Simon, Tony J.

Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

Schneider, M., Debbané, M., Bassett, A. S., Chow, E. W. C., Fung, W. L. A., van den Bree, M. B. M., Owen, M., Murphy, K. C., Niarchou, M., Kates, W. R., et al. (2014) · American Journal of Psychiatry

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 779

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

Karayiorgou, M., Simon, T. J., & Gogos, J. A. (2010) · Nature Reviews Neuroscience

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 474

Assessment of the Prodromal Questionnaire–Brief Child Version for Measurement of Self-reported Psychoticlike Experiences in Childhood

Karcher, N. R., Barch, D. M., Avenevoli, S., Savill, M., Huber, R. S., Simon, T. J., Leckliter, I. N., Sher, K. J., & Loewy, R. L. (2018) · JAMA Psychiatry

Schizophrenia research and treatmentChild and Adolescent Psychosocial and Emotional Development

Cited by 198

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

International 22q11.2 Brain and Behavior Consortium, Davies, R. W., Fiksinski, A. M., Breetvelt, E. J., Williams, N. M., Hooper, S. R., Monfeuga, T., Bassett, A. S., Owen, M. J., Gur, R. E., et al. (2020) · Nature Medicine

Schizophrenia research and treatmentGenomic variations and chromosomal abnormalities

Cited by 139

Mapping Cortical Thickness in Children with 22q11.2 Deletions

Bearden, C. E., van Erp, T. G. M., Dutton, R. A., Tran, H., Zimmermann, L., Sun, D., Geaga, J. A., Simon, T. J., Glahn, D. C., Cannon, T. D., et al. (2007) · Cerebral Cortex

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 92

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Mlynarski, E. E., Sheridan, M. B., Xie, M., Guo, T., Racedo, S. E., McDonald-McGinn, D. M., Gai, X., Chow, E. W. C., Vorstman, J., Swillen, A., et al. (2015) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesCongenital heart defects research

Cited by 74

Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

DeBoer, T., Wu, Z., Lee, A., & Simon, T. J. (2007) · Behavioral and Brain Functions

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 67

Effects of Comt Genotype on Behavioral Symptomatology in the 22q11.2 Deletion Syndrome

Bearden, C. E., Jawad, A. F., Lynch, D. R., Monterossso, J. R., Sokol, S., McDonald-McGinn, D. M., Saitta, S. C., Harris, S. E., Moss, E., Wang, P. P., et al. (2005) · Child Neuropsychology

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 42

Bullying and psychosis: The impact of chronic traumatic stress on psychosis risk in 22q11.2 deletion syndrome—A uniquely vulnerable population

Mayo, D., Bolden, K. A., Simon, T. J., & Niendam, T. A. (2019) · Journal of Psychiatric Research

Bullying, Victimization, and AggressionSchizophrenia research and treatment

Cited by 32