ArXiv TLDR

The Genetic and Environmental Architecture of the Human Functional Connectome

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2604.24614

Tanu Raghav, Daniel Guerrero, Uttara Tipnis, Julie Sara Benny, Mintao Liu + 6 more

q-bio.NC

TLDR

This paper improves twin models by explicitly accounting for measurement error to better understand genetic and environmental influences on the human functional connectome.

Key contributions

  • Extends classical twin models (ACE/ADE) to include measurement error from repeated fMRI sessions.
  • Analyzes monozygotic and dizygotic twins from HCP to estimate genetic and environmental variance.
  • Identifies distinct functional modules influenced by shared environment, additive, or dominant genetics.
  • Reveals that genetic and environmental influences are structured into coherent, multiscale brain networks.

Why it matters

This research refines how we study genetic and environmental contributions to brain function by improving twin model accuracy. It provides a clearer picture of how nature and nurture shape the human connectome, opening new avenues for understanding brain disorders.

Original Abstract

Functional connectivity varies across individuals due to genetic and environmental factors, yet classical twin models typically confound non-shared environment with measurement error and are largely limited to resting-state analyses. We hypothesized that: i) explicitly modeling measurement error from repeated fMRI sessions enables more accurate application of classical twin models (ACE/ADE) to functional connectivity; ii) model applicability depends on scan-length and parcellation granularity; iii) genetic and environmental effects on functional connectomes show differentiated functional modules across conditions. We extended ACE/ADE models to include a repeated-scan derived error term by analyzing monozygotic and dizygotic twins from the Young-Adult Human Connectome Project dataset. Genetic and environment variance components were estimated for all functional couplings across resting-state and task conditions, integrated across conditions using a minimum-error criterion, and analyzed using multilayer community detection across resolution scales. Functional couplings segregated into distinct categories characterized by shared environmental, additive, dominant, or epistatic influences, with a substantial fraction not meeting twin-model assumptions. Integrating across conditions revealed hierarchical community structure in genetic and environmental components observed across community resolution scales. Incorporating measurement error into twin models improves interpretability and applicability at the functional connectome level, revealing that genetic and environmental influences are structured into coherent, multiscale brain networks.

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