Publications

Found 82 results
Author Title Type [ Year(Desc)]
Filters: Author is Eran Halperin  [Clear All Filters]
2010
Preuss, M., König I. R., Thompson J. R., Erdmann J., Absher D., Assimes T. L., et al. (2010).  Design of the Coronary Artery Disease Genome-Wide Replication and Meta-Analysis (CARDIoGRAM) Study--A Genome-Wide Association Meta-Analysis Involving More than 22,000 Cases and 60,000 Controls. Circulation: Cardiovascular Genetics. 3, 475-483.
Pasaniuc, B., Avinery R.., Gur T., Skibola C. F., Bracci P. M., & Halperin E. (2010).  A Generic Coalescent-Based Framework for the Selection of a Reference Panel for Imputation. Genetic Epidemiology. 34(8), 773-782.
Conde, L., Halperin E., Akers N.. K., Brown K. M., Smedby K.. E., & Rothman N.. (2010).  Genome-Wide Association Study of Follicular Lymphoma Identifies a Risk Locus at 6p21.32. Nature Genetics. 42(8), 661-664.
Sankararaman, S., Obozinski G., Jordan M. I., & Halperin E. (2010).  Genomic Privacy and Limits of Individual Detection in a Pool.
Kirkpatrick, B., Halperin E., & Karp R. M. (2010).  Haplotype Inference in Complex Pedigrees. Journal of Computational Biology. 17(3), 269-280.
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.
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.
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,
2011
Pasaniuc, B., Zaitlen N., & Halperin E. (2011).  Accurate Estimation of Expression Levels of Homologous Genes in RNA-Seq Experiments. 18(3), 459-468.
Kovacs, A.., Ben-Jacob N.., Tayem H.., Halperin E., Iraqi F.. A., & Gophna U.. (2011).  Genotype Is a Stronger Determinant than Sex of the Mouse Gut Microbiota. Microbial Ecology. 61(2), 423-428.
He, D., Zaitlen N., Pasaniuc B., Eskin E., & Halperin E. (2011).  Genotyping Common and Rare Variation Using Overlapping Pool Sequencing. BMC Informatics. 12,
He, D., Zaitlen N., Pasaniuc B., Eskin E., & Halperin E. (2011).  Genotyping Common and Rare Variation Using Overlapping Pool Sequencing. Proceedings of the First Annual RECOMB Satellite Workshop on Massively Parallel Sequencing (RECOMB-seq). 26-27.
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.
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. 136-152.
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.
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.
2012
Wang, Z., Hormozdiari F., Yang W-Y., Halperin E., & Eskin E. (2012).  CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping. 326-340.
Slager, S.. L., Skibola C. F., & Halperin E. (2012).  Common Variation at 6p21.31 (BAK1) Influences the Risk of Chronic Lymphocytic Leukemia. Blood. 120(4), 843-846.
Baran, Y., Pasaniuc B., Sankararaman S., Torgerson D. G., Gignoux C., Eng C., et al. (2012).  Fast and Accurate Inference of Local Ancestry in Latino Populations. Bioinformatics. 28(10), 1359-1367.
Efros, A., & Halperin E. (2012).  Haplotype Reconstruction Using Perfect Phylogeny and Sequence Data. 13,
Baran, Y., & Halperin E. (2012).  Joint Analysis of Multiple Metagenomic Samples. PLoS Computational Biology. 8(2), 
Rozov, R., Halperin E., & Shamir R. (2012).  MGMR: Leveraging RNA-Seq Population Data to Optimize Expression Estimation. 13,
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.

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