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Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation., , , , , , and . PLoS Comput. Biol., (2012)Analysis of case-control association studies with known risk variants., , , , , , , , , and 6 other author(s). Bioinform., 28 (13): 1729-1737 (2012)Transferability of Tag SNPs to Capture Common Genetic Variation in DNA Repair Genes Across Multiple Populations., , , , and . Pacific Symposium on Biocomputing, page 478-486. World Scientific, (2006)A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population, , , , , , , , , and 168 other author(s). Nature genetics, 42 (10): 885–892 (2010)Human Genome Sequence Variation and the Inherited Basis of Common Disease.. RECOMB, volume 3500 of Lecture Notes in Computer Science, page 601-602. Springer, (2005)Characterization of single-nucleotide polymorhisms in coding regions of human genes, , , , , , , , , and 7 other author(s). Nature Genetics, 22 (3): 231--238 (1999)Copy number variation: New insights in genome diversity, , , , , , , , , and 3 other author(s). Genome Research, (2006)