Author: George Dedoussis

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Preprints

A reference panel of 64,976 haplotypes for genotype imputation

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Very low depth whole genome sequencing in complex trait association studies

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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

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Whole genome sequencing analysis of the cardiometabolic proteome

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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

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Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

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The transferability of lipid loci across African, Asian and European cohorts

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume

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Mendelian Randomization analysis reveals a causal influence of circulating sclerostin levels on bone mineral density and fractures

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Maternal and fetal genetic contribution to gestational weight gain

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Population-wide copy number variation calling using variant call format files from 6,898 individuals

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