Chantal Kemner

Nature Genetics · 2007–2015

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

Papers from Chantal Kemner's perspective

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

  1. Mixed-effects modeling with crossed random effects for subjects and items
  2. R: A language and environment for statistical computing.
  3. A Kenward-Roger approximation and parametric bootstrap methods for tests in linear mixed models: The R Package pbkrtest
  4. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
  5. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome (Nature Genetics)
  6. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (Nature Genetics)
  7. Global variation in copy number in the human genome (Nature)
  8. Principal components analysis corrects for stratification in genome-wide association studies
  9. Diagnostic genome profiling in mental retardation. (American Journal of Human Genetics)
  10. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. (American Journal of Human Genetics)

Their papers