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    <title>Recent ucistat items</title>
    <link>https://escholarship.org/uc/ucistat/rss</link>
    <description>Recent eScholarship items from Department of Statistics</description>
    <pubDate>Sat, 13 Jun 2026 05:04:14 +0000</pubDate>
    <item>
      <title>Genetic Variation and Stroke Recovery: The STRONG Study</title>
      <link>https://escholarship.org/uc/item/8184b81p</link>
      <description>BACKGROUND: Genetic association studies can reveal biology and treatment targets but have received limited attention for stroke recovery. STRONG (Stroke, Stress, Rehabilitation, and Genetics) was a prospective, longitudinal (1-year), genetic study in adults with stroke at 28 US stroke centers. The primary aim was to examine the association that candidate genetic variants have with (1) motor/functional outcomes and (2) stress-related outcomes.
METHODS: For motor/functional end points, 3 candidate gene variants (ApoE ε4, BDNF [brain-derived neurotrophic factor], and a dopamine polygenic score) were analyzed for associations with change in grip strength (3 months-baseline), function (3-month Stroke Impact Scale-Activities of Daily Living), mood (3-month Patient Health Questionnaire-8), and cognition (12-month telephone-Montreal Cognitive Assessment). For stress-related outcomes, 7 variants (serotonin transporter gene-linked promoter region, ACE [angiotensin-converting enzyme], oxytocin...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8184b81p</guid>
      <pubDate>Tue, 12 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cramer, Steven C</name>
      </author>
      <author>
        <name>Parodi, Livia</name>
      </author>
      <author>
        <name>Moslemi, Zahra</name>
      </author>
      <author>
        <name>Braun, Robynne G</name>
      </author>
      <author>
        <name>Aldridge, Chad M</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Rosand, Jonathan</name>
      </author>
      <author>
        <name>Holman, E Alison</name>
        <uri>https://orcid.org/0000-0001-5076-8403</uri>
      </author>
      <author>
        <name>Shah, Shreyansh</name>
      </author>
      <author>
        <name>Griessenauer, Christoph J</name>
      </author>
      <author>
        <name>Patel, Nirav</name>
      </author>
      <author>
        <name>Anderson, Christopher</name>
      </author>
      <author>
        <name>Henry, Jonathan</name>
      </author>
      <author>
        <name>Kourkoulis, Christina</name>
      </author>
      <author>
        <name>Lin, David J</name>
      </author>
      <author>
        <name>Zaba, Natalie</name>
      </author>
      <author>
        <name>Gee, Joey</name>
      </author>
      <author>
        <name>Moon, Johnson</name>
      </author>
      <author>
        <name>Schwertfeger, Julie</name>
      </author>
      <author>
        <name>Jayaraman, Arun</name>
      </author>
      <author>
        <name>Lee, Robert</name>
      </author>
      <author>
        <name>Lansberg, Maarten G</name>
      </author>
      <author>
        <name>Kemp, Stephanie</name>
      </author>
      <author>
        <name>Huang, Emily</name>
      </author>
      <author>
        <name>Bingham, Elijah</name>
      </author>
      <author>
        <name>Lugo, Leonel</name>
      </author>
      <author>
        <name>Eun, Da Eun Katie</name>
      </author>
      <author>
        <name>Payne, Jeremy</name>
      </author>
      <author>
        <name>Patten, Carolynn</name>
        <uri>https://orcid.org/0000-0002-9948-0045</uri>
      </author>
      <author>
        <name>Ng, Kwan</name>
      </author>
      <author>
        <name>Cao, Madelyn</name>
      </author>
      <author>
        <name>Jubb, Ashley</name>
      </author>
      <author>
        <name>McGee, Breann</name>
      </author>
      <author>
        <name>Shahbaba, Ryan</name>
      </author>
      <author>
        <name>Agrawal, Kunal</name>
      </author>
      <author>
        <name>Kissela, Brett</name>
      </author>
      <author>
        <name>DeJong, Stacey</name>
      </author>
      <author>
        <name>Cole, John</name>
      </author>
      <author>
        <name>Silver, Brian</name>
      </author>
      <author>
        <name>Manxhari, Christina</name>
      </author>
      <author>
        <name>Cucchiara, Brett</name>
      </author>
      <author>
        <name>Busza, Ania</name>
      </author>
      <author>
        <name>Hepple, Jennifer Paige</name>
      </author>
      <author>
        <name>Liew, Sook-Lei</name>
      </author>
      <author>
        <name>Alderman, Susan</name>
      </author>
      <author>
        <name>Beauchamp, Jennifer</name>
      </author>
      <author>
        <name>Mathew, Nitha Joseph</name>
      </author>
      <author>
        <name>Hayes, Heather</name>
      </author>
      <author>
        <name>Majersik, Jennifer J</name>
      </author>
      <author>
        <name>Worrall, Bradford B</name>
      </author>
      <author>
        <name>Tirschwell, David</name>
      </author>
      <author>
        <name>Bushnell, Cheryl</name>
      </author>
      <author>
        <name>Husseini, Nada El</name>
      </author>
      <author>
        <name>Lee, Jin-Moo</name>
      </author>
      <author>
        <name>Falcone, Guido J</name>
      </author>
    </item>
    <item>
      <title>Neurodatascience: Past, Present, and Future</title>
      <link>https://escholarship.org/uc/item/9d3867jx</link>
      <description>The study of the brain is a compelling example of the power of convergent science. Over the last few decades, advances in neuroscience techniques and experimentation, as well as in data science tools to analyze the resulting data, have dramatically furthered our understanding of fundamental brain functions. Historically, it has been common for analytical approaches to have a considerable lag in development following the availability of new neuroscience techniques. However, this relationship has not simply been unidirectional, as there have been examples in which analytical developments have directly led to new scientific questions and experiments. Here we review how this interplay between neuroscience and data science advances has unfolded in the past and into the present, with a focus on electrophysiology and calcium imaging. Applying lessons learned from the past and present, we then discuss expected developments, challenges, and opportunities in the future. We end by providing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9d3867jx</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Cooper, Keiland W</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Fortin, Norbert J</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
    </item>
    <item>
      <title>Hippocampal ensembles represent sequential relationships among discrete nonspatial events</title>
      <link>https://escholarship.org/uc/item/93c9q82h</link>
      <description>ABSTRACT The hippocampus is critical to the temporal organization of our experiences, including the ability to remember past event sequences and predict future ones. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain poorly understood. Here we recorded hippocampal ensemble activity as rats remembered a sequence of nonspatial events (5 odor presentations unfolding over several seconds), using a task with established parallels in humans. Using novel statistical methods and deep learning techniques, we then identified new forms of sequential organization in hippocampal activity linked with task performance. We discovered that sequential firing fields (“time cells”) provided temporal information within and across events in the sequence, and that distinct types of task-critical information (stimulus identity, temporal order, and trial outcome) were also sequentially differentiated within event presentations. Finally,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/93c9q82h</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Li, Lingge</name>
      </author>
      <author>
        <name>Agostinelli, Forest</name>
      </author>
      <author>
        <name>Saraf, Mansi</name>
      </author>
      <author>
        <name>Elias, Gabriel A</name>
      </author>
      <author>
        <name>Baldi, Pierre</name>
        <uri>https://orcid.org/0000-0003-0636-7930</uri>
      </author>
      <author>
        <name>Fortin, Norbert J</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
    </item>
    <item>
      <title>Modeling Local Field Potentials with Regularized Matrix Data Clustering</title>
      <link>https://escholarship.org/uc/item/5vx0v6rv</link>
      <description>In this paper, we propose a novel regularized mixture model for clustering matrix-valued image data. The new framework introduces a sparsity structure (e.g., low rank, spatial sparsity) and separable covariance structure motivated by scientific interpretability. We formulate the problem as a fi-nite mixture model of matrix-normal distributions with regularization terms, and then develop an Expectation-Maximization-type of algorithm for efficient computation. Simulation results and analysis on brain signals show the excellent performance of the proposed method in terms of a better prediction accuracy than the competitors and the scientific interpretability of the solution.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5vx0v6rv</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gao, Xu</name>
      </author>
      <author>
        <name>Shen, Weining</name>
        <uri>https://orcid.org/0000-0003-3137-1085</uri>
      </author>
      <author>
        <name>Hu, Jianhua</name>
      </author>
      <author>
        <name>Fortin, Norbert</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Ombao, Hernando</name>
      </author>
    </item>
    <item>
      <title>Unity by Diversity: Improved Representation Learning for Multimodal VAEs</title>
      <link>https://escholarship.org/uc/item/5vb1n9mb</link>
      <description>Variational Autoencoders for multimodal data hold promise for many tasks in data analysis, such as representation learning, conditional generation, and imputation. Current architectures either share the encoder output, decoder input, or both across modalities to learn a shared representation. Such architectures impose hard constraints on the model. In this work, we show that a better latent representation can be obtained by replacing these hard constraints with a soft constraint. We propose a new mixture-of-experts prior, softly guiding each modality's latent representation towards a shared aggregate posterior. This approach results in a superior latent representation and allows each encoding to preserve information better from its uncompressed original features. In extensive experiments on multiple benchmark datasets and two challenging real-world datasets, we show improved learned latent representations and imputation of missing data modalities compared to existing methods.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5vb1n9mb</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Sutter, TM</name>
      </author>
      <author>
        <name>Meng, Y</name>
      </author>
      <author>
        <name>Agostini, A</name>
      </author>
      <author>
        <name>Chopard, D</name>
      </author>
      <author>
        <name>Fortin, N</name>
      </author>
      <author>
        <name>Vogt, JE</name>
      </author>
      <author>
        <name>Shahbaba, B</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Mandt, S</name>
      </author>
    </item>
    <item>
      <title>A Model-Agnostic Graph Neural Network for Integrating Local and Global Information</title>
      <link>https://escholarship.org/uc/item/54c5s9m8</link>
      <description>Graph Neural Networks (GNNs) have achieved promising performance in a variety of graph-focused tasks. Despite their success, however, existing GNNs suffer from two significant limitations: a lack of interpretability in their results due to their black-box nature, and an inability to learn representations of varying orders. To tackle these issues, we propose a novel &lt;b&gt;M&lt;/b&gt;odel-&lt;b&gt;a&lt;/b&gt;gnostic &lt;b&gt;G&lt;/b&gt;raph Neural &lt;b&gt;Net&lt;/b&gt;work (MaGNet) framework, which is able to effectively integrate information of various orders, extract knowledge from high-order neighbors, and provide meaningful and interpretable results by identifying influential compact graph structures. In particular, MaGNet consists of two components: an estimation model for the latent representation of complex relationships under graph topology, and an interpretation model that identifies influential nodes, edges, and node features. Theoretically, we establish the generalization error bound for MaGNet via empirical Rademacher...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/54c5s9m8</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Zhou, Wenzhuo</name>
      </author>
      <author>
        <name>Qu, Annie</name>
      </author>
      <author>
        <name>Cooper, Keiland W</name>
      </author>
      <author>
        <name>Fortin, Norbert</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
    </item>
    <item>
      <title>A scalable reinforcement learning framework inspired by hippocampal memory mechanisms for efficient contextual and sequential decision making</title>
      <link>https://escholarship.org/uc/item/4zm8452k</link>
      <description>Efficient decision-making in context-dependent, sequential tasks remains a fundamental challenge in reinforcement learning (RL). Inspired by the function of the brain’s hippocampal system, we introduce Hippocampal-Augmented Memory Integration (HAMI), a biologically inspired memory-based RL framework that leverages symbolic indexing, hierarchical memory refinement, and structured episodic retrieval to enhance both learning efficiency and adaptability. We also propose Hierarchical Contextual Sequences (HiCoS), a structured RL environment grounded in neuroscience studies on episodic and sequence memory and context-driven decision-making, which serves as a controlled testbed for evaluating biologically inspired memory-based decision-making systems. Our experimental results demonstrate that HAMI achieves high decision accuracy and improved sample efficiency while maintaining low memory utilization. HAMI’s architecture exhibits significantly lower inference latency than baseline memory-based...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4zm8452k</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Poursiami, Hamed</name>
      </author>
      <author>
        <name>Moshruba, Ayana</name>
      </author>
      <author>
        <name>Cooper, Keiland W</name>
      </author>
      <author>
        <name>Gobin, Derek</name>
      </author>
      <author>
        <name>Kaiser, Md Abdullah-Al</name>
      </author>
      <author>
        <name>Singh, Ankur</name>
      </author>
      <author>
        <name>Noor, Rouhan</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Jaiswal, Akhilesh</name>
      </author>
      <author>
        <name>Fortin, Norbert J</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Parsa, Maryam</name>
      </author>
    </item>
    <item>
      <title>Optimal Transport based Cross-Domain Integration for Heterogeneous Data</title>
      <link>https://escholarship.org/uc/item/47t8571q</link>
      <description>Detecting dynamic patterns shared across heterogeneous datasets is a critical yet challenging task in many scientific domains, particularly within the biomedical sciences. Systematic heterogeneity inherent in diverse data sources can significantly hinder the effectiveness of existing machine learning methods in uncovering shared underlying dynamics. Additionally, practical and technical constraints in real-world experimental designs often limit data collection to only a small number of subjects, even when rich, time-dependent measurements are available for each individual. These limited sample sizes further diminish the power to detect common dynamic patterns across subjects. In this article, we propose a novel heterogeneous data integration framework based on optimal transport to extract shared patterns in the conditional mean dynamics of target responses. The key advantage of the proposed method is its ability to enhance discriminative power by reducing heterogeneity unrelated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/47t8571q</guid>
      <pubDate>Thu, 7 May 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yuan, Yubai</name>
      </author>
      <author>
        <name>Zhang, Yijiao</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Fortin, Norbert</name>
        <uri>https://orcid.org/0000-0002-6793-6984</uri>
      </author>
      <author>
        <name>Cooper, Keiland</name>
      </author>
      <author>
        <name>Nie, Qing</name>
        <uri>https://orcid.org/0000-0002-8804-3368</uri>
      </author>
      <author>
        <name>Qu, Annie</name>
      </author>
    </item>
    <item>
      <title>Evaluating the potential of acupuncture for Alzheimer’s disease treatment: A meta-analysis and systematic review of mouse model studies</title>
      <link>https://escholarship.org/uc/item/0sd9c8sj</link>
      <description>Acupuncture is an ancient practice that was developed within the framework of traditional Chinese medicine. While acupuncture has been recently proposed as a therapy for Alzheimer’s disease (AD), acupuncture effects are not well understood in terms of neural mechanisms. Here, we review and examine the studies that used AD mouse models and analyze the experiments where researchers administered electroacupuncture (EA) to AD mice to assess the potential therapeutic impact of acupuncture on disease pathology and cognitive function in controlled laboratory settings. We analyzed 29 relevant PubMed articles published between January 2014 and July 2025. Our results reveal that EA significantly reduces both amyloid-beta (Aβ) and phosphorylated tau (p-tau) levels and neuroinflammatory biomarkers, including molecular signatures for activated microglia and astrocytes in the brain. EA also enhances cognitive functions. While no study directly compared acupoint strategies, the indirect comparisons...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0sd9c8sj</guid>
      <pubDate>Wed, 8 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Yang, Mohan</name>
      </author>
      <author>
        <name>Tong, Liqi</name>
      </author>
      <author>
        <name>Guo, Zhiling</name>
      </author>
      <author>
        <name>Tan, Zhiqun</name>
      </author>
      <author>
        <name>Holmes, Todd C</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
    </item>
    <item>
      <title>How much we express love predicts how much we feel loved in daily life</title>
      <link>https://escholarship.org/uc/item/9hb4139s</link>
      <description>Feeling and expressing love in daily life are interconnected and perhaps mutually influential experiences. In this study we examined the reciprocal dynamics of feeling and expressing love and its relation to well-being using an ecological momentary assessment design. Over a four-week period, we asked participants (N = 52; 67% Female; 80% White) to report their levels of feeling loved and expressing love six times a day. Using a continuous-time process model, we explored individual differences in inertia (i.e., persistence of a process over time) and cross-influences of felt and expressed love over time. We found that increases in expressing love led to increased feelings of being loved over time; however, increases in felt love did not lead to increases in expressing love. Notably, participants who experienced more persistent feelings of love (that is, greater inertia over time) indicated higher levels of flourishing. These results suggest new avenues for psychological well-being...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9hb4139s</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Williams, Lindy</name>
      </author>
      <author>
        <name>Kim, Sharon H</name>
      </author>
      <author>
        <name>Li, Yanling</name>
      </author>
      <author>
        <name>Heshmati, Saida</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Roeser, Robert W</name>
      </author>
      <author>
        <name>Oravecz, Zita</name>
      </author>
    </item>
    <item>
      <title>An Expert Guide to Planning Experimental Tasks For Evidence-Accumulation Modeling</title>
      <link>https://escholarship.org/uc/item/8mn5z2kf</link>
      <description>Evidence-accumulation models (EAMs) are powerful tools for making sense of human and animal decision-making behavior. EAMs have generated significant theoretical advances in psychology, behavioral economics, and cognitive neuroscience and are increasingly used as a measurement tool in clinical research and other applied settings. Obtaining valid and reliable inferences from EAMs depends on knowing how to establish a close match between model assumptions and features of the task/data to which the model is applied. However, this knowledge is rarely articulated in the EAM literature, leaving beginners to rely on the private advice of mentors and colleagues and inefficient trial-and-error learning. In this article, we provide practical guidance for designing tasks appropriate for EAMs, relating experimental manipulations to EAM parameters, planning appropriate sample sizes, and preparing data and conducting an EAM analysis. Our advice is based on prior methodological studies and the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8mn5z2kf</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Boag, Russell J</name>
      </author>
      <author>
        <name>Innes, Reilly J</name>
      </author>
      <author>
        <name>Stevenson, Niek</name>
      </author>
      <author>
        <name>Bahg, Giwon</name>
      </author>
      <author>
        <name>Busemeyer, Jerome R</name>
      </author>
      <author>
        <name>Cox, Gregory E</name>
      </author>
      <author>
        <name>Donkin, Chris</name>
      </author>
      <author>
        <name>Frank, Michael J</name>
      </author>
      <author>
        <name>Hawkins, Guy E</name>
      </author>
      <author>
        <name>Heathcote, Andrew</name>
      </author>
      <author>
        <name>Hedge, Craig</name>
      </author>
      <author>
        <name>Lerche, Veronika</name>
      </author>
      <author>
        <name>Lilburn, Simon D</name>
      </author>
      <author>
        <name>Logan, Gordon D</name>
      </author>
      <author>
        <name>Matzke, Dora</name>
      </author>
      <author>
        <name>Miletić, Steven</name>
      </author>
      <author>
        <name>Osth, Adam F</name>
      </author>
      <author>
        <name>Palmeri, Thomas J</name>
      </author>
      <author>
        <name>Sederberg, Per B</name>
      </author>
      <author>
        <name>Singmann, Henrik</name>
      </author>
      <author>
        <name>Smith, Philip L</name>
      </author>
      <author>
        <name>Stafford, Tom</name>
      </author>
      <author>
        <name>Steyvers, Mark</name>
      </author>
      <author>
        <name>Strickland, Luke</name>
      </author>
      <author>
        <name>Trueblood, Jennifer S</name>
      </author>
      <author>
        <name>Tsetsos, Konstantinos</name>
      </author>
      <author>
        <name>Turner, Brandon M</name>
      </author>
      <author>
        <name>Usher, Marius</name>
      </author>
      <author>
        <name>van Maanen, Leendert</name>
      </author>
      <author>
        <name>van Ravenzwaaij, Don</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Voss, Andreas</name>
      </author>
      <author>
        <name>Weichart, Emily R</name>
      </author>
      <author>
        <name>Weindel, Gabriel</name>
      </author>
      <author>
        <name>White, Corey N</name>
      </author>
      <author>
        <name>Evans, Nathan J</name>
      </author>
      <author>
        <name>Brown, Scott D</name>
      </author>
      <author>
        <name>Forstmann, Birte U</name>
      </author>
    </item>
    <item>
      <title>Optimizing the Color Shapes Task for Ambulatory Assessment and Drift Diffusion Modeling: A Factorial Experiment</title>
      <link>https://escholarship.org/uc/item/5772z52z</link>
      <description>BACKGROUND: Recent advances in cognitive digital assessment methodology, including high-frequency, ambulatory assessments, promise to improve the detection of subtle cognitive changes. Computational modeling approaches may further improve the sensitivity of digital cognitive assessments to detect subtle cognitive changes by capturing features that map onto core cognitive processes.
