| Challenges in multi-task learning for fMRI-based diagnosis: Benefits for psychiatric conditions and CNVs would likely require thousands of patients A Harvey, CA Moreau, K Kumar, G Huguet, SGW Urchs, H Sharmarke, ... Imaging Neuroscience 2, 1-20, 2024 | | 2024 |
| Neurocognitive profiles of 22q11. 2 and 16p11. 2 deletions and duplications RC Gur, CE Bearden, S Jacquemont, A Swillen, T van Amelsvoort, ... Molecular Psychiatry, 1-9, 2024 | 1 | 2024 |
| Pathogenic variants in KMT2C result in a neurodevelopmental disorder distinct from Kleefstra and Kabuki syndromes D Rots, S Choufani, V Faundes, AJM Dingemans, S Joss, N Foulds, ... The American Journal of Human Genetics, 2024 | 1 | 2024 |
| Longitudinal follow-up of metformin treatment in Fragile X Syndrome P Seng, FAM Montanaro, HMB Biag, MJ Salcedo-Arellano, K Kim, ... Frontiers in Psychology 15, 1305597, 2024 | | 2024 |
| Modelling Co-Occurring Mental Health Conditions Among Autistic Individuals Using Polygenic Scores A Okewole, VR Bourque, S Jacquemont, V Warrier, S Baron-Cohen BJPsych Open 10 (S1), S69-S69, 2024 | | 2024 |
| 295. Rare Variant Genetic Architecture of the Human Cortical MRI Phenotypes in General Population K Kumar, S Kazem, Z Liao, J Kopal, G Huguet, T Renne, M Jean-Louis, ... Biological Psychiatry 95 (10), S220-S221, 2024 | | 2024 |
| Subcortical Brain Alterations Across Copy Number Variants Converge With Those in Severe Mental Illnesses K Kumar, C Modenato, C Moreau, C Ching, C Bearden, PM Thompson, ... Biological Psychiatry 95 (10), S58-S59, 2024 | | 2024 |
| Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability Z Schmilovich, VR Bourque, E Douard, G Huguet, C Poulain, JP Ross, ... Frontiers in Psychiatry 15, 1369767, 2024 | | 2024 |
| Analyzing the Quality of Life in Individuals with Fragile X Syndrome in Relation to Sleep and Mental Health A Minhas, K Whitlock, C Rosenfelt, J Shatto, B Finlay, J Zwicker, S Lippe, ... Journal of Autism and Developmental Disorders, 1-13, 2024 | | 2024 |
| Investigating the convergence of resting-state functional connectivity profiles in Alzheimer’s disease with neuropsychiatric symptoms and schizophrenia N Clarke, C Moreau, HT Wang, A Harvey, P Orban, Z Ismail, ... OSF, 2024 | | 2024 |
| Clinical correlates of diagnostic certainty in children and youths with Autistic Disorder EM Rødgaard, B Rodríguez-Herreros, A Zeribi, K Jensen, V Courchesne, ... Molecular Autism 15 (1), 15, 2024 | | 2024 |
| Genetic and phenotypic similarity across major psychiatric disorders: a systematic review and quantitative assessment VR Bourque, C Poulain, C Proulx, CA Moreau, R Joober, B Forgeot d’Arc, ... Translational Psychiatry 14 (1), 171, 2024 | 1 | 2024 |
| Using rare genetic mutations to revisit structural brain asymmetry J Kopal, K Kumar, K Shafighi, K Saltoun, C Modenato, CA Moreau, ... nature communications 15 (1), 2639, 2024 | | 2024 |
| Thalamocortical organoids enable in vitro modeling of 22q11. 2 microdeletion associated with neuropsychiatric disorders D Shin, CN Kim, J Ross, KM Hennick, SR Wu, N Paranjape, R Leonard, ... Cell Stem Cell 31 (3), 421-432. e8, 2024 | 3 | 2024 |
| Pervasive alterations of intra-axonal volume and network organization in young children with a 16p11. 2 deletion AM Maillard, D Romascano, JE Villalón-Reina, CA Moreau, ... Translational Psychiatry 14 (1), 95, 2024 | 1 | 2024 |
| Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients … K Szakszon, CM Lourenco, BL Callewaert, D Geneviève, F Rouxel, ... Journal of medical genetics 61 (2), 132-141, 2024 | 1 | 2024 |
| Specific EEG resting state biomarkers in FXS and ASD M Proteau-Lemieux, IS Knoth, S Davoudi, CO Martin, AM Bélanger, ... | | 2024 |
| Beyond the global brain differences: intraindividual variability differences in 1q21. 1 distal and 15q11. 2 BP1-BP2 deletion carriers R Boen, T Kaufmann, D Van der Meer, O Frei, I Agartz, D Ames, ... Biological psychiatry 95 (2), 147-160, 2024 | 2 | 2024 |
| Spliceosome malfunction causes neurodevelopmental disorders with overlapping features D Li, Q Wang, A Bayat, MR Battig, Y Zhou, DGM Bosch, G van Haaften, ... The Journal of Clinical Investigation 134 (1), 2024 | 8 | 2024 |
| Integrating genomic variants and developmental milestones to predict cognitive and adaptive outcomes in autistic children VR Bourque, Z Schmilovich, G Huguet, J England, A Okewole, C Poulain, ... medRxiv, 2024.07. 31.24311250, 2024 | | 2024 |
