Evidence map›Paper›PMID 41053002›Full record

ArticleTranslational psychiatry2025

The interplay between genomic copy number variants, sleep, and cognition in the general population.

Cecile Poulain, Rackeb Tesfaye, Elise Douard, Jean-Louis Martineau, Zohra Saci, Aurelie Labbe, David C Glahn, Laura Almasy, Mayada Elsabbagh, Guillaume Huguet and 1 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Cecile Poulain *Centre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, QC, Canada. cecile.poulain@umontreal.ca.
Rackeb Tesfaye *Department of Neurology and Neurosurgery, McGill University, Montreal Neurological Institute, Azrieli Centre for Autism Research, Montréal, QC, Canada.
Elise DouardCentre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, QC, Canada.ORCID http://orcid.org/0000-0003-4205-8828
Jean-Louis MartineauCentre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, QC, Canada.
Zohra SaciCentre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, QC, Canada.ORCID http://orcid.org/0000-0003-2788-1306
Aurelie LabbeHEC Montreal, Department of Decision Sciences, Université de Montréal, Montréal, QC, Canada.
David C GlahnDepartment of Psychiatry, Boston Children's Hospital, Boston, MA, USA.
Laura AlmasyDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Mayada ElsabbaghDepartment of Neurology and Neurosurgery, McGill University, Montreal Neurological Institute, Azrieli Centre for Autism Research, Montréal, QC, Canada.ORCID http://orcid.org/0000-0002-7311-9059
Guillaume HuguetCentre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, QC, Canada.ORCID http://orcid.org/0000-0002-4746-6030
Sebastien JacquemontCentre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, QC, Canada. sebastien.jacquemont@umontreal.ca.ORCID http://orcid.org/0000-0001-6838-8767

Funding

Large-Scale Evaluation of the Effect of Rare Genetic Variants on Psychiatric Symptoms and Cognitive AbilityU01MH119690 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI ALMASY, LAURA A., GLAHN, DAVID C · 2019 to 2023
$5.9M
NIMH NIH HHS U01 MH119690
6 · The paper itself

Abstract

Genomic Copy Number variants (CNVs) increase risk for neurodevelopmental disorders (NDDs) and affect cognition, but their impact on sleep remains understudied despite the well-established link between sleep disturbances, NDDs, and cognition. We investigated the relationship between CNVs, sleep traits, cognitive ability, and executive function in 498,852 individuals from an unselected population in the UK Biobank. We replicated the U-shape relationship between measures of cognitive ability and sleep duration. The effects of CNVs on sleep duration were evident at the genome-wide level; CNV-burden analyses showed that overall, CNVs with an increasing number of intolerant genes were associated with increased or decreased sleep duration in a U-shape pattern (p < 2e

Indexed as

CognitionDNA Copy Number VariationsExecutive FunctionSleepSleep Wake DisordersAdultAgedFemaleGenome-Wide Association StudyHumansMaleMiddle AgedSleep Initiation and Maintenance DisordersUnited Kingdom

Identifiers

PMID41053002
PMCPMC12501278

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.