| | Title | Authors / Editors | Date |
|
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:124260 |
A Mentalization-Informed Staging Approach to Clinical High Risk for Psychosis |
Armando, Marco; Hutsebaut, Joost; Debbané, Martin |
2019 |
|
unige:97037 |
Adolescence is the starting point of sex-dichotomous COMT genetic effects |
Sannino, S; Padula, Maria; Managò, F; Schaer, Marie; ... Papaleo, F |
2017 |
|
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:139055 |
Associations between schizotypal personality features, mentalizing difficulties and thought problems in a sample of community adolescents |
Salaminios, George; Morosan, Larisa; Toffel, Elodie; Tanzer, Michal; ... Debbané, Martin |
2020 |
|
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: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: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: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: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 |
2018 |
|
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 |
2018 |
|
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 |
2017 |
|
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 |
2013 |
|
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 |
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: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:154208 |
La maturation cérébrale chez les jeunes et la transition des patients consultants en pédopsychiatrie: y-a-t-il une incohérence? |
Kilicel, Deniz; Badoud, Deborah Myriam; von Plessen, Kerstin Jessica; Armando, Marco |
2021 |
|
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: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 |
2017 |
|
unige:134856 |
Pituitary dysmaturation affects psychopathology and neurodevelopment in 22q11.2 Deletion Syndrome |
Sandini, Corrado; Chambaz, Maëlle; Schneider, Maude; Armando, Marco; ... Eliez, Stéphan |
2020 |
Armando, Marco
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