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The American Journal of Psychiatry|March 4, 2006
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndromeBronwyn Glaser, Martin Debbane, Christine Hinard, et al.Journal of Pediatric Psychology|April 28, 2018
Early Adaptive Functioning Trajectories in Preschoolers With Autism Spectrum DisordersMartina Franchini, Daniela Zöller, Edouard Gentaz, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|August 14, 2003
Factors associated with parenting stress in mothers of children with fragile X syndromeCindy Johnston, David Hessl, Chistine Blasey, et al.Journal of Neurodevelopmental Disorders|December 3, 2010
Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndromeMarie Schaer, Bronwyn Glaser, Marie-Christine Ottet, et al.Journal of the American Academy of Child and Adolescent Psychiatry|March 12, 2002
Genetic and environmental influences on the cognitive outcomes of children with fragile X syndromeJennifer Dyer-Friedman, Bronwyn Glaser, David Hessl, et al.Journal of the American Academy of Child and Adolescent Psychiatry|October 26, 2013
Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site studyDoron Gothelf, Maude Schneider, Tamar Green, et al.The Journal of Pediatrics|June 20, 2002
Language skills in children with velocardiofacial syndrome (deletion 22q11.2)Bronwyn Glaser, Donna L Mumme, Christine Blasey, et al.Journal of Neurodevelopmental Disorders|November 16, 2016
Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal studyMathilde Bostelmann, Maude Schneider, Maria Carmela Padula, et al.Psychiatry Research|March 2, 2012
Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndromeMaude Schneider, Martial Van der Linden, Bronwyn Glaser, et al.Pageof 4