Ge, Ruiyang, Ching, Christopher R. K., Craig, Michael, Crossley, Nicolas A., Cunningham, Adam, Daly, Eileen, Doherty, Joanne L., Durdle, Courtney A., Emanuel, Beverly S., Fiksinski, Ania, Forsyth, Jennifer K., Fremont, Wanda, Bassett, Anne S., Goodrich-Hunsaker, Naomi J., Gudbrandsen, M, Gur, RE, Jalbrzikowski, M, Kates, WR, Lin, A, Linden, DEJ, McCabe, Kathryn L., McDonald-McGinn, D, Moss, H, Kushan, Leila, Murphy, DG, Murphy, KC, Owen, MJ, Villalon-Reina, JE, Repetto, GM, Roalf, DR, Ruparel, K, Schmitt, JE, Schuite-Koops, S, Angkustsiri, K, Antshel, Kevin M., Sun, D, Vajdi, A, van den Bree, M, Vorstman, J, Thompson, PM, Vila-Rodriguez, F, Bearden, CE, van Amelsvoort, Therese, Bakker, Geor, Butcher, Nancy J., Campbell, Linda E., Chow, Eva W. C.. John Wiley & Sons; 2024. Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome.

Zhao, Yingjie, Wang, Yujue, Johnston, H. Richard, Chow, Eva W. C., Vorstman, Jacob A. S., Vingerhoets, Claudia, van Amelsvoort, Therese, Gothelf, Doron, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Eliez, Stephan, Shi, Lijie, Schneider, Maude, van den Bree, MBM, Owen, MJ, Kates, WR, Repetto, GM, Shashi, V, Schoch, K, Bearden, CE, Digilio, MC, Unolt, M, McDonald-McGinn, Donna M., Putotto, C, Marino, B, Pontillo, M, Armando, M, Vicari, S, Angkustsiri, K, Campbell, Linda, Busa, T, Heine-Suñer, D, Murphy, KC, Crowley, T. Blaine, Murphy, D, García-Miñaúr, S, Fernández, L, International 22q11.2 Brain and Behavior Consortium (IBBC),, Zhang, ZD, Goldmuntz, E, Gur, RE, Emanuel, BS, Zheng, D, Marshall, CR, McGinn, Daniel E., Bassett, AS, Wang, T, Morrow, BE, Tran, Oanh T., Miller, Daniella, Lin, Jhih-Rong, Zackai, Elaine. Nature Publishing Group; 2023. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS..