Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome

Author:

Thompson Carlie A.1,Karelis Jason1,Middleton Frank A.12,Gentile Karen2,Coman Ioana L.3,Radoeva Petya D.4,Mehta Rashi5,Fremont Wanda P.1,Antshel Kevin M.16,Faraone Stephen V.1,Kates Wendy R.1

Affiliation:

1. Department of Psychiatry and Behavioral Sciences; SUNY Upstate Medical University; Syracuse New York

2. Department of Neuroscience; SUNY Upstate Medical University; Syracuse New York

3. Department of Computer Science; SUNY Oswego; Oswego New York

4. Department of Psychiatry; University of Washington; Seattle Washington

5. Department of Radiology; SUNY Upstate Medical University; Syracuse New York

6. Department of Psychology; Syracuse University; Syracuse New York

Funder

National Institutes of Health

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference112 articles.

1. Allelic and genotype frequencies of catechol-O-methyltransferase (Val158Met) and CYP2D6*10 (Pro34Ser) single nucleotide polymorphisms in the philippines;Baclig;Int J Mol Epidemiol Genet,2012

2. Update on the treatment of spinal cord injury;Baptiste;Prog Brain Res,2007

3. Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome;Bassett;Biol Psychiatry,2007

4. Mapping cortical thickness in children with 22q11.2 deletions;Bearden;Cereb Cortex,2007

5. The neurocognitive phenotype of the 22q11. 2 deletion syndrome: Selective deficit in visual-spatial memory;Bearden;J Clin Exp Neuropsychol,2001

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