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
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
- Creator: 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.
- Resource Type: journal article
- Date: 2020
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
- Creator: 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.
- Resource Type: journal article
- Date: 2020
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects
- Creator: 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
- Resource Type: journal article
- Date: 2018
Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome
- Creator: 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
- Resource Type: journal article
- Date: 2017
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome
- Creator: 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.
- Resource Type: journal article
- Date: 2015
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
- Creator: 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.
- Resource Type: journal article
- Date: 2014