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Craig A Erickson

Biographic Data

ID7387871
NAMECraig A Erickson
GIVEN NAMESCraig A
FAMILY NAMEErickson
SIGNATUREERICKSON C A
AFFILIATIONSUniversity of Cincinnati Medical Center
ORCID0000-0003-4512-398X
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS0
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Beyond the Fragile X protein

    Open Access•Walker S McKinney, Austin Corsmeier et al.•ARTICLE•Frontiers in Psychiatry•2025

    Our finding of stronger links between neighborhood resources and clinical outcomes in males with FXS is consistent with previous work and may reflect increased reliance on social-environmental supports in males who typically have more significant intellectual and adaptive deficits than females. Consistent associations between greater social resources, higher IQ, and stronger adaptive skills suggest social support (e.g., social cohesion, resource …

  • Co-designing a communication app to enhance collaborative communication support for secondary students with autism

    Open Access•John O’rourke, Christopher Kueh et al.•ARTICLE•Educational Technology Research…•2023

  • Gabaa Alpha 2,3 Modulation Improves Select Phenotypes in a Mouse Model of Fragile X Syndrome

    Open Access•Tori L Schaefer, Amy A Ashworth et al.•ARTICLE•Frontiers in Psychiatry•2021

    Fragile X syndrome (FXS) is the most common cause of inherited intellectual disability. FXS is caused by functional loss of the Fragile X Protein (FXP), also known as Fragile X Mental Retardation Protein (FMRP). In humans and animal models, loss of FXP leads to sensory hypersensitivity, increased susceptibility to seizures and cortical hyperactivity. Several components of the GABAergic system, the major inhibitory system in the brain, are dysregu…

No prominent works on this page.

  • Gabaa Alpha 2,3 Modulation Improves Select Phenotypes in a Mouse Model of Fragile X Syndrome

    Open Access•Tori L Schaefer, Amy A Ashworth et al.•ARTICLE•Frontiers in Psychiatry•2021

    Fragile X syndrome (FXS) is the most common cause of inherited intellectual disability. FXS is caused by functional loss of the Fragile X Protein (FXP), also known as Fragile X Mental Retardation Protein (FMRP). In humans and animal models, loss of FXP leads to sensory hypersensitivity, increased susceptibility to seizures and cortical hyperactivity. Several components of the GABAergic system, the major inhibitory system in the brain, are dysregu…

  • Co-designing a communication app to enhance collaborative communication support for secondary students with autism

    Open Access•John O’rourke, Christopher Kueh et al.•ARTICLE•Educational Technology Research…•2023

  • Beyond the Fragile X protein

    Open Access•Walker S McKinney, Austin Corsmeier et al.•ARTICLE•Frontiers in Psychiatry•2025

    Our finding of stronger links between neighborhood resources and clinical outcomes in males with FXS is consistent with previous work and may reflect increased reliance on social-environmental supports in males who typically have more significant intellectual and adaptive deficits than females. Consistent associations between greater social resources, higher IQ, and stronger adaptive skills suggest social support (e.g., social cohesion, resource …

Autism Spectrum Disorder Research (3 works) · Fragile x (2 works) · Fragile X syndrome (2 works) · Genetics and Neurodevelopmental Disorders (2 works) · Medicine (2 works) · Psychology (2 works) · Adaptive behavior (1 work) · Adaptive functioning (1 work) · Agonist (1 work) · Anxiety (1 work)

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