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Publications

Examining the role of common variants in rare neurodevelopmental conditions

Journal article

Huang QQ. et al, (2024), Nature

Substantial role of rare inherited variation in individuals with developmental disorders

Preprint

Samocha KE. et al, (2024)

Genome-wide association meta-analysis of age at onset of walking

Preprint

Gui A. 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)

Investigating the role of commoncis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders

Preprint

Wigdor EM. 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 Genomics, 2

The female protective effect against autism spectrum disorder

Journal article

Wigdor EM. et al, (2022), Cell Genomics, 2, 100134 - 100134

The female protective effect against autism spectrum disorder

Preprint

Wigdor EM. et al, (2021)

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)

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Journal article

Satterstrom FK. et al, (2019), Nature Neuroscience, 22, 1961 - 1965

Paternal-age-related de novo mutations and risk for five disorders

Journal article

Taylor JL. et al, (2019), Nature Communications, 10

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

Journal article

Weiner DJ. et al, (2017), Nat Genet, 49, 978 - 985