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Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.
New England Journal of Medicine. Feb 2008;2008 Feb 28;358(9):956-61.

Genome-wide detection and characterization of positive selection in human populations .
Nature. 2007 Oct 18;449(7164):913-8.

A second generation human haplotype map of over 3.1 million SNPs.
Nature. 2007 Oct 18;449(7164):851-61.

The genomic landscapes of human breast and colorectal cancers.
Science. 2007 Oct 11; [Epub ahead of print]

New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
Nature Genetics. 2007 Sep;39(9):1045-51.

Genome-wide association study identifies novel breast cancer susceptibility loci
Nature. 28 June 2007;447:1087-1093.

A Common Allele on Chromosome 9 Associated with Coronary Heart Disease
Science. EPub May 3, 2007.

Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs.
Human Molecular Genetics. 2007 Jan 1;16(1):36-49. Epub 2006 Nov 29

Novel genes identified in a high-density genome wide association study for nicotine dependence.
Human Molecular Genetics. 2007 Jan 1;16(1):24-35. Epub 2006 Dec 7.

Design and validation of a population-based definition of the metabolic syndrome.
Diabetes Care. 2006 Nov;29(11):2420-6.

Perspectives on development of a combination pharmacogenomic diagnostic and drug product.
Pharmacogenomics. 2006 Oct;7(7):1045-9. Review.

A genomewide single-nucleotide-polymorphism panel with high ancestry information for African American admixture mapping.
American Journal Human Genetics. 2007 Jun;80(6):1014-23.
2006 Aug 15

Allele-specific KRT1 expression is a complex trait.
PLoS Genetics. 2006 Jun;2(6):e93. Epub 2006 Jun 9.

Analysis of allelic differential expression in human white blood cells. Genome Research.arch. 2006 Mar;16(3):331-9. Epub 2006 Feb 8.

Common deletions and SNPs are in linkage disequilibrium in the human genome.
Nature Genetics. 2006 Jan;38(1):82-5. Epub 2005 Dec 4.

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles.
Genome Research.arch. 2005 November; 15(11): 1511-1518.

XA haplotype map of the human genome.
Nature. 2005 October 27; 437: 1299-1320.

High-Resolution Whole-Genome Association Study of Parkinson Disease (109k PDF full text)
American Journal of Human Genetics. 2005;77:685–693.

Fine-scale recombination patterns differ between chimpanzees and humans.
Nature Genetics. 2005 Apr;37(4):429-34. Epub 2005 Feb 18.

Whole Genome Patterns of Common DNA Variation in Three Human Populations
Science. 2005 Feb 18;307(5712):1072-1079.
 [Genotype Browser]

Application of Pooled Genotyping to Scan Candidate Regions for Association with HDL Cholesterol Levels
Human Genomics. 2004 Oct;1(6).
[Supplemental Tables]

Segmental Phylogenetic Relationships of Inbred Mouse Strains Revealed by Fine-Scale Analysis of Sequence Variation Across 4.6 Mb of Mouse Genome.
Genome Research.arch. 2004 Aug;14(8):1493-1500.

VISTA: Computational Tools for Comparative Genomics.
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W273-9.

Noncoding sequences conserved in a limited number of mammals
in the SIM2 interval are frequently functional.
Genome Research.arch. 2004 Mar;14(3):367-72.

Matching strategies for genetic association studies in structured populations.
American Journal of Human Genetics. 2004 Feb;74(2):317-25.

Multi-species sequence comparison: the next frontier in genome annotation.
Genome Biology. 2003, 4:122.

Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates.
Genome Research. 2003 Mar;13(3):341-6.

Cross-species sequence comparisons: a review of methods and available resources.
Genome Research. 2003 Jan;13(1):1-12. Review.

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
Science. 2001 Nov 23;294(5547):1719-23.

Evolutionarily conserved sequences on human chromosome 21.
Genome Research. 2001 Oct;11(10):1651-9.