Publications
Identifying Personal Genomes by Surname Inference.
Science. 339(6117), 321-324.
(2013). Increasing the Power of Association Studies by Imputation-Based Sparse Tag SNP Selection.
Communications in Information and Systems. 9(3), 269-282.
(2009). Inference and Analysis of Haplotypes from Combined Genotyping Studies Deposited in dbSNP.
Genome Research. 15(11), 1594-1600.
(2005). Inhibition of Activated Pericentromeric SINE/Alu Repeat Transcription in Senescent Human Adult Stem Cells Reinstates Self-Renewal.
Cell Cycle. 10(17), 3016-3030.
(2011). Joint Analysis of Multiple Metagenomic Samples.
PLoS Computational Biology. 8(2),
(2012). LAMP: Local Ancestry in adMixed Populations.
American Journal of Human Genetics. 82(2), 290-303.
(2008). Leveraging Genetic Variability Across Populations for the Identification of Causal Variants.
The American Journal of Human Genetics. 86(1), 23-33.
(2010). Leveraging the HapMap Correlation Structure in Association Studies.
American Journal of Human Genetics. 80, 683-691.
(2007). Maximizing Power in Association Studies.
Nature Biotechnology. 27(3), 255-256.
(2009). The Minimum-Entropy Set Cover Problem.
Theoretical Computer Science. 348(2), 240-250.
(2005). miRNAkey: A Software for microRNA Deep Sequencing Analysis.
Bioinformatics. 26(20), 2615-2616.
(2010). A Model-Based Approach for Analysis of Spatial Structure in Genetic Data.
Nature Genetics. 44, 725-731.
(2012). A Model-Based Approach for Analysis of Spatial Structure in Genetic Data.
Nature Genetics. 44, 725-731.
(2012). A Note on Optimally Phasing Long Genomic Regions Using Local Haplotype Predictions.
Journal of Bioinformatics and Computational Biology. 4(3), 639-647.
(2006). Novel Associations for Coronary Artery Disease Derived from Genome Wide Association Studies Are Not Associated with Increased Carotid Intima-Media Thickness.....
Atherosclerosis. 219(2), 684-689.
(2011). Pedigree Reconstruction Using Identity by Descent.
Journal of Computational Biology. 18(11), 1481-1493.
(2011). Performance Aspects of Distributed Caches Using TTL-Based Consistency.
Theoretical Computer Science. 331(1), 73-96.
(2005). Polymorphisms in the Estrogen Receptor 1 and Vitamin C and Matrix Metalloproteinase Gene Families Are Associated with Susceptibility to Lymphoma.
PLoS ONE. 3(7),
(2008).
(2010). Probabilistic Inference of Viral Quasispecies Subject to Recombination.
Journal of Computational Biology. 20(2), 113-123.
(2013). A Randomization Test for Controlling Population Stratification in Whole-Genome Association Studies.
American Journal of Human Genetics. 81(5), 895-905.
(2007). A Search for Overlapping Genetic Susceptibility Loci Between Non-Hodgkin Lymphoma and Autoimmune Diseases.
Genomics. 98(1), 9-14.
(2011). SNP Imputation in Association Studies.
Nature Biotechnology. 27(4), 349-351.
(2009). Using DNA Pools for Genotyping Trios.
Nucleic Acids Research. 34(19),
(2006). Whole-Genome Patterns of Common DNA Variation in Three Human Populations.
Science. 307(5712), 1072-1079.
(2005).