PubRank

Eran Halperin

Author PubWeight™ 134.24‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Whole-genome patterns of common DNA variation in three human populations. Science 2005 21.22
2 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011 13.25
3 A comparison of phasing algorithms for trios and unrelated individuals. Am J Hum Genet 2006 12.45
4 Identifying personal genomes by surname inference. Science 2013 10.79
5 Estimating local ancestry in admixed populations. Am J Hum Genet 2008 5.90
6 Leveraging the HapMap correlation structure in association studies. Am J Hum Genet 2007 3.57
7 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. Circ Cardiovasc Genet 2010 3.15
8 Inhibition of activated pericentromeric SINE/Alu repeat transcription in senescent human adult stem cells reinstates self-renewal. Cell Cycle 2011 3.11
9 Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. Nat Genet 2009 2.73
10 Genomic privacy and limits of individual detection in a pool. Nat Genet 2009 2.60
11 Inference of locus-specific ancestry in closely related populations. Bioinformatics 2009 2.54
12 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Nat Genet 2010 2.37
13 Fast and accurate inference of local ancestry in Latino populations. Bioinformatics 2012 2.30
14 On the inference of ancestries in admixed populations. Genome Res 2008 2.27
15 A model-based approach for analysis of spatial structure in genetic data. Nat Genet 2012 2.02
16 Leveraging genetic variability across populations for the identification of causal variants. Am J Hum Genet 2010 2.00
17 Efficient reconstruction of haplotype structure via perfect phylogeny. J Bioinform Comput Biol 2003 1.96
18 An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biol 2014 1.95
19 Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Nat Genet 2011 1.92
20 A randomization test for controlling population stratification in whole-genome association studies. Am J Hum Genet 2007 1.73
21 Accurate estimation of expression levels of homologous genes in RNA-seq experiments. J Comput Biol 2011 1.69
22 Genotype is a stronger determinant than sex of the mouse gut microbiota. Microb Ecol 2010 1.63
23 Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma. PLoS One 2008 1.61
24 miRNAkey: a software for microRNA deep sequencing analysis. Bioinformatics 2010 1.41
25 Probabilistic inference of viral quasispecies subject to recombination. J Comput Biol 2013 1.40
26 Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. Blood 2012 1.26
27 A generic coalescent-based framework for the selection of a reference panel for imputation. Genet Epidemiol 2010 1.26
28 A New Stress-Based Model of Political Extremism: Personal Exposure to Terrorism, Psychological Distress, and Exclusionist Political Attitudes. J Conflict Resolut 2009 1.17
29 Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation. Bioinformatics 2013 1.11
30 Matrin 3 binds and stabilizes mRNA. PLoS One 2011 1.11
31 Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP. Genome Res 2005 1.05
32 HAPLOPOOL: improving haplotype frequency estimation through DNA pools and phylogenetic modeling. Bioinformatics 2007 0.98
33 Dynamic network topology changes in functional modules predict responses to oxidative stress in yeast. Mol Biosyst 2009 0.96
34 A note on phasing long genomic regions using local haplotype predictions. J Bioinform Comput Biol 2006 0.93
35 Joint analysis of multiple metagenomic samples. PLoS Comput Biol 2012 0.93
36 Haplotype reconstruction using perfect phylogeny and sequence data. BMC Bioinformatics 2012 0.93
37 Algorithms for efficient near-perfect phylogenetic tree reconstruction in theory and practice. IEEE/ACM Trans Comput Biol Bioinform 2007 0.92
38 Pedigree reconstruction using identity by descent. J Comput Biol 2011 0.91
39 Presymptomatic risk assessment for chronic non-communicable diseases. PLoS One 2010 0.90
40 Fast lossless compression via cascading Bloom filters. BMC Bioinformatics 2014 0.90
41 A search for overlapping genetic susceptibility loci between non-Hodgkin lymphoma and autoimmune diseases. Genomics 2011 0.90
42 Enhanced localization of genetic samples through linkage-disequilibrium correction. Am J Hum Genet 2013 0.89
43 PRRC2A and BCL2L11 gene variants influence risk of non-Hodgkin lymphoma: results from the InterLymph consortium. Blood 2012 0.89
44 Rare variant association testing under low-coverage sequencing. Genetics 2013 0.88
45 CNVeM: copy number variation detection using uncertainty of read mapping. J Comput Biol 2013 0.87
46 Association mapping and significance estimation via the coalescent. Am J Hum Genet 2008 0.87
47 Novel associations for coronary artery disease derived from genome wide association studies are not associated with increased carotid intima-media thickness, suggesting they do not act via early atherosclerosis or vessel remodeling. Atherosclerosis 2011 0.86
48 Learning natural selection from the site frequency spectrum. Genetics 2013 0.85
49 Haplotype inference in complex pedigrees. J Comput Biol 2010 0.85
50 Chemokine polymorphisms and lymphoma: a pooled analysis. Leuk Lymphoma 2010 0.84
51 Using DNA pools for genotyping trios. Nucleic Acids Res 2006 0.84
52 eALPS: estimating abundance levels in pooled sequencing using available genotyping data. J Comput Biol 2013 0.79
53 MGMR: leveraging RNA-Seq population data to optimize expression estimation. BMC Bioinformatics 2012 0.78
54 Genotyping common and rare variation using overlapping pool sequencing. BMC Bioinformatics 2011 0.78
55 Relation of genetic profile and novel circulating biomarkers with coronary plaque phenotype as determined by intravascular ultrasound: rationale and design of the ATHEROREMO-IVUS study. EuroIntervention 2014 0.77
56 Detection of molecular paths associated with insulitis and type 1 diabetes in non-obese diabetic mouse. PLoS One 2009 0.77
57 Affirmation, acknowledgment of in-group responsibility, group-based guilt, and support for reparative measures. J Pers Soc Psychol 2011 0.77
58 GLINT: a user-friendly toolset for the analysis of high-throughput DNA-methylation array data. Bioinformatics 2017 0.76
59 Authoritarianism, perceived threat and exclusionism on the eve of the Disengagement: Evidence from Gaza. Int J Intercult Relat 2009 0.75
60 When Ideology Meets Conflict-Related Content: Influences on Emotion Generation and Regulation. Emotion 2017 0.75