The genetic architecture of the human cerebral cortex.
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Date
2020
Authors
Grasby, Katrina L
Jahanshad, Neda
Painter, Jodie N
Colodro-Conde, Lucía
Bralten, Janita
Hibar, Derrek P
Lind, Penelope A
Pizzagalli, Fabrizio
Ching, Christopher R K
McMahon, Mary Agnes B
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Abstract
The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the specific genetic loci that influence human cortical structure. To identify genetic variants that affect cortical structure, we conducted a genome-wide association meta-analysis of brain magnetic resonance imaging data from 51,665 individuals. We analyzed the surface area and average thickness of the whole cortex and 34 regions with known functional specializations. We identified 199 significant loci and found significant enrichment for loci influencing total surface area within regulatory elements that are active during prenatal cortical development, supporting the radial unit hypothesis. Loci that affect regional surface area cluster near genes in Wnt signaling pathways, which influence progenitor expansion and areal identity. Variation in cortical structure is genetically correlated with cognitive function, Parkinson's disease, insomnia, depression, neuroticism, and attention deficit hyperactivity disorder.
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MeSH Terms
Attention Deficit Disorder with Hyperactivity
Brain Mapping
Cerebral Cortex
Cognition
Genetic Loci
Genetic Variation
Genome-Wide Association Study
Humans
Magnetic Resonance Imaging
Organ Size
Parkinson Disease
Brain Mapping
Cerebral Cortex
Cognition
Genetic Loci
Genetic Variation
Genome-Wide Association Study
Humans
Magnetic Resonance Imaging
Organ Size
Parkinson Disease