David A. Hinds

Genetics · 2005–2019

A researcher in the Science corpus: 18 papers; trusts 7 researchers and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

Whom David A. Hinds trusts overall

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

  1. Bryan N. Howie
  2. Brian L. Browning
  3. Jonathan Marchini
  4. Sharon R. Browning

Who trusts David A. Hinds overall

  1. Frank Steemers
  2. Graham P. McVicker
  3. Jonathan Marchini
  4. Kevin L. Gunderson
  5. Reedik Mägi
  6. Kenneth L. McNally

Papers from David A. Hinds's perspective

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

  1. Defining the role of common variation in the genomic and biological architecture of adult human height
  2. Genotype Imputation (Annual review of genomics and human genetics (Print))
  3. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. (American Journal of Human Genetics)
  4. Generating samples under a Wright-Fisher neutral model of genetic variation (Bioinform.)
  5. Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
  6. Genome-wide genetic data on ~500,000 UK Biobank participants (bioRxiv)
  7. PLINK: a tool set for whole-genome association and population-based linkage analyses.
  8. Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics (PLoS Genetics)
  9. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
  10. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (The Lancet)

Their papers