., & 30 othersRepetto, G. M., Simon, T., Boot, E., Heung, T., Evers, R., Vingerhoets, C., van Duin, E., Zackai, E., Vergaelen, E., Devriendt, K., Vermeesch, J. R., Owen, M., Murphy, C., Michaelovosky, E., Kushan, L., Schneider, M., Fremont, W., Busa, T., Hooper, S., McCabe, K., Duijff, S., Isaev, K., Pellecchia, G., Wei, J., Gazzellone, M. J., Scherer, S. W., Emanuel, B. S., Guo, T., Morrow, B. E. & Marshall, C. R., 28 Jul 2017, In: The American Journal of Psychiatry.

  Research output: Contribution to journal › Article › peer-review

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