OBJECTIVE: We explored the validity of a brief smartphone-based adaptation of a visual working memory task that has shown sensitivity for detecting preclinical Alzheimer disease risk. We aimed to optimize properties of the task for computational cognitive feature extraction with drift diffusion modeling.
METHODS: We analyzed data from 68 participants (n=47, 69% women; n=55, 81% White; mean age 49, SD 14; range 24-80 years) who completed 60 trials for each of 16 variations of a visual working memory binding task (the Color Shapes task) on smartphones, over an 8-day period. A drift diffusion model was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5772z52z</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Sharon Haeun</name>
      </author>
      <author>
        <name>Hakun, Jonathan G</name>
      </author>
      <author>
        <name>Li, Yanling</name>
      </author>
      <author>
        <name>Harrington, Karra D</name>
      </author>
      <author>
        <name>Elbich, Daniel B</name>
      </author>
      <author>
        <name>Sliwinski, Martin J</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Oravecz, Zita</name>
      </author>
    </item>
    <item>
      <title>Partially Observable Predictor Models for Identifying Cognitive Markers</title>
      <link>https://escholarship.org/uc/item/1wn7g523</link>
      <description>Repeated assessments of cognitive performance yield rich data from which we can extract markers of cognitive performance. Computational cognitive process models are often fit to repeated cognitive assessments to quantify individual differences in terms of substantively meaningful cognitive markers and link them to other person-level variables. Most studies stop at this point and do not test whether these cognitive markers have utility for predicting some meaningful outcomes. Here, we demonstrate a partially observable predictor modeling approach that can fill this gap. Using this approach, we can simultaneously extract cognitive markers from repeated assessment data and use these together with demographic covariates for predictive modeling of a clinically interesting outcome in a Bayesian multilevel modeling framework. We describe this approach by constructing a predictive process model in which features of learning are combined with demographic variables to predict mild cognitive...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1wn7g523</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Oravecz, Zita</name>
      </author>
      <author>
        <name>Sliwinski, Martin</name>
      </author>
      <author>
        <name>Kim, Sharon H</name>
      </author>
      <author>
        <name>Williams, Lindy</name>
      </author>
      <author>
        <name>Katz, Mindy J</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>An EZ Bayesian hierarchical drift diffusion model for response time and accuracy</title>
      <link>https://escholarship.org/uc/item/03k3219c</link>
      <description>The EZ-diffusion model is a simplification of the popular drift diffusion model of choice response times that allows researchers to calculate diffusion model parameters directly from data with no need for expensive computations. The EZ-diffusion model is based on a system of equations in which the diffusion model’s drift rate, boundary separation, and nondecision time parameters are jointly used to predict three summary statistics (the accuracy rate and the mean and variance of the correct response times). These equations can then be inverted to obtain estimators for the three parameters from these summary statistics. Here, we describe a probabilistic formulation of the EZ-diffusion model that can serve as a hyper-efficient proxy model to the drift diffusion model. The new formulation is based on sampling distributions of summary statistics and consists only of normal and binomial distributions. It can easily be implemented in any probabilistic programming language. We demonstrate...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/03k3219c</guid>
      <pubDate>Wed, 25 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Chávez De la Peña, Adriana F</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Prediction Interval Transfer Learning for Linear Regression Using an Empirical Bayes Approach</title>
      <link>https://escholarship.org/uc/item/7wg6k8xn</link>
      <description>ABSTRACT  Current literature on transfer learning has been focused on improving the predictive performance corresponding to a small dataset by transferring information to it from a larger but possibly biassed dataset. However, the transfer learning methods currently available do not allow the computation of prediction intervals, and hence, one has to rely on using either the small dataset alone or combining it with the possibly biassed dataset to obtain prediction intervals using traditional linear regression methods. In this article, we propose an E mpirical B ayes approach for P rediction I nterval T ransfer L earning (EB‐PITL), to compute prediction intervals for transfer learning in linear regression tasks. We have proved that the Gibbs sampler associated with EB‐PITL is geometrically ergodic, so EB‐PITL can also quantify the Monte Carlo uncertainty associated with its predicted value. The efficiency of EB‐PITL against currently available methods is demonstrated using simulation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7wg6k8xn</guid>
      <pubDate>Wed, 11 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dixit, Anand</name>
      </author>
      <author>
        <name>Shen, Weining</name>
        <uri>https://orcid.org/0000-0003-3137-1085</uri>
      </author>
      <author>
        <name>Zhang, Min</name>
      </author>
      <author>
        <name>Zhang, Dabao</name>
        <uri>https://orcid.org/0000-0003-0629-8672</uri>
      </author>
    </item>
    <item>
      <title>Accuracy of Continuous Noninvasive Hemoglobin Monitoring</title>
      <link>https://escholarship.org/uc/item/44z478nq</link>
      <description>BACKGROUND: Noninvasive hemoglobin (Hb) monitoring devices are available in the clinical setting, but their accuracy and precision against central laboratory Hb measurements have not been evaluated in a systematic review and meta-analysis.
METHODS: We conducted a comprehensive search of the literature (2005 to August 2013) with PubMed, Web of Science and the Cochrane Library, reviewed references of retrieved articles, and contacted manufactures to identify studies assessing the accuracy of noninvasive Hb monitoring against central laboratory Hb measurements. Two independent reviewers assessed the quality of studies using recommendations for reporting guidelines and quality criteria for method comparison studies. Pooled mean difference and standard deviation (SD) (95% limits of agreement) across studies were calculated using the random-effects model. Heterogeneity was assessed using the I statistic.
RESULTS: A total of 32 studies (4425 subjects, median sample size of 44, ranged...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/44z478nq</guid>
      <pubDate>Thu, 26 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Sang-Hyun</name>
      </author>
      <author>
        <name>Lilot, Marc</name>
      </author>
      <author>
        <name>Murphy, Linda Suk-Ling</name>
        <uri>https://orcid.org/0000-0003-2948-0792</uri>
      </author>
      <author>
        <name>Sidhu, Kulraj S</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Rinehart, Joseph</name>
      </author>
      <author>
        <name>Cannesson, Maxime</name>
      </author>
    </item>
    <item>
      <title>Estimating causal effects for binary outcomes using per-decision inverse probability weighting</title>
      <link>https://escholarship.org/uc/item/8wp4v5h2</link>
      <description>Micro-randomized trials are commonly conducted for optimizing mobile health interventions such as push notifications for behavior change. In analyzing such trials, causal excursion effects are often of primary interest, and their estimation typically involves inverse probability weighting (IPW). However, in a micro-randomized trial, additional treatments can often occur during the time window over which an outcome is defined, and this can greatly inflate the variance of the causal effect estimator because IPW would involve a product of numerous weights. To reduce variance and improve estimation efficiency, we propose two new estimators using a modified version of IPW, which we call "per-decision IPW." The second estimator further improves efficiency using the projection idea from the semiparametric efficiency theory. These estimators are applicable when the outcome is binary and can be expressed as the maximum of a series of sub-outcomes defined over sub-intervals of time. We...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8wp4v5h2</guid>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Bao, Yihan</name>
      </author>
      <author>
        <name>Bell, Lauren</name>
      </author>
      <author>
        <name>Williamson, Elizabeth</name>
      </author>
      <author>
        <name>Garnett, Claire</name>
      </author>
      <author>
        <name>Qian, Tianchen</name>
        <uri>https://orcid.org/0000-0003-4282-7826</uri>
      </author>
    </item>
    <item>
      <title>Distal causal excursion effects: modeling long-term effects of time-varying treatments in micro-randomized trials</title>
      <link>https://escholarship.org/uc/item/8vd1c18h</link>
      <description>Micro-randomized trials (MRTs) play a crucial role in optimizing digital interventions. In an MRT, each participant is sequentially randomized among treatment options hundreds of times. While the interventions tested in MRTs target short-term behavioral responses (proximal outcomes), their ultimate goal is to drive long-term behavior change (distal outcomes). However, existing causal inference methods, such as the causal excursion effect, are limited to proximal outcomes, making it challenging to quantify the long-term impact of interventions. To address this gap, we introduce the distal causal excursion effect (DCEE), a novel estimand that quantifies the long-term effect of time-varying treatments. The DCEE contrasts distal outcomes under two excursion policies while marginalizing over most treatment assignments, enabling a parsimonious and interpretable causal model even with a large number of decision points. We propose two estimators for the DCEE-one with cross-fitting and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8vd1c18h</guid>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Qian, Tianchen</name>
        <uri>https://orcid.org/0000-0003-4282-7826</uri>
      </author>
    </item>
    <item>
      <title>Ambulatory assessment to predict problem anger in trauma-affected adults: Study protocol</title>
      <link>https://escholarship.org/uc/item/8717t3xr</link>
      <description>BACKGROUND: Problem anger is common after experiencing a traumatic event. Current evidence-driven treatment options are limited, and problem anger negatively affects an individual's capacity to engage with traditional psychological treatments. Smartphone interventions hold significant potential in mental health because of their ability to deliver low-intensity, precision support for individuals at the time and place they need it most. While wearable technology has the capacity to augment smartphone-delivered interventions, there is a dearth of evidence relating to several key areas, including feasibility of compliance in mental health populations; validity of in vivo anger assessment; ability to predict future mood states; and delivery of timely and appropriate interventions.
METHODS: This protocol describes a cohort study that leverages 10 days of ambulatory assessment in the form of ecological momentary assessment and a wearable. Approximately 100 adults with problem anger will...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8717t3xr</guid>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Metcalf, Olivia</name>
      </author>
      <author>
        <name>Finlayson-Short, Laura</name>
      </author>
      <author>
        <name>Lamb, Karen E</name>
      </author>
      <author>
        <name>Zaloumis, Sophie</name>
      </author>
      <author>
        <name>O’Donnell, Meaghan L</name>
      </author>
      <author>
        <name>Qian, Tianchen</name>
        <uri>https://orcid.org/0000-0003-4282-7826</uri>
      </author>
      <author>
        <name>Varker, Tracey</name>
      </author>
      <author>
        <name>Cowlishaw, Sean</name>
      </author>
      <author>
        <name>Brotman, Melissa</name>
      </author>
      <author>
        <name>Forbes, David</name>
      </author>
    </item>
    <item>
      <title>Autoimmune antibodies and systemic inflammatory markers are prevalent and associated with cognition in individuals aged 90+</title>
      <link>https://escholarship.org/uc/item/5n0973jm</link>
      <description>BackgroundWhile recent studies have found associations between markers of autoimmunity/inflammation and cognitive performance in individuals aged 60-90, these findings remain unexplored in individuals aged 90 and above.ObjectiveTo examine the prevalence of autoimmune antibodies and raised inflammatory markers and their associations with cognition in participants aged 90 + .MethodsWe included participants with serological testing from The 90+ Study, a community-based longitudinal study in southern California. For measures of autoimmunity, we evaluated antinuclear, antineutrophil cytoplasmic (ANCA), rheumatoid factor, double stranded DNA, antithyroglobulin, and thyroid peroxidase antibodies. For inflammatory markers, we examined interleukin-6 (IL-6) and erythrocyte sedimentation rate (ESR). To examine the relationship between autoimmune antibodies and inflammatory markers with cognitive performance, we ran linear mixed effects models.ResultsAmong 201 participants (mean age 94.8...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5n0973jm</guid>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Farahmand, Ghasem</name>
      </author>
      <author>
        <name>Leiby, Anne-Marie C</name>
      </author>
      <author>
        <name>Yu, Jiaxin</name>
      </author>
      <author>
        <name>Ramanathan, Aanan</name>
      </author>
      <author>
        <name>Javaheri, Rojan</name>
      </author>
      <author>
        <name>Kawas, Claudia H</name>
      </author>
      <author>
        <name>Woodworth, Davis C</name>
      </author>
      <author>
        <name>Corrada, Maria M</name>
      </author>
      <author>
        <name>Qian, Tianchen</name>
        <uri>https://orcid.org/0000-0003-4282-7826</uri>
      </author>
      <author>
        <name>Sajjadi, S Ahmad</name>
        <uri>https://orcid.org/0000-0002-8960-2213</uri>
      </author>
    </item>
    <item>
      <title>Predicting high anger intensity using ecological momentary assessment and wearable-derived physiological data in a trauma-affected sample</title>
      <link>https://escholarship.org/uc/item/11t2k02h</link>
      <description>&lt;b&gt;Background:&lt;/b&gt; Digital technologies offer tremendous potential to predict dysregulated mood and behavior within an individual's environment, and in doing so can support the development of new digital health interventions. However, no prediction models have been built in trauma-exposed populations that leverage real-world data.&lt;b&gt;Objective:&lt;/b&gt; This project aimed to determine if wearable-derived physiological data can predict anger intensity in trauma-exposed adults.&lt;b&gt;Method:&lt;/b&gt; Heart rate variability (i.e. a commercial wearable stress score) was combined with ecological momentary assessment (EMA) data collected over 10 days (&lt;i&gt;n&lt;/i&gt; = 84). Five summary measures from stress scores collected 10 min prior to each EMA were selected using factor analysis of 24 candidates.&lt;b&gt;Results:&lt;/b&gt; A high area under the receiver operating curve (AUC) was found for a logistic mixed effects model including these measures as predictors, ranging 0.761 (95% CI:0.569-0.921) to 0.899 (95% CI:0.784-0.980)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/11t2k02h</guid>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Metcalf, Olivia</name>
      </author>
      <author>
        <name>Lamb, Karen E</name>
      </author>
      <author>
        <name>Forbes, David</name>
      </author>
      <author>
        <name>O’Donnell, Meaghan L</name>
      </author>
      <author>
        <name>Qian, Tianchen</name>
        <uri>https://orcid.org/0000-0003-4282-7826</uri>
      </author>
      <author>
        <name>Varker, Tracey</name>
      </author>
      <author>
        <name>Cowlishaw, Sean</name>
      </author>
      <author>
        <name>Zaloumis, Sophie</name>
      </author>
    </item>
    <item>
      <title>A Framework for Variational Inference and Data Assimilation of Soil Biogeochemical Models Using Normalizing Flows</title>
      <link>https://escholarship.org/uc/item/8fb053sp</link>
      <description>Soil biogeochemical models (SBMs) represent soil variables and their responses to global change. Data assimilation approaches help determine whether SBMs accurately represent soil processes consistent with soil pool and flux measurements. Bayesian inference is commonly used in data assimilation procedures that estimate posterior parameter distributions with Markov chain Monte Carlo (MCMC) methods. The ability to account for data and parameter uncertainty is a strength of MCMC inference, but the computational inefficiency of MCMC methods remains a barrier to their wider application, especially with large data sets. Given the limitations of MCMC approaches, we developed an alternative variational inference framework that uses a method called normalizing flows from the field of machine learning. Normalizing flows rely on deep learning to map probability distributions and approximate SBMs that have been discretized into state space models. As a test of our method, we fit approximated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8fb053sp</guid>
      <pubDate>Thu, 2 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Xie, HW</name>
      </author>
      <author>
        <name>Sujono, D</name>
      </author>
      <author>
        <name>Ryder, T</name>
      </author>
      <author>
        <name>Sudderth, EB</name>
      </author>
      <author>
        <name>Allison, SD</name>
        <uri>https://orcid.org/0000-0003-4629-7842</uri>
      </author>
    </item>
    <item>
      <title>Single-cell spatial transcriptomics reveals distinct patterns of dysregulation in non-neuronal and neuronal cells induced by the Trem2R47H Alzheimer’s risk gene mutation</title>
      <link>https://escholarship.org/uc/item/71v7f231</link>
      <description>The R47H missense mutation of the TREM2 gene is a known risk factor for development of Alzheimer’s Disease. In this study, we analyze the impact of the Trem2R47H mutation on specific cell types in multiple cortical and subcortical brain regions in the context of wild-type and 5xFAD mouse background. We profile 19 mouse brain sections consisting of wild-type, Trem2R47H, 5xFAD and Trem2R47H; 5xFAD genotypes using MERFISH spatial transcriptomics, a technique that enables subcellular profiling of spatial gene expression. Spatial transcriptomics and neuropathology data are analyzed using our custom pipeline to identify plaque and Trem2R47H-induced transcriptomic dysregulation. We initially analyze&amp;nbsp;cell type-specific transcriptomic alterations induced by plaque proximity. Next, we analyze spatial distributions of disease associated microglia and astrocytes, and how they vary between 5xFAD and Trem2R47H; 5xFAD mouse models. Finally, we analyze the impact of the Trem2R47H mutation&amp;nbsp;on...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/71v7f231</guid>
      <pubDate>Thu, 11 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Johnston, Kevin G</name>
      </author>
      <author>
        <name>Berackey, Bereket T</name>
      </author>
      <author>
        <name>Tran, Kristine M</name>
      </author>
      <author>
        <name>Gelber, Alon</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>MacGregor, Grant R</name>
        <uri>https://orcid.org/0000-0001-7598-9501</uri>
      </author>
      <author>
        <name>Mukamel, Eran A</name>
        <uri>https://orcid.org/0000-0003-3203-9535</uri>
      </author>
      <author>
        <name>Tan, Zhiqun</name>
      </author>
      <author>
        <name>Green, Kim N</name>
        <uri>https://orcid.org/0000-0002-6049-6744</uri>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
    </item>
    <item>
      <title>From images to detection: Machine learning for blood pattern classification</title>
      <link>https://escholarship.org/uc/item/56x1x1v8</link>
      <description>Bloodstain Pattern Analysis (BPA) helps us understand how bloodstains form, with a focus on their size, shape, and distributions. This aids in crime scene reconstruction and provides insight into victim positions and crime investigation. One challenge in BPA is distinguishing between different types of bloodstains, such as those from firearms, impacts, or other mechanisms. Our study focuses on differentiating impact spatter bloodstain patterns from gunshot backward spatter bloodstain patterns. We distinguish patterns by extracting well-designed individual stain features, applying effective data consolidation methods, and selecting boosting classifiers. As a result, our model exhibits competitive accuracy and efficiency on the tested dataset, suggesting its potential in similar scenarios.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/56x1x1v8</guid>
      <pubDate>Thu, 14 Aug 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Yilin</name>
      </author>
      <author>
        <name>Shen, Weining</name>
        <uri>https://orcid.org/0000-0003-3137-1085</uri>
      </author>
    </item>
    <item>
      <title>A Bayesian Time-Varying Psychophysiological Interaction Model</title>
      <link>https://escholarship.org/uc/item/0bq7z39h</link>
      <description>A Bayesian Time-Varying Psychophysiological Interaction Model</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0bq7z39h</guid>
      <pubDate>Thu, 3 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schetzsle, Brian</name>
      </author>
      <author>
        <name>Lee, Jaylen</name>
      </author>
      <author>
        <name>Bornstein, Aaron</name>
        <uri>https://orcid.org/0000-0001-6251-6000</uri>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Guindani, Michele</name>
        <uri>https://orcid.org/0000-0002-6363-9907</uri>
      </author>
    </item>
    <item>
      <title>Beyond the Surface: Mapping DDE's Metabolic Footprint on Adolescent Obesity.</title>
      <link>https://escholarship.org/uc/item/8b81r54h</link>
      <description>BACKGROUND: Bariatric surgery is an intervention for severe obesity, leading to significant weight loss and metabolic improvements. However, the release of lipophilic chemicals accumulated in adipose tissue during weight loss presents a unique clinical challenge and research opportunity. Dichlorodiphenyldichloroethylene (DDE) is a persistent organic pollutant increasingly recognized as obesogen, while the biological mechanisms through which DDE influences body mass index (BMI) and waist circumference remain underexplored.
