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
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