Evidence map›Paper›PMID 39964619›Full record

ArticleBehavior genetics2025

The Genetic Specificity of Cognitive Tests After Controlling for General Cognitive Ability.

Francesca Procopio, Engin Keser, Jacob Knyspel, Margherita Malanchini, Kaili Rimfeld, Robert Plomin

Abstract read
In one paragraph

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

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Francesca ProcopioSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK. francesca.procopio@kcl.ac.uk.ORCID 0000-0001-9750-3947
Engin KeserSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Jacob KnyspelSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Margherita MalanchiniSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Kaili RimfeldSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Robert PlominSocial, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

Funding

Colorado Adoption/Twin Study of Lifespan behavioral development & cognitive aging (CATSLife2)R01AG046938 · NIA · UNIVERSITY OF COLORADO · PI REYNOLDS, CHANDRA A, WADSWORTH, SALLY J · 2015 to 2024
$18.5M
NIA NIH HHS R01 AG046938NIH HHS AG046938
6 · The paper itself

Abstract

Diverse tests of cognitive abilities correlate about 0.30 phenotypically and about 0.60 genetically. Their phenotypic overlap defines general cognitive ability (g), driven largely by genetic overlap. Consequently, much of our understanding of the genetic landscape of specific cognitive tests likely reflects g rather than the tests themselves. Removing this g-associated genetic variance will sharpen research on cognitive tests. Here, we use Genomic Structural Equation Modelling (Genomic SEM) to remove shared genetic variance among 12 diverse cognitive tests that capture verbal and nonverbal cognitive domains. We applied Genomic SEM to summary statistics from the largest genome-wide association studies of verbal tests (GenLang Consortium, five tests) and largely nonverbal tests (UK Biobank, seven tests) to chart the genetic landscape of the 12 tests independent of g as compared to uncorrected cognitive tests. We found that SNP heritabilities were nearly as high for the tests corrected for g as uncorrected: the average SNP heritability was 0.16 (SE = 0.02) for the uncorrected tests and 0.13 (SE = 0.02) for the tests corrected for g. Despite this, the genetic landscape of the cognitive tests transformed after controlling for genomic g. The matrix of positive genetic correlations for the cognitive tests (average 0.45) disappeared after g-correction, and some strong negative correlations emerged; for instance, Memory and Word (-0.72), Fluid and Symbol (-0.72), and Tower and Spelling (-0.79). The summary statistics for these g-corrected cognitive tests can be used by researchers to create polygenic scores that focus on the specificity of the tests.

Indexed as

CognitionFemaleGenome-Wide Association StudyHumansIntelligenceMaleNeuropsychological TestsPhenotypePolymorphism, Single NucleotideCognitive testsGeneral cognitive abilityGenetic specificityGenomic SEM

Identifiers

PMID39964619
PMCPMC11882725

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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.