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10.3280/QPC2017-040003

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Finger E.C., Marsh A.A., Mitchell D.G., Reid M.E., Sims C., Bhdhani S., Kosson D.S, Chen G., Towbin K.E., Leibenluft, E., Pine, D.S., Blair, J.R. (2008). Abnormal ventromedial prefrontal cortex function in children with psychopathic traits during reversal learning. Arch. Gen. Psychiatry, 65: 586-594.

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Gerdes M., Solot C., Wang P.P., Moss E., LaRossa D., Randall P., Goldmuntz E., Clark B.J., Driscoll D.A., Jawad A., Emanuel B.S., McDonald-McGinn D.M., Batshaw M.L., Zackai E.H. (1999). Cognitive and Behavior Profile of Preschool Children With Chromosome 22q11.2 Deletion. American Journal of Medical Genetics, 85: 127-133.

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Itami S., Uno H. (2002). Orbitofrontal cortex dysfunction in attention-deficit hyperactivity disorder revealed by reversal and extinction tasks. NeuroReport, 13(18): 2453-2457.

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Jawad A.F., McDonald-McGinn D.M., Zackai E., Sullivan K.E. (2001). Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge/Velocardiofacial syndrome). J. Pediatr., 139: 715-723.

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Jolinn E.M., Weller R.A., Jessani N.R., Zackai E.H., McDonald-McGinn D.M., Weller E.B. (2009). Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion Syndrome. J. of Affective Disorders, 9, 119: 177-180.

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Kates W.R., Antshel K.M., AbdulSabur N., Colgan D., Funke B., Fremont W., Higgins A.M., Kucherlapati R., Shprintzen R.J. (2006). A Gender-Moderated Effect of a Functional COMT Polymorphism on Prefrontal Brain Morphology and Function in Velo-cardio-facial Syndrome (22q11.2 Deletion Syndrome). Am. J. Med. Genet. B. Neuropsychiatr. Genet., 141B(3): 274-280.

Unstructured Citation

Kates W.R., Krauss B.R., AbdulSabur N., Colgan D., Antshel K.M., Higgins A.M., Shprintzen R.J. (2007) The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome). Neuropsychologia, 45(12): 2863-2873.

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Kates W.R, Antshel K.M., Faraone S.V., Fremont W.P., Higgins A.M., Shprintzen R.J., Botti J., Kelchner L., McCarthy C. (2011). Neuroanatomic predictors to prodomal psychosis in Velocardiofacial syndrome (22q11.2 deletion syndrome): A longitudinal study. Biol. Psychiatry, 69: 945-952

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Shaikh T.H., Kurahashi H., Saitta S.C., O’Hare A.M., Hu P., Roe B.A., Driscoll D.A., McDonald-McGinn D.M., Zackai E.H., Budarf M.L. et al. (2000). Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: Genomic organization and deletion endpoint analysis. Hum. Mol. Genet., 9: 489-501.

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Unstructured Citation

Simon T.J. (2008). A New Account of the Neurocognitive Foundations of Impairments in Space, Time and Number Processing in Children with Chromosome 22q11.2 Deletion Syndrome. Dev. Disabil. Res. Rev., 14(1): 52-58.

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Unstructured Citation

Sobin C., Kiley-Brabeck K., Karayiorgou M. (2005). Lower Prepulse Inhibition in Children With the 22q11 Deletion Syndrome. Am. J. Psychiatry, 162: 1090-1099.

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Unstructured Citation

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