The genetic architecture of the human cerebral cortex.
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dc.contributor.author | Alzheimer’s Disease Neuroimaging Initiative | |
dc.contributor.author | CHARGE Consortium | |
dc.contributor.author | EPIGEN Consortium | |
dc.contributor.author | IMAGEN Consortium | |
dc.contributor.author | SYS Consortium | |
dc.contributor.author | Parkinson’s Progression Markers Initiative | |
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dc.contributor.author | Martin, Nicholas G | |
dc.contributor.author | Martinot, Jean-Luc | |
dc.contributor.author | McDonald, Colm | |
dc.contributor.author | McMahon, Katie L | |
dc.contributor.author | Meyer-Lindenberg, Andreas | |
dc.contributor.author | Michie, Patricia T | |
dc.contributor.author | Morey, Rajendra A | |
dc.contributor.author | Mowry, Bryan | |
dc.contributor.author | Nyberg, Lars | |
dc.contributor.author | Oosterlaan, Jaap | |
dc.contributor.author | Ophoff, Roel A | |
dc.contributor.author | Pantelis, Christos | |
dc.contributor.author | Paus, Tomas | |
dc.contributor.author | Pausova, Zdenka | |
dc.contributor.author | Penninx, Brenda W J H | |
dc.contributor.author | Polderman, Tinca J C | |
dc.contributor.author | Posthuma, Danielle | |
dc.contributor.author | Rietschel, Marcella | |
dc.contributor.author | Roffman, Joshua L | |
dc.contributor.author | Rowland, Laura M | |
dc.contributor.author | Sachdev, Perminder S | |
dc.contributor.author | Sämann, Philipp G | |
dc.contributor.author | Schall, Ulrich | |
dc.contributor.author | Schumann, Gunter | |
dc.contributor.author | Scott, Rodney J | |
dc.contributor.author | Sim, Kang | |
dc.contributor.author | Sisodiya, Sanjay M | |
dc.contributor.author | Smoller, Jordan W | |
dc.contributor.author | Sommer, Iris E | |
dc.contributor.author | St Pourcain, Beate | |
dc.contributor.author | Stein, Dan J | |
dc.contributor.author | Toga, Arthur W | |
dc.contributor.author | Trollor, Julian N | |
dc.contributor.author | Van der Wee, Nic J A | |
dc.contributor.author | van 't Ent, Dennis | |
dc.contributor.author | Völzke, Henry | |
dc.contributor.author | Walter, Henrik | |
dc.contributor.author | Weber, Bernd | |
dc.contributor.author | Weinberger, Daniel R | |
dc.contributor.author | Wright, Margaret J | |
dc.contributor.author | Zhou, Juan | |
dc.contributor.author | Stein, Jason L | |
dc.contributor.author | Thompson, Paul M | |
dc.contributor.author | Medland, Sarah E | |
dc.contributor.author | Enhancing NeuroImaging Genetics through Meta-Analysis Consortium (ENIGMA)—Genetics working group | |
dc.date.accessioned | 2025-01-07T16:21:14Z | |
dc.date.available | 2025-01-07T16:21:14Z | |
dc.date.issued | 2020 | |
dc.description.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. | |
dc.identifier.doi | 10.1126/science.aay6690 | |
dc.identifier.essn | 1095-9203 | |
dc.identifier.pmc | PMC7295264 | |
dc.identifier.pmid | 32193296 | |
dc.identifier.pubmedURL | https://pmc.ncbi.nlm.nih.gov/articles/PMC7295264/pdf | |
dc.identifier.unpaywallURL | http://www.bristol.ac.uk/alspac/external/documents/grant-acknowledgements.pdf | |
dc.identifier.uri | https://hdl.handle.net/10668/27761 | |
dc.issue.number | 6484 | |
dc.journal.title | Science (New York, N.Y.) | |
dc.journal.titleabbreviation | Science | |
dc.language.iso | en | |
dc.organization | SAS - Hospital Universitario Virgen del Rocío | |
dc.organization | Instituto de Investigación Biomédica de Sevilla (IBIS) | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Meta-Analysis | |
dc.pubmedtype | Research Support, N.I.H., Extramural | |
dc.pubmedtype | Research Support, N.I.H., Intramural | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.pubmedtype | Research Support, U.S. Gov't, Non-P.H.S. | |
dc.rights.accessRights | open access | |
dc.subject.mesh | Attention Deficit Disorder with Hyperactivity | |
dc.subject.mesh | Brain Mapping | |
dc.subject.mesh | Cerebral Cortex | |
dc.subject.mesh | Cognition | |
dc.subject.mesh | Genetic Loci | |
dc.subject.mesh | Genetic Variation | |
dc.subject.mesh | Genome-Wide Association Study | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Organ Size | |
dc.subject.mesh | Parkinson Disease | |
dc.title | The genetic architecture of the human cerebral cortex. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 367 |
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