Author: Elise B Robinson

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Preprints

Partitioning gene-mediated disease heritability without eQTLs

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An Atlas of Genetic Correlations across Human Diseases and Traits

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Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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Common risk variants identified in autism spectrum disorder

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

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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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ASD and ADHD have a similar burden of rare protein-truncating variants

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

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Gene family information facilitates variant interpretation and identification of disease-associated genes

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Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples

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

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The female protective effect against autism spectrum disorder

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Higher genetic risk of schizophrenia is associated with lower cognitive performance in healthy individuals

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Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups.

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