OBJECTIVES: We aimed to identify metabolic signatures mediating the association between DDE exposure and weight loss by plasma and adipose tissue metabolomics.
METHODS: We conducted a longitudinal study involving 60 adolescents with severe obesity undergoing bariatric surgery. We quantified &lt;i&gt;p,p'&lt;/i&gt;-DDE concentrations in visceral adipose tissue collected during surgery and analyzed metabolic profiles from both adipose tissues collected at surgery and plasma...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8b81r54h</guid>
      <pubDate>Wed, 2 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Zhenjiang</name>
      </author>
      <author>
        <name>Pan, Shudi</name>
      </author>
      <author>
        <name>Baumert, Brittney O</name>
      </author>
      <author>
        <name>Chen, Jiawen Carmen</name>
      </author>
      <author>
        <name>Goodrich, Jesse A</name>
      </author>
      <author>
        <name>Wang, Hongxu</name>
      </author>
      <author>
        <name>Rock, Sarah</name>
      </author>
      <author>
        <name>Ryder, Justin</name>
      </author>
      <author>
        <name>Valvi, Damaskini</name>
      </author>
      <author>
        <name>Jenkins, Todd</name>
      </author>
      <author>
        <name>Sisley, Stephanie</name>
      </author>
      <author>
        <name>Lin, Xiangping</name>
      </author>
      <author>
        <name>Bartell, Scott M</name>
        <uri>https://orcid.org/0000-0001-7797-2906</uri>
      </author>
      <author>
        <name>Inge, Thomas H</name>
      </author>
      <author>
        <name>Xanthakos, Stavra</name>
      </author>
      <author>
        <name>McNeil, Brooklynn</name>
      </author>
      <author>
        <name>Robuck, Anna R</name>
      </author>
      <author>
        <name>Mullins, Catherine E</name>
      </author>
      <author>
        <name>Eckel, Sandrah P</name>
      </author>
      <author>
        <name>McConnell, Rob S</name>
      </author>
      <author>
        <name>La Merrill, Michele A</name>
      </author>
      <author>
        <name>Walker, Douglas I</name>
      </author>
      <author>
        <name>Conti, David V</name>
      </author>
      <author>
        <name>Chatzi, Lida</name>
      </author>
    </item>
    <item>
      <title>Who benefits from mobile health interventions? A dynamical systems analysis of psychological well‐being in early adults</title>
      <link>https://escholarship.org/uc/item/0xz5d3z9</link>
      <description>Research shows that skills for improving Psychological Well-Being (PWB) may be learned through PWB interventions; however, the dynamic mechanisms underlying this learning process are not well understood. Using an Ecological Momentary Intervention (EMI) design, we conducted an 8-week Randomized Controlled Trial (N = 160; aged 18-22 years), implemented in a mobile Health (mHealth) platform to characterize these dynamical mechanisms. College-attending early adults were randomized to three groups: an active control group (N = 55); an intervention group (N = 51) with positive practices intervention; and a second intervention group (N = 54) with positive practices and meditation intervention. The mHealth implementation allowed us to introduce the interventions in participants' daily lives while also assessing their PWB (in terms of positive emotions and relationship quality) several times a day. We used a Bayesian process model to analyze changes in PWB in terms of the underlying dynamical...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0xz5d3z9</guid>
      <pubDate>Fri, 20 Jun 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Heshmati, Saida</name>
      </author>
      <author>
        <name>Muth, Chelsea</name>
      </author>
      <author>
        <name>Li, Yanling</name>
      </author>
      <author>
        <name>Roeser, Robert W</name>
      </author>
      <author>
        <name>Smyth, Joshua M</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Chow, Sy‐Miin</name>
      </author>
      <author>
        <name>Oravecz, Zita</name>
      </author>
    </item>
    <item>
      <title>Geospatial Access to Extracorporeal Membrane Oxygenation in the United States</title>
      <link>https://escholarship.org/uc/item/1tp4z4sb</link>
      <description>OBJECTIVES: To conduct a Geospatial Information System analysis of extracorporeal membrane oxygenation (ECMO) centers in the United States utilizing data from the U.S. Census Bureau to better understand access to ECMO care and identify potential disparities.
DESIGN: A cross-sectional descriptive and statistical analysis of geospatial access to ECMO-capable centers in the United States, accounting for demographic variables.
SETTING: The unit of analysis were U.S. Census block groups and demographic variables of interest obtained from the American Community Survey.
PATIENTS: Patients accounted for in the U.S. Census data.
INTERVENTIONS: None.
MEASUREMENTS AND MAIN RESULTS: Sixty-seven percent of the U.S. population had direct access to ECMO-capable centers. Disparities were present, with Puerto Rico, Wyoming, North Dakota, and Alaska having no access. Poverty, increased age, and lower population density consistently correlated with limited access. We identified significant racial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1tp4z4sb</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gottula, Adam L</name>
      </author>
      <author>
        <name>Van Wyk, Hannah</name>
      </author>
      <author>
        <name>Qi, Man</name>
      </author>
      <author>
        <name>Vogelsong, Melissa A</name>
      </author>
      <author>
        <name>Shaw, Chris R</name>
      </author>
      <author>
        <name>Tonna, Joseph E</name>
      </author>
      <author>
        <name>Johnson, Nicholas J</name>
      </author>
      <author>
        <name>Condella, Anna</name>
      </author>
      <author>
        <name>Bartos, Jason A</name>
      </author>
      <author>
        <name>Berrocal, Veronica J</name>
        <uri>https://orcid.org/0000-0003-0304-7202</uri>
      </author>
      <author>
        <name>Benoit, Justin L</name>
      </author>
      <author>
        <name>Hsu, Cindy H</name>
      </author>
    </item>
    <item>
      <title>Metabolic Signatures in Adipose Tissue Linking Lipophilic Persistent Organic Pollutant Mixtures to Blood Pressure Five Years After Bariatric Surgery Among Adolescents</title>
      <link>https://escholarship.org/uc/item/2mz2x4nq</link>
      <description>Persistent organic pollutants (POPs) are lipophilic environmental contaminants accumulated in the adipose tissue. Weight loss interventions, such as bariatric surgery, can mobilize POPs from adipose tissue into the bloodstream. We hypothesized that this mobilization could contribute to increases in blood pressure among 57 adolescents with severe obesity undergoing bariatric surgery. POPs and metabolic features were measured from visceral adipose tissue collected during surgery using gas and liquid chromatography, coupled with high-resolution mass spectrometry. Blood pressure was assessed at baseline, 6 months, and 5 years post-surgery. We used quantile g-computation to estimate associations of POP mixtures with blood pressure changes. With one quartile increase in POP mixtures, systolic blood pressure (SBP) increased by 6.4% five years after bariatric surgery compared to baseline SBP [95% confidence interval (CI): 0.4%, 12.4%]. The meet-in-the-middle approach identified overlapping...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2mz2x4nq</guid>
      <pubDate>Wed, 2 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pan, Shudi</name>
      </author>
      <author>
        <name>Li, Zhenjiang</name>
      </author>
      <author>
        <name>Walker, Douglas I</name>
      </author>
      <author>
        <name>Baumert, Brittney O</name>
      </author>
      <author>
        <name>Wang, Hongxu</name>
      </author>
      <author>
        <name>Goodrich, Jesse A</name>
      </author>
      <author>
        <name>Rock, Sarah</name>
      </author>
      <author>
        <name>Inge, Thomas H</name>
      </author>
      <author>
        <name>Jenkins, Todd M</name>
      </author>
      <author>
        <name>Sisley, Stephanie</name>
      </author>
      <author>
        <name>Bartell, Scott M</name>
        <uri>https://orcid.org/0000-0001-7797-2906</uri>
      </author>
      <author>
        <name>Xanthakos, Stavra</name>
      </author>
      <author>
        <name>Lin, Xiangping</name>
      </author>
      <author>
        <name>McNeil, Brooklynn</name>
      </author>
      <author>
        <name>Robuck, Anna R</name>
      </author>
      <author>
        <name>Mullins, Catherine E</name>
      </author>
      <author>
        <name>La Merill, Michele A</name>
      </author>
      <author>
        <name>Garcia, Erika</name>
      </author>
      <author>
        <name>Aung, Max T</name>
      </author>
      <author>
        <name>Eckel, Sandrah P</name>
      </author>
      <author>
        <name>McConnell, Rob</name>
      </author>
      <author>
        <name>Conti, David V</name>
      </author>
      <author>
        <name>Ryder, Justin R</name>
      </author>
      <author>
        <name>Chatzi, Lida</name>
      </author>
    </item>
    <item>
      <title>Exposure to per- and polyfluoroalkyl substances and alterations in plasma microRNA profiles in children</title>
      <link>https://escholarship.org/uc/item/1nm4t5fm</link>
      <description>BACKGROUND: Per- and polyfluoroalkyl substances (PFAS) are synthetic chemicals that persist in the environment and can accumulate in humans, leading to adverse health effects. MicroRNAs (miRNAs) are emerging biomarkers that can advance the understanding of the mechanisms of PFAS effects on human health. However, little is known about the associations between PFAS exposures and miRNA alterations in humans.
OBJECTIVE: To investigate associations between PFAS concentrations and miRNA levels in children.
METHODS: Data from two distinct cohorts were utilized: 176 participants (average age 17.1 years; 75.6% female) from the Teen-Longitudinal Assessment of Bariatric Surgery (Teen-LABS) cohort in the United States, and 64 participants (average age 6.5 years, 39.1% female) from the Rhea study, a mother-child cohort in Greece. PFAS concentrations and miRNA levels were assessed in plasma samples from both studies. Associations between individual PFAS and plasma miRNA levels were examined...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1nm4t5fm</guid>
      <pubDate>Fri, 21 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Yijie</name>
      </author>
      <author>
        <name>Baumert, Brittney O</name>
      </author>
      <author>
        <name>Stratakis, Nikos</name>
      </author>
      <author>
        <name>Goodrich, Jesse A</name>
      </author>
      <author>
        <name>Wu, Haotian</name>
      </author>
      <author>
        <name>Liu, Shelley H</name>
      </author>
      <author>
        <name>Wang, Hongxu</name>
      </author>
      <author>
        <name>Beglarian, Emily</name>
      </author>
      <author>
        <name>Bartell, Scott M</name>
        <uri>https://orcid.org/0000-0001-7797-2906</uri>
      </author>
      <author>
        <name>Eckel, Sandrah Proctor</name>
      </author>
      <author>
        <name>Walker, Douglas</name>
      </author>
      <author>
        <name>Valvi, Damaskini</name>
      </author>
      <author>
        <name>La Merrill, Michele Andrea</name>
        <uri>https://orcid.org/0000-0002-5720-5862</uri>
      </author>
      <author>
        <name>Inge, Thomas H</name>
      </author>
      <author>
        <name>Jenkins, Todd</name>
      </author>
      <author>
        <name>Ryder, Justin R</name>
      </author>
      <author>
        <name>Sisley, Stephanie</name>
      </author>
      <author>
        <name>Kohli, Rohit</name>
      </author>
      <author>
        <name>Xanthakos, Stavra A</name>
      </author>
      <author>
        <name>Vafeiadi, Marina</name>
      </author>
      <author>
        <name>Margetaki, Aikaterini</name>
      </author>
      <author>
        <name>Roumeliotaki, Theano</name>
      </author>
      <author>
        <name>Aung, Max</name>
      </author>
      <author>
        <name>McConnell, Rob</name>
      </author>
      <author>
        <name>Baccarelli, Andrea</name>
      </author>
      <author>
        <name>Conti, David</name>
      </author>
      <author>
        <name>Chatzi, Lida</name>
      </author>
    </item>
    <item>
      <title>Computational Phenotyping of Cognitive Decline With Retest Learning</title>
      <link>https://escholarship.org/uc/item/4wv7g79c</link>
      <description>OBJECTIVES: Cognitive change is a complex phenomenon encompassing both retest-related performance gains and potential cognitive decline. Disentangling these dynamics is necessary for effective tracking of subtle cognitive change and risk factors for Alzheimer's Disease and Related Dementias (ADRD).
METHOD: We applied a computational cognitive model of learning and forgetting to data from Einstein Aging Study (EAS; n = 316). EAS participants completed multiple bursts of ultra-brief, high-frequency cognitive assessments on smartphones. Analyzing response time data from a measure of visual short-term working memory, the Color Shapes task, and from a measure of processing speed, the Symbol Search task, we extracted several key cognitive markers: short-term intraindividual variability in performance, within-burst retest learning and asymptotic (peak) performance, across-burst change in asymptote and forgetting of retest gains.
