Roger Staff

Prof. Roger Staff


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
24 February 2025 in Nuclear Medicine and Molecular Imaging
Verified
Journal Article
Closed access
PDF file
STShailendra Mohan Tripathi
Shailendra Mohan Tripathi
CMChristopher J. McNeil
Christopher J. McNeil
Roger StaffRoger Staff
Roger Staff
AMAlison D Murray
Alison D Murray
Claude M. WischikClaude M. Wischik
Claude M. Wischik
GWGordon Waiter
Gordon Waiter

26 July 2025 in Brain Sciences
Verified
Journal Article
Open access
PDF file
Moses O. SokunbiMoses O. Sokunbi
Moses O. Sokunbi
Oumayma SOULAOumayma SOULA
Oumayma SOULA
BOBertha Ochieng
Bertha Ochieng
Roger StaffRoger Staff
Roger Staff
Background: Autism spectrum disorder (ASD) is characterised by atypical behavioural and cognitive diversity, yet the neural underpinnings linking brain activity and individual presentations remain poorly understood. In this study, we investigated the relationship between resting-state functional magnetic resonance imaging (fMRI) signal complexity and intelligence (full-scale intelligence quotient (FIQ); verbal intelligence quotient (VIQ); and performance intelligence quotient (PIQ)) in male adults with ASD (n = 14) and matched neurotypical controls (n = 15). Methods: We used three complexity-based metrics: Hurst exponent (H), fuzzy approximate entropy (fApEn), and fuzzy sample entropy (fSampEn) to characterise resting-state fMRI signal dynamics, and correlated these measures with standardised intelligence scores. Results: Using a whole-brain measure, ASD participants showed significant negative correlations between PIQ and both fApEn and fSampEn, suggesting that increased neural irregularity may relate to reduced cognitive–perceptual performance in autistic individuals. No significant associations between entropy (fApEn and fSampEn) and PIQ were found in the control group. Group differences in brain–behaviour associations were confirmed through formal interaction testing using Fisher’s r-to-z transformation, which showed significantly stronger correlations in the ASD group. Complementary regression analyses with interaction terms further demonstrated that the entropy (fApEn and fSampEn) and PIQ relationship was significantly moderated by group, reinforcing evidence for autism-specific neural mechanisms underlying cognitive function. Conclusions: These findings provide insight into how cognitive functions in autism may not only reflect deficits but also an alternative neural strategy, suggesting that distinct temporal patterns may be associated with intelligence in ASD. These preliminary findings could inform clinical practice and influence health and social care policies, particularly in autism diagnosis and personalised support planning.

19 June 2025 in Preprints.org
Verified
Preprint
Open access
PDF file
Moses O. SokunbiMoses O. Sokunbi
Moses O. Sokunbi
Oumayma SOULAOumayma SOULA
Oumayma SOULA
BOBertha Ochieng
Bertha Ochieng
Roger StaffRoger Staff
Roger Staff
Autism Spectrum Disorder (ASD) is characterised by atypical behavioural and cognitive diversity, yet the neural underpinnings linking brain activity and individual presentations remain poorly understood. In this study, we investigated the relationship between resting-state functional magnetic resonance imaging (fMRI) signal complexity and intelligence (full-scale intelligence quotient (FIQ); verbal intelligence quotient (VIQ); and performance intelligence quotient (PIQ); in male adults with ASD (n = 14) and matched neurotypical controls (n = 15), using three complexity-based metrics: Hurst Exponent (H), fuzzy approximate entropy (fApEn), and fuzzy sample entropy (fSampEn). Using a whole-brain measure, ASD participants showed significant negative correlations between PIQ and both fApEn and fSampEn, suggesting that increased neural irregularity may relate to reduced cognitive-perceptual performance in autistic individuals. No significant group association with complexity were found in the control group. These findings provide insight into how cognitive functions in autism may not only reflect deficits but also an alternative neural strategy, suggesting that distinct temporal patterns may influence intelligence in ASD. These preliminary findings could inform clinical practice and influence health and social care policies, particularly in autism diagnosis and personalised support planning.