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Variations in Dysbindin-1 are associated with cognitive response to antipsychotic drug treatment Scheggia, Diego; Mastrogiacomo, Rosa; Mereu, Maddalena; Sannino, Sara; ... Papaleo, Francesco 2018
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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
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Ultra high risk status and transition to psychosis in 22q11.2 deletion syndrome Schneider, Maude; Armando, Marco; Pontillo, Maria; Vicari, Stefano; ... Eliez, Stéphan 2016
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The contribution of a neurodevelopment and genetic perspective to our understanding of the pathogenesis of psychotic disorders: the case of 22q11ds and of youth populations Armando, Marco 2017
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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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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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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
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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
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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 2017
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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
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Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes Delio, Maria; Schneider, Maude; Dahoun, Sophie; Eliez, Stéphan; Armando, Marco 2013
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Détection et traitement précoce des sujets à haut risque clinique depsychose : définitions et recommandations Michel, Christoph; Toffel, Elodie; Schmidt, S J; Eliez, Stéphan; ... Debbané, Martin 2017
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Cortical morphology development in patients with 22q11.2 deletion syndrome at ultra-high risk of psychosis Padula, Maria; Schaer, Marie; Armando, Marco; Sandini, Corrado; ... Eliez, Stéphan 2018
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Coping Strategies Mediate the Effect of Stressful Life Events on Schizotypal Traits and Psychotic Symptoms in 22q11.2 Deletion Syndrome Armando, Marco; Sandini, Corrado; Chambaz, Maëlle; Schaer, Marie; ... Eliez, Stéphan 2018
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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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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
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Adolescence is the starting point of sex-dichotomous COMT genetic effects Sannino, S; Padula, Maria; Managò, F; Schaer, Marie; ... Papaleo, F 2017
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A Mentalization-Informed Staging Approach to Clinical High Risk for Psychosis Armando, Marco; Hutsebaut, Joost; Debbané, Martin 2019
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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