RESULTS: Asymptotic performance was related to both mild...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4wv7g79c</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Oravecz, Zita</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Hakun, Jonathan G</name>
      </author>
      <author>
        <name>Kim, Sharon H</name>
      </author>
      <author>
        <name>Katz, Mindy J</name>
      </author>
      <author>
        <name>Wang, Cuiling</name>
      </author>
      <author>
        <name>Lipton, Richard B</name>
      </author>
      <author>
        <name>Derby, Carol A</name>
      </author>
      <author>
        <name>Roque, Nelson A</name>
      </author>
      <author>
        <name>Sliwinski, Martin J</name>
      </author>
    </item>
    <item>
      <title>Quantitative Measurement of Cyber Resilience: Modeling and Experimentation</title>
      <link>https://escholarship.org/uc/item/3x54t0rf</link>
      <description>Cyber resilience is the ability of a system to resist and recover from a cyber attack, thereby restoring the system's functionality. Effective design and development of a cyber resilient system requires experimental methods and tools for quantitative measuring of cyber resilience. This article describes an experimental method and test bed for obtaining resilience-relevant data as a system (in our case - a truck) traverses its route, in repeatable, systematic experiments. We model a truck equipped with an autonomous cyber-defense system and which also includes inherent physical resilience features. When attacked by malware, this ensemble of cyber-physical features (i.e., "bonware") strives to resist and recover from the performance degradation caused by the malware's attack. We propose parsimonious mathematical models to aid in quantifying systems' resilience to cyber attacks. Using the models, we identify quantitative characteristics obtainable from experimental data and show...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3x54t0rf</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Weisman, Michael J</name>
      </author>
      <author>
        <name>Kott, Alexander</name>
      </author>
      <author>
        <name>Ellis, Jason E</name>
      </author>
      <author>
        <name>Murphy, Brian J</name>
      </author>
      <author>
        <name>Parker, Travis W</name>
      </author>
      <author>
        <name>Smith, Sidney</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Serological inflammation markers and their association with cognition in the oldest old; The 90+ Study</title>
      <link>https://escholarship.org/uc/item/0hb517c3</link>
      <description>AbstractBackground&lt;p&gt;Recent studies in the younger old have identified associations between cognitive performance and markers of inflammation, including interleukin‐6 (IL‐6) and erythrocyte sedimentation rate (ESR). These associations remain unexplored in the oldest old (age 90+), an age group most vulnerable to dementia. In addition, no studies have examined if amyloid burden impacts these associations. This study aims to: (1) examine the associations between inflammatory markers (IL‐6, ESR) and cognitive performance in individuals age 90+ and (2) to examine if amyloid burden impacts these associations.&lt;/p&gt;Method&lt;p&gt;Participants with at least one plasma measure of inflammation and amyloid burden measured by positron emission tomography (PET) were selected from 
The 90+ Study
 (n = 112 for IL‐6, n = 123 for ESR). Cognitive measures included (1) global cognitive score defined as the average of the standardized scores of Mini‐Mental State Examination (MMSE) and Modified MMSE (3MS),...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0hb517c3</guid>
      <pubDate>Thu, 20 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Leiby, Anne‐Marie C</name>
      </author>
      <author>
        <name>Farahmand, Ghasem</name>
      </author>
      <author>
        <name>Ramanathan, Aanan</name>
      </author>
      <author>
        <name>Woodworth, Davis C</name>
      </author>
      <author>
        <name>Jiang, Luohua</name>
        <uri>https://orcid.org/0000-0002-2281-7260</uri>
      </author>
      <author>
        <name>Yu, Jiaxin</name>
      </author>
      <author>
        <name>Qian, Tianchen</name>
        <uri>https://orcid.org/0000-0003-4282-7826</uri>
      </author>
      <author>
        <name>Corrada, María MM</name>
      </author>
      <author>
        <name>Kawas, Claudia H</name>
      </author>
      <author>
        <name>Sajjadi, S Ahmad</name>
        <uri>https://orcid.org/0000-0002-8960-2213</uri>
      </author>
    </item>
    <item>
      <title>Individual differences in cortical processing speed predict cognitive abilities: A model-based cognitive neuroscience account</title>
      <link>https://escholarship.org/uc/item/9cx7n446</link>
      <description>&lt;p&gt;Previous research has shown that individuals with greater cognitive abilities display a greater speed of higher-order cognitive processing. These results suggest that speeded neural information processing may facilitate evidence accumulation during decision making and memory updating and thus yield advantages in general cognitive abilities. We used a hierarchical Bayesian cognitive modeling approach to test the hypothesis that individual differences in the velocity of evidence accumulation mediate the relationship between neural processing speed and cognitive abilities. We found that a higher neural speed predicted both the velocity of evidence accumulation across behavioral tasks and cognitive ability test scores. However, only a negligible part of the association between neural processing speed and cognitive abilities was mediated by individual differences in the velocity of evidence accumulation. The model demonstrated impressive forecasting abilities by predicting 36% of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9cx7n446</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schubert, Anna-Lena</name>
      </author>
      <author>
        <name>Nunez, Michael D</name>
      </author>
      <author>
        <name>Hagemann, Dirk</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Cultural Consensus Theory for the evaluation of patients’ mental health scores in forensic psychiatric hospitals</title>
      <link>https://escholarship.org/uc/item/97d782vk</link>
      <description>In many forensic psychiatric hospitals, patients’ mental health is monitored at regular intervals. Typically, clinicians score patients using a Likert scale on multiple criteria including hostility. Having an overview of patients’ scores benefits staff members in at least three ways. First, the scores may help adjust treatment to the individual patient; second, the change in scores over time allows an assessment of treatment effectiveness; third, the scores may warn staff that particular patients are at high risk of turning violent, either before or after release. Practical importance notwithstanding, current practices for the analysis of mental health scores are suboptimal: evaluations from different clinicians are averaged (as if the Likert scale were linear and the clinicians identical), and patients are analyzed in isolation (as if they were independent). Uncertainty estimates of the resulting score are often ignored. Here we outline a quantitative program for the analysis...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/97d782vk</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>van den Bergh, Don</name>
      </author>
      <author>
        <name>Bogaerts, Stefan</name>
      </author>
      <author>
        <name>Spreen, Marinus</name>
      </author>
      <author>
        <name>Flohr, Rob</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Batchelder, William H</name>
      </author>
      <author>
        <name>Wagenmakers, Eric-Jan</name>
      </author>
    </item>
    <item>
      <title>Poor stimulus discriminability as a common neuropsychological deficit between ADHD and reading ability in young children: a moderated mediation model</title>
      <link>https://escholarship.org/uc/item/8z66g1qw</link>
      <description>BACKGROUND: Attention deficit hyperactivity disorder (ADHD) is frequently associated with poorer reading ability; however, the specific neuropsychological domains linking this co-occurrence remain unclear. This study evaluates information-processing characteristics as possible neuropsychological links between ADHD symptoms and RA in a community-based sample of children and early adolescents with normal IQ (⩾70).
METHOD: The participants (n = 1857, aged 6-15 years, 47% female) were evaluated for reading ability (reading single words aloud) and information processing [stimulus discriminability in the two-choice reaction-time task estimated using diffusion models]. ADHD symptoms were ascertained through informant (parent) report using the Development and Well-Being Assessment (DAWBA). Verbal working memory (VWM; digit span backwards), visuospatial working memory (VSWM, Corsi Blocks backwards), sex, socioeconomic status, and IQ were included as covariates.
RESULTS: In a moderated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8z66g1qw</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lúcio, PS</name>
      </author>
      <author>
        <name>Salum, GA</name>
      </author>
      <author>
        <name>Rohde, LA</name>
      </author>
      <author>
        <name>Swardfager, W</name>
      </author>
      <author>
        <name>Gadelha, A</name>
      </author>
      <author>
        <name>Vandekerckhove, J</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Pan, PM</name>
      </author>
      <author>
        <name>Polanczyk, GV</name>
      </author>
      <author>
        <name>do Rosário, MC</name>
      </author>
      <author>
        <name>Jackowski, AP</name>
      </author>
      <author>
        <name>Mari, JJ</name>
      </author>
      <author>
        <name>Cogo-Moreira, H</name>
      </author>
    </item>
    <item>
      <title>Cortico-Brainstem Mechanisms of Biased Perceptual Decision-Making in the Context of Pain</title>
      <link>https://escholarship.org/uc/item/8w40w272</link>
      <description>Prior expectations can bias how we perceive pain. Using a drift diffusion model, we recently showed that this influence is primarily based on changes in perceptual decision-making (indexed as shift in starting point). Only during unexpected application of high-intensity noxious stimuli, altered information processing (indexed as increase in drift rate) explained the expectancy effect on pain processing. Here, we employed functional magnetic resonance imaging to investigate the neural basis of both these processes in healthy volunteers. On each trial, visual cues induced the expectation of high- or low-intensity noxious stimulation or signaled equal probability for both intensities. Participants categorized a subsequently applied electrical stimulus as either low- or high-intensity pain. A shift in starting point towards high pain correlated negatively with right dorsolateral prefrontal cortex activity during cue presentation underscoring its proposed role of "keeping pain out...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8w40w272</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wiech, Katja</name>
      </author>
      <author>
        <name>Eippert, Falk</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Zaman, Jonas</name>
      </author>
      <author>
        <name>Placek, Katerina</name>
      </author>
      <author>
        <name>Tuerlinckx, Francis</name>
      </author>
      <author>
        <name>Vlaeyen, Johan WS</name>
      </author>
      <author>
        <name>Tracey, Irene</name>
      </author>
    </item>
    <item>
      <title>How can we make sound replication decisions?</title>
      <link>https://escholarship.org/uc/item/7rr2c989</link>
      <description>Replication and the reported crises impacting many fields of research have become a focal point for the sciences. This has led to reforms in publishing, methodological design and reporting, and increased numbers of experimental replications coordinated across many laboratories. While replication is rightly considered an indispensable tool of science, financial resources and researchers' time are quite limited. In this perspective, we examine different values and attitudes that scientists can consider when deciding whether to replicate a finding and how. We offer a conceptual framework for assessing the usefulness of various replication tools, such as preregistration.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7rr2c989</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Davis-Stober, Clintin P</name>
      </author>
      <author>
        <name>Sarafoglou, Alexandra</name>
      </author>
      <author>
        <name>Aczel, Balazs</name>
      </author>
      <author>
        <name>Chandramouli, Suyog H</name>
      </author>
      <author>
        <name>Errington, Timothy M</name>
      </author>
      <author>
        <name>Field, Sarahanne M</name>
      </author>
      <author>
        <name>Fishbach, Ayelet</name>
      </author>
      <author>
        <name>Freire, Juliana</name>
      </author>
      <author>
        <name>Ioannidis, John PA</name>
      </author>
      <author>
        <name>Oberauer, Klaus</name>
      </author>
      <author>
        <name>Pestilli, Franco</name>
      </author>
      <author>
        <name>Ressl, Susanne</name>
      </author>
      <author>
        <name>Schad, Daniel J</name>
      </author>
      <author>
        <name>Schure, Judith ter</name>
      </author>
      <author>
        <name>Tentori, Katya</name>
      </author>
      <author>
        <name>van Ravenzwaaij, Don</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Gundersen, Odd Erik</name>
      </author>
    </item>
    <item>
      <title>What does it mean to feel loved: Cultural consensus and individual differences in felt love</title>
      <link>https://escholarship.org/uc/item/797154dq</link>
      <description>Cultural consensus theory is a statistical framework (CCT) for the study of individual differences in the knowledge of culturally shared opinions. In this article, we demonstrate how a CCT analysis can be used to study individual differences and cultural consensus on what makes people feel loved, or more generally any social behaviors that are governed by cognitive schemata. To highlight the advantages of the method, we describe a study in which people reported on their everyday experiences of feeling loved. Our unique approach to understanding this topic is to focus on people’s cognitive evaluations on what feeling loved (both romantically and nonromantically) entails by exploring the shared agreement regarding when one is most likely to feel loved and the individual differences that influence knowledge of these shared agreements. Our results reveal that people converge on a consensus about indicators of expressed love and that these scenarios are both romantic and nonromantic....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/797154dq</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Heshmati, Saeideh</name>
      </author>
      <author>
        <name>Oravecz, Zita</name>
      </author>
      <author>
        <name>Pressman, Sarah</name>
        <uri>https://orcid.org/0000-0003-1576-6466</uri>
      </author>
      <author>
        <name>Batchelder, William H</name>
      </author>
      <author>
        <name>Muth, Chelsea</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Robust Modeling in Cognitive Science</title>
      <link>https://escholarship.org/uc/item/4wz7142v</link>
      <description>In an attempt to increase the reliability of empirical findings, psychological scientists have recently proposed a number of changes in the practice of experimental psychology. Most current reform efforts have focused on the analysis of data and the reporting of findings for empirical studies. However, a large contingent of psychologists build models that explain psychological processes and test psychological theories using formal psychological models. Some, but not all, recommendations borne out of the broader reform movement bear upon the practice of behavioral or cognitive modeling. In this article, we consider which aspects of the current reform movement are relevant to psychological modelers, and we propose a number of techniques and practices aimed at making psychological modeling more transparent, trusted, and robust.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4wz7142v</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, Michael D</name>
        <uri>https://orcid.org/0000-0001-7538-0720</uri>
      </author>
      <author>
        <name>Criss, Amy H</name>
      </author>
      <author>
        <name>Devezer, Berna</name>
      </author>
      <author>
        <name>Donkin, Christopher</name>
      </author>
      <author>
        <name>Etz, Alexander</name>
      </author>
      <author>
        <name>Leite, Fábio P</name>
      </author>
      <author>
        <name>Matzke, Dora</name>
      </author>
      <author>
        <name>Rouder, Jeffrey N</name>
      </author>
      <author>
        <name>Trueblood, Jennifer S</name>
      </author>
      <author>
        <name>White, Corey N</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Dialogues about the practice of science</title>
      <link>https://escholarship.org/uc/item/4wg265qv</link>
      <description>Dialogues about the practice of science</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4wg265qv</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Shiffrin, Richard M</name>
      </author>
      <author>
        <name>Trueblood, Jennifer S</name>
      </author>
      <author>
        <name>Kellen, David</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Psychological well-being and personality traits are associated with experiencing love in everyday life</title>
      <link>https://escholarship.org/uc/item/3086j2nn</link>
      <description>Everyday life presents many experiences that can make people feel connected to another and leave them feeling loved. We conducted two ecological momentary assessment studies (N = 52 and N = 160) to examine people's subjective perceptions of the impact of these experiences by capturing the extent to which they felt loved at several randomly sampled times during their daily life. Individual differences in loving feelings were characterized by baseline levels, within-person variabilities, and slow and fast time scale indicators of change. Results showed that there were considerable individual differences in these characteristics and these individual differences related systematically to both psychological well-being and personality: across two studies, higher felt love baseline levels were related to greater psychological well-being as well as to higher Extraversion personality scores, while people scoring high on Neuroticism showed lower baseline levels.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3086j2nn</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Oravecz, Zita</name>
      </author>
      <author>
        <name>Dirsmith, Jessica</name>
      </author>
      <author>
        <name>Heshmati, Saeideh</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Brick, Timothy R</name>
      </author>
    </item>
    <item>
      <title>Is It Worthy to Take Account of the “Guessing” in the Performance of the Raven Test? Calling for the Principle of Parsimony for Test Validation</title>
      <link>https://escholarship.org/uc/item/2q70q3f4</link>
      <description>The present study compares the fit of two- and three-parameter logistic (2PL and 3PL) models of item response theory in the performance of preschool children on the Raven’s Colored Progressive Matrices. The test of Raven is widely used for evaluating nonverbal intelligence of factor g. Studies comparing models with real data are scarce on the literature and this is the first to compare models of two and three parameters for the test of Raven, evaluating the informational gain of considering guessing probability. Participants were 582 Brazilian’s preschool children (Mage = 57 months; SD = 7 months; 46% female) who responded individually to the instrument. The model fit indices suggested that the 2PL fit better to the data. The difficulty and ability parameters were similar between the models, with almost perfect correlations. Differences were observed in terms of discrimination and test information. The principle of parsimony must be called for comparing models.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2q70q3f4</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lúcio, Patrícia Silva</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Polanczyk, Guilherme V</name>
      </author>
      <author>
        <name>Cogo-Moreira, Hugo</name>
      </author>
    </item>
    <item>
      <title>Bayesian Inference and Testing Any Hypothesis You Can Specify</title>
      <link>https://escholarship.org/uc/item/2g1141km</link>
      <description>Hypothesis testing is a special form of model selection. Once a pair of competing models is fully defined, their definition immediately leads to a measure of how strongly each model supports the data. The ratio of their support is often called the likelihood ratio or the Bayes factor. Critical in the model-selection endeavor is the specification of the models. In the case of hypothesis testing, it is of the greatest importance that the researcher specify exactly what is meant by a “null” hypothesis as well as the alternative to which it is contrasted, and that these are suitable instantiations of theoretical positions. Here, we provide an overview of different instantiations of null and alternative hypotheses that can be useful in practice, but in all cases the inferential procedure is based on the same underlying method of likelihood comparison. An associated app can be found at https://osf.io/mvp53/. This article is the work of the authors and is reformatted from the original,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2g1141km</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Etz, Alexander</name>
      </author>
      <author>
        <name>Haaf, Julia M</name>
      </author>
      <author>
        <name>Rouder, Jeffrey N</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>A joint process model of consensus and longitudinal dynamics</title>
      <link>https://escholarship.org/uc/item/1bx321db</link>
      <description>&lt;p&gt;The Extended Condorcet Model allows us to explore interindividual consensus concerning culturally held knowledge. At the same time, it enables a process-level description of interindividual differences in the knowledge a person has of the consensus, their willingness to guess in the absence of knowledge, and their bias in guessing. These person-specific characteristics potentially have an influence on one's everyday life experiences. Here, we develop a cognitive latent variable model in which dynamic process parameters from intensive longitudinal daily life data are systematically linked to parameters of the Extended Condorcet Model. We apply this joint model of consensus and longitudinal dynamics to study whether subjective beliefs on what makes people feel loved are linked to daily life experiences of love.&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1bx321db</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Oravecz, Zita</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Individual Differences in Cortical Processing Speed Predict Cognitive Abilities: a Model-Based Cognitive Neuroscience Account</title>
      <link>https://escholarship.org/uc/item/01j2h74d</link>
      <description>Previous research has shown that individuals with greater cognitive abilities display a greater speed of higher-order cognitive processing. These results suggest that speeded neural information processing may facilitate evidence accumulation during decision making and memory updating and thus yield advantages in general cognitive abilities. We used a hierarchical Bayesian cognitive modeling approach to test the hypothesis that individual differences in the velocity of evidence accumulation mediate the relationship between neural processing speed and cognitive abilities. We found that a higher neural speed predicted both the velocity of evidence accumulation across behavioral tasks and cognitive ability test scores. However, only a negligible part of the association between neural processing speed and cognitive abilities was mediated by individual differences in the velocity of evidence accumulation. The model demonstrated impressive forecasting abilities by predicting 36% of individual...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/01j2h74d</guid>
      <pubDate>Wed, 19 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Schubert, Anna-Lena</name>
      </author>
      <author>
        <name>Nunez, Michael D</name>
      </author>
      <author>
        <name>Hagemann, Dirk</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>How can we make sound replication decisions?</title>
      <link>https://escholarship.org/uc/item/8s45445d</link>
      <description>Replication and the reported crises impacting many fields of research have become a focal point for the sciences. This has led to reforms in publishing, methodological design and reporting, and increased numbers of experimental replications coordinated across many laboratories. While replication is rightly considered an indispensable tool of science, financial resources and researchers' time are quite limited. In this perspective, we examine different values and attitudes that scientists can consider when deciding whether to replicate a finding and how. We offer a conceptual framework for assessing the usefulness of various replication tools, such as preregistration.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8s45445d</guid>
      <pubDate>Thu, 13 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Davis-Stober, Clintin P</name>
      </author>
      <author>
        <name>Sarafoglou, Alexandra</name>
      </author>
      <author>
        <name>Aczel, Balazs</name>
      </author>
      <author>
        <name>Chandramouli, Suyog H</name>
      </author>
      <author>
        <name>Errington, Timothy M</name>
      </author>
      <author>
        <name>Field, Sarahanne M</name>
      </author>
      <author>
        <name>Fishbach, Ayelet</name>
      </author>
      <author>
        <name>Freire, Juliana</name>
      </author>
      <author>
        <name>Ioannidis, John PA</name>
      </author>
      <author>
        <name>Oberauer, Klaus</name>
      </author>
      <author>
        <name>Pestilli, Franco</name>
      </author>
      <author>
        <name>Ressl, Susanne</name>
      </author>
      <author>
        <name>Schad, Daniel J</name>
      </author>
      <author>
        <name>Schure, Judith ter</name>
      </author>
      <author>
        <name>Tentori, Katya</name>
      </author>
      <author>
        <name>van Ravenzwaaij, Don</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Gundersen, Odd Erik</name>
      </author>
    </item>
    <item>
      <title>Debiased lasso for stratified Cox models with application to the national kidney transplant data.</title>
      <link>https://escholarship.org/uc/item/1jf1q0q9</link>
      <description>The Scientific Registry of Transplant Recipients (SRTR) system has become a rich resource for understanding the complex mechanisms of graft failure after kidney transplant, a crucial step for allocating organs effectively and implementing appropriate care. As transplant centers that treated patients might strongly confound graft failures, Cox models stratified by centers can eliminate their confounding effects. Also, since recipient age is a proven non-modifiable risk factor, a common practice is to fit models separately by recipient age groups. The moderate sample sizes, relative to the number of covariates, in some age groups may lead to biased maximum stratified partial likelihood estimates and unreliable confidence intervals even when samples still outnumber covariates. To draw reliable inference on a comprehensive list of risk factors measured from both donors and recipients in SRTR, we propose a de-biased lasso approach via quadratic programming for fitting stratified Cox...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1jf1q0q9</guid>
      <pubDate>Mon, 16 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Xia, Lu</name>
      </author>
      <author>
        <name>Nan, Bin</name>
      </author>
      <author>
        <name>Li, Yi</name>
      </author>
    </item>
    <item>
      <title>Incorporating testing volume into estimation of effective reproduction number dynamics</title>
      <link>https://escholarship.org/uc/item/0m226329</link>
      <description>Branching process inspired models are widely used to estimate the effective reproduction number-a useful summary statistic describing an infectious disease outbreak-using counts of new cases. Case data is a real-time indicator of changes in the reproduction number, but is challenging to work with because cases fluctuate due to factors unrelated to the number of new infections. We develop a new model that incorporates the number of diagnostic tests as a surveillance model covariate. Using simulated data and data from the SARS-CoV-2 pandemic in California, we demonstrate that incorporating tests leads to improved performance over the state of the art.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0m226329</guid>
      <pubDate>Mon, 16 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Goldstein, Isaac H</name>
      </author>
      <author>
        <name>Wakefield, Jon</name>
      </author>
      <author>
        <name>Minin, Volodymyr M</name>
        <uri>https://orcid.org/0000-0002-1917-9288</uri>
      </author>
    </item>
    <item>
      <title>HOW CLOSE AND HOW MUCH? LINKING HEALTH OUTCOMES TO BUILT ENVIRONMENT SPATIAL DISTRIBUTIONS.</title>
      <link>https://escholarship.org/uc/item/1b18k8c4</link>
      <description>Built environment features (BEFs) refer to aspects of the human constructed environment, which may in turn support or restrict health related behaviors and thus impact health. In this paper we are interested in understanding whether the spatial distribution and quantity of fast food restaurants (FFRs) influence the risk of obesity in schoolchildren. To achieve this goal, we propose a two-stage Bayesian hierarchical modeling framework. In the first stage, examining the position of FFRs relative to that of some reference locations - in our case, schools - we model the distances of FFRs from these reference locations as realizations of Inhomogenous Poisson processes (IPP). With the goal of identifying representative spatial patterns of exposure to FFRs, we model the intensity functions of the IPPs using a Bayesian non-parametric model, specifying a Nested Dirichlet Process prior. The second stage model relates exposure patterns to obesity. We offer two different approaches to carry...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1b18k8c4</guid>
      <pubDate>Mon, 2 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Peterson, Adam</name>
      </author>
      <author>
        <name>Berrocal, Veronica</name>
      </author>
      <author>
        <name>Sanchez-Vaznaugh, Emma</name>
      </author>
      <author>
        <name>SÁnchez, Brisa</name>
      </author>
    </item>
    <item>
      <title>Across ages and places: Unpredictability of maternal sensory signals and child internalizing behaviors</title>
      <link>https://escholarship.org/uc/item/4n11f05q</link>
      <description>BACKGROUND: Patterns of sensory inputs early in life play an integral role in shaping the maturation of neural circuits, including those implicated in emotion and cognition. In both experimental animal models and observational human research, unpredictable sensory signals have been linked to aberrant developmental outcomes, including poor memory and effortful control. These findings suggest that sensitivity to unpredictable sensory signals is conserved across species and sculpts the developing brain. The current study provides a novel investigation of unpredictable maternal sensory signals in early life and child internalizing behaviors. We tested these associations in three independent cohorts to probe the generalizability of associations across continents and cultures.
