Danielle A. Baribeau
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 38 publications
Characterizing ARID1B-related disorders and variants of uncertain significance using DNA methylation.
Journal: European journal of human genetics : EJHG
Published: February 10, 2026
Traumatic Experiences and Major Life Stressors in Children and Youth With Neurodevelopmental Disorders.
Journal: Journal of autism and developmental disorders
Published: December 17, 2025
An n-of-1 gene-directed drug repurposing trial for an ultrarare genetic condition.
Journal: Epilepsia
Published: October 24, 2025
A precision health approach to medication management in neurodevelopmental conditions: a model development and validation study using four international cohorts.
Journal: medRxiv : the preprint server for health sciences
Published: March 31, 2025
Psychopharmacology in children with genetic disorders of epigenetic and chromatin regulation.
Journal: Journal of neurodevelopmental disorders
Published: November 27, 2024
Clinical Genetic Testing in Schizophrenia: A Systematic Review and Meta-Analysis.
Journal: Biological psychiatry
Published: November 18, 2024
Predictors of Depressive Symptoms in Autistic Youth-A Longitudinal Study From the Province of Ontario Neurodevelopmental Disorders (POND) Network: Prédicteurs des symptômes dépressifs chez les jeunes autistes-une étude longitudinale du Réseau des troubles neurodéveloppementaux de la province de l'Ontario (réseau POND).
Journal: Canadian journal of psychiatry. Revue canadienne de psychiatrie
Published: July 25, 2024
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia.
Journal: Brain : a journal of neurology
Published: June 25, 2024
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure.
Journal: Journal of neurodevelopmental disorders
Published: September 28, 2023
Selective Serotonin Reuptake Inhibitor Treatment Post Gene Therapy for an Ultrarare Neurometabolic Disorder (AADC Deficiency).
Journal: Journal of the American Academy of Child and Adolescent Psychiatry
Published: September 26, 2023
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions.
Journal: NPJ genomic medicine
Published: September 26, 2023
Support to caregivers who have received genetic information about neurodevelopmental and psychiatric vulnerability in their young children: A narrative review.
Journal: Clinical genetics
Published: March 19, 2023
Last Updated: 09/26/2026