Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

- 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.

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

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

- Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A. S., Bearden, Carrie E., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J., Chopra, Pankaj, Campbell, Linda E., McCabe, Kathryn L.

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

- Davies, Robert W., Fiksinski, Ania M., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E., Breetvelt, Elemi J., Cubells, Joseph F., Eliez, Stephan, Garcia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan G., Philip, Nicole, Repetto, Gabriela M., Williams, Nigel M., Shashi, Vandana, Simon, Tony J., Suñer, Damiàn Heine, Vicari, Stefano, Scherer, Stephen W., Epstein, Michael P., Warren, Stephen T., Morrison, Sinead, Chawner, Samuel, Vingerhoets, Claudia, Hooper, Stephen R., Breckpot, Jeroen, Vergaelen, Elfi, Vogels, Annick, Monks, Stephen, Prasad, Sarah E., Sandini, Corrado, Schneider, Maude, Maeder, Johanna, Fraguas, David, Evers, Rens, Monfeuga, Thomas, Tassone, Flora, Morey-Canyelles, Jaume, Ousley, Opal Y., Antshel, Kevin M., Fremont, Wanda, Fritsch, Rosemarie, Ornstein, Claudia, Daly, Eileen M., Costain, Gregory A., Boot, Erik, Bassett, Anne S., Heung, Tracy, Crowley, T. Blaine, Zackai, Elaine H., Calkins, Monica E., Gur, Ruben C., McCabe, Kathryn L., Busa, Tiffany, Schoch, Kelly, Pontillo, Maria, Duijff, Sasja N., Owen, Michael J., Kahn, René S., Houben, Michiel, Kushan, Leila, Jalbrzikowski, Maria, Carmel, Miri, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Bearden, Carrie E., Vorstman, Jacob A. S., Gur, Raquel E., Morrow, Bernice E.

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

- Zhao, Yingjie, Guo, Tingwei, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, van Amelsvoort, Thérèse, van den Bree, Marianne, Owen, Michael, Niarchou, Maria, Fiksinski, Ania, Campbell, Linda, Breetvelt, Elemi, McDonald-McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann

Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome

- Bassett, Anne S., Lowther, Chelsea, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van den Bree, Marianne

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome

- Vorstman, Jacob A. S., Breetvelt, Elemi J., Chow, Eva W. C., Fung, Wai Lun Alan, Butcher, Nancy J., Young, Donald A., McDonald-McGinn, Donna M., Vogels, Annick, van Amelsvoort, Therese, Gothelf, Doron, Weinberger, Ronnie, Weizman, Abraham, Duijff, Sasja N., Klaassen, Petra W. J., Koops, Sanne, Kates, Wendy R., Antshel, Kevin M., Simon, Tony J., Ousley, Opal Y., Swillen, Ann, Gur, Raquel E., Bearden, Carrie E., Kahn, René S., Eliez, Stephan, Bassett, Anne S., Emanuel, Beverly S., Zackai, Elaine H., Kushan, Leila, Fremont, Wanda, Schoch, Kelly, Stoddard, Joel, Cubells, Joseph, Fu, Fiona, Campbell, Linda E., Schneider, Maude, Fritsch, Rosemarie, Vergaelen, Elfi, Neeleman, Marjolein, Boot, Erik, Debbané, Martin, Philip, Nicole, Green, Tamar, van den Bree, Marianne B. M., Murphy, Declan, Canyelles, Jaume Morey, Jalbrzikowski, Maria, Arango, Celso, Murphy, Kieran C., Pontillo, Maria, Armando, Marco, Vicari, Stefano, Shashi, Vandana, Hooper, Stephen R.

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 deletion syndrome

- Schneider, Maude, Debbané, Martin, Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W. J., Swillen, Ann, Gothelf, Doron, Bassett, Anne S., Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Chow, Eva W. C., Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J., Eliez, Stephan, Fung, Wai Lun Alan, van den Bree, Marianne B. M., Owen, Michael, Murphy, Kieran C., Niarchou, Maria, Kates, Wendy R.