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Author: Eleftheria Zeggini

Rankings

  • All-time downloads: 35,901 (rank: 3,328 out of 513,392)
  • Categories:
    • bioinformatics: 198 (rank: 32,689 (tie) out of 37,058)
    • genetic and genomic medicine: 706 (rank: 1,441 (tie) out of 6,816)
    • genetics: 26,903 (rank: 211 out of 38,777)
    • genomics: 6,293 (rank: 3,066 (tie) out of 45,811)
    • systems biology: 1,801 (rank: 1,900 (tie) out of 12,917)

Downloads per author, site-wide

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

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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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Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank

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New genetic signals for lung function highlight pathways and pleiotropy, and chronic obstructive pulmonary disease associations across multiple ancestries

genomics more details view paper
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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The genetic architecture of osteoarthritis: insights from UK Biobank

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

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Integrative epigenomics, transcriptomics and proteomics of patient chondrocytes reveal genes and pathways involved in osteoarthritis

systems biology more details view paper
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Whole genome sequencing analysis of the cardiometabolic proteome

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Decoding the genomic basis of osteoarthritis

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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

genetics more details view paper
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Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

genomics more details view paper
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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Osteocyte Transcriptome Mapping Identifies a Molecular Landscape Controlling Skeletal Homeostasis and Susceptibility to Skeletal Disease

systems biology more details view paper
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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

genetic and genomic medicine more details view paper
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The transferability of lipid loci across African, Asian and European cohorts

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Accelerating functional gene discovery in osteoarthritis

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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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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The Genetic Epidemiology of Developmental Dysplasia of the Hip: A Genome-Wide Association Study Harnessing National Clinical Audit Data

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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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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The influence of rare variants in circulating metabolic biomarkers

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Genome-wide association and functional analyses identify CASC20 and KIF26B as target loci in heterotopic ossification

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Maternal and fetal genetic contribution to gestational weight gain

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

bioinformatics more details view paper
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The transcriptome of regenerating zebrafish scales identifies genes involved in human bone disease

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