Publications by authors named "Mohsen Soltanifar"

It is common practice to use hierarchical Bayesian model for the informing of a pediatric randomized controlled trial (RCT) by adult data, using a prespecified borrowing fraction parameter (BFP). This implicitly assumes that the BFP is intuitive and corresponds to the degree of similarity between the populations. Generalizing this model to any historical studies, naturally leads to empirical Bayes meta-analysis.

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This research evaluated standard Weibull mixture cure (WMC) network meta-analysis (NMA) with Bayesian hierarchical (BH) WMC NMA to inform long-term survival of therapies. Four trials in previously treated metastatic non-small-cell lung cancer with PD-L1 >1% were used comparing docetaxel with nivolumab, pembrolizumab and atezolizumab. Cure parameters related to a certain treatment class were assumed to share a common distribution.

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Effect modification (EM) may cause bias in network meta-analysis (NMA). Existing population adjustment NMA methods use individual patient data to adjust for EM but disregard available subgroup information from aggregated data in the evidence network. Additionally, these methods often rely on the shared effect modification (SEM) assumption.

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Measurements of response inhibition components of reactive inhibition and proactive inhibition within the stop-signal paradigm have been of particular interest to researchers since the 1980s. While frequentist nonparametric and Bayesian parametric methods have been proposed to precisely estimate the entire distribution of reactive inhibition, quantified by stop signal reaction times (SSRT), there is no method yet in the stop signal task literature to precisely estimate the entire distribution of proactive inhibition. We identify the proactive inhibition as the difference of go reaction times for go trials following stop trials versus those following go trials and introduce an Asymmetric Laplace Gaussian (ALG) model to describe its distribution.

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Article Synopsis
  • - The study examines how single Stop Signal Reaction Times (SSRT) in stop signal tasks have been modeled using nonparametric and Bayesian methods, emphasizing the need to consider the impact of trial types on SSRT estimations.
  • - It introduces a two-state mixture model for SSRT distributions and compares it to traditional single SSRT distributions, finding that the mixture model is more varied and exhibits distinct statistical characteristics such as positive skewness and high kurtosis.
  • - The findings indicate that the mixture SSRT indices are consistently larger than the single SSRT counterparts, suggesting that this approach offers significant improvements in estimating SSRTs in cognitive tasks.
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Article Synopsis
  • The Stop Signal Reaction Time (SSRT) is a measurement related to how quickly the brain can stop a response, initially proposed by Logan in 1994 without considering trial types.
  • In 2017, two new indices—mixture SSRT and weighted SSRT—were introduced to better analyze SSRT over time, but a time series approach was still lacking.
  • A recent study compared a time series-based SSRT to Logan's original SSRT, finding that the new approach yields significantly larger SSRT estimates by incorporating factors like reactive and proactive inhibition effects.
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The negative impact of school absenteeism on children's academic performance has been documented in the educational literature, yet few studies have used validated development indicators, or investigated individual and neighborhood characteristics to illuminate potential moderating factors. Using cross-sectional Early Development Instrument (EDI) panel data (2001-2005) we constructed multilevel linear and logistic regression models to examine the association between school absenteeism and early childhood development, moderated by Aboriginal status, length of school absence, neighborhood-level income inequality, and children's sex assigned at birth. Our study included 3572 children aged four to eight in 56 residential neighborhoods in Saskatoon, Canada.

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