Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Walker S, McKinney"'
Publikováno v:
Journal of Clinical and Translational Science, Vol 8 (2024)
Despite having the same underlying genetic etiology, individuals with the same syndromic form of intellectual developmental disability (IDD) show a large degree of interindividual differences in cognition and IQ. Research indicates that up to 80% of
Externí odkaz:
https://doaj.org/article/911192e3613e4418ba9e01e2290d25cf
Autor:
Walker S. McKinney, Shannon E. Kelly, Kathryn E. Unruh, Robin L. Shafer, John A. Sweeney, Martin Styner, Matthew W. Mosconi
Publikováno v:
Frontiers in Integrative Neuroscience, Vol 16 (2022)
Externí odkaz:
https://doaj.org/article/7d06a0419d674f039c241bd75aae9a8f
Autor:
Kathryn E. Unruh, Walker S. McKinney, Erin K. Bojanek, Kandace K. Fleming, John A. Sweeney, Matthew W. Mosconi
Publikováno v:
Molecular Autism, Vol 12, Iss 1, Pp 1-25 (2021)
Abstract Background Sensorimotor issues are common in autism spectrum disorder (ASD), related to core symptoms, and predictive of worse functional outcomes. Deficits in rapid behaviors supported primarily by feedforward mechanisms, and continuous, fe
Externí odkaz:
https://doaj.org/article/ad9143ad0b604f8bb95c868b0c28107b
Autor:
Walker S. McKinney, Shannon E. Kelly, Kathryn E. Unruh, Robin L. Shafer, John A. Sweeney, Martin Styner, Matthew W. Mosconi
Publikováno v:
Frontiers in Integrative Neuroscience, Vol 16 (2022)
BackgroundSensorimotor issues are common in autism spectrum disorder (ASD), though their neural bases are not well understood. The cerebellum is vital to sensorimotor control and reduced cerebellar volumes in ASD have been documented. Our study exami
Externí odkaz:
https://doaj.org/article/9464492f9ba9463a90e8bc8af1ba28b3
Autor:
Walker S. McKinney, James Bartolotti, Pravin Khemani, Jun Yi Wang, Randi J. Hagerman, Matthew W. Mosconi
Publikováno v:
NeuroImage: Clinical, Vol 27, Iss , Pp 102332- (2020)
Introduction: Premutation carriers of the FMR1 gene are at risk of developing fragile X-associated tremor/ataxia syndrome (FXTAS), a neurodegenerative disease characterized by motor, cognitive, and psychiatric decline as well as cerebellar and cerebr
Externí odkaz:
https://doaj.org/article/9b35238d39f44a789e32a2c1ed811579
Autor:
Kathryn E Unruh, James V Bartolotti, Walker S McKinney, Lauren M Schmitt, John A Sweeney, Matthew W Mosconi
Publikováno v:
Cerebral Cortex.
Sensorimotor issues are present in the majority of individuals with autism spectrum disorder (ASD) and are associated with core symptoms. The neural systems associated with these impairments remain unclear. Using a visually guided precision gripping
Autor:
Mehar N. Singh, Michael C. Roberts, Walker S. McKinney, Shannon Kelly, Adrian Ortega, Rachel Doyle, Elizabeth C. Tampke
Publikováno v:
Training and Education in Professional Psychology.
Autor:
Walker S. McKinney, Zheng Wang, Shannon Kelly, Pravin Khemani, Su Lui, Stormi P. White, Matthew W. Mosconi
Publikováno v:
Frontiers in Integrative Neuroscience, Vol 13 (2019)
BackgroundIndividuals with premutation alleles of the FMR1 gene are at risk of developing fragile X-associated tremor/ataxia syndrome (FXTAS), a neurodegenerative condition affecting sensorimotor function. Information on quantitative symptom traits a
Externí odkaz:
https://doaj.org/article/85a41bb191b541d3b9bafed6a7726bfb
Autor:
Zheng Wang, Callie Lane, Matthew Terza, Pravin Khemani, Su Lui, Walker S. McKinney, Matthew W. Mosconi
Publikováno v:
Brain Sciences, Vol 11, Iss 1, p 13 (2020)
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a neurodegenerative disorder associated with a premutation cytosine-guanine-guanine (CGG) trinucleotide repeat expansion of the FMR1 gene. FXTAS is estimated to be the most common single-gene for
Externí odkaz:
https://doaj.org/article/7de2833889b24db6b326dfbaee9792af
Autor:
Grant C. Magnon, Walker S. McKinney, John A. Sweeney, Rebecca J. Lepping, Stephen A. Coombes, Zheng Wang, Matthew W. Mosconi, Sarah K. Keedy, David E. Vaillancourt
Publikováno v:
Human Brain Mapping
Sensorimotor abnormalities are common in autism spectrum disorder (ASD) and predictive of functional outcomes, though their neural underpinnings remain poorly understood. Using functional magnetic resonance imaging, we examined both brain activation