Author: Laura J. Scott

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Preprints

Genomewide association study identifies 30 loci associated with bipolar disorder

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A reference panel of 64,976 haplotypes for genotype imputation

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Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Influence of genetic variants on gene expression in human pancreatic islets – implications for type 2 diabetes

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Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

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Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores

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Interactions between genetic variation and cellular environment in skeletal muscle gene expression

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A powerful subset-based gene-set analysis method identifies novel associations and improves interpretation in UK Biobank

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