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Analysis of protein-coding genetic variation in 60,706 humans
The case for selection at CCR5-Delta32
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
Methods for high-density admixture mapping of disease genes
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Genome-wide detection and characterization of positive selection in human populations
A second generation human haplotype map of over 3.1 million SNPs
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region