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        <datestamp>2026-09-28T14:58:59Z</datestamp>
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          <dc:title>Structure-Adaptive E-Value Filter for Detecting Regional Signals in Brain Imaging</dc:title>
          <dc:creator>Jingcheng He (9046971)</dc:creator>
          <dc:creator>Hangjin Jiang (10164692)</dc:creator>
          <dc:creator>Wenguang Sun (4173823)</dc:creator>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Neuroscience</dc:subject>
          <dc:subject>Mental Health</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>False discovery rate</dc:subject>
          <dc:subject>Conformal inference</dc:subject>
          <dc:subject>Partial conjunction hypothesis</dc:subject>
          <dc:subject>Neuroimaging</dc:subject>
          <dc:subject>Cognitive impairment</dc:subject>
          <dc:description>&lt;p&gt;Structural MRI provides a noninvasive view of the neuroanatomical differences associated with cognitive impairment and dementia. Using data from the Alzheimer’s Disease Neuroimaging Initiative, we investigate which anatomical regions exhibit widespread gray-matter differences and how these regional patterns vary across the clinical spectrum. Addressing this goal requires translating spatially dependent voxel-level evidence into regional conclusions while controlling multiplicity across anatomical regions. We propose the Structure-adaptive E-value FilTer (SEFT), which uses flexible working models to construct spatially adaptive voxel-level scores and aggregates them into regional partial-conjunction e-values. When combined with the e-value Benjamini–Hochberg (e-BH) procedure, these e-values provide finite-sample control of the set-wise false discovery rate under arbitrary interregional dependence. The ADNI analysis reveals a coherent neuroanatomical pattern: the exploratory analysis shows that differences between normal cognition and mild cognitive impairment are concentrated in medial-temporal regions, whereas the differences between mild cognitive impairment and dementia extend more broadly into temporal–limbic and posterior association regions. Both patterns largely overlap the normal-cognition–dementia benchmark, identifying a shared anatomical core across the clinical comparisons.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T14:58:59Z</dc:date>
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