METHOD: The three prospective longitudinal cohorts were based in Orange, USA (n&amp;nbsp;=&amp;nbsp;163, 47.2&amp;nbsp;% female, M&lt;sub&gt;age&lt;/sub&gt;&amp;nbsp;=&amp;nbsp;1&amp;nbsp;year); Turku, Finland (n&amp;nbsp;=&amp;nbsp;239, 44.8&amp;nbsp;% female,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4n11f05q</guid>
      <pubDate>Wed, 27 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Aran, Özlü</name>
      </author>
      <author>
        <name>Swales, Danielle A</name>
      </author>
      <author>
        <name>Bailey, Natasha A</name>
      </author>
      <author>
        <name>Korja, Riikka</name>
      </author>
      <author>
        <name>Holmberg, Eeva</name>
      </author>
      <author>
        <name>Eskola, Eeva</name>
      </author>
      <author>
        <name>Nolvi, Saara</name>
      </author>
      <author>
        <name>Perasto, Laura</name>
      </author>
      <author>
        <name>Nordenswan, Elisabeth</name>
      </author>
      <author>
        <name>Karlsson, Hasse</name>
      </author>
      <author>
        <name>Karlsson, Linnea</name>
      </author>
      <author>
        <name>Sandman, Curt A</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
    </item>
    <item>
      <title>Impact of Unpredictable Maternal Sensory Signals During Early Development on Adolescent Functional Connectivity of the Paraventricular Nucleus of the Thalamus</title>
      <link>https://escholarship.org/uc/item/2nz86954</link>
      <description>Background: Emotional circuit maturation is shaped by sensory signals in the environment during early life. For example, unpredictable parental and environmental sensory signals (high entropy) during early life result in increased hippocampal synaptic pruning and enduring changes in emotional circuitry in rodents. In humans, exposure to such high entropy during infancy is associated with deficits in memory and executive control during childhood and adolescence. Maturation of emotional circuitry is dependent on the integration of numerous processes in several circuits, all involving the paraventricular nucleus of the thalamus (PVT). Indeed, there is growing evidence that the PVT contributes to storing memories of salient experiences over long durations, such as memories of early life adversity. However, PVT connectivity in humans has not yet been evaluated prior to adulthood, and the impact of early life entropy on the development of PVT connectivity to key nodes of emotional circuitry...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2nz86954</guid>
      <pubDate>Wed, 27 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Leonard, Bianca</name>
      </author>
      <author>
        <name>Rasmussen, Jerod M</name>
        <uri>https://orcid.org/0000-0002-9400-7750</uri>
      </author>
      <author>
        <name>Small, Steven L</name>
      </author>
      <author>
        <name>Sandman, Curt A</name>
      </author>
      <author>
        <name>Stern, Hal</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
      <author>
        <name>Yassa, Michael A</name>
        <uri>https://orcid.org/0000-0002-8635-1498</uri>
      </author>
    </item>
    <item>
      <title>Infant hedonic/anhedonic processing index (HAPI-Infant): Assessing infant anhedonia and its prospective association with adolescent depressive symptoms</title>
      <link>https://escholarship.org/uc/item/98q922v9</link>
      <description>BACKGROUND: Anhedonia, an impairment in the motivation for or experience of pleasure, is a well-established transdiagnostic harbinger and core symptom of mental illness. Given increasing recognition of early life origins of mental illness, we posit that anhedonia should, and could, be recognized earlier if appropriate tools were available. However, reliable diagnostic instruments prior to childhood do not currently exist.
METHODS: We developed an assessment instrument for anhedonia/reward processing in infancy, the Infant Hedonic/Anhedonic Processing Index (HAPI-Infant). Exploratory factor and psychometric analyses were conducted using data from 6- and 12-month-old infants from two cohorts (N&amp;nbsp;=&amp;nbsp;188, N&amp;nbsp;=&amp;nbsp;212). Then, associations were assessed between infant anhedonia and adolescent self-report of depressive symptoms.
RESULTS: The HAPI-Infant (47-items), exhibited excellent psychometric properties. Higher anhedonia scores at 6 (r&amp;nbsp;=&amp;nbsp;0.23, p&amp;nbsp;&amp;lt;&amp;nbsp;.01)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/98q922v9</guid>
      <pubDate>Fri, 22 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Irwin, Jessica L</name>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
      <author>
        <name>Sandman, Curt A</name>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
    </item>
    <item>
      <title>Addendum: Exposure to unpredictability and mental health: Validation of the brief version of the Questionnaire of Unpredictability in Childhood (QUIC-5) in English and Spanish</title>
      <link>https://escholarship.org/uc/item/8kc53733</link>
      <description>Addendum: Exposure to unpredictability and mental health: Validation of the brief version of the Questionnaire of Unpredictability in Childhood (QUIC-5) in English and Spanish</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8kc53733</guid>
      <pubDate>Fri, 22 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lindert, Natasha G</name>
      </author>
      <author>
        <name>Maxwell, Megan Y</name>
      </author>
      <author>
        <name>Liu, Sabrina R</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
      <author>
        <name>Risbrough, Victoria B</name>
      </author>
      <author>
        <name>Baker, Dewleen G</name>
        <uri>https://orcid.org/0000-0002-1736-9838</uri>
      </author>
      <author>
        <name>Nievergelt, Caroline M</name>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
    </item>
    <item>
      <title>Within-subject changes in methylome profile identify individual signatures of early-life adversity, with a potential to predict neuropsychiatric outcome</title>
      <link>https://escholarship.org/uc/item/3w95r9wm</link>
      <description>Background: Adverse early-life experiences (ELA), including poverty, trauma and neglect, affect a majority of the world's children. Whereas the impact of ELA on cognitive and emotional health throughout the lifespan is well-established, it is not clear how distinct types of ELA influence child development, and there are no tools to predict for an individual child their vulnerability or resilience to the consequences of ELAs. Epigenetic markers including DNA-methylation profiles of peripheral cells may encode ELA and provide a predictive outcome marker. However, the rapid dynamic changes in DNA methylation in childhood and the inter-individual variance of the human genome pose barriers to identifying profiles predicting outcomes of ELA exposure. Here, we examined the relation of several dimensions of ELA to changes of DNA methylation, using a longitudinal within-subject design and a high threshold for methylation changes in the hope of mitigating the above challenges.
Methods:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3w95r9wm</guid>
      <pubDate>Fri, 22 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Short, Annabel K</name>
      </author>
      <author>
        <name>Weber, Ryan</name>
      </author>
      <author>
        <name>Kamei, Noriko</name>
      </author>
      <author>
        <name>Thai, Christina Wilcox</name>
      </author>
      <author>
        <name>Arora, Hina</name>
      </author>
      <author>
        <name>Mortazavi, Ali</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Glynn, Laura</name>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
    </item>
    <item>
      <title>Evaluating predicted heart mass in adolescent heart transplantation</title>
      <link>https://escholarship.org/uc/item/5c08n8z6</link>
      <description>BACKGROUND: Predicted Heart Mass (PHM) has emerged as an attractive size matching metric in adult cardiac transplantation. However, since PHM was derived from a healthy adult cohort, its generalizability to the pediatric population is unclear. We hypothesize that PHM can be extended to older adolescents, and potentially broaden the donor pool available to this group.
METHODS: The United Network for Organ Sharing database was retrospectively analyzed for patients aged 13 to 18 undergoing heart transplantation. Recipients were divided into quintiles (Q1-Q5) based on donor-to-recipient predicted heart mass ratios (PHMR). Primary end-point was graft survival at 5 years.
RESULTS: Two thousand sixty-one adolescent heart transplant recipients between January 1994 and September 2019 were retrospectively analyzed. The median PHMR's for each quintile was 0.84 (0.59-0.92), 0.97 (0.92-1.02), 1.08 (1.02-1.14), 1.21 (1.14-1.30), and 1.44 (1.30-2.31). Kaplan-Meier survival curves demonstrated...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5c08n8z6</guid>
      <pubDate>Thu, 21 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, James Y</name>
      </author>
      <author>
        <name>Zawadzki, Roy S</name>
      </author>
      <author>
        <name>Kidambi, Sumanth</name>
      </author>
      <author>
        <name>Rosenthal, David N</name>
      </author>
      <author>
        <name>Dykes, John C</name>
      </author>
      <author>
        <name>Nasirov, Teimour</name>
      </author>
      <author>
        <name>Ma, Michael</name>
      </author>
    </item>
    <item>
      <title>Weight Matching in Infant Heart Transplantation: A National Registry Analysis</title>
      <link>https://escholarship.org/uc/item/35g019vb</link>
      <description>BACKGROUND: Infants account for a significant proportion of pediatric heart transplantation but also suffer from a high waitlist mortality. Donor oversizing by weight-based criteria is common practice in transplantation and is prevalent in this group. We sought to analyze the impact of oversizing on outcomes in infants.
METHODS: Infant heart transplantations reported to the United Network for Organ Sharing from January 1994 to September 2019 were retrospectively analyzed. 2384 heart transplantation recipients were divided into quintiles (Q1-Q5) on the basis of donor-to-recipient weight ratio (DRWR). Multivariate Cox regression was used to estimate the effect of DRWR. The primary end point was graft survival at 1 year.
RESULTS: The median DRWR for each quintile was 0.90 (0.37-1.04), 1.17 (1.04-1.29), 1.43 (1.29-1.57), 1.74 (1.58-1.97), and 2.28 (1.97-5.00). Pairwise comparisons showed improved survival for Q3 and Q4 over each of the bottom 2 quintiles and the top quintile. Regression...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/35g019vb</guid>
      <pubDate>Thu, 21 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lee, James Y</name>
      </author>
      <author>
        <name>Kidambi, Sumanth</name>
      </author>
      <author>
        <name>Zawadzki, Roy S</name>
      </author>
      <author>
        <name>Rosenthal, David N</name>
      </author>
      <author>
        <name>Dykes, John C</name>
      </author>
      <author>
        <name>Nasirov, Teimour</name>
      </author>
      <author>
        <name>Ma, Michael</name>
      </author>
    </item>
    <item>
      <title>Geographic variation in the use of continuous outpatient inotrope infusion therapy and beta blockers</title>
      <link>https://escholarship.org/uc/item/25r6n6gt</link>
      <description>BACKGROUND: Continuous outpatient inotrope infusion therapy (COIIT) can be used as palliative or interim treatment in patients with advanced heart failure (AHF). Despite widespread use, there is a relative lack of data informing best practices. This study aimed to examine whether patterns of COIIT use differed by region and to explore whether observed differences influenced clinical outcomes.
METHODS: Retrospective study of AHF patients receiving COIIT from May 2009 through June 2016. The primary outcome was regional difference, the secondary outcome was persistence (duration) on therapy. Cox proportional hazards model was used to calculate hazard ratios for treatment regimens.
RESULTS: There were 3,286 patients, mean (SD) age 61.9 (14.4) years and 74.0% (2,433) male. Inotrope selection and beta blocker use varied by region by chi square (χ2 (21)&amp;nbsp;=&amp;nbsp;166.9, p&amp;nbsp;&amp;lt;&amp;nbsp;0.001). Persistence was greater on milrinone compared to dobutamine (HR (for discontinuation) 0.54,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/25r6n6gt</guid>
      <pubDate>Thu, 21 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Grazette, Luanda</name>
      </author>
      <author>
        <name>Tran, Jeffrey S</name>
      </author>
      <author>
        <name>Zawadzki, Nadine K</name>
      </author>
      <author>
        <name>Zawadzki, Roy S</name>
      </author>
      <author>
        <name>McLeod, Jennifer M</name>
      </author>
      <author>
        <name>Fong, Michael W</name>
      </author>
      <author>
        <name>Wilson, Melissa L</name>
      </author>
      <author>
        <name>Havakuk, Ofer</name>
      </author>
      <author>
        <name>Hay, Joel W</name>
      </author>
    </item>
    <item>
      <title>Development and evaluation of a novel dietary bisphenol A (BPA) exposure risk tool</title>
      <link>https://escholarship.org/uc/item/0c48x9bj</link>
      <description>BackgroundExposure to endocrine disrupting chemicals such as bisphenol A (BPA) is primarily from the diet through canned foods. Characterizing dietary exposures can be conducted through biomonitoring and dietary surveys; however, these methods can be time-consuming and challenging to implement.MethodsWe developed a novel dietary exposure risk questionnaire to evaluate BPA exposure and compared these results to 24-hr dietary recall data from participants (n = 404) of the Diet Intervention Examining The Factors Interacting with Treatment Success (DIETFITS) study, a dietary clinical trial, to validate questionnaire responses. High BPA exposure foods were identified from the dietary recalls and used to estimate BPA exposure. Linear regression models estimated the association between exposure to BPA and questionnaire responses. A composite risk score was developed to summarize questionnaire responses.ResultsIn questionnaire data, 65% of participants ate canned food every week. A composite...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0c48x9bj</guid>
      <pubDate>Thu, 21 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Hartle, Jennifer C</name>
      </author>
      <author>
        <name>Zawadzki, Roy S</name>
      </author>
      <author>
        <name>Rigdon, Joseph</name>
      </author>
      <author>
        <name>Lam, Juleen</name>
      </author>
      <author>
        <name>Gardner, Christopher D</name>
      </author>
    </item>
    <item>
      <title>Parsing memory and nonmemory contributions to age-related declines in mnemonic discrimination performance: a hierarchical Bayesian diffusion decision modeling approach</title>
      <link>https://escholarship.org/uc/item/99h7p2cz</link>
      <description>The mnemonic discrimination task (MDT) is a widely used cognitive assessment tool. Performance in this task is believed to indicate an age-related deficit in episodic memory stemming from a decreased ability to pattern-separate among similar experiences. However, cognitive processes other than memory ability might impact task performance. In this study, we investigated whether nonmnemonic decision-making processes contribute to the age-related deficit in the MDT. We applied a hierarchical Bayesian version of the Ratcliff diffusion model to the MDT performance of 26 younger and 31 cognitively normal older adults. It allowed us to decompose decision behavior in the MDT into different underlying cognitive processes, represented by specific model parameters. Model parameters were compared between groups, and differences were evaluated using the Bayes factor. Our results suggest that the age-related decline in MDT performance indicates a predominantly mnemonic deficit rather than differences...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/99h7p2cz</guid>
      <pubDate>Tue, 19 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Chwiesko, Caroline</name>
      </author>
      <author>
        <name>Janecek, John</name>
      </author>
      <author>
        <name>Doering, Stephanie</name>
      </author>
      <author>
        <name>Hollearn, Martina</name>
      </author>
      <author>
        <name>McMillan, Liv</name>
        <uri>https://orcid.org/0000-0001-5077-7799</uri>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Lee, Michael D</name>
        <uri>https://orcid.org/0000-0001-7538-0720</uri>
      </author>
      <author>
        <name>Ratcliff, Roger</name>
      </author>
      <author>
        <name>Yassa, Michael A</name>
        <uri>https://orcid.org/0000-0002-8635-1498</uri>
      </author>
    </item>
    <item>
      <title>Associations of reproductive and breastfeeding history with anti-Müllerian hormone concentration among African-American women of reproductive age</title>
      <link>https://escholarship.org/uc/item/3pc397z3</link>
      <description>RESEARCH QUESTION: Are gravidity, parity and breastfeeding history associated with anti-Müllerian hormone concentration among African-American women of reproductive age?
