| Title | Authors / Editors | Date |
unige:8763 |
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 |
unige:8764 |
Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome |
Gothelf, Doron; Hoeft, Fumiko; Hinard, Christine; Hallmayer, J. F.; ... Reiss, A. L. |
2007 |
unige:5348 |
Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome |
Green, Tamar; Gothelf, Doron; Glaser, Bronwyn; Debbané, Martin; ... Eliez, Stéphan |
2009 |
unige:32574 |
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 |
unige:35806 |
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 |
unige:55310 |
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 |
unige:82909 |
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 |
unige:93285 |
Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study |
Weisman, Omri; Guri, Yael; Gur, Raquel E; McDonald-McGinn, Donna M; ... Gothelf, Doron |
2017 |
unige:102778 |
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 |
unige:126967 |
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects |
Zhao, Yingjie; Guo, Tingwei; Fiksinski, Ania; Breetvelt, Elemi; ... Morrow, Bernice E |
2018 |
unige:109045 |
Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome |
Fiksinski, Ania M; Schneider, Maude; Murphy, CM; Armando, Marco; ... Vorstman, Jacob A S |
2018 |
unige:109047 |
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 |
2019 |
unige:137334 |
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; ... Morrow, Bernice E |
2020 |
unige:138349 |
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion |
Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S; Heung, Tracy; ... Bassett, Anne S |
2020 |