Publications

Found 82 results
Author Title [ Type(Desc)] Year
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Journal Article
Gymrek, M., McGuire A. L., Golan D., Halperin E., & Erlich Y. (2013).  Identifying Personal Genomes by Surname Inference. Science. 339(6117), 321-324.
Davidovich, O.., Kimmel G., Halperin E., & Shamir R. (2009).  Increasing the Power of Association Studies by Imputation-Based Sparse Tag SNP Selection. Communications in Information and Systems. 9(3), 269-282.
Zaitlen, N., Kang H. Min, Feolo M. L., Sherry S. T., Halperin E., & Eskin E. (2005).  Inference and Analysis of Haplotypes from Combined Genotyping Studies Deposited in dbSNP. Genome Research. 15(11), 1594-1600.
Wang, J., Geesman G. J., Hostikka S. Liisa, Atallah M., Blackwell B., Lee E., et al. (2011).  Inhibition of Activated Pericentromeric SINE/Alu Repeat Transcription in Senescent Human Adult Stem Cells Reinstates Self-Renewal. Cell Cycle. 10(17), 3016-3030.
Baran, Y., & Halperin E. (2012).  Joint Analysis of Multiple Metagenomic Samples. PLoS Computational Biology. 8(2), 
Sankararaman, S., Sridhar S., Kimmel G., & Halperin E. (2008).  LAMP: Local Ancestry in adMixed Populations. American Journal of Human Genetics. 82(2), 290-303.
Zaitlen, N., Pasaniuc B., Gur T., Ziv E., & Halperin E. (2010).  Leveraging Genetic Variability Across Populations for the Identification of Causal Variants. The American Journal of Human Genetics. 86(1), 23-33.
Zaitlen, N., Kang H. Min, Eskin E., & Halperin E. (2007).  Leveraging the HapMap Correlation Structure in Association Studies. American Journal of Human Genetics. 80, 683-691.
Halperin, E., & Stephan D. A. (2009).  Maximizing Power in Association Studies. Nature Biotechnology. 27(3), 255-256.
Halperin, E., & Karp R. M. (2005).  The Minimum-Entropy Set Cover Problem. Theoretical Computer Science. 348(2), 240-250.
Ronen, R.., Gan I.., Modai S.., Sukacheov A.., Dror G.., Halperin E., et al. (2010).  miRNAkey: A Software for microRNA Deep Sequencing Analysis. Bioinformatics. 26(20), 2615-2616.
Yang, W-Y., Novembre J., Eskin E., & Halperin E. (2012).  A Model-Based Approach for Analysis of Spatial Structure in Genetic Data. Nature Genetics. 44, 725-731.
Yang, W-Y., Novembre J., Eskin E., & Halperin E. (2012).  A Model-Based Approach for Analysis of Spatial Structure in Genetic Data. Nature Genetics. 44, 725-731.
Eskin, E., Halperin E., & Sharan R. (2006).  A Note on Optimally Phasing Long Genomic Regions Using Local Haplotype Predictions. Journal of Bioinformatics and Computational Biology. 4(3), 639-647.
Conde, L., Bevan S.., Sitzer M.., Klopp N.., Illig T.., Thiery J.., et al. (2011).  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.
Kirkpatrick, B., Li S. Cheng, Karp R. M., & Halperin E. (2011).  Pedigree Reconstruction Using Identity by Descent. Journal of Computational Biology. 18(11), 1481-1493.
Cohen, E., Halperin E., & Kaplan H.. (2005).  Performance Aspects of Distributed Caches Using TTL-Based Consistency. Theoretical Computer Science. 331(1), 73-96.
Skibola, C. F., Bracci P. M., Halperin E., Nieters A., Hubbard A., Paynter R. A., et al. (2008).  Polymorphisms in the Estrogen Receptor 1 and Vitamin C and Matrix Metalloproteinase Gene Families Are Associated with Susceptibility to Lymphoma. PLoS ONE. 3(7), 
Padhukasahasram, B.., Halperin E., Wessel J.., Thomas D.. J., Silver E.., Trumbower H.., et al. (2010).  Presymptomatic Risk Assessment for Chronic Non-Communicable Diseases. PLoS ONE. 5,
Töpfer, A., Zagordi O., Prabhakaran S., Roth V., Halperin E., & Beerenwinkel N. (2013).  Probabilistic Inference of Viral Quasispecies Subject to Recombination. Journal of Computational Biology. 20(2), 113-123.
Kimmel, G., Jordan M. I., Halperin E., Shamir R., & Karp R. M. (2007).  A Randomization Test for Controlling Population Stratification in Whole-Genome Association Studies. American Journal of Human Genetics. 81(5), 895-905.
Conde, L., Bracci P. M., Halperin E., & Skibola C. F. (2011).  A Search for Overlapping Genetic Susceptibility Loci Between Non-Hodgkin Lymphoma and Autoimmune Diseases. Genomics. 98(1), 9-14.
Halperin, E., & Stephan D. A. (2009).  SNP Imputation in Association Studies. Nature Biotechnology. 27(4), 349-351.
Beckman, K.. B., Abel K.. A., Braun A.., & Halperin E. (2006).  Using DNA Pools for Genotyping Trios. Nucleic Acids Research. 34(19), 
Hinds, D.. A., Stuve L.. L., Nilsen G.. B., Halperin E., Eskin E., Ballinger D.. G., et al. (2005).  Whole-Genome Patterns of Common DNA Variation in Three Human Populations. Science. 307(5712), 1072-1079.

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