DESIGN: This study included baseline data from the Study of the Environment, Lifestyle and Fibroids, a 5-year longitudinal study of African-American women. Within this community cohort, data from 1392 women aged 25-35 years were analysed. The primary outcome was serum anti-Müllerian hormone concentration measured using the Ansh Labs picoAMH assay, an enzyme-linked immunosorbent assay. Multivariable linear regression models were used to estimate mean differences in anti-Müllerian hormone concentration (β) and 95% CI by self-reported gravidity, parity and breastfeeding history, with adjustment for potential confounders.
RESULTS: Of the 1392 participants, 1063 had a history of gravidity (76.4%). Of these, 891 (83.8%) were parous and 564 had breastfed. Multivariable-adjusted regression analyses found no appreciable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3pc397z3</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Komorowski, Allison S</name>
      </author>
      <author>
        <name>Jiang, Charley</name>
      </author>
      <author>
        <name>Berrocal, Veronica J</name>
        <uri>https://orcid.org/0000-0003-0304-7202</uri>
      </author>
      <author>
        <name>Neff, Lisa M</name>
      </author>
      <author>
        <name>Wise, Lauren A</name>
      </author>
      <author>
        <name>Harmon, Quaker E</name>
      </author>
      <author>
        <name>Baird, Donna D</name>
      </author>
      <author>
        <name>Marsh, Erica E</name>
      </author>
      <author>
        <name>Bernardi, Lia A</name>
      </author>
    </item>
    <item>
      <title>Reasons for undergoing amyloid imaging among diverse enrollees in the A4 study</title>
      <link>https://escholarship.org/uc/item/0vv2n63q</link>
      <description>INTRODUCTION: Understanding attitudes toward participation among diverse preclinical Alzheimer's disease (AD) trial participants could yield insights to instruct future recruitment.
METHODS: Using data from the Anti-Amyloid Treatment in Asymptomatic AD (A4) Study, we examined differences among mutually exclusive racial and ethnic groups in views and perceptions of amyloid imaging (VPAI), a measure of motivations to undergo amyloid biomarker testing in the setting of preclinical AD. We used linear regression to quantify differences at baseline.
RESULTS: Compared to non-Hispanic or Latino (NH) White participants, Hispanic or Latino (3.52 points, 95% confidence interval [CI]: [2.61, 4.42]); NH Asian (2.97 points, 95% CI: [1.71, 4.22]); and NH Black participants (2.79 points, 95% CI: [1.96, 3.63]) participants demonstrated higher levels of endorsement of the VPAI items at baseline.
DISCUSSION: Differences may exist among participants from differing ethnic and racial groups in motivations...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0vv2n63q</guid>
      <pubDate>Thu, 7 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Magana‐Ramirez, Christina M</name>
      </author>
      <author>
        <name>Irizarry‐Martinez, Gimarie</name>
      </author>
      <author>
        <name>Gillen, Daniel L</name>
      </author>
      <author>
        <name>Grill, Joshua D</name>
        <uri>https://orcid.org/0000-0002-4215-7589</uri>
      </author>
    </item>
    <item>
      <title>Comparative analysis of thermal adaptations of extremophilic prolyl oligopeptidases</title>
      <link>https://escholarship.org/uc/item/18z2t66d</link>
      <description>Prolyl oligopeptidases from psychrophilic, mesophilic, and thermophilic organisms found in a range of natural environments are studied using a combination of protein structure prediction, atomistic molecular dynamics, and trajectory analysis to determine how the S9 protease family adapts to extreme thermal conditions. We compare our results with hypotheses from the literature regarding structural adaptations that allow proteins to maintain structure and function at extreme temperatures, and we find that, in the case of prolyl oligopeptidases, only a subset of proposed adaptations are employed for maintaining stability. The catalytic and propeller domains are highly structured, limiting the range of mutations that can be made to enhance hydrophobicity or form disulfide bonds without disrupting the formation of necessary secondary structure. Rather, we observe a pattern in which overall prevalence of bound interactions (salt bridges and hydrogen bonds) is conserved by using increasing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/18z2t66d</guid>
      <pubDate>Tue, 5 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Diessner, Elizabeth M</name>
      </author>
      <author>
        <name>Takahashi, Gemma R</name>
      </author>
      <author>
        <name>Butts, Carter T</name>
      </author>
      <author>
        <name>Martin, Rachel W</name>
      </author>
    </item>
    <item>
      <title>Nonstationary spatial prediction of soil organic carbon: Implications for stock assessment decision making</title>
      <link>https://escholarship.org/uc/item/88654309</link>
      <description>The Rapid Carbon Assessment (RaCA) project was conducted by the US Department of Agriculture's National Resources Conservation Service between 2010-2012 in order to provide contemporaneous measurements of soil organic carbon (SOC) across the US. Despite the broad extent of the RaCA data collection effort, direct observations of SOC are not available at the high spatial resolution needed for studying carbon storage in soil and its implications for important problems in climate science and agriculture. As a result, there is a need for predicting SOC at spatial locations not included as part of the RaCA project. In this paper, we compare spatial prediction of SOC using a subset of the RaCA data for a variety of statistical methods. We investigate the performance of methods with off-the-shelf software available (both stationary and nonstationary) as well as a novel nonstationary approach based on partitioning relevant spatially-varying covariate processes. Our new method addresses...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/88654309</guid>
      <pubDate>Mon, 16 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Risser, Mark D</name>
        <uri>https://orcid.org/0000-0003-1956-1783</uri>
      </author>
      <author>
        <name>Calder, Catherine A</name>
      </author>
      <author>
        <name>Berrocal, Veronica J</name>
        <uri>https://orcid.org/0000-0003-0304-7202</uri>
      </author>
      <author>
        <name>Berrett, Candace</name>
      </author>
    </item>
    <item>
      <title>Exploratory assessment: Nurse‐led community health worker delivered HCV intervention for people experiencing homelessness</title>
      <link>https://escholarship.org/uc/item/53v996vr</link>
      <description>BACKGROUND: Getting and maintaining Hepatitis C Virus (HCV) cure is challenging among people experiencing homelessness (PEH) as a result of critical social determinants of health such as unstable housing, mental health disorders, and drug and alcohol use.
OBJECTIVES: The purpose of this exploratory pilot study was to compare a registered nurse/community health worker (RN/CHW)-led HCV intervention tailored for PEH, "I am HCV Free," with a clinic-based standard of care (cbSOC) for treating HCV. Efficacy was measured by sustained virological response at 12 weeks after stopping antivirals (SVR12), and improvement in mental health, drug and alcohol use, and access to healthcare.
METHODS: An exploratory randomized controlled trial design was used to assign PEH recruited from partner sites in the Skid Row Area of Los Angeles, California, to the RN/CHW or cbSOC programs. All received direct-acting antivirals. The RN/CHW group received directly observed therapy in community-based settings,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/53v996vr</guid>
      <pubDate>Mon, 16 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Nyamathi, Adeline</name>
        <uri>https://orcid.org/0000-0003-4979-6620</uri>
      </author>
      <author>
        <name>Salem, Benissa E</name>
      </author>
      <author>
        <name>Lee, Darlene</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Hudson, Angela</name>
      </author>
      <author>
        <name>Saab, Sammy</name>
      </author>
      <author>
        <name>Shin, Sanghyuk S</name>
        <uri>https://orcid.org/0000-0001-9982-4373</uri>
      </author>
      <author>
        <name>Jones‐Patten, Alexandria</name>
      </author>
      <author>
        <name>Yadav, Kartik</name>
        <uri>https://orcid.org/0000-0001-7873-2808</uri>
      </author>
      <author>
        <name>Alikhani, Mitra</name>
      </author>
      <author>
        <name>Clarke, Richard</name>
      </author>
      <author>
        <name>Chang, Alicia</name>
      </author>
      <author>
        <name>White, Kathryn</name>
      </author>
      <author>
        <name>Gelberg, Lillian</name>
        <uri>https://orcid.org/0000-0001-9772-0116</uri>
      </author>
    </item>
    <item>
      <title>How Trustworthy Is Your Tree? Bayesian Phylogenetic Effective Sample Size Through the Lens of Monte Carlo Error</title>
      <link>https://escholarship.org/uc/item/1t6947wm</link>
      <description>Bayesian inference is a popular and widely-used approach to infer phylogenies (evolutionary trees). However, despite decades of widespread application, it remains difficult to judge how well a given Bayesian Markov chain Monte Carlo (MCMC) run explores the space of phylogenetic trees. In this paper, we investigate the Monte Carlo error of phylogenies, focusing on high-dimensional summaries of the posterior distribution, including variability in estimated edge/branch (known in phylogenetics as "split") probabilities and tree probabilities, and variability in the estimated summary tree. Specifically, we ask if there is any measure of effective sample size (ESS) applicable to phylogenetic trees which is capable of capturing the Monte Carlo error of these three summary measures. We find that there are some ESS measures capable of capturing the error inherent in using MCMC samples to approximate the posterior distributions on phylogenies. We term these tree ESS measures, and identify...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1t6947wm</guid>
      <pubDate>Sat, 31 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Magee, Andrew</name>
      </author>
      <author>
        <name>Karcher, Michael</name>
      </author>
      <author>
        <name>Matsen, Frederick A</name>
      </author>
      <author>
        <name>Minin, Volodymyr M</name>
        <uri>https://orcid.org/0000-0002-1917-9288</uri>
      </author>
    </item>
    <item>
      <title>Individual longitudinal changes in DNA-methylome identify signatures of early-life adversity and correlate with later outcome</title>
      <link>https://escholarship.org/uc/item/7bc2m1ss</link>
      <description>Adverse early-life experiences (ELA) affect a majority of the world's children. Whereas the enduring impact of ELA on cognitive and emotional health is established, there are no tools to predict vulnerability to ELA consequences in an individual child. Epigenetic markers including peripheral-cell DNA-methylation profiles may encode ELA and provide predictive outcome markers, yet the interindividual variance of the human genome and rapid changes in DNA methylation in childhood pose significant challenges. Hoping to mitigate these challenges we examined the relation of several ELA dimensions to DNA methylation changes and outcome using a within-subject longitudinal design and a high methylation-change threshold. DNA methylation was analyzed in buccal swab/saliva samples collected twice (neonatally and at 12 months) in 110 infants. We identified CpGs differentially methylated across time for each child and determined whether they associated with ELA indicators and executive function...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7bc2m1ss</guid>
      <pubDate>Sat, 20 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Short, Annabel K</name>
      </author>
      <author>
        <name>Weber, Ryan</name>
      </author>
      <author>
        <name>Kamei, Noriko</name>
      </author>
      <author>
        <name>Thai, Christina Wilcox</name>
      </author>
      <author>
        <name>Arora, Hina</name>
      </author>
      <author>
        <name>Mortazavi, Ali</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Glynn, Laura</name>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
    </item>
    <item>
      <title>The Current State of Undergraduate Bayesian Education and Recommendations for the Future</title>
      <link>https://escholarship.org/uc/item/33d0496n</link>
      <description>As a result of the increased emphasis on mis- and over-use of p-values in scientific research and the rise in popularity of Bayesian statistics, Bayesian education is becoming more important at the undergraduate level. With the advances in computing tools, Bayesian statistics is also becoming more accessible for undergraduates. This study focuses on analyzing Bayesian courses for undergraduates. We explored whether an undergraduate Bayesian course is offered in our sample of 152 high-ranking research universities and liberal arts colleges. For each identified Bayesian course, we examined how it fits into the institution’s undergraduate curricula, such as majors and prerequisites. Through a series of course syllabi analyses, we explored the topics covered and their popularity in these courses, and the adopted teaching and learning tools, such as software. This article presents our findings on the current practices of teaching full Bayesian courses at the undergraduate level. Based...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/33d0496n</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dogucu, Mine</name>
      </author>
      <author>
        <name>Hu, Jingchen</name>
      </author>
    </item>
    <item>
      <title>Reproducibility in the Classroom</title>
      <link>https://escholarship.org/uc/item/25b54425</link>
      <description>Difficulties in reproducing results from scientific studies have lately been referred to as a reproducibility crisis. Scientific practice depends heavily on scientific training. What gets taught in the classroom is often practiced in labs, fieldwork, and data analysis. The importance of reproducibility in the classroom has gained momentum in statistics education in recent years. In this article, we review the existing literature on reproducibility education. We delve into the relationship between computing tools and reproducibility through visiting historical developments in this area. We share examples for teaching reproducibility and reproducible teaching while discussing the pedagogical opportunities created by these examples as well as challenges that the instructors should be aware of. We detail the use of teaching reproducibility and reproducible teaching practices in an introductory data science course. Lastly, we provide recommendations on reproducibility education for...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/25b54425</guid>
      <pubDate>Fri, 19 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Dogucu, Mine</name>
      </author>
    </item>
    <item>
      <title>From the Great Depression to the Great Recession: A Model‐Based Ranking of U.S. Recessions</title>
      <link>https://escholarship.org/uc/item/87j0k5rh</link>
      <description>From the Great Depression to the Great Recession: A Model‐Based Ranking of U.S. Recessions</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/87j0k5rh</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Rui</name>
      </author>
      <author>
        <name>Jeliazkov, Ivan</name>
      </author>
    </item>
    <item>
      <title>Information Processing Pattern and Propensity to Buy: An Investigation of Online Point-of-Purchase Behavior</title>
      <link>https://escholarship.org/uc/item/0ps8v3q1</link>
      <description>The information processing literature provides a wealth of laboratory evidence on the effects that the choice task and individual characteristics have on the extent to which consumers engage in alternative-based versus attribute-based information processing. Less attention has been paid to studying how the processing pattern at the point of purchase is associated with a consumer's propensity to buy in shopping settings. To understand this relationship, we formulate a discrete choice model and perform formal model comparisons to distinguish among several possible dependence structures. We consider models involving an existing measure of information processing, PATTERN; a latent variable version of this measure; and several new refinements and generalizations. Analysis of a unique data set of 895 shoppers on a popular electronics website supports the latent variable specification and provides validation for several hypotheses and modeling components. We find a positive relationship...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0ps8v3q1</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Mintz, Ofer</name>
      </author>
      <author>
        <name>Currim, Imran S</name>
      </author>
      <author>
        <name>Jeliazkov, Ivan</name>
      </author>
    </item>
    <item>
      <title>Nonparametric Vector Autoregressions: Specification, Estimation, and Inference</title>
      <link>https://escholarship.org/uc/item/07h0g04r</link>
      <description>For over three decades, vector autoregressions have played a central role in empirical macroeconomics. These models are general, can capture sophisticated dynamic behavior, and can be extended to include features such as structural instability, time-varying parameters, dynamic factors, threshold-crossing behavior, and discrete outcomes. Building upon growing evidence that the assumption of linearity may be undesirable in modeling certain macroeconomic relationships, this article seeks to add to recent advances in VAR modeling by proposing a nonparametric dynamic model for multivariate time series. In this model, the problems of modeling and estimation are approached from a hierarchical Bayesian perspective. The article considers the issues of identification, estimation, and model comparison, enabling nonparametric VAR (or NPVAR) models to be fit efficiently by Markov chain Monte Carlo (MCMC) algorithms and compared to parametric and semiparametric alternatives by marginal likelihoods...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/07h0g04r</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Jeliazkov, Ivan</name>
      </author>
    </item>
    <item>
      <title>Clinical decision support improves physician guideline adherence for laboratory monitoring of chronic kidney disease: a matched cohort study</title>
      <link>https://escholarship.org/uc/item/6g2316gd</link>
      <description>BackgroundGuidelines exist for chronic kidney disease (CKD) but are not well implemented in clinical practice. We evaluated the impact of a guideline-based clinical decision support system (CDSS) on laboratory monitoring and achievement of laboratory targets in stage 3–4 CKD patients.MethodsWe performed a matched cohort study of 12,353 stage 3–4 CKD patients whose physicians opted to receive an automated guideline-based CDSS with CKD-related lab results, and 42,996 matched controls whose physicians did not receive the CDSS. Physicians were from US community-based physician practices utilizing a large, commercial laboratory (LabCorp®).We compared the percentage of laboratory tests obtained within guideline-recommended intervals and the percentage of results within guideline target ranges between CDSS and non-CDSS patients. Laboratory tests analyzed included estimated glomerular filtration rate, plasma parathyroid hormone, serum calcium, phosphorus, 25-hydroxy vitamin D (25-D),...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6g2316gd</guid>
      <pubDate>Tue, 16 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ennis, Jennifer</name>
      </author>
      <author>
        <name>Gillen, Daniel</name>
      </author>
      <author>
        <name>Rubenstein, Arthur</name>
      </author>
      <author>
        <name>Worcester, Elaine</name>
      </author>
      <author>
        <name>Brecher, Mark E</name>
      </author>
      <author>
        <name>Asplin, John</name>
      </author>
      <author>
        <name>Coe, Fredric</name>
      </author>
    </item>
    <item>
      <title>Childhood unpredictability is associated with increased risk for long- and short-term depression and anhedonia symptoms following combat deployment</title>
      <link>https://escholarship.org/uc/item/0mk6x14n</link>
      <description>High unpredictability has emerged as a dimension of early-life adversity that may contribute to a host of deleterious consequences later in life. Early-life unpredictability affects development of limbic and reward circuits in both rodents and humans, with a potential to increase sensitivity to stressors and mood symptoms later in life. Here, we examined the extent to which unpredictability during childhood was associated with changes in mood symptoms (anhedonia and general depression) after two adult life stressors, combat deployment and civilian reintegration, which were assessed ten years apart. We also examined how perceived stress and social support mediated and /or moderated links between childhood unpredictability and mood symptoms. To test these hypotheses, we leveraged the Marine Resiliency Study, a prospective longitudinal study of the effects of combat deployment on mental health in Active-Duty Marines and Navy Corpsman. Participants (&lt;i&gt;N&lt;/i&gt; = 273) were assessed for...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mk6x14n</guid>
      <pubDate>Mon, 8 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Hunt, Christopher</name>
      </author>
      <author>
        <name>Vinograd, Meghan</name>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Stern, Hal</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Nievergelt, Caroline</name>
      </author>
      <author>
        <name>Cuccurazzu, Bruna</name>
      </author>
      <author>
        <name>Napan, Cindy</name>
      </author>
      <author>
        <name>Delmar, Dylan</name>
      </author>
      <author>
        <name>Baker, Dewleen G</name>
        <uri>https://orcid.org/0000-0002-1736-9838</uri>
      </author>
      <author>
        <name>Risbrough, Victoria B</name>
      </author>
    </item>
    <item>
      <title>A Statistical Model for Event Sequence Data.</title>
      <link>https://escholarship.org/uc/item/1018271b</link>
      <description>The identification of recurring patterns within a sequence of events is an important task in behavior research. In this paper, we consider a general probabilistic framework for identifying such patterns, by distinguishing between events that belong to a pattern and events that occur as part of background processes. The event processes, both for background events and events that are part of recurring patterns, are modeled as competing renewal processes. Using this framework, we develop an inference procedure to detect the sequences present in observed data. Our method is compared to a current approach used within the ethology literature on both simulated data and data collected to study the impact of fragmented and unpredictable maternal behavior on cognitive development of children.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1018271b</guid>
      <pubDate>Wed, 3 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Heins, Kevin</name>
      </author>
      <author>
        <name>Stern, Hal</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
    </item>
    <item>
      <title>Scaling up the evaluation of psychotherapy: evaluating motivational interviewing fidelity via statistical text classification</title>
      <link>https://escholarship.org/uc/item/9dv2f776</link>
      <description>BackgroundBehavioral interventions such as psychotherapy are leading, evidence-based practices for a variety of problems (e.g., substance abuse), but the evaluation of provider fidelity to behavioral interventions is limited by the need for human judgment. The current study evaluated the accuracy of statistical text classification in replicating human-based judgments of provider fidelity in one specific psychotherapy— motivational interviewing (MI).MethodParticipants (n = 148) came from five previously conducted randomized trials and were either primary care patients at a safety-net hospital or university students. To be eligible for the original studies, participants met criteria for either problematic drug or alcohol use. All participants received a type of brief motivational interview, an evidence-based intervention for alcohol and substance use disorders. The Motivational Interviewing Skills Code is a standard measure of MI provider fidelity based on human ratings that was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9dv2f776</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Atkins, David C</name>
      </author>
      <author>
        <name>Steyvers, Mark</name>
      </author>
      <author>
        <name>Imel, Zac E</name>
      </author>
      <author>
        <name>Smyth, Padhraic</name>
      </author>
    </item>
    <item>
      <title>Impact of stepwise hyperventilation on cerebral tissue oxygen saturation in anesthetized patients: a mechanistic study</title>
      <link>https://escholarship.org/uc/item/8sd3g0dd</link>
      <description>BACKGROUND: While the decrease in blood carbon dioxide (CO2 ) secondary to hyperventilation is generally accepted to play a major role in the decrease of cerebral tissue oxygen saturation (SctO2 ), it remains unclear if the associated systemic hemodynamic changes are also accountable.
