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Author: Stephen Burgess

  • ORCiD: http://orcid.org/0000-0001-5365-8760
  • Most recently observed institution: MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK.

Rankings

  • All-time downloads: 28,925 (rank: 1,518 out of 380,283)
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    • bioinformatics: 401 (rank: 21,552 (tie) out of 32,581)
    • epidemiology: 8,464 (rank: 11 out of 9,542)
    • genetics: 15,016 (rank: 724 out of 35,172)
    • genomics: 5,044 (rank: 3,470 (tie) out of 40,588)

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Preprints

Consequences Of Natural Perturbations In The Human Plasma Proteome

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MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations

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Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases

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A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits

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Selecting causal risk factors from high-throughput experiments using multivariable Mendelian randomization

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Cross-platform genetic discovery of small molecule products of metabolism and application to clinical outcomes

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A Comparison Of Robust Mendelian Randomization Methods Using Summary Data

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Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases

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A robust and efficient method for Mendelian randomization with hundreds of genetic variants: unravelling mechanisms linking HDL-cholesterol and coronary heart disease

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Use of polygenic risk scores and other molecular markers to enhance cardiovascular risk prediction: Prospective cohort study and modelling analysis

genomics more details view paper
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Power calculator for instrumental variable analysis in pharmacoepidemiology

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Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD

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Birthweight, Type 2 Diabetes and Cardiovascular Disease: Addressing the Barker Hypothesis with Mendelian randomization

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Disentangling genetically confounded polygenic associations between Attention-Deficit/Hyperactivity Disorder, literacy and language

genetics more details view paper
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Factorial Mendelian randomization: using genetic variants to assess interactions

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Dissecting causal pathways using Mendelian randomization with summarized genetic data: application to age at menarche and risk of breast cancer

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Genetic determinants of lipids and cardiovascular disease outcomes: a wide-angled Mendelian randomization investigation

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Genetic Analyses of Blood Cell Structure for Biological and Pharmacological Inference

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What explains the effect of education on cardiovascular disease? Applying Mendelian randomization to identify the consequences of education inequality

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Improving on a modal-based estimation method: model averaging for consistent and efficient estimation in Mendelian randomization when a plurality of candidate instruments are valid

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Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohort

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MR-Clust: Clustering of genetic variants in Mendelian randomization with similar causal estimates

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Bayesian variable selection with a pleiotropic loss function in Mendelian randomization

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Urinary biomarkers and cardiovascular outcomes in the UK Biobank: observational and Mendelian randomization analyses

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Semiparametric methods for estimation of a non-linear exposure-outcome relationship using instrumental variables with application to Mendelian randomization

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Body size and composition and site-specific cancers in UK Biobank: a Mendelian randomisation study

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The association between low-density lipoprotein cholesterol predicted by HMGCR genetic variants and breast cancer risk may be mediated by body mass index

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The association between weight at birth and breast cancer risk revisited using Mendelian randomisation

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Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans

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