| | Title | Authors / Editors | Date |
|
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 |
|
unige:125307 |
22q11 microdeletion syndrome and ultra-high risk for psychosis: The role of neurological soft signs as an independent marker of vulnerability for psychosis |
Pitzianti, Mariabernarda; Pontillo, Maria; Vicari, Stefano; Armando, Marco; Pasini, Augusto |
2019 |
|
unige:132509 |
Individualized prediction of transition to psychosis in 1,676 individuals at clinical high risk: development and validation of a multivariable prediction model based on individual patient data meta-analysis |
Malda, Aaltsje; Boonstra, Nynke; Barf, Hans; de Jong, Steven; ... Pijnenborg, Gerdina Hendrika Maria |
2019 |
|
unige:132728 |
Antipsychotics do not influence neurological soft signs in children and adolescents at ultra-high risk for psychosis: a pilot study |
Pitzianti, Mariabernarda; Casarelli, Livia; Pontillo, Maria; Vicari, Stefano; ... Pasini, Augusto |
2019 |
|
unige:132729 |
Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome |
Niarchou, Maria; Chawner, Samuel J R A; Fiksinski, Ania; Vorstman, Jacob A S; ... Thapar, Anita |
2019 |
|
unige:120114 |
Prevalence, course and psychosis-predictive value of negative symptoms in 22q11.2 deletion syndrome |
Schneider, Maude; Armando, Marco; Schultze-Lutter, Frauke; Pontillo, Maria; ... Eliez, Stéphan |
2019 |
|
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:112258 |
Prevalence and Clinical Significance of Symptoms at Ultra High Risk for Psychosis in Children and Adolescents with Obsessive⁻Compulsive Disorder: Is There an Association with Global, Role, and Social Functioning? |
Averna, Roberto; Pontillo, Maria; Demaria, Francesco; Armando, Marco; ... Vicari, Stefano |
2018 |
|
unige:112259 |
Variations in Dysbindin-1 are associated with cognitive response to antipsychotic drug treatment |
Scheggia, Diego; Mastrogiacomo, Rosa; Mereu, Maddalena; Sannino, Sara; ... Papaleo, Francesco |
2018 |
|
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:97042 |
No age effect in the prevalence and clinical significance of ultra-high risk symptoms and criteria for psychosis in 22q11 deletion syndrome: Confirmation of the genetically driven risk for psychosis? |
Armando, Marco; Schneider, Maude; Pontillo, Maria; Vicari, Stefano; ... Eliez, Stéphan |
2017 |
|
unige:97044 |
Clinical presentation of Attenuated Psychosis Syndrome in children and adolescents: Is there an age effect? |
Ribolsi, Michele; Lin, Ashleigh; Wardenaar, Klaas J; Pontillo, Maria; ... Armando, Marco |
2017 |
|
unige:93286 |
Ultra high risk status and transition to psychosis in 22q11.2 deletion syndrome |
Schneider, Maude; Armando, Marco; Pontillo, Maria; Vicari, Stefano; ... Eliez, Stéphan |
2016 |
|
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: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:34338 |
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome |
Sailani, Mohammad Reza; Makrythanasis, Periklis; Valsesia, Armand; Santoni, Federico; ... Antonarakis, Stylianos |
2013 |
Vicari, Stefano
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