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Author: Manuel A. Rivas

Rankings

  • All-time downloads: 38,434 (rank: 1,047 out of 393,396)
  • Categories:
    • bioinformatics: 5,151 (rank: 1,847 out of 33,499)
    • epidemiology: 1,175 (rank: 1,130 (tie) out of 9,544)
    • genetics: 27,047 (rank: 193 out of 36,121)
    • genomics: 5,061 (rank: 3,650 (tie) out of 41,868)

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Preprints

Genetics of 38 blood and urine biomarkers in the UK Biobank

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Transcriptome-wide association studies: opportunities and challenges

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A Fast and Scalable Framework for Large-scale and Ultrahigh-dimensional Sparse Regression with Application to the UK Biobank

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Medical relevance of protein-truncating variants across 337,208 individuals in the UK Biobank study

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GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background

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Bayesian model comparison for rare variant association studies of multiple phenotypes

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Landscape of X chromosome inactivation across human tissues

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Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight novel adipocyte biology

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Phenome-wide burden of copy number variation in UK Biobank

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

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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

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FasTag: automatic text classification of unstructured medical narratives

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Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics

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Large-scale phenome-wide association study of PCSK9 loss-of-function variants demonstrates protection against ischemic stroke

genetics more details view paper
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Sex-specific genetic effects across biomarkers

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Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

genetics more details view paper
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Polygenic risk modeling with latent trait-related genetic components

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Mosaic Mutations in Blood DNA Sequence Are Associated with Solid Tumor Cancers

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Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide

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Assessing digital phenotyping to enhance genetic studies of human diseases

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Constraint-based analysis for causal discovery in population-based biobanks

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Large-Scale Sparse Regression for Multiple Responses with Applications to UK Biobank

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Reported CCR5-∆32 deviation from Hardy-Weinberg equilibrium is explained by poor genotyping of rs62625034

genetics more details view paper
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Pervasive additive and non-additive effects within the HLA region contribute to disease risk in the UK Biobank

genetics more details view paper
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Fast Sparse-Group Lasso Method for Multi-response Cox Model with Applications to UK Biobank

bioinformatics more details view paper
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