David Clayton

Genetics · 2001–2013

A researcher in the Science corpus: 10 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

Whom David Clayton trusts overall

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

  1. J. K. Pritchard

Who trusts David Clayton overall

  1. J. Wakefield

Papers from David Clayton's perspective

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

  1. High-resolution haplotype structure in the human genome (Nature Genetics)
  2. Haplotype tagging for the identification of common disease genes (Nature Genetics)
  3. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
  4. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (Nature Genetics)
  5. Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease (Nature Genetics)
  6. On the allelic spectrum of human disease. (Trends in Genetics)
  7. Genome-wide association studies for complex traits: consensus, uncertainty and challenges (Nature reviews genetics)
  8. Complement Factor H Polymorphism and Age-Related Macular Degeneration (Science)
  9. Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium. (American Journal of Human Genetics)
  10. Linkage disequilibrium in humans: models and data. (American Journal of Human Genetics)

Their papers