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    <responseDate>2026-10-14T03:53:47Z</responseDate>
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    <identifier>10.57760/sciencedb.psych.00846</identifier>
    <datestamp>2026-05-06T17:59:01Z</datestamp>
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  <dc:date>2026-05-06</dc:date>
  <dc:title>Dataset for the paper &amp;ldquo;Shared Neurogenetic Substrates of Non-planning Impulsivity and Procrastination&amp;rdquo;</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.psych.00846</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Procrastination has maladaptive impact on health and survival, yet it remains moderately heritable, presenting a biological paradox. Procrastination has been conceptualized as a byproduct of impulsivity, explaining its prevalence despite no discernible adaptive benefit. However, the shared neurobiological substrates underlying the association between impulsivity and procrastination have yet to be elucidated. Using a longitudinal twin cohort (N = 154), we show that non-planning impulsivity (NPI) during late adolescence and early adulthood is prospectively associated with procrastination in later life. This effect was independently replicated in two cross-sectional cohorts (N = 327; N = 1,543). Twin modeling using an additive genetic and non-shared environmental (AE) framework, together with a meta-analysis of twin studies (N = 3,656 twin pairs) revealed significant shared genetic contributions (rg = 0.51). Beyond genetic overlap, neuroimaging meta-analysis (NeuroSynth meta‑analysis for impulsivity: k = 198 studies, 5855 loci; mini meta-analysis for procrastination: k = 5 studies, 7 independent samples, Ncumulative = 893 participants), normative modeling (N = 37,407), and seed-based d mapping (SDM) converged on the left dorsolateral prefrontal cortex (DLPFC) as the region of maximal overlap between NPI and procrastination. The transcriptional profiles of the left DLPFC and impulsivity-associated genes exhibited functional convergence on regulation of biological and cellular processes. These genes showed brain-specific expression and associations with cortical metabolism, neurodegenerative disease, and developmental expression peaks, indicating a shared molecular basis for the neurogenetic architecture of procrastination. Together, our findings delineate a cross-scale characterization of the shared neurogenetic substrates linking NPI and procrastination, offering empirical evidence that elucidates the biological origins of procrastination.This dataset includes the de-identified summary data and analysis scripts for the paper &amp;ldquo;Shared Neurogenetic Substrates of Non-planning Impulsivity and Procrastination&amp;rdquo; compiled in the order in which the results are presented.</dc:description>
  <dc:subject>procrastination; non-planning impulsivity; twin studies; dorsolateral prefrontal cortex; behavioral genetics</dc:subject>
  <dc:creator>Yuanyuan Hu</dc:creator>
  <dc:creator>Jie Xiang</dc:creator>
  <dc:creator>Yuening Jin</dc:creator>
  <dc:creator>Qingchen Fan</dc:creator>
  <dc:creator>Changshuo Wang</dc:creator>
  <dc:creator>Yihan Wu</dc:creator>
  <dc:creator>Dang Zheng</dc:creator>
  <dc:creator>Yancheng Tang</dc:creator>
  <dc:creator>Wei Li</dc:creator>
  <dc:creator>Bowen Hu</dc:creator>
  <dc:creator>Tingyong Feng</dc:creator>
  <dc:creator>Yuan Zhou</dc:creator>
  <dc:creator>Zhiyi Chen</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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