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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/11899| Title: | Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry | Authors: | Gui, A.;Hollowell, A.;Wigdor, E. M.;Morgan, M. J.;Hannigan, L. J.;Corfield, E. C.;Odintsova, V.;Hottenga, J. J.;Wong, A.;Pool, R.;Cullen, H.;Wilson, S. ;Warrier, V.;Eilertsen, E. M.;Andreassen, O. A.;Middeldorp, C. M. ;St Pourcain, B.;Bartels, M.;Boomsma, D. I.;Hartman, C. A.;Robinson, E. B.;Arichi, T.;Edwards, A. D.;Johnson, M. H.;Dudbridge, F.;Sanders, S. J.;Havdahl, A.;Ronald, A. | Issue Date: | 2025 | Source: | Nat Hum Behav, 2025 (9) 7 p.1470-1487 | Pages: | 1470-1487 | Journal Title: | Nat Hum Behav | 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. | DOI: | 10.1038/s41562-025-02145-1 |
| Appears in Sites: | Children's Health Queensland Publications Queensland Health Publications |
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