Andrew G. Clark

TL;DR: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and has reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-generation sequencing, deep exome sequencing, and dense microarray genotyping.

TL;DR: Comparative genomic analysis indicates vertebrate expansions of genes associated with neuronal function, with tissue-specific developmental regulation, and with the hemostasis and immune systems are indicated.

TL;DR: This paper examined potential sources of missing heritability and proposed research strategies, including and extending beyond current genome-wide association approaches, to illuminate the genetics of complex diseases and enhance its potential to enable effective disease prevention or treatment.

TL;DR: Genetic and Phenotypic Variation Organisation of Genetic Variation Random Genetic Drift Mutation and the Neutral Theory Darwinian Selection Inbreeding, Population Subdivision, and Migration Molecular Population Genetics Evolutionary Quantitative Genetics Population Genomics Human Population Genetics