Francisco M. De La Vega

发表

A high-density admixture map for disease gene discovery in african americans.

Scott M. Williams, Jason H. Moore, D. Altshuler, 2004, American journal of human genetics.

An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels

Gabriel Silva, Francisco M De La Vega, Rick Kittles, 2009, BMC Genetics.

Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples

Francisco M De La Vega, Kenneth K Kidd, Judith R Kidd, 2011, Investigative Genetics.

The SNPlex genotyping system: a flexible and scalable platform for SNP genotyping.

Nicolas Peyret, Francisco M De La Vega, K. Hayashibara, 2005, Journal of biomolecular techniques : JBT.

Identifying Selected Regions from Heterozygosity and Divergence Using a Light-Coverage Genomic Dataset from Two Human Populations

Francisco M. De La Vega, Stephen J. O'Brien, S. O’Brien, 2008, PloS one.

Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America

Gabriel Silva, Francisco M De La Vega, Rick Kittles, 2009, Human mutation.

The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern.

Hadar I. Isaac, Bjarni V. Halldórsson, B. Halldórsson, 2005, Genome research.

Optimal Selection of SNP Markers for Disease Association Studies

Sorin Istrail, Francisco M. De La Vega, Bjarni V. Halldórsson, 2005, Human Heredity.

Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies.

Bjarni V. Halldórsson, V. Bafna, S. Istrail, 2004, Genome research.

A second-generation combined linkage physical map of the human genome.

Francisco M De La Vega, Fiona C L Hyland, Steven Buyske, 2007, Genome research.

Assessment of two flexible and compatible SNP genotyping platforms: TaqMan SNP Genotyping Assays and the SNPlex Genotyping System.

M. Rhodes, F. M. De La Vega, K. Lazaruk, 2005, Mutation research.

Power and Sample Size Calculations for Genetic Case/Control Studies Using Gene-Centric SNP Maps: Application to Human Chromosomes 6, 21, and 22 in Three Populations

Derek Gordon, Charles Scafe, Hadar I. Isaac, 2005, Human Heredity.

Patterns of linkage disequilibrium in the MHC region on human chromosome 6p

J. Hampe, M. Krawczak, T. Lu, 2004, Human Genetics.

Mapping Genes for Common Diseases: The Case for Genetic (LD) Maps

F. M. De La Vega, A. Collins, W. Lau, 2004, Human Heredity.

New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies.

Francisco M De La Vega, F. M. De La Vega, J. Ziegle, 2002, BioTechniques.