about
Developing psychosis and its risk states through the lens of schizotypy.Reduced fronto-temporal and limbic connectivity in the 22q11.2 deletion syndrome: vulnerability markers for developing schizophrenia?Neuroanatomic variation in monozygotic twin pairs discordant for the narrow phenotype for autismPsychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implicationsIncreased gyrification in Williams syndrome: evidence using 3D MRI methods.Neural correlates of auditory perception in Williams syndrome: an fMRI study.Regional analysis of hippocampal activation during memory encoding and retrieval: fMRI study.The French Version of the Reflective Functioning Questionnaire: Validity Data for Adolescents and Adults and Its Association with Non-Suicidal Self-InjuryFrom genes to brain: understanding brain development in neurogenetic disorders using neuroimaging techniques.Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.Brain activity underlying negative self- and other-perception in adolescents: The role of attachment-derived self-representations.Prefrontal plasticity and stress inoculation-induced resilience.Clinical and cognitive risk factors for psychotic symptoms in 22q11.2 deletion syndrome: a transversal and longitudinal approachSocial orienting and joint attention in preschoolers with autism spectrum disorders.Adaptive strategy for the statistical analysis of connectomes.Adolescent resting state networks and their associations with schizotypal trait expression.Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndromeA volumetric study of parietal lobe subregions in Turner syndromeBrain development in Turner syndrome: a magnetic resonance imaging study.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.Testing measurement invariance of the schizotypal personality questionnaire-brief scores across Spanish and Swiss adolescents.Strange-face-in-the-mirror illusion and schizotypy during adolescence.Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndromeStructural and functional connectivity in the default mode network in 22q11.2 deletion syndrome.How to measure cortical folding from MR images: a step-by-step tutorial to compute local gyrification index.Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.Disentangling resting-state BOLD variability and PCC functional connectivity in 22q11.2 deletion syndrome.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?An affected core drives network integration deficits of the structural connectome in 22q11.2 deletion syndrome.Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.Developmental trajectories of executive functions in 22q11.2 deletion syndromeRare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeAction simulation in hallucination-prone adolescents.Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal studyGraph theory reveals dysconnected hubs in 22q11DS and altered nodal efficiency in patients with hallucinations.Early adversity and combat exposure interact to influence anterior cingulate cortex volume in combat veterans.Brief Report: A Preference for Biological Motion Predicts a Reduction in Symptom Severity 1 Year Later in Preschoolers with Autism Spectrum Disorders.Converging evidence for abnormalities of the prefrontal cortex and evaluation of midsagittal structures in pediatric posttraumatic stress disorder: an MRI study.Ultra high risk status and transition to psychosis in 22q11.2 deletion syndromeDecreased frontal gyrification correlates with altered connectivity in children with autism.
P50
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P50
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