• 3794 Citations
  • 34 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.

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

1 Citation (Scopus)

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

Villalón-Reina, J. E., Martínez, K., Qu, X., Ching, C. R. K., Nir, T. M., Kothapalli, D., Corbin, C., Sun, D., 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. & 32 others, Campbell, L. E., McCabe, K. L., Daly, E., Gudbrandsen, M., Murphy, C. M., Murphy, D., Craig, M., Emanuel, B., McDonald-McGinn, D. M., Vorstman, J. A. S., Fiksinski, A. M., Koops, S., Ruparel, K., Roalf, D., Gur, R. E., Eric Schmitt, J., Simon, T. J., Goodrich-Hunsaker, N. J., Durdle, C. A., Doherty, J. L., Cunningham, A. C., van den Bree, M., Linden, D. E. J., Owen, M., Moss, H., Kelly, S., Donohoe, G., Murphy, K. C., Arango, C., Jahanshad, N., Thompson, P. M. & Bearden, C. E., Jan 1 2019, (Accepted/In press) In : Molecular Psychiatry.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Diffusion Tensor Imaging
Internal Capsule
Diffusion Magnetic Resonance Imaging
Corpus Callosum
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

Seeing eye to eye with threat: Atypical Threat Bias in Children with 22q11.2 Deletion Syndrome

Popa, A. M., Cruz, J. R., Wong, L. M., Harvey, D. J., Angkustsiri, K., Leckliter, I. N., Perez-Edgar, K. & Simon, T. J., Jan 1 2019, In : American journal on intellectual and developmental disabilities. 124, 6, p. 549-567 19 p.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Anxiety
Reaction Time
Schizophrenia
Syndrome
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