Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease
Genetic Variants Associated with von Willebrand Factor Levels in Healthy Men and Women Identified Using the HumanCVD BeadChip
Selection and Mutation for α Thalassemia in Nonmalarial and Malarial Environments
Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population
Identification and In Silico Analysis of Novel von Hippel-Lindau ( VHL ) Gene Variants from a Large Population
Diversification of the ADH1B Gene during Expansion of Modern Humans
Ancestral Heterogeneity in a Biethnic Stroke Population
Successful Aging Shows Linkage to Chromosomes 6, 7, and 14 in the Amish
Wide Disparity in Genetic Admixture Among Mexican Americans from San Antonio, TX
Selecting SNPs to Identify Ancestry
A Report of the First Biennial Meeting on Capita Selecta in Complex Disease Analysis (CSCDA2010), Leuven, Belgium, August 25–27, 2010