| unige:97037 | Adolescence is the starting point of sex-dichotomous COMT genetic effects | Sannino, S; Padula, Maria; Managò, F; Schaer, Marie; ... Papaleo, F |
| unige:97036 | Altered structural network architecture is predictive of the presence of psychotic symptoms in patients with 22q11.2 deletion syndrome | Padula, Maria; Scariati Jaussi, Elisa; Schaer, Marie; Sandini, Corrado; ... Eliez, Stéphan |
| unige:102774 | Does differential visual exploration contribute to visual memory impairments in 22q11.2 microdeletion syndrome? | Bostelmann, Mathilde; Glaser, Bronwyn; Zaharia, Alexandra; Eliez, Stéphan; Schneider, Maude |
| unige:102591 | Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in theGPR98Locus on 5q14.3 | Guo, Tingwei; Repetto, Gabriela M; McDonald McGinn, Donna M; Chung, Jonathan H; ... Morrow, Bernice E |
| unige:93295 | Implication of reward alterations in the expression of negative symptoms in 22q11.2 deletion syndrome: a behavioural and DTI study | Dubourg, Lydia; Schneider, Maude; Padula, Maria; Chambaz, Léa; ... Eliez, Stéphan |
| unige:93290 | Morphological brain changes associated with negative symptoms in patients with 22q11.2 Deletion Syndrome | Mihailov, Angéline; Padula, Maria; Scariati Jaussi, Elisa; Schaer, Marie; ... Eliez, Stéphan |
| unige:93288 | Multimodal investigation of triple network connectivity in patients with 22q11DS and association with executive functions | Padula, Maria; Schaer, Marie; Scariati Jaussi, Elisa; Maeder, Johanna; ... Eliez, Stéphan |
| unige:55003 | Negative and paranoid symptoms are associated with negative performance beliefs and social cognition in 22q11.2 deletion syndrome | Schneider, Maude; Van der Linden, Martial; Menghetti, Sarah; Debbané, Martin; Eliez, Stéphan |
| 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 |
| unige:97043 | No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients | Guipponi, Michel; Santoni, Federico; Schneider, Maude; Gehrig, C; ... Antonarakis, Stylianos |
| unige:97033 | Psychotic symptoms influence the development of anterior cingulate BOLD variability in 22q11.2 deletion syndrome | Zoeller, Daniela; Padula, Maria; Sandini, Corrado; Schneider, Maude; ... Eliez, Stéphan |
| unige:102776 | Quantifying indices of short- and long-range white matter connectivity at each cortical vertex | Padula, Maria; Schaer, Marie; Scariati Jaussi, Elisa; Mutlu, Aytac Kadir; ... Eliez, Stéphan |
| unige:97041 | Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome | Bassett, Anne S; Lowther, Chelsea; Merico, Daniele; Costain, Gregory; ... Marshall, Christian R |
| 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 |
| unige:102773 | Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome | Souchay, Céline; Dubourg, Lydia; Ballhausen, Nicola; Schneider, Maude; ... Eliez, Stéphan |
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