Proposal Title
Identify genes that influence movement disorders, including Parkinson disease, in 22q11.2DS
Pregnancy and birth complications as risk factors for schizophrenia in 22q11.2DS
Do polygenic risk scores account for variable effects of schizophrenia and autism spectrum disorders in 22q11.2 microdeletion syndrome?
Molecular genetics of CRKL in cardiovascular development
Identify genes on 22q11.2 that influence IQ in children, aged 8 or older, and adolescents with 22q11.2DS
The Relationship of Executive Functions to Psychosis in Patients with 22q11.2 Deletion Syndrome
The Relationship of Verbal Memory and Learning Abilities to Psychosis in Patients with 22q11.2 Deletion Syndrome
Examining Attention Deficit Hyperactivity Disorder (ADHD) inattention symptoms as antecedents of psychosis risk in 22q11.2 Deletion Syndrome (22q11.2DS).
Analysis of iPSC phenotype and mitochondrial haplotype in 22q11 deletion syndrome
A polygenic score analysis of 22q11 deletion syndrome
Aberrant recombination as a risk factor for 22q11.2 deletions.
Genetic modifiers of congenital heart disease in 22q11DS: whole exome analysis.
A multisite study of cortical development in 22q11.2 deletion syndrome
Examining the genetic risk underlying development of Attention Deficit Hyperactivity Disorder in children with 22q11.2 Deletion Syndrome.
Characterizing the autism spectrum disorder (ASD) profile of 22q11.2 Deletion Syndrome (22q11.2DS) – a comparison with non-syndromic ASD and individuals at high genetic risk of ASD.
Prodromal symptoms in 22q11DS
Examining genetic risk underlying development of anxiety and negative symptoms in 22q11.2 Deletion Syndrome.
Prodrome and conversion rates to psychosis in 22q11.2DS
Psychopathology in parents of children with 22q11.2 Deletion Syndrome – a comparison with population-based rates
LCR subunit copy number variance influences the 22q11.2DS phenotype
Delineation of deletion size in 22q11.2 deletion syndrome related to extreme cognitive phenotypes
Processing speed, Cognitive Decline and Psychotic Disorders in the 22q11.2 Deletion Syndrome. A Longitudinal Study.