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Genome-wide analysis of social behaviour across social domains, reporters and developmental stages: a meta-regression approach

Lucía de Hoyos, Fenja Schlag, Sanjeevan Jahagirdar, Elizabeth C. Corfield, Andrea G. Allegrini, D. Admiraal, E. De Zeeuw, Ilja Maria Nolte, Natalia Llonga, Alexander Neumann, K. Lange, Simone van den Bedem, Ebba Du Rietz, E. Motazedi, Else Eising, Nicole Ying Ting Ng, Teemu Palviainen, Carol A. Wang, E. Thiering, Sofia Scatolin, P. Choudhary, N. Vilor-Tejedor, Z. Liao, S. Alemany, Casper‐Emil Tingskov Pedersen, N. Fernandez-Jimenez, M. Campbell, P. Girchenko, Eli Barthome, L. Caitlin Martin, Hanna Seelemeyer, Afsheen Kumar, Aimée Jeanne, Tarunveer S. Ahluwalia, Melissa H. Black, Jan K. Buitelaar, Simon E. Fisher, Anni Heiskala, María Hernández‐Lorca, Vincent W. V. Jaddoe, Marjo‐Riitta Järvelin, Sheri‐Michelle Koopowitz, Marilyn T. Lake, Paul Lichtenstein, Sabrina Llop, Mannan Luo, Anni Malmberg, Sergi Marí, Albertine J. Oldehinkel, Zdenka Pausová and 10 more

Peer-reviewed journal

In the authors' words

Abstract Social behaviour is a heritable trait linked to well-being and mental health, yet it varies across social context, including social domains, informants and development, which may shape its underlying genomic architecture. Here, we conducted a genome-wide meta-regression meta-analysis of social behaviour from infancy to early adulthood, studying ~500,000 repeated measures in European-ancestry cohorts ( N = 73,321). We modelled heterogeneity in single-variant associations across social domains (low prosocial behaviour and peer/social difficulties), multiple informants (parents, teachers and self-reports) and ages (2–29 years), identifying 6 associated loci, including variation within CADM2 ( P = 2.51 × 10 −9 ). Single nucleotide polymorphism-based heritability ranged from 2% to 7%, and the genetic architecture comprised 4 factors reflecting differences in either social domains or informants. Polygenic scores ( N = 16,305) accurately predicted contextual variation in independent cohorts, with some cross-ancestry transferability. Context-specific patterns of genetic correlations, particularly when estimating the developmental onset of associations, offer opportunities to disentangle shared trajectories linking social behaviour with later-life and mental health outcomes.

Main resultLimitation the authors admit

Appeared: Wednesday, September 23. Nature Human Behaviour. Peer-reviewed journal.

DOI: 10.1038/s41562-026-02551-z