Study uncovers brain's timing system for cognition

Researchers at Rutgers Health have identified how the brain integrates fast and slow processing through white matter connections, influencing cognitive abilities. Published in Nature Communications, the study analyzed data from nearly 1,000 people to map these neural timescales. Variations in this system may explain differences in thinking efficiency and hold promise for mental health research.

The human brain juggles information arriving at vastly different speeds, from immediate environmental cues to deliberate reflections on context and intent. A new investigation from Rutgers Health, detailed in Nature Communications, reveals how it achieves this balance via intrinsic neural timescales—unique processing windows for each brain region—and the white matter networks that link them.

Led by Linden Parkes, an assistant professor of psychiatry at Rutgers Health, the team examined brain imaging from 960 individuals to construct detailed connectomes. They employed mathematical models to trace information flow across these networks. "To affect our environment through action, our brains must combine information processed over different timescales," Parkes explained. "The brain achieves this by leveraging its white matter connectivity to share information across regions, and this integration is crucial for human behavior."

The findings show that the arrangement of these timescales across the cerebral cortex determines how smoothly the brain transitions between activity patterns linked to behavior. Not everyone has the same setup: "We found that differences in how the brain processes information at different speeds help explain why people vary in their cognitive abilities," Parkes noted. Those with better-aligned wiring for fast and slow signals tend to exhibit higher cognitive capacity.

These patterns also tie into genetic, molecular, and cellular brain features, with parallels observed in mice, indicating evolutionary conservation. "Our work highlights a fundamental link between the brain's white matter connectivity and its local computational properties," Parkes added.

Looking ahead, the researchers plan to apply this framework to disorders like schizophrenia, bipolar disorder, and depression to explore disruptions in temporal processing. Collaborators included Avram Holmes, Ahmad Beyh, Amber Howell, and Jason Z. Kim from Cornell University. The study appeared in Nature Communications (2025; 16(1)), with DOI: 10.1038/s41467-025-66542-w.

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Illustration of glowing whole-brain neural networks coordinating efficiently, representing a University of Notre Dame study on general intelligence.
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Study points to whole-brain network coordination as a key feature of general intelligence

በAI የተዘገበ በ AI የተሰራ ምስል እውነት ተፈትሸ

University of Notre Dame researchers report evidence that general intelligence is associated with how efficiently and flexibly brain networks coordinate across the whole connectome, rather than being localized to a single “smart” region. The findings, published in Nature Communications, are based on neuroimaging and cognitive data from 831 Human Connectome Project participants and an additional 145 adults from the INSIGHT Study.

A common belief that the frontal lobe fully develops by age 25 has been challenged by recent neuroscience findings. New brain-imaging studies reveal that key neural wiring and network efficiency evolve well into the early 30s. This extended timeline highlights ongoing maturation processes in the brain.

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Researchers have identified brain connectivity patterns tied to autism symptom severity in children diagnosed with either autism or ADHD. The findings, from a study led by the Child Mind Institute, suggest shared biological mechanisms across these conditions regardless of formal diagnosis. These patterns align with genetic activity involved in neural development.

Researchers at the University of California, Irvine report that a machine-learning system called SIGNET can infer cause-and-effect links between genes in human brain tissue, revealing extensive rewiring of gene regulation—especially in excitatory neurons—in Alzheimer’s disease.

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