Abstract is: Eleazar Eskin is a computer scientist and geneticist, professor and Chair of the Department of Computational Medicine, and professor of computer science and human genetics at the University of California, Los Angeles. His research focuses on bioinformatics, genomics, and machine learning. A primary research focus is on developing statistical and computational techniques to probe the genetic basis of human disease.
| human | Q5 |
| P2456 | DBLP author ID | e/EEskin |
| P2671 | Google Knowledge Graph ID | /g/11fq8sdjzf |
| P8189 | J9U ID | 987007421399305171 |
| P549 | Mathematics Genealogy Project ID | 191292 |
| P4955 | MR Author ID | 721273 |
| P691 | NL CR AUT ID | xx0033823 |
| P856 | official website | https://web.cs.ucla.edu/~eeskin/ |
| P496 | ORCID iD | 0000-0003-1149-4758 |
| P214 | VIAF cluster ID | 29814544 |
| P1556 | zbMATH author ID | eskin.eleazar |
| P184 | doctoral advisor | Salvatore J. Stolfo | Q20652360 |
| P185 | doctoral student | Noah Zaitlen | Q84099574 |
| P69 | educated at | Columbia University | Q49088 |
| P108 | employer | University of California, Los Angeles | Q174710 |
| P6104 | maintained by WikiProject | WikiProject Mathematics | Q8487137 |
| P106 | occupation | university teacher | Q1622272 |
| P21 | sex or gender | male | Q6581097 |
| Q36191266 | "Good enough solutions" and the genetics of complex diseases |
| Q92205417 | A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity |
| Q34399031 | A comparison of phasing algorithms for trios and unrelated individuals |
| Q28386760 | A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping |
| Q30435297 | A high-resolution association mapping panel for the dissection of complex traits in mice |
| Q34275393 | A model-based approach for analysis of spatial structure in genetic data |
| Q51135552 | A note on phasing long genomic regions using local haplotype predictions |
| Q43787849 | A sequence-based variation map of 8.27 million SNPs in inbred mouse strains |
| Q35586817 | A spatial haplotype copying model with applications to genotype imputation |
| Q35946156 | Accounting for Population Structure in Gene-by-Environment Interactions in Genome-Wide Association Studies Using Mixed Models |
| Q35689818 | Accurate and fast multiple-testing correction in eQTL studies |
| Q37011323 | Accurate discovery of expression quantitative trait loci under confounding from spurious and genuine regulatory hotspots |
| Q33760353 | Accurate viral population assembly from ultra-deep sequencing data |
| Q38673440 | Addressing the Digital Divide in Contemporary Biology: Lessons from Teaching UNIX. |
| Q33870832 | Allele-specific expression and eQTL analysis in mouse adipose tissue |
| Q35060063 | An Optimal Weighted Aggregated Association Test for Identification of Rare Variants Involved in Common Diseases |
| Q46096644 | An ancestry-based approach for detecting interactions |
| Q55341329 | An integrated -omics analysis of the epigenetic landscape of gene expression in human blood cells. |
| Q37269736 | Analysis of allele-specific expression in mouse liver by RNA-Seq: a comparison with Cis-eQTL identified using genetic linkage |
| Q30840823 | Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping |
| Q42697286 | Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes |
| Q34046655 | Assembly of non-unique insertion content using next-generation sequencing |
| Q28301463 | Assessing computational tools for the discovery of transcription factor binding sites |
| Q58706567 | BayesCCE: a Bayesian framework for estimating cell-type composition from DNA methylation without the need for methylation reference |
| Q36664429 | CNVeM: Copy Number Variation Detection Using Uncertainty of Read Mapping |
| Q46523364 | Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension |
| Q36017055 | Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder |
| Q37480692 | Colocalization of GWAS and eQTL Signals Detects Target Genes |
| Q30431821 | Comparative analysis of proteome and transcriptome variation in mouse |
| Q38937326 | Correcting for cell-type heterogeneity in DNA methylation: a comprehensive evaluation |
| Q42625494 | Correction: Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains |
| Q42475607 | Correction: Genome-Wide Association Study Identifies Nox3 as a Critical Gene for Susceptibility to Noise-Induced Hearing Loss |
| Q55551655 | Correction: Mapping Genetic Variants Associated with Beta-Adrenergic Responses in Inbred Mice. |
| Q35415471 | Detecting the presence and absence of causal relationships between expression of yeast genes with very few samples |
| Q33776290 | Detection and reconstruction of tandemly organized de novo copy number variations |
| Q31138145 | Discovering Single Nucleotide Polymorphisms Regulating Human Gene Expression Using Allele Specific Expression from RNA-seq Data |
| Q31094471 | Discovering tightly regulated and differentially expressed gene sets in whole genome expression data |
| Q33244586 | Discrete profile comparison using information bottleneck |
| Q37460669 | Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis |
| Q35415373 | EMINIM: an adaptive and memory-efficient algorithm for genotype imputation |
| Q34778524 | Effectively Identifying eQTLs from Multiple Tissues by Combining Mixed Model and Meta-analytic Approaches |
| Q33742044 | Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies |
