David M. Evans

Genetics · Nature Genetics · 2008–2018

A researcher in the Science corpus: 11 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Whom David M. Evans trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. Subir Ghosh
  2. Bryan N. Howie
  3. Pan Du

Papers from David M. Evans's perspective

Ordered by how strongly the researchers David M. Evans trusts endorse each paper. Same corpus, a different order for every researcher.

  1. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
  2. Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
  3. Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
  4. Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
  5. A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
  6. Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Genetic Epidemiology)
  7. Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology (Statistics in Medicine)
  8. Efficient Design for Mendelian Randomization Studies: Subsample and 2-Sample Instrumental Variable Estimators (American Journal of Epidemiology)
  9. Major Lipids, Apolipoproteins, and Risk of Vascular Disease
  10. Genome-wide genetic data on ~500,000 UK Biobank participants (bioRxiv)

Their papers