METHODS: Twenty-six patients (American Society of Anesthesiologists I-II) undergoing nonneurosurgical procedures were anesthetized with either propofol-remifentanil (n = 13) or sevoflurane (n = 13). During a stable intraoperative period, ventilation was adjusted stepwise from hypoventilation to hyperventilation to achieve a progressive change in end-tidal CO2 (ETCO2 ) from 55 to 25 mmHg. Minute ventilation, SctO2 , ETCO2 , mean arterial pressure (MAP), and cardiac output (CO) were recorded.
RESULTS: Hyperventilation led to a SctO2 decrease from 78 ± 4% to 69 ± 5% (Δ = -9 ± 4%, P &amp;lt; 0.001) in the propofol-remifentanil group and from 81 ± 5% to 71 ± 7% (Δ = -10 ± 3%, P &amp;lt; 0.001) in the sevoflurane...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8sd3g0dd</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>ALEXANDER, BS</name>
        <uri>https://orcid.org/0000-0003-3657-0673</uri>
      </author>
      <author>
        <name>GELB, AW</name>
        <uri>https://orcid.org/0000-0001-7004-4410</uri>
      </author>
      <author>
        <name>MANTULIN, WW</name>
      </author>
      <author>
        <name>CERUSSI, AE</name>
      </author>
      <author>
        <name>TROMBERG, BJ</name>
        <uri>https://orcid.org/0000-0002-7481-7975</uri>
      </author>
      <author>
        <name>YU, Z</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>LEE, C</name>
      </author>
      <author>
        <name>MENG, L</name>
      </author>
    </item>
    <item>
      <title>Biomarker-Based Calibration of Retrospective Exposure Predictions of Perfluoro­octanoic Acid</title>
      <link>https://escholarship.org/uc/item/10v658sf</link>
      <description>Estimated historical exposures and serum concentrations of perfluorooctanoic acid (PFOA) have been extensively used in epidemiologic studies that examined associations between PFOA exposures and adverse health outcomes among residents in highly exposed areas in the Mid-Ohio Valley. Using measured serum PFOA levels in 2005-2006, we applied two calibration methods to these retrospective exposure predictions: (1) multiplicative calibration and (2) Bayesian pharmacokinetic calibration with larger adjustments to more recent exposure estimates and smaller adjustments to exposure estimates for years farther in the past. We conducted simulation studies of various hypothetical exposure scenarios and compared hypothetical true historical intake rates with estimates based on mis-specified baseline exposure and pharmacokinetic models to find the method with the least bias. The Bayesian method outperformed the multiplicative method if a change to bottled water consumption was not reported...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/10v658sf</guid>
      <pubDate>Mon, 17 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shin, Hyeong-Moo</name>
      </author>
      <author>
        <name>Steenland, Kyle</name>
      </author>
      <author>
        <name>Ryan, P Barry</name>
      </author>
      <author>
        <name>Vieira, Verónica M</name>
        <uri>https://orcid.org/0000-0001-7153-4606</uri>
      </author>
      <author>
        <name>Bartell, Scott M</name>
        <uri>https://orcid.org/0000-0001-7797-2906</uri>
      </author>
    </item>
    <item>
      <title>Estimation for General Birth-Death Processes</title>
      <link>https://escholarship.org/uc/item/5jk564q2</link>
      <description>Birth-death processes (BDPs) are continuous-time Markov chains that track the number of "particles" in a system over time. While widely used in population biology, genetics and ecology, statistical inference of the instantaneous particle birth and death rates remains largely limited to restrictive linear BDPs in which per-particle birth and death rates are constant. Researchers often observe the number of particles at discrete times, necessitating data augmentation procedures such as expectation-maximization (EM) to find maximum likelihood estimates. For BDPs on finite state-spaces, there are powerful matrix methods for computing the conditional expectations needed for the E-step of the EM algorithm. For BDPs on infinite state-spaces, closed-form solutions for the E-step are available for some linear models, but most previous work has resorted to time-consuming simulation. Remarkably, we show that the E-step conditional expectations can be expressed as convolutions of computable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5jk564q2</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Crawford, Forrest W</name>
      </author>
      <author>
        <name>Minin, Vladimir N</name>
        <uri>https://orcid.org/0000-0002-1917-9288</uri>
      </author>
      <author>
        <name>Suchard, Marc A</name>
      </author>
    </item>
    <item>
      <title>A Semiparametric Bayesian Model for Detecting Synchrony Among Multiple Neurons</title>
      <link>https://escholarship.org/uc/item/48c82996</link>
      <description>We propose a scalable semiparametric Bayesian model to capture dependencies among multiple neurons by detecting their cofiring (possibly with some lag time) patterns over time. After discretizing time so there is at most one spike at each interval, the resulting sequence of 1s (spike) and 0s (silence) for each neuron is modeled using the logistic function of a continuous latent variable with a gaussian process prior. For multiple neurons, the corresponding marginal distributions are coupled to their joint probability distribution using a parametric copula model. The advantages of our approach are as follows. The nonparametric component (i.e., the gaussian process model) provides a flexible framework for modeling the underlying firing rates, and the parametric component (i.e., the copula model) allows us to make inferences regarding both contemporaneous and lagged relationships among neurons. Using the copula model, we construct multivariate probabilistic models by separating the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/48c82996</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Zhou, Bo</name>
      </author>
      <author>
        <name>Lan, Shiwei</name>
      </author>
      <author>
        <name>Ombao, Hernando</name>
      </author>
      <author>
        <name>Moorman, David</name>
      </author>
      <author>
        <name>Behseta, Sam</name>
      </author>
    </item>
    <item>
      <title>Travel patterns during pregnancy: comparison between Global Positioning System (GPS) tracking and questionnaire data</title>
      <link>https://escholarship.org/uc/item/34r1b7d2</link>
      <description>BackgroundMaternal exposures to traffic-related air pollution have been associated with adverse pregnancy outcomes. Exposures to traffic-related air pollutants are strongly influenced by time spent near traffic. However, little is known about women’s travel activities during pregnancy and whether questionnaire-based data can provide reliable information on travel patterns during pregnancy.ObjectivesExamine women’s in-vehicle travel behavior during pregnancy and examine the difference in travel data collected by questionnaire and global positioning system (GPS) and their potential for exposure error.MethodsWe measured work-related travel patterns in 56 pregnant women using a questionnaire and one-week GPS tracking three times during pregnancy (&amp;lt;20&amp;nbsp;weeks, 20–30&amp;nbsp;weeks, and &amp;gt;30&amp;nbsp;weeks of gestation). We compared self-reported activities with GPS-derived trip distance and duration, and examined potentially influential factors that may contribute to differences. We...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/34r1b7d2</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Wu, Jun</name>
        <uri>https://orcid.org/0000-0002-2693-7112</uri>
      </author>
      <author>
        <name>Jiang, Chengsheng</name>
      </author>
      <author>
        <name>Jaimes, Guillermo</name>
      </author>
      <author>
        <name>Bartell, Scott</name>
        <uri>https://orcid.org/0000-0001-7797-2906</uri>
      </author>
      <author>
        <name>Dang, Andy</name>
      </author>
      <author>
        <name>Baker, Dean</name>
      </author>
      <author>
        <name>Delfino, Ralph J</name>
      </author>
    </item>
    <item>
      <title>Family studies of type 1 diabetes reveal additive and epistatic effects between MGAT1 and three other polymorphisms</title>
      <link>https://escholarship.org/uc/item/30m8j7x8</link>
      <description>In a recent study on multiple sclerosis (MS), we observed additive effects and epistatic interactions between variants of four genes that converge to induce T-cell hyperactivity by altering Asn-(N)-linked protein glycosylation: namely, the Golgi enzyme MGAT1, cytotoxic T-lymphocyte antigen 4 (CTLA-4), interleukin-2 receptor-α (IL2RA) and interleukin-7 receptor-α (IL7RA). As the CTLA-4, IL2RA and IL7RA variants are associated with type 1 diabetes (T1D), we examined for joint effects in T1D. Employing a novel conditional logistic regression for family-based data sets, epistatic and additive effects were observed using 1423 multiplex families from the Type 1 Diabetes Genetic Consortium data set. The IL2RA and IL7RA variants had univariate association in MS and T1D, whereas the MGAT1 and CTLA-4 variants associated with only MS or T1D, respectively. However, similar to MS, the MGAT1 variant haplotype interacted with CTLA4 (P=0.03), and a combination of IL2RA and IL7RA (P=0.01). The...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/30m8j7x8</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Yu, Z</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Li, CF</name>
      </author>
      <author>
        <name>Mkhikian, H</name>
      </author>
      <author>
        <name>Zhou, RW</name>
      </author>
      <author>
        <name>Newton, BL</name>
      </author>
      <author>
        <name>Demetriou, M</name>
        <uri>https://orcid.org/0000-0001-8547-5774</uri>
      </author>
    </item>
    <item>
      <title>Obesity Paradox in End-Stage Kidney Disease Patients</title>
      <link>https://escholarship.org/uc/item/1w09074q</link>
      <description>In the general population, obesity is associated with increased cardiovascular risk and decreased survival. In patients with end-stage renal disease (ESRD), however, an "obesity paradox" or "reverse epidemiology" (to include lipid and hypertension paradoxes) has been consistently reported, i.e. a higher body mass index (BMI) is paradoxically associated with better survival. This survival advantage of large body size is relatively consistent for hemodialysis patients across racial and regional differences, although published results are mixed for peritoneal dialysis patients. Recent data indicate that both higher skeletal muscle mass and increased total body fat are protective, although there are mixed data on visceral (intra-abdominal) fat. The obesity paradox in ESRD is unlikely to be due to residual confounding alone and has biologic plausibility. Possible causes of the obesity paradox include protein-energy wasting and inflammation, time discrepancy among competitive risk factors...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1w09074q</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Park, Jongha</name>
      </author>
      <author>
        <name>Ahmadi, Seyed-Foad</name>
      </author>
      <author>
        <name>Streja, Elani</name>
      </author>
      <author>
        <name>Molnar, Miklos Z</name>
      </author>
      <author>
        <name>Flegal, Katherine M</name>
      </author>
      <author>
        <name>Gillen, Daniel</name>
      </author>
      <author>
        <name>Kovesdy, Csaba P</name>
      </author>
      <author>
        <name>Kalantar-Zadeh, Kamyar</name>
        <uri>https://orcid.org/0000-0002-8666-0725</uri>
      </author>
    </item>
    <item>
      <title>Maternal psychosocial stress during pregnancy is associated with newborn leukocyte telomere length</title>
      <link>https://escholarship.org/uc/item/1vn8597n</link>
      <description>OBJECTIVE: In adults, one of the major determinants of leukocyte telomere length (LTL), a predictor of age-related diseases and mortality, is cumulative psychosocial stress exposure. More recently we reported that exposure to maternal psychosocial stress during intrauterine life is associated with LTL in young adulthood. The objective of the present study was to determine how early in life this effect of stress on LTL is apparent by quantifying the association of maternal psychosocial stress during pregnancy with newborn telomere length.
STUDY DESIGN: In a prospective study of N = 27 mother-newborn dyads maternal pregnancy-specific stress was assessed in early gestation and cord blood peripheral blood mononuclear cells were subsequently collected and analyzed for LTL measurement.