| Q35007795 | Efficient algorithms for tandem copy number variation reconstruction in repeat-rich regions |
| Q31138389 | Efficient and Accurate Multiple-Phenotype Regression Method for High Dimensional Data Considering Population Structure |
| Q36515832 | Efficient control of population structure in model organism association mapping |
| Q35579859 | Efficient multiple-trait association and estimation of genetic correlation using the matrix-variate linear mixed model |
| Q34338267 | Efficient reconstruction of haplotype structure via perfect phylogeny |
| Q37216430 | Efficiently identifying significant associations in genome-wide association studies |
| Q37005099 | Fast and Accurate Construction of Confidence Intervals for Heritability |
| Q37482147 | Fast pairwise IBD association testing in genome-wide association studies |
| Q34007867 | Fine mapping in 94 inbred mouse strains using a high-density haplotype resource |
| Q37079498 | ForestPMPlot: A Flexible Tool for Visualizing Heterogeneity Between Studies in Meta-analysis |
| Q37297966 | Functional genomic assessment of phosgene-induced acute lung injury in mice |
| Q46134806 | Further evidence for association of GRK3 to bipolar disorder suggests a second disease mutation |
| Q30432771 | Gene networks associated with conditional fear in mice identified using a systems genetics approach |
| Q35667376 | Gene-Gene Interactions Detection Using a Two-stage Model |
| Q27309881 | Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred Strains |
| Q35742093 | Genetic and environmental control of host-gut microbiota interactions |
| Q34322168 | Genetic control of obesity and gut microbiota composition in response to high-fat, high-sucrose diet in mice |
| Q46837858 | Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate |
| Q34569552 | Genome reassembly with high-throughput sequencing data |
| Q33798453 | Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease |
| Q41974219 | Genome-wide association mapping of blood cell traits in mice |
| Q34267434 | Genome-wide association mapping with longitudinal data |
| Q36763587 | Genome-wide association studies in mice |
| Q33568411 | Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysis |
| Q30413835 | Genome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss |
| Q33862938 | Genome-wide case/control studies in hypertension: only the 'tip of the iceberg'. |
| Q34046617 | Genotyping common and rare variation using overlapping pool sequencing |
| Q30587068 | Hap-seq: An Optimal Algorithm for Haplotype Phasing with Imputation Using Sequencing Data |
| Q30583329 | Hap-seqX: Expedite algorithm for haplotype phasing with imputation using sequence data |
| Q30908816 | Haplotype reconstruction from genotype data using Imperfect Phylogeny |
| Q36119879 | High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping |
| Q36459127 | High-Resolution Association Mapping of Atherosclerosis Loci in Mice |
| Q33358669 | High-resolution mapping of gene expression using association in an outbred mouse stock |
| Q30422039 | Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits |
| Q28822408 | Hypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genes |
| Q38860719 | IPED2: Inheritance Path based Pedigree Reconstruction Algorithm for Complicated Pedigrees |
| Q41632927 | IPED2X: a robust pedigree reconstruction algorithm for complicated pedigrees |
| Q30671349 | IPED: inheritance path-based pedigree reconstruction algorithm using genotype data |
| Q28477846 | Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum |
| Q35975057 | Identification of causal genes for complex traits |
| Q28507726 | Identification of novel genes that mediate innate immunity using inbred mice |
| Q34336624 | Identifying causal variants at loci with multiple signals of association |
| Q37683472 | Identifying genetic relatives without compromising privacy |
| Q36683291 | Improved linear mixed models for genome-wide association studies |
| Q39356415 | Improved methods for multi-trait fine mapping of pleiotropic risk loci |
| Q57057122 | Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies |
| Q36742595 | Improving the Accuracy and Efficiency of Partitioning Heritability into the Contributions of Genomic Regions |
| Q35007657 | Imputation aware meta-analysis of genome-wide association studies |
| Q37218478 | Imputing Phenotypes for Genome-wide Association Studies |
| Q34661915 | In silico QTL mapping of basal liver iron levels in inbred mouse strains |
| Q45998545 | Incorporating homologues into sequence embeddings for protein analysis. |
| Q36022170 | Incorporating prior information into association studies |
| Q47864609 | Incorporation of Biological Knowledge Into the Study of Gene-Environment Interactions |
| Q34505622 | Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population |
| Q35065465 | Increasing Power of Genome-Wide Association Studies by Collecting Additional Single-Nucleotide Polymorphisms |
| Q30418487 | Increasing association mapping power and resolution in mouse genetic studies through the use of meta-analysis for structured populations |
| Q36517959 | Increasing power in association studies by using linkage disequilibrium structure and molecular function as prior information |
| Q35550128 | Increasing power of groupwise association test with likelihood ratio test |
