Thesis Vault

Deep phenotyping of language, cognition, and behaviour in school-aged children with recurrent copy number variants

Jente Verbesselt, KU Leuven, Leuven, Belgium, 2024

A Genetics-First Approach to Understanding Variation in Neuropsychiatric Outcomes: The 22q11.2 Deletion Syndrome

Ania Fiksinski, Utrecht University, 2021

Expression of Parkinson's disease and associated neurophenotypes in 22q11.2 deletion syndrome

Nancy Butcher, University of Toronto, 2015

Understanding Speech Problems in 22q11.2 Deletion Syndrome for Outcome Prediction

Nicole Spruit, UMC Utrecht, 2014

The Role of Putative Tbx1 Target Genes in the Pathogenesis of the 22q11 Deletion Syndrome Phenotype

Catherine Roberts, University College London, 2013

Increased Medical Interventions in Children with 22q11.2 Deletion Syndrome (Velocardiofacial Syndrome)

Emily King, University of Cincinnati, 2011

22q11 Deletion syndrome and neurotransmitter systems in unchallenged and challenged conditions

Erik Boot, University of Amsterdam, 2010

Retrospective Chart Review of Hospitalizations and Health Problems of Children with Velocardiofacial Syndrome

Michelle Wojtasiak, University of Cincinnati, 2002

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