David R Cox

发表

High-resolution whole-genome association study of Parkinson disease.

Mariza de Andrade, Demetrius M Maraganore, D. Cox, 2005, American journal of human genetics.

A meta-analysis of genome-wide linkage scans for hypertension: the National Heart, Lung and Blood Institute Family Blood Pressure Program.

Eric Boerwinkle, Stephen T Turner, Steven C Hunt, 2003, American journal of hypertension.

High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology.

Henk Neefs, Michael Olivier, Scott Law, 2002, Nucleic acids research.

Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

D. Cox, K. Frazer, D. Ballinger, 2004, Human Genomics.

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

Stefan Johansson, Jason Flannick, Christopher J O'Donnell, 2013, Nature Genetics.

Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates.

D. Cox, N. Patil, K. Frazer, 2003, Genome research.

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Thomas Meitinger, Pierre Fontanillas, Stefan Johansson, 2014, Nature Genetics.

Analysis of allelic differential expression in human white blood cells.

D. Cox, K. Frazer, D. Ballinger, 2006, Genome research.

A genomewide association study of skin pigmentation in a South Asian population.

D. Cox, R. Stokowski, David Cox, 2007, American journal of human genetics.

Allele-Specific KRT1 Expression Is a Complex Trait

D. Cox, K. Frazer, H. Tao, 2006, PLoS genetics.