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Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome Gothelf, Doron; Hoeft, Fumiko; Hinard, Christine; Hallmayer, J. F.; ... Reiss, A. L. 2007
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Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome Vorstman, Jacob A S; Breetvelt, Elemi J; Duijff, Sasja N; Eliez, Stéphan; ... Bassett, Anne S 2015
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COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome Gothelf, Doron; Eliez, Stéphan; Thompson, Tracy; Hinard, Christine; ... Reiss, A. L. 2005
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Deletion size analysis of 1,680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2 Guo, Tingwei; Diacou, Alexander; Hiroko, Nomaru; McDonald-McGinn, Donna M; ... Morrow, Bernice E 2018
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Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome Mosheva, Mariela; Pouillard, Virginie; Fishman, Yael; Dubourg, Lydia; ... Schneider, Maude 2018
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Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome Green, Tamar; Gothelf, Doron; Glaser, Bronwyn; Debbané, Martin; ... Eliez, Stéphan 2009
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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; Bassett, Anne S.; Chow, Eva W.C.; ... Eliez, Stéphan 2014
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Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome Mlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; ... Emanuel, Beverly S. 2016
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Risk Factors and the Evolution of Psychosis in 22q11.2 Deletion Syndrome: A Longitudinal 2-Site Study Gothelf, Doron; Schneider, Maude; Green, Tamar; Debbané, Martin; ... Eliez, Stéphan 2013
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Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study Weisman, Omri; Guri, Yael; Gur, Raquel E; McDonald-McGinn, Donna M; ... Gothelf, Doron 2017
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Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome Fiksinski, Ania M; Schneider, Maude; Murphy, CM; Armando, Marco; ... Vorstman, Jacob A S 2018