Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome
- Creator: 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.
- Resource Type: journal article
- Date: 2024
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.
- Creator: 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
- Resource Type: journal article
- Date: 2023