Projects per year
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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.
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Projects
- 7 Finished
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Cognitive-Affective Psychosis Proneness Risk and protective factors in 22q11.2DS
8/1/15 → 7/31/20
Project: Research project
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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.
9/24/13 → 6/30/18
Project: Research project
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Fragile X Spectrum as Model for Neurogenetic Mechanisms of Cognitive Dysfunction
9/30/07 → 6/30/13
Project: Research project
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Research output
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Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis
Wigby, K., Cordeiro, L., Wilson, R., Angkustsiri, K., Simon, T. J. & Tartaglia, N., Jun 1 2020, In: American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. 184, 2, p. 456-468 13 p.Research output: Contribution to journal › Article › peer-review
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At-home self-administration of an immersive virtual reality therapeutic game for post-stroke upper limb rehabilitation
Salisbury, J. P., Aronson, T. M. & Simon, T. J., Nov 2 2020, CHI PLAY 2020 - Extended Abstracts of the 2020 Annual Symposium on Computer-Human Interaction in Play. Association for Computing Machinery, Inc, p. 114-121 8 p. (CHI PLAY 2020 - Extended Abstracts of the 2020 Annual Symposium on Computer-Human Interaction in Play).Research output: Chapter in Book/Report/Conference proceeding › Conference contribution
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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
International 22q11.2 Brain and Behavior Consortium, Jan 2 2020, In: American Journal of Human Genetics. 106, 1, p. 26-40 15 p.Research output: Contribution to journal › Article › peer-review
10 Scopus citations -
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
International 22q11.2DS Brain and Behavior Consortium, Jan 1 2020, (Accepted/In press) In: Molecular Psychiatry.Research output: Contribution to journal › Article › peer-review
21 Scopus citations -
Mapping subcortical brain alterations in 22q11.2 deletion syndrome: Effects of deletion size and convergence with idiopathic neuropsychiatric illness
Ching, C. R. K., Gutman, B. A., Sun, D., Reina, J. V., Ragothaman, A., Isaev, D., Zavaliangos-Petropulu, A., Lin, A., Jonas, R. K., Kushan, L., Pacheco-Hansen, L., Vajdi, A., Forsyth, J. K., Jalbrzikowski, M., Bakker, G., Van Amelsvoort, T., Antshel, K. M., Fremont, W., Kates, W. R., Campbell, L. E. & 35 others, , Jul 1 2020, In: American Journal of Psychiatry. 177, 7, p. 589-600 12 p.Research output: Contribution to journal › Article › peer-review
18 Scopus citations