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Publications

Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions

Huang QQ. et al, (2024)

AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms.

Ljungdahl A. et al, (2023)

Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populations

Chundru VK. et al, (2023)

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

Wigdor EM. et al, (2023)

Analysis of genetic dominance in the UK Biobank

Palmer DS. et al, (2023), Science, 379, 1341 - 1348

The genetics of cortical organisation and development: a study of 2,347 neuroimaging phenotypes

Warrier V. et al, (2022)

The female protective effect against autism spectrum disorder

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

The female protective effect against autism spectrum disorder

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

The female protective effect against autism spectrum disorder

Wigdor EM. et al, (2021)

The Polygenic and Monogenic Basis of Blood Traits and Diseases.

Vuckovic D. et al, (2020), Cell, 182, 1214 - 1231.e11

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Vuckovic D. et al, (2020)

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

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

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

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.

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

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