Publications

Found 82 results
Author Title Type [ Year(Asc)]
Filters: Author is Eran Halperin  [Clear All Filters]
2010
Bracci, P. M., Skibola C. F., Conde L., Halperin E., Lightfoot T., Smith A., et al. (2010).  Chemokine Polymorphisms and Lymphoma: A Pooled Analysis. Leukemia and Lymphoma. 51(3), 497-506.
Halperin, E. (2010).  Deciphering the Genetic Components of Human Diseases.
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,
2009
Lindfors, E., Gopalacharyulu P. V., Halperin E., & Orešič M. (2009).  Detection of Molecular Paths Associated with Insulitis and Type 1 Diabetes in Non-Obese Diabetic Mouse. PLoS ONE. 4(10), 
Gopalacharyulu, P. V., Velagapudi V.. R., Lindfors E., Halperin E., & Orešič M. (2009).  Dynamic Network Topology Changes in Functional Modules Predict Responses to Oxidative Stress in Yeast. Molecular BioSystems. 5(3), 276-287.
Skibola, C. F., Bracci P. M., Halperin E., Conde L., Craig D. W., Agana L., et al. (2009).  Genetic Variants at 6p21.33 Are Associated with Susceptibility to Follicular Lymphoma. Nature Genetics. 41(8), 873-875.
Sankararaman, S., Obozinski G., Jordan M. I., & Halperin E. (2009).  Genomic Privacy and Limits of Individual Detection in a Pool. Nature Genetics. 41(9), 965-967.
Kirkpatrick, B., Rosa J.., Halperin E., & Karp R. M. (2009).  Haplotype Inference in Complex Pedigrees. 108-120.
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.
Pasaniuc, B., Sankararaman S., Kimmel G., & Halperin E. (2009).  Inference of Locus-Specific Ancestry in Closely Related Populations. 25(12), 213-221.
Halperin, E., & Stephan D. A. (2009).  Maximizing Power in Association Studies. Nature Biotechnology. 27(3), 255-256.
Halperin, E., & Stephan D. A. (2009).  SNP Imputation in Association Studies. Nature Biotechnology. 27(4), 349-351.

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