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Robust inference and correlates from genetic associations with personality

  • Estonian Biobank Research Team
  • , COGA Collaborators
  • , The Spit for Science Working Group
  • Department of Psychology
  • Michigan State University
  • Washington University St. Louis
  • Department of Biological Psychology
  • Vrije Universiteit Amsterdam
  • Amsterdam UMC
  • University of Tartu
  • Texas State University
  • Laboratoire de Sciences Cognitives et Psycholinguistique
  • University of Texas at Austin
  • Population Research Center
  • Department of Psychiatry
  • Massachusetts General Hospital
  • Psychiatric and Neurodevelopmental Genetics Unit
  • Harvard University
  • Broad Institute
  • School of Biological and Behavioral Sciences
  • Queen Mary University of London
  • University of Bristol
  • Yale University
  • University of California at San Diego
  • Institute of Psychology
  • University of Tartu
  • Department of Psychology
  • University of Warwick
  • Tallinn University
  • Department of Psychology
  • University of Edinburgh
  • McGill University
  • deCODE Genetics
  • Department of Psychology
  • University of Oslo
  • School of Psychology and Neuroscience
  • PsychGen Centre for Genetic Epidemiology and Mental Health
  • Norwegian Institute of Public Health
  • Psychiatric Genetic Epidemiology Group
  • Lovisenberg Diakonale Hospital
  • Centre for Fertility and Health
  • Centre for Research on Equality in Education
  • Department of Mental Health
  • Department of Psychiatry
  • Østfold Hospital
  • Department of Complex Trait Genetics
  • University of Groningen
  • Centre for Genomic and Experimental Medicine

Research output: Contribution to journal › Article › peer-review

Abstract

Personality traits describe stable differences in how people think, feel and behave, and how they interact with and experience their social and physical environments1,2. Many questions remain unanswered about associations between DNA and personality traits, such as their robustness, their generalizability and the biological and social pathways through which they act. Here we meta-analyse data across 46 cohorts comprising 611,037 to 1.14 million participants with European-like and African-like genomes for genome-wide association studies (GWAS) of the Big Five personality traits (extraversion, agreeableness, conscientiousness, neuroticism and openness to experience), and data from up to 50,725 participants for within-family GWAS. We identify 1,260 lead genetic variants associated with personality, including 824 novel variants3. Common genetic variants explain a moderate 4.8–9.3% of the variance in measures of each trait, and 9.3–13.3% among instruments with typical measurement reliability. Genetic associations with personality are highly consistent but not identical across geography, reporter (self versus close other), age group and measurement instrument, and we find minimal spousal assortment for personality in recent history. In contrast to many other social and behavioural traits4,5, within-family GWAS and polygenic index analyses indicate that genetic associations with personality are minimally confounded by the shared family environment. Polygenic prediction, genetic correlation and Mendelian randomization analyses indicate that personality traits have widespread, potentially causal associations with consequential behaviours and life outcomes. Overall, we find that the genetic architecture of personality is robustly generalizable, minimally confounded and widely relevant to human experience.

Original languageEnglish
JournalNature
Early online dateSept 2026
DOIs
Publication statusE-pub ahead of print - Sept 2026
Externally publishedYes

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