Abstract
Age at onset of walking is an important early childhood milestone which is used clinically and in public health screening. In this genome-wide association study meta-analysis of age at onset of walking (N = 70,560 European-ancestry infants), we identified 11 independent genome-wide significant loci. SNP-based heritability was 24.13% (95% confidence intervals = 21.86–26.40) with ~11,900 variants accounting for about 90% of it, suggesting high polygenicity. One of these loci, in gene RBL2, co-localized with an expression quantitative trait locus (eQTL) in the brain. Age at onset of walking (in months) was negatively genetically correlated with ADHD and body-mass index, and positively genetically correlated with brain gyrification in both infant and adult brains. The polygenic score showed out-of-sample prediction of 3–5.6%, confirmed as largely due to direct effects in sib-pair analyses, and was separately associated with volume of neonatal brain structures involved in motor control. This study offers biological insights into a key behavioural marker of neurodevelopment.
| Original language | English |
|---|---|
| Pages (from-to) | 1470-1487 |
| Number of pages | 18 |
| Journal | Nature Human Behaviour |
| Volume | 9 |
| Issue number | 7 |
| Early online date | May 2025 |
| DOIs | |
| Publication status | Published - Jul 2025 |
| Externally published | Yes |
Keywords
- Child cohort
- Cohort profile
- Enrichment
- Genetic correlation
- Heritability
- Milestones
- Netherlands twin register
- Norwegian mother
- Set
- Tool