2020

Scientific Articles

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
unige:137245	Favorable effects of omega-3 polyunsaturated fatty acids in attentional control and conversion rate to psychosis in 22q11.2 deletion syndrome	Armando, Marco; Ciampoli, Mariasole; Padula, Maria; Amminger, Paul; ... Papaleo, Francesco
unige:134856	Pituitary dysmaturation affects psychopathology and neurodevelopment in 22q11.2 Deletion Syndrome	Sandini, Corrado; Chambaz, Maëlle; Schneider, Maude; Armando, Marco; ... Eliez, Stéphan

2019

Scientific Articles

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
unige:124260	A Mentalization-Informed Staging Approach to Clinical High Risk for Psychosis	Armando, Marco; Hutsebaut, Joost; Debbané, Martin;
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
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
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
unige:132734	Prevalence of Non-Affective Psychoses in Individuals with Autism Spectrum Disorders: A Systematic Review	De Giorgi, Riccardo; De Crescenzo, Franco; D'Alò, Gian Loreto; Rizzo Pesci, Nicola; ... Armando, Marco
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

2018

Scientific Articles

unige:106658	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
unige:102777	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
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
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
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
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

2017

Scientific Articles

unige:97037	Adolescence is the starting point of sex-dichotomous COMT genetic effects	Sannino, S; Padula, Maria; Managò, F; Schaer, Marie; ... Papaleo, F
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
unige:97040	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
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:93285	Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic Study	Weisman, Omri; Guri, Yael; Gur, Raquel E; McDonald-McGinn, Donna M; ... Gothelf, Doron

Privat-docent Thesis

unige:98848

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;

2016

Scientific Articles

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

2015

Scientific Articles

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

2014

Scientific Articles

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

2013

Scientific Articles

unige:29136

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes

Delio, Maria; Schneider, Maude; Dahoun, Sophie; Eliez, Stéphan; Armando, Marco