Search results (18)
« Back to PublicationsGenome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry.
Journal article
Gui A. et al, (2025), Nat Hum Behav, 9, 1470 - 1487
Examining the role of common variants in rare neurodevelopmental conditions.
Journal article
Huang QQ. et al, (2024), Nature, 636, 404 - 411
Substantial role of rare inherited variation in individuals with developmental disorders
Preprint
Samocha KE. et al, (2024)
Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions
Preprint
Huang QQ. et al, (2024)
AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms.
Preprint
Ljungdahl A. et al, (2023)
Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populations
Preprint
Chundru VK. et al, (2023)
Analysis of genetic dominance in the UK Biobank.
Journal article
Palmer DS. et al, (2023), Science, 379, 1341 - 1348
The genetics of cortical organisation and development: a study of 2,347 neuroimaging phenotypes
Preprint
Warrier V. et al, (2022)
The female protective effect against autism spectrum disorder.
Conference paper
Wigdor EM. et al, (2022), Cell Genom, 2
The female protective effect against autism spectrum disorder
Journal article
Wigdor EM. et al, (2022), Cell Genomics, 2, 100134 - 100134
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
Journal article
Vuckovic D. et al, (2020), Cell, 182, 1214 - 1231.e11
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Journal article
Vuckovic D. et al, (2020)