• 3704 Citations
  • 33 h-Index
1976 …2020
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Fingerprint Dive into the research topics where Tony J Simon is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
DiGeorge Syndrome Medicine & Life Sciences
Chromosome Deletion Medicine & Life Sciences
Brain Medicine & Life Sciences
Cognition Medicine & Life Sciences
Psychotic Disorders Medicine & Life Sciences
Corpus Callosum Medicine & Life Sciences
Schizophrenia Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences

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Projects 1976 2020

Psychotic Affective Disorders
DiGeorge Syndrome
Psychotic Disorders
Schizophrenia
Anxiety

MIND Institute Intellectual and Developmental Disabilities Research Center

Hertz-Picciotto, I., Hagerman, R. J., Simon, T., van De Water, J. A., Crawley, J., Ozonoff, S., Abbeduto, L. J., Abbeduto, L. J., Crawley, J., Ozonoff, S. J., Van de Water, J. A. & Simon, T. J.

National Institutes of Health

9/24/136/30/18

Project: Research project

Developmental Disabilities
Fragile X Syndrome
Intellectual Disability
Research Personnel
Rodentia
Magnetic Resonance Imaging
Phenotype
Fragile X Mental Retardation Protein
RNA
Genes
Inborn Genetic Diseases
Research Personnel
DiGeorge Syndrome
Fragile X Syndrome
Cognition
DiGeorge Syndrome
Parietal Lobe
Cognition
Chromosome Deletion
Brain

Research Output 1985 2019

DiGeorge Syndrome
Bullying
Vulnerable Populations
Psychotic Disorders
Chromosome Deletion

Interrelationship Between Cognitive Control, Anxiety, and Restricted and Repetitive Behaviors in Children with 22q11.2 Deletion Syndrome

Uljarević, M., McCabe, K. L., Angkustsiri, K., Simon, T. J. & Hardan, A. Y., Jan 1 2019, (Accepted/In press) In : Autism Research.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Child Behavior
Anxiety
Communication
Social Problems
3 Citations (Scopus)

A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome

Jensen, M., Kooy, R. F., Simon, T. J., Reyniers, E., Girirajan, S. & Tassone, F., Apr 1 2018, In : European Journal of Medical Genetics. 61, 4, p. 209-212 4 p.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Intellectual Disability
Phenotype
Genome
Chromosomes, Human, Pair 22

Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome

Villalon-Reina, J. E., Ching, C. R. K., Kothapalli, D., Sun, D., Nir, T., Lin, A., Forsyth, J. K., Kushan, L., Vajdi, A., Jalbrzikowski, M., Hansen, L., Jonas, R. K., Van Amelsvoort, T., Bakker, G., Kates, W. R., Antshel, K. M., Fremont, W., Campbell, L. E., McCabe, K. L., Daly, E. & 22 others, Gudbrandsen, M., Murphy, C., Murphy, D., Craig, M., Emanuel, B., McDonald-Mcginn, D., Ruparel, K., Roalf, D., Gur, R. E., Schmitt, J. E., Simon, T. J., Goodrich-Hunsaker, N. J., Durdle, C. A., Doherty, J., Cunningham, A. C., Van Den Bree, M., Linden, D. E. J., Owen, M., Moss, H., Jahanshad, N., Bearden, C. E. & Thompson, P. M., Jan 1 2018, 14th International Symposium on Medical Information Processing and Analysis. Lepore, N., Romero, E. & Brieva, J. (eds.). SPIE, 109750U. (Proceedings of SPIE - The International Society for Optical Engineering; vol. 10975).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

deletion
Deletion
Anisotropy
anisotropy
Alternatives
5 Citations (Scopus)

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., Sher, K. J. & Loewy, R. L., Aug 1 2018, In : JAMA Psychiatry. 75, 8, p. 853-861 9 p.

Research output: Contribution to journalArticle

Psychotic Disorders
Neuropsychological Tests
Psychometrics
Self Report
Brain Waves