| 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 M Schneider, M Debbané, AS Bassett, EWC Chow, WLA Fung, ... American Journal of Psychiatry 171 (6), 627-639, 2014 | 774* | 2014 |
| Psycho-social factors associated with mental resilience in the Corona lockdown IM Veer, A Riepenhausen, M Zerban, C Wackerhagen, LMC Puhlmann, ... Translational psychiatry 11 (1), 67, 2021 | 275* | 2021 |
| Cognitive decline preceding the onset of psychosis in patients with 22q11. 2 deletion syndrome JAS Vorstman, EJ Breetvelt, SN Duijff, S Eliez, M Schneider, ... JAMA psychiatry 72 (4), 377-385, 2015 | 242* | 2015 |
| Sex differences in thickness, and folding developments throughout the cortex AK Mutlu, M Schneider, M Debbané, D Badoud, S Eliez, M Schaer Neuroimage 82, 200-207, 2013 | 224 | 2013 |
| Deviant dynamics of EEG resting state pattern in 22q11. 2 deletion syndrome adolescents: a vulnerability marker of schizophrenia? MI Tomescu, TA Rihs, R Becker, J Britz, A Custo, F Grouiller, M Schneider, ... Schizophrenia research 157 (1-3), 175-181, 2014 | 141 | 2014 |
| Risk factors and the evolution of psychosis in 22q11. 2 deletion syndrome: a longitudinal 2-site study D Gothelf, M Schneider, T Green, M Debbané, A Frisch, B Glaser, H Zilkha, ... Journal of the American Academy of Child & Adolescent Psychiatry 52 (11 …, 2013 | 131 | 2013 |
| Genetic contributors to risk of schizophrenia in the presence of a 22q11. 2 deletion I Cleynen, W Engchuan, MS Hestand, T Heung, AM Holleman, ... Molecular psychiatry 26 (8), 4496-4510, 2021 | 109 | 2021 |
| Rare genome-wide copy number variation and expression of schizophrenia in 22q11. 2 deletion syndrome AS Bassett, C Lowther, D Merico, G Costain, EWC Chow, ... American Journal of Psychiatry 174 (11), 1054-1063, 2017 | 94 | 2017 |
| Schizophrenia patients and 22q11. 2 deletion syndrome adolescents at risk express the same deviant patterns of resting state EEG microstates: a candidate endophenotype of … MI Tomescu, TA Rihs, M Roinishvili, FI Karahanoglu, M Schneider, ... Schizophrenia Research: Cognition 2 (3), 159-165, 2015 | 87 | 2015 |
| Enhanced maternal origin of the 22q11. 2 deletion in velocardiofacial and DiGeorge syndromes M Delio, T Guo, DM McDonald-McGinn, E Zackai, S Herman, ... The American Journal of Human Genetics 92 (3), 439-447, 2013 | 83 | 2013 |
| Does the Social Functioning Scale reflect real-life social functioning? An experience sampling study in patients with a non-affective psychotic disorder and healthy control … M Schneider, U Reininghaus, M van Nierop, M Janssens, I Myin-Germeys, ... Psychological Medicine 47 (16), 2777-2786, 2017 | 77 | 2017 |
| Preliminary structure and predictive value of attenuated negative symptoms in 22q11. 2 deletion syndrome M Schneider, M Van der Linden, B Glaser, E Rizzi, SP Dahoun, C Hinard, ... Psychiatry research 196 (2-3), 277-284, 2012 | 76 | 2012 |
| Clinical and cognitive risk factors for psychotic symptoms in 22q11. 2 deletion syndrome: a transversal and longitudinal approach M Schneider, M Schaer, AK Mutlu, S Menghetti, B Glaser, M Debbané, ... European child & adolescent psychiatry 23, 425-436, 2014 | 74 | 2014 |
| Ultra high risk status and transition to psychosis in 22q11. 2 deletion syndrome M Schneider, M Armando, M Pontillo, S Vicari, M Debbané, ... World Psychiatry 15 (3), 259-265, 2016 | 67 | 2016 |
| Developmental trajectories of executive functions in 22q11. 2 deletion syndrome J Maeder, M Schneider, M Bostelmann, M Debbané, B Glaser, ... Journal of Neurodevelopmental Disorders 8, 1-12, 2016 | 65 | 2016 |
| Resting-state networks in adolescents with 22q11. 2 deletion syndrome: associations with prodromal symptoms and executive functions M Debbané, M Lazouret, AL Lagioia, M Schneider, D Van De Ville, ... Schizophrenia research 139 (1-3), 33-39, 2012 | 65 | 2012 |
| Understanding the pediatric psychiatric phenotype of 22q11. 2 deletion syndrome AM Fiksinski, M Schneider, CM Murphy, M Armando, S Vicari, ... American Journal of Medical Genetics Part A 176 (10), 2182-2191, 2018 | 63 | 2018 |
| Altered auditory processing in frontal and left temporal cortex in 22q11. 2 deletion syndrome: a group at high genetic risk for schizophrenia TA Rihs, MI Tomescu, J Britz, V Rochas, A Custo, M Schneider, ... Psychiatry Research: Neuroimaging 212 (2), 141-149, 2013 | 59 | 2013 |
| Complete sequence of the 22q11. 2 allele in 1,053 subjects with 22q11. 2 deletion syndrome reveals modifiers of conotruncal heart defects Y Zhao, A Diacou, HR Johnston, FI Musfee, DM McDonald-McGinn, ... The American Journal of Human Genetics 106 (1), 26-40, 2020 | 56 | 2020 |
| Positive psychotic symptoms are associated with divergent developmental trajectories of hippocampal volume during late adolescence in patients with 22q11DS V Mancini, C Sandini, MC Padula, D Zöller, M Schneider, M Schaer, ... Molecular Psychiatry 25 (11), 2844-2859, 2020 | 55 | 2020 |
