Author: Lili Milani

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Preprints

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

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Genomewide association study identifies 30 loci associated with bipolar disorder

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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Genome-wide association study identifies 48 common genetic variants associated with handedness

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Cell specific eQTL analysis without sorting cells

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Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Lifelong genetically lowered sclerostin and risk of cardiovascular disease.

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An epigenome-wide association study of educational attainment (n = 10,767)

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Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

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An interaction map of circulating metabolites, immune gene networks and their genetic regulation

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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

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Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing

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Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

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Genome-wide study identifies association between HLA-B*55:01 and penicillin allergy

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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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