| Q34206593 | Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP |
| Q36305467 | Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome |
| Q30865659 | Integrating functional data to prioritize causal variants in statistical fine-mapping studies |
| Q34187048 | Interpreting meta-analyses of genome-wide association studies |
| Q51687139 | Laplace Propagation |
| Q30653340 | Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data |
| Q35752524 | Leveraging the HapMap correlation structure in association studies |
| Q36709919 | Limited RNA editing in exons of mouse liver and adipose |
| Q33869927 | Linkage effects and analysis of finite sample errors in the HapMap |
| Q61443677 | Local genetic effects on gene expression across 44 human tissues |
| Q40449556 | Long Single-Molecule Reads Can Resolve the Complexity of the Influenza Virus Composed of Rare, Closely Related Mutant Variants. |
| Q28481719 | Mapping genetic variants associated with beta-adrenergic responses in inbred mice |
| Q41555517 | Memory efficient assembly of human genome |
| Q37458267 | Meta-analysis identifies gene-by-environment interactions as demonstrated in a study of 4,965 mice |
| Q42620879 | Mismatch string kernels for discriminative protein classification |
| Q43662455 | Mixed models can correct for population structure for genomic regions under selection |
| Q35051928 | Mixed-model coexpression: calculating gene coexpression while accounting for expression heterogeneity |
| Q28593424 | Mouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesis |
| Q45843642 | Multi-marker tagging single nucleotide polymorphism selection using estimation of distribution algorithms |
| Q36758653 | Multiple testing correction in linear mixed models |
| Q37416447 | Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs |
| Q33597308 | Optimal algorithms for haplotype assembly from whole-genome sequence data |
| Q45984379 | Polymorphisms and haplotypes of the regulator of G protein signaling-2 gene in normotensives and hypertensives. |
| Q60932187 | Population structure in genetic studies: Confounding factors and mixed models |
| Q43683512 | Postassociation cleaning using linkage disequilibrium information |
| Q33760332 | Privacy preserving protocol for detecting genetic relatives using rare variants |
| Q96609249 | Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing |
| Q47837919 | Protein family classification using sparse markov transducers |
| Q35807550 | Quantitative analysis of 3-dimensional facial soft tissue photographic images: technical methods and clinical application |
| Q52352531 | ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues |
| Q35136958 | Random-Effects Model Aimed at Discovering Associations in Meta-Analysis of Genome-wide Association Studies |
| Q33432685 | Rapid and accurate multiple testing correction and power estimation for millions of correlated markers |
| Q36972245 | Rare Variant Association Testing Under Low-Coverage Sequencing |
| Q46071518 | Searching genomes for noncoding RNA using FastR. |
| Q33698614 | Selection in Europeans on Fatty Acid Desaturases Associated with Dietary Changes |
| Q57087867 | Selection on the FADS region in Europeans |
| Q38993486 | Simultaneous Modeling of Disease Status and Clinical Phenotypes To Increase Power in Genome-Wide Association Studies |
| Q39886245 | Sparse PCA corrects for cell type heterogeneity in epigenome-wide association studies |
| Q34714023 | Spatial localization of recent ancestors for admixed individuals |
| Q99250720 | Swab-Seq: A high-throughput platform for massively scaled up SARS-CoV-2 testing |
| Q30422958 | Systems genetic analysis of osteoblast-lineage cells |
| Q27347732 | The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic Determinants |
| Q30371907 | The Genetic Architecture of Noise-Induced Hearing Loss: Evidence for a Gene-by-Environment Interaction |
| Q27468697 | The Genetic Basis of Host Preference and Resting Behavior in the Major African Malaria Vector, Anopheles arabiensis |
| Q41984817 | The Genetic Landscape of Hematopoietic Stem Cell Frequency in Mice |
| Q30276950 | The Hybrid Mouse Diversity Panel: a resource for systems genetics analyses of metabolic and cardiovascular traits |
| Q36580787 | The Minnesota Center for Twin and Family Research genome-wide association study |
| Q52043503 | The spectrum kernel: a string kernel for SVM protein classification |
| Q55245667 | Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia. |
| Q37005532 | Using genomic annotations increases statistical power to detect eGenes |
| Q33419808 | Using network component analysis to dissect regulatory networks mediated by transcription factors in yeast |
| Q48603899 | Using substitution matrices to estimate probability distributions for biological sequences |
| Q34971144 | Variance component model to account for sample structure in genome-wide association studies |
| Q28770097 | Whole-genome analysis of Alu repeat elements reveals complex evolutionary history |
| Q40213493 | Widespread Allelic Heterogeneity in Complex Traits |
| Q30681290 | eALPS: estimating abundance levels in pooled sequencing using available genotyping data |
| Q84099574 | Noah Zaitlen | doctoral advisor | P184 |
| Q20652360 | Salvatore J. Stolfo | doctoral student | P185 |
| Eleazar Eskin | wikipedia |
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