Publications by authors named "Hyoungshin Choi"

Objective: Social anxiety disorder (SAD) is characterized by heightened sensitivity to social interactions or settings, which disrupts daily activities and social relationships. This study aimed to explore the feasibility of utilizing digital phenotypes for predicting the severity of these symptoms and to elucidate how the main predictive digital phenotypes differed depending on the symptom severity.

Method: We collected 511 behavioral and physiological data over 7 to 13 weeks from 27 SAD and 31 healthy individuals using smartphones and smartbands, from which we extracted 76 digital phenotype features.

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Article Synopsis
  • Autism spectrum disorder is linked to sensory and social communication challenges, and previous research suggests that brain organization differences in individuals with autism correlate with their behaviors.
  • This study used advanced autoencoder techniques to analyze structural connectivity in the brains of 80 individuals with autism and 61 neurotypical controls, focusing on low-dimensional features from diffusion MRI data.
  • The results revealed significant differences in brain connectivity, particularly in regions associated with sensory and emotional processing, and showed that these differences are related to communication skills in individuals with autism, highlighting potential biomarkers for the condition.
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Eating behavior is highly heterogeneous across individuals and cannot be fully explained using only the degree of obesity. We utilized unsupervised machine learning and functional connectivity measures to explore the heterogeneity of eating behaviors measured by a self-assessment instrument using 424 healthy adults (mean ± standard deviation [SD] age = 47.07 ± 18.

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Clinical heterogeneity has been one of the main barriers to develop effective biomarkers and therapeutic strategies in autism spectrum disorder (ASD). Recognizing this challenge, much effort has been made in recent neuroimaging studies to find biologically more homogeneous subgroups (called 'neurosubtypes') in autism. However, most approaches have rarely evaluated how much the employed features in subtyping represent the core anomalies of ASD, obscuring its utility in actual clinical diagnosis.

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