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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Cognitive-Affective Psychosis Proneness Risk and protective factors in 22q11.2DS
Project: Research project
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Fragile X Spectrum as Model for Neurogenetic Mechanisms of Cognitive Dysfunction
Project: Research project
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Cognitive-Affective Psychosis Proneness Risk and protective factors in 22q11.2DS
8/1/15 → 7/31/20
Project: Research project
Research output
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Atypical attentional filtering of visual information in youth with chromosome 22q11.2 deletion syndrome as indexed by event-related potentials
Linton, S. R., Popa, A. M., Luck, S. J., Bolden, K., Angkustsiri, K., Carter, C. S., Niendam, T. A. & Simon, T. J., Jan 2021, In: NeuroImage: Clinical. 32, 102877.Research output: Contribution to journal › Article › peer-review
Open Access -
The Importance of Understanding Individual Differences of Emotion Regulation Abilities in 22q11.2 Deletion Syndrome
Campbell, L. E., Swaab, L., Freeman, E. E., McCormack, L., Simon, T. J., Angkustsiri, K. & McCabe, K. L., 2021, (Accepted/In press) In: Journal of Autism and Developmental Disorders.Research output: Contribution to journal › Article › peer-review
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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
1 Scopus citations -
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
2 Scopus citations -
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
21 Scopus citations