Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.

- 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

Exercise Intolerance, Benefits, and Prescription for People Living With a Fontan Circulation: The Fontan Fitness Intervention Trial (F-FIT)—Rationale and Design

- Tran, Derek L., Gibson, Hannah, Maiorana, Andrew J., Verrall, Charlotte E., Baker, David W., Clode, Melanie, Lubans, David R., Zannino, Diana, Bullock, Andrew, Ferrie, Suzie, Briody, Julie, Simm, Peter, Wijesekera, Vishva, D'Almeida, Michelle, Gosbell, Sally E., Davis, Glen M., Weintraub, Robert, Keech, Anthony, Puranik, Rajesh, Ugander, Martin, Justo, Robert, Zentner, D, Majumdar, A, Grigg, L, Coombes, JS, d'Udekem, Y, Morris, NR, Ayer, J, Celermajer, DS, Cordina, R

Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects

- Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Campbell, Linda, Moss, Hayley, Owen, Michael J., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, Maria Angeles, Epstein, Michael P., Evers, Rens, Fernandez, L, Fritsch, Rosemarie, Algas, Fernando Garcia, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Terese, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D. A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A. S., Gothelf, Doron, Zackai, Elaine, Agopian, A. J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E.

Sleep-disordered breathing in patients with pulmonary valve incompetence complicating congenital heart disease

- Miles, Susan, Ahmad, Waheed, Bailey, Amy, Hatton, Rachael, Boyle, Andrew, Collins, Nicholas