RESULTS: After accounting for the effects of potential determinants of newborn LTL (gestational age at birth, weight, sex, and exposure to antepartum obstetric complications), there was a significant,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1vn8597n</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Entringer, Sonja</name>
      </author>
      <author>
        <name>Epel, Elissa S</name>
      </author>
      <author>
        <name>Lin, Jue</name>
        <uri>https://orcid.org/0000-0001-7216-1610</uri>
      </author>
      <author>
        <name>Buss, Claudia</name>
        <uri>https://orcid.org/0000-0002-8738-3133</uri>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Blackburn, Elizabeth H</name>
      </author>
      <author>
        <name>Simhan, Hyagriv N</name>
      </author>
      <author>
        <name>Wadhwa, Pathik D</name>
      </author>
    </item>
    <item>
      <title>Markov Chain Monte Carlo from Lagrangian Dynamics</title>
      <link>https://escholarship.org/uc/item/0qn744zs</link>
      <description>Hamiltonian Monte Carlo (HMC) improves the computational e ciency of the Metropolis-Hastings algorithm by reducing its random walk behavior. Riemannian HMC (RHMC) further improves the performance of HMC by exploiting the geometric properties of the parameter space. However, the geometric integrator used for RHMC involves implicit equations that require fixed-point iterations. In some cases, the computational overhead for solving implicit equations undermines RHMC's benefits. In an attempt to circumvent this problem, we propose an explicit integrator that replaces the momentum variable in RHMC by velocity. We show that the resulting transformation is equivalent to transforming Riemannian Hamiltonian dynamics to Lagrangian dynamics. Experimental results suggests that our method improves RHMC's overall computational e ciency in the cases considered. All computer programs and data sets are available online (http://www.ics.uci.edu/~babaks/Site/Codes.html) in order to allow replication...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0qn744zs</guid>
      <pubDate>Sun, 16 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Lan, Shiwei</name>
      </author>
      <author>
        <name>Stathopoulos, Vasileios</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Girolami, Mark</name>
      </author>
    </item>
    <item>
      <title>The anticancer compound JTE-607 reveals hidden sequence specificity of the mRNA 3′ processing machinery</title>
      <link>https://escholarship.org/uc/item/2621z0j2</link>
      <description>JTE-607 is an anticancer and anti-inflammatory compound and its active form, compound 2, directly binds to and inhibits CPSF73, the endonuclease for the cleavage step in pre-messenger RNA (pre-mRNA) 3′ processing. Surprisingly, compound 2-mediated inhibition of pre-mRNA cleavage is sequence specific and the drug sensitivity is predominantly determined by sequences flanking the cleavage site (CS). Using massively parallel in vitro assays, we identified key sequence features that determine drug sensitivity. We trained a machine learning model that can predict poly(A) site (PAS) relative sensitivity to compound 2 and provide the molecular basis for understanding the impact of JTE-607 on PAS selection and transcription termination genome wide. We propose that CPSF73 and associated factors bind to the CS region in a sequence-dependent manner and the interaction affinity determines compound 2 sensitivity. These results have not only elucidated the mechanism of action of JTE-607, but...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2621z0j2</guid>
      <pubDate>Tue, 11 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Liu, Liang</name>
      </author>
      <author>
        <name>Yu, Angela M</name>
      </author>
      <author>
        <name>Wang, Xiuye</name>
      </author>
      <author>
        <name>Soles, Lindsey V</name>
      </author>
      <author>
        <name>Teng, Xueyi</name>
        <uri>https://orcid.org/0000-0001-7258-3477</uri>
      </author>
      <author>
        <name>Chen, Yiling</name>
      </author>
      <author>
        <name>Yoon, Yoseop</name>
      </author>
      <author>
        <name>Sarkan, Kristianna SK</name>
      </author>
      <author>
        <name>Valdez, Marielle Cárdenas</name>
      </author>
      <author>
        <name>Linder, Johannes</name>
      </author>
      <author>
        <name>England, Whitney</name>
      </author>
      <author>
        <name>Spitale, Robert</name>
        <uri>https://orcid.org/0000-0002-3511-8098</uri>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Marazzi, Ivan</name>
        <uri>https://orcid.org/0000-0003-3376-0922</uri>
      </author>
      <author>
        <name>Qiao, Feng</name>
        <uri>https://orcid.org/0000-0002-1704-7257</uri>
      </author>
      <author>
        <name>Li, Wei</name>
      </author>
      <author>
        <name>Seelig, Georg</name>
      </author>
      <author>
        <name>Shi, Yongsheng</name>
      </author>
    </item>
    <item>
      <title>The HDI + ROPE Decision Rule Is Logically Incoherent But We Can Fix It</title>
      <link>https://escholarship.org/uc/item/88h1s355</link>
      <description>The Bayesian highest-density interval plus region of practical equivalence (HDI + ROPE) decision rule is an increasingly common approach to testing null parameter values. The decision procedure involves a comparison between a posterior highest-density interval (HDI) and a prespecified region of practical equivalence. One then accepts or rejects the null parameter value depending on the overlap (or lack thereof) between these intervals. Here, we demonstrate, both theoretically and through examples, that this procedure is logically incoherent. Because the HDI is not transformation invariant, the ultimate inferential decision depends on statistically arbitrary and scientifically irrelevant properties of the statistical model. The incoherence arises from a common confusion between probability density and probability proper. The HDI + ROPE procedure relies on characterizing posterior densities as opposed to being based directly on probability. We conclude with recommendations for alternative...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/88h1s355</guid>
      <pubDate>Wed, 5 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Etz, Alexander</name>
      </author>
      <author>
        <name>de la Peña, Adriana F Chávez</name>
      </author>
      <author>
        <name>Baroja, Luis</name>
      </author>
      <author>
        <name>Medriano, Kathleen</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
    </item>
    <item>
      <title>Geographical variability and network structure</title>
      <link>https://escholarship.org/uc/item/789291wg</link>
      <description>In this paper, we explore the potential implications of geographical variability for the structure of social networks. Beginning with some basic simplifying assumptions, we derive a number of ways in which local network structure should be expected to vary across a region whose population is unevenly distributed. To examine the manner in which these effects would be expected to manifest given realistic population distributions, we then perform an exploratory simulation study that examines the features of large-scale interpersonal networks generated using block-level data from the 2000 U.S. Census. Using a stratified sample of micropolitan and metropolitan areas with populations ranging from approximately 1000 to 1,000,000 persons, we extrapolatively simulate network structure using spatial network models calibrated to two fairly proximate social relations. From this sample of simulated networks, we examine the effect of both within-location and between-location heterogeneity on...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/789291wg</guid>
      <pubDate>Wed, 5 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Butts, Carter T</name>
      </author>
      <author>
        <name>Acton, Ryan M</name>
      </author>
      <author>
        <name>Hipp, John R</name>
        <uri>https://orcid.org/0000-0001-9006-2587</uri>
      </author>
      <author>
        <name>Nagle, Nicholas N</name>
      </author>
    </item>
    <item>
      <title>Where’s Waldo, Ohio? Using Cognitive Models to Improve the Aggregation of Spatial Knowledge</title>
      <link>https://escholarship.org/uc/item/1s3960gj</link>
      <description>We apply cognitive modeling to improve the wisdom of the crowd in a spatial knowledge task. Participants provided point estimates for where 48 US cities are located and then, using the point estimate as a center point, chose a radius large enough that they believed the resulting circle was certain to contain the city’s location. Simple and radius-weighted arithmetic averages of the individuals’ point estimates produced more accurate group answers than the majority of individuals. These statistical aggregates, however, assume there are no differences in individual expertise nor in the difficulty of locating different cities. Accordingly, we develop a set of cognitive models to infer group estimates that make various assumptions about individual expertise and differences in city difficulty. The model-based estimates generally outperform the statistical averages. The models are especially accurate if they allow for individual differences in expertise that can vary city by city. We...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1s3960gj</guid>
      <pubDate>Wed, 5 Jun 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Montgomery, Lauren E</name>
      </author>
      <author>
        <name>Baldini, Charles M</name>
      </author>
      <author>
        <name>Vandekerckhove, Joachim</name>
        <uri>https://orcid.org/0000-0003-2600-5937</uri>
      </author>
      <author>
        <name>Lee, Michael D</name>
      </author>
    </item>
    <item>
      <title>A Novel Approach to Integrate Human Biomonitoring Data with Model Predicted Dietary Exposures: A Crop Protection Chemical Case Study Using Lambda-Cyhalothrin</title>
      <link>https://escholarship.org/uc/item/40r9n0rg</link>
      <description>The appropriate use of human biomonitoring data to model population chemical exposures is challenging, especially for rapidly metabolized chemicals, such as agricultural chemicals. The objective of this study is to demonstrate a novel approach integrating model predicted dietary exposures and biomonitoring data to potentially inform regulatory risk assessments. We use lambda-cyhalothrin as a case study, and for the same representative U.S. population in the National Health and Nutrition Examination Survey (NHANES), an integrated exposure and pharmacokinetic model predicted exposures are calibrated to measurements of the urinary metabolite 3-phenoxybenzoic acid (3PBA), using an approximate Bayesian computing (ABC) methodology. We demonstrate that the correlation between modeled urinary 3PBA and the NHANES 3PBA measurements more than doubled as ABC thresholding narrowed the acceptable tolerance range for predicted versus observed urinary measurements. The median predicted urinary...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/40r9n0rg</guid>
      <pubDate>Tue, 28 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Cuvelier, Nicholas</name>
      </author>
      <author>
        <name>Avanasi, Raga</name>
      </author>
      <author>
        <name>Grunenwald, Mark</name>
      </author>
      <author>
        <name>Ramanarayanan, Tharacad</name>
      </author>
      <author>
        <name>Wolf, Douglas C</name>
      </author>
      <author>
        <name>Bartell, Scott M</name>
        <uri>https://orcid.org/0000-0001-7797-2906</uri>
      </author>
    </item>
    <item>
      <title>tauFisher predicts circadian time from a single sample of bulk and single-cell pseudobulk transcriptomic data</title>
      <link>https://escholarship.org/uc/item/09x2q576</link>
      <description>As the circadian clock regulates fundamental biological processes, disrupted clocks are often observed in patients and diseased tissues. Determining the circadian time of the patient or the tissue of focus is essential in circadian medicine and research. Here we present tauFisher, a computational pipeline that accurately predicts circadian time from a single transcriptomic sample by finding correlations between rhythmic genes within the sample. We demonstrate tauFisher’s performance in adding timestamps to both bulk and single-cell transcriptomic samples collected from multiple tissue types and experimental settings. Application of tauFisher at a cell-type level in a single-cell RNAseq dataset collected from mouse dermal skin implies that greater circadian phase heterogeneity may explain the dampened rhythm of collective core clock gene expression in dermal immune cells compared to dermal fibroblasts. Given its robustness and generalizability across assay platforms, experimental...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/09x2q576</guid>
      <pubDate>Mon, 27 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Duan, Junyan</name>
      </author>
      <author>
        <name>Ngo, Michelle N</name>
      </author>
      <author>
        <name>Karri, Satya Swaroop</name>
      </author>
      <author>
        <name>Tsoi, Lam C</name>
      </author>
      <author>
        <name>Gudjonsson, Johann E</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Lowengrub, John</name>
      </author>
      <author>
        <name>Andersen, Bogi</name>
        <uri>https://orcid.org/0000-0001-7181-2768</uri>
      </author>
    </item>
    <item>
      <title>Anatomical and molecular characterization of parvalbumin-cholecystokinin co-expressing inhibitory interneurons: implications for neuropsychiatric conditions</title>
      <link>https://escholarship.org/uc/item/2cz59398</link>
      <description>Inhibitory interneurons are crucial to brain function and their dysfunction is implicated in neuropsychiatric conditions. Emerging evidence indicates that cholecystokinin (CCK)-expressing interneurons (CCK+) are highly heterogenous. We find that a large subset of parvalbumin-expressing (PV+) interneurons express CCK strongly;&amp;nbsp;between 40 and 56% of PV+ interneurons in mouse hippocampal CA1&amp;nbsp;express CCK. Primate interneurons also exhibit substantial PV/CCK co-expression. Mouse PV+/CCK+ and PV+/CCK- cells show distinguishable electrophysiological and molecular characteristics. Analysis of single nuclei RNA-seq and ATAC-seq data shows that PV+/CCK+ cells are a subset of PV+ cells, not of synuclein gamma positive (SNCG+) cells, and that they strongly express oxidative phosphorylation (OXPHOS) genes. We find that mitochondrial complex I and IV-associated OXPHOS gene expression is&amp;nbsp;strongly correlated with CCK expression in PV+ interneurons at both the transcriptomic and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cz59398</guid>
      <pubDate>Sat, 11 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Grieco, Steven F</name>
      </author>
      <author>
        <name>Johnston, Kevin G</name>
      </author>
      <author>
        <name>Gao, Pan</name>
      </author>
      <author>
        <name>Garduño, B Maximiliano</name>
      </author>
      <author>
        <name>Tang, Bryan</name>
      </author>
      <author>
        <name>Yi, Elsie</name>
      </author>
      <author>
        <name>Sun, Yanjun</name>
      </author>
      <author>
        <name>Horwitz, Gregory D</name>
      </author>
      <author>
        <name>Yu, Zhaoxia</name>
        <uri>https://orcid.org/0000-0001-9700-1795</uri>
      </author>
      <author>
        <name>Holmes, Todd C</name>
      </author>
      <author>
        <name>Xu, Xiangmin</name>
        <uri>https://orcid.org/0000-0002-5828-1533</uri>
      </author>
    </item>
    <item>
      <title>Comment</title>
      <link>https://escholarship.org/uc/item/98q9r4c3</link>
      <description>Comment</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/98q9r4c3</guid>
      <pubDate>Tue, 7 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Stern, Hal</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
    </item>
    <item>
      <title>Recognition of overlapping elliptical objects in a binary image</title>
      <link>https://escholarship.org/uc/item/6m4395w9</link>
      <description>Recognition of overlapping objects is required in many applications in the field of computer vision. Examples include cell segmentation, bubble detection and bloodstain pattern analysis. This paper presents a method to identify overlapping objects by approximating them with ellipses. The method is intended to be applied to complex-shaped regions which are believed to be composed of one or more overlapping objects. The method has two primary steps. First, a pool of candidate ellipses are generated by applying the Euclidean distance transform on a compressed image and the pool is filtered by an overlaying method. Second, the concave points on the contour of the region of interest are extracted by polygon approximation to divide the contour into segments. Then, the optimal ellipses are selected from among the candidates by choosing a minimal subset that best fits the identified segments. We propose the use of the adjusted Rand index, commonly applied in clustering, to compare the...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6m4395w9</guid>
      <pubDate>Tue, 7 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zou, Tong</name>
      </author>
      <author>
        <name>Pan, Tianyu</name>
      </author>
      <author>
        <name>Taylor, Michael</name>
      </author>
      <author>
        <name>Stern, Hal</name>
      </author>
    </item>
    <item>
      <title>Statistical Methods for the Forensic Analysis of Geolocated Event Data</title>
      <link>https://escholarship.org/uc/item/66v3r3hj</link>
      <description>A common question in forensic analysis is whether two observed data sets originated from the same
source or from different sources. Statistical approaches to addressing this question have been widely
adopted within the forensics community, particularly for DNA evidence. Here we investigate the
application of statistical approaches to same-source forensic questions for spatial event data, such as
determining the likelihood that two sets of observed GPS locations were generated by the same individual. We develop two approaches to quantify the strength of evidence in this setting. The first is a
likelihood ratio approach based on modeling the spatial event data directly. The second approach is to
instead measure the similarity of the two observed data sets via a score function and then assess the
strength of the observed score resulting in the score-based likelihood ratio. A comparative evaluation
using geolocated Twitter event data from two large metropolitan areas shows the potential...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/66v3r3hj</guid>
      <pubDate>Tue, 7 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Galbraith, Christopher</name>
      </author>
      <author>
        <name>Smyth, Padhraic</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
    </item>
    <item>
      <title>Towards a likelihood ratio approach for bloodstain pattern analysis</title>
      <link>https://escholarship.org/uc/item/493686zj</link>
      <description>In this work, we explore the application of likelihood ratio as a forensic evidence assessment tool to evaluate the causal mechanism of a bloodstain pattern. It is assumed that there are two competing hypotheses regarding the cause of a bloodstain pattern. The bloodstain patterns are represented as a collection of ellipses with each ellipse characterized by its location, size and orientation. Quantitative measures and features are derived to summarize key aspects of the patterns. A bivariate Gaussian model is chosen to estimate the distribution of features under a given hypothesis and thus approximate the likelihood of a pattern. Published data with 59 impact patterns and 55 gunshot patterns is used to train and evaluate the model. Results demonstrate the feasibility of the likelihood ratio approach for bloodstain pattern analysis. The results also hint at some of the challenges that need to be addressed for future use of the likelihood ratio approach for bloodstain pattern analysis.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/493686zj</guid>
      <pubDate>Tue, 7 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Zou, Tong</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
    </item>
    <item>
      <title>Fully Bayesian Autoencoders with Latent Sparse Gaussian Processes.</title>
      <link>https://escholarship.org/uc/item/47m3r5v9</link>
      <description>We present a fully Bayesian autoencoder model that treats both local latent variables and global decoder parameters in a Bayesian fashion. This approach allows for flexible priors and posterior approximations while keeping the inference costs low. To achieve this, we introduce an amortized MCMC approach by utilizing an implicit stochastic network to learn sampling from the posterior over local latent variables. Furthermore, we extend the model by incorporating a Sparse Gaussian Process prior over the latent space, allowing for a fully Bayesian treatment of inducing points and kernel hyperparameters and leading to improved scalability. Additionally, we enable Deep Gaussian Process priors on the latent space and the handling of missing data. We evaluate our model on a range of experiments focusing on dynamic representation learning and generative modeling, demonstrating the strong performance of our approach in comparison to existing methods that combine Gaussian Processes and autoencode...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/47m3r5v9</guid>
      <pubDate>Wed, 1 May 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Tran, Ba-Hien</name>
      </author>
      <author>
        <name>Shahbaba, Babak</name>
        <uri>https://orcid.org/0000-0002-8102-1609</uri>
      </author>
      <author>
        <name>Mandt, Stephan</name>
      </author>
      <author>
        <name>Filippone, Maurizio</name>
      </author>
    </item>
    <item>
      <title>Regression analysis of longitudinal data with outcome‐dependent sampling and informative censoring</title>
      <link>https://escholarship.org/uc/item/5qv1d1q2</link>
      <description>We consider regression analysis of longitudinal data in the presence of outcome-dependent observation times and informative censoring. Existing approaches commonly require correct specification of the joint distribution of the longitudinal measurements, observation time process and informative censoring time under the joint modeling framework, and can be computationally cumbersome due to the complex form of the likelihood function. In view of these issues, we propose a semi-parametric joint regression model and construct a composite likelihood function based on a conditional order statistics argument. As a major feature of our proposed methods, the aforementioned joint distribution is not required to be specified and the random effect in the proposed joint model is treated as a nuisance parameter. Consequently, the derived composite likelihood bypasses the need to integrate over the random effect and offers the advantage of easy computation. We show that the resulting estimators...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5qv1d1q2</guid>
      <pubDate>Sun, 7 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Shen, Weining</name>
        <uri>https://orcid.org/0000-0003-3137-1085</uri>
      </author>
      <author>
        <name>Liu, Suyu</name>
      </author>
      <author>
        <name>Chen, Yong</name>
      </author>
      <author>
        <name>Ning, Jing</name>
      </author>
    </item>
    <item>
      <title>Unpredictable maternal behavior is associated with a blunted infant cortisol response</title>
      <link>https://escholarship.org/uc/item/40c0n8gj</link>
      <description>BACKGROUND: Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis is associated with poor physical and mental health. Early-life adversity may dysregulate cortisol response to subsequent stress. This study examines the association between patterns of maternal behavior and infant stress response to a challenge. Specifically, we test whether infant exposure to unpredictable maternal sensory signals is related to the cortisol response to a painful stressor.
METHOD: Participants were 102 mothers and their children enrolled in a longitudinal study. Patterns of maternal sensory signals were evaluated at 6 and 12&amp;nbsp;months during a 10-min mother-infant play episode. Entropy rate was calculated as a quantitative measure of the degree of unpredictability of maternal sensory signals (visual, auditory, and tactile) exhibited during the play episode. Infant saliva samples were collected for cortisol analysis before and after inoculation at 12&amp;nbsp;months.
RESULTS: Unpredictable...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/40c0n8gj</guid>
      <pubDate>Sun, 7 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Noroña‐Zhou, Amanda N</name>
      </author>
      <author>
        <name>Morgan, Alyssa</name>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
      <author>
        <name>Sandman, Curt A</name>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
    </item>
    <item>
      <title>Prenatal Maternal Mood Entropy Is Associated With Child Neurodevelopment</title>
      <link>https://escholarship.org/uc/item/3jv205k4</link>
      <description>Emerging evidence indicates that the predictability of signals early in life may influence the developing brain. This study examines links between a novel indicator of maternal mood dysregulation, mood entropy, and child neurodevelopmental outcomes. Associations between prenatal maternal mood entropy and child neurodevelopment were assessed in 2 longitudinal cohorts. Maternal mood was measured several times over pregnancy beginning as early as 15 weeks' gestation. Shannon's mood entropy was applied to distributions of mothers' responses on mood questionnaires. Child cognitive and language development were evaluated at 2 and 6-9 years of age. Higher prenatal maternal mood entropy was associated with lower cognitive development scores at 2 years of age and lower expressive language scores at 6-9 years of age. These associations persisted after adjusting for maternal pre and postnatal mood levels and for other relevant sociodemographic factors. Our findings identify maternal mood...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3jv205k4</guid>
      <pubDate>Sun, 7 Apr 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Howland, Mariann A</name>
      </author>
      <author>
        <name>Sandman, Curt A</name>
      </author>
      <author>
        <name>Davis, Elysia Poggi</name>
      </author>
      <author>
        <name>Stern, Hal S</name>
        <uri>https://orcid.org/0000-0002-5657-2820</uri>
      </author>
      <author>
        <name>Phelan, Michael</name>
      </author>
      <author>
        <name>Baram, Tallie Z</name>
        <uri>https://orcid.org/0000-0003-0771-8616</uri>
      </author>
      <author>
        <name>Glynn, Laura M</name>
      </author>
    </item>
  </channel>
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