Genetic Architecture of Atherosclerosis in Mice: A Systems Genetics Analysis of Common Inbred StrainsThe Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic DeterminantsThe Genetic Basis of Host Preference and Resting Behavior in the Major African Malaria Vector, Anopheles arabiensisAssessing computational tools for the discovery of transcription factor binding sitesA general framework for meta-analyzing dependent studies with overlapping subjects in association mappingIdentification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparumMapping genetic variants associated with beta-adrenergic responses in inbred miceIdentification of novel genes that mediate innate immunity using inbred miceMouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesisWhole-genome analysis of Alu repeat elements reveals complex evolutionary historyHypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genesThe Hybrid Mouse Diversity Panel: a resource for systems genetics analyses of metabolic and cardiovascular traits.The Genetic Architecture of Noise-Induced Hearing Loss: Evidence for a Gene-by-Environment InteractionGenome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss.Increasing association mapping power and resolution in mouse genetic studies through the use of meta-analysis for structured populations.Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits.Systems genetic analysis of osteoblast-lineage cellsComparative analysis of proteome and transcriptome variation in mouse.Gene networks associated with conditional fear in mice identified using a systems genetics approach.A high-resolution association mapping panel for the dissection of complex traits in miceHap-seqX: expedite algorithm for haplotype phasing with imputation using sequence data.Hap-seq: an optimal algorithm for haplotype phasing with imputation using sequencing dataLeveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing dataIPED: inheritance path-based pedigree reconstruction algorithm using genotype data.eALPS: estimating abundance levels in pooled sequencing using available genotyping dataAnalysis of genetic variation in Ashkenazi Jews by high density SNP genotyping.Integrating functional data to prioritize causal variants in statistical fine-mapping studies.Haplotype reconstruction from genotype data using Imperfect Phylogeny.Discovering tightly regulated and differentially expressed gene sets in whole genome expression data.Discovering Single Nucleotide Polymorphisms Regulating Human Gene Expression Using Allele Specific Expression from RNA-seq Data.Efficient and Accurate Multiple-Phenotype Regression Method for High Dimensional Data Considering Population Structure.Discrete profile comparison using information bottleneckHigh-resolution mapping of gene expression using association in an outbred mouse stock.Using network component analysis to dissect regulatory networks mediated by transcription factors in yeast.Rapid and accurate multiple testing correction and power estimation for millions of correlated markers.Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysisOptimal algorithms for haplotype assembly from whole-genome sequence data.Selection in Europeans on Fatty Acid Desaturases Associated with Dietary ChangesEffectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies.Privacy preserving protocol for detecting genetic relatives using rare variants.
P50
Q27309881-EF40EBD1-EB1A-4FF3-A603-C0627DB55626Q27347732-CEE0F933-7076-4678-B416-E910C988CF87Q27468697-C50F1844-6DFC-4D1B-9EAD-FB7124C5DC2EQ28301463-20210F19-2F5A-4D1E-8B20-F1FD88E5BC4CQ28386760-E260877C-83C5-4C50-BFE9-E2AED8B1DD01Q28477846-0709440C-A632-4DB3-B506-B1FB8AC4A5FCQ28481719-EDC4395F-FF3D-4FC4-AA3F-DC5D352197C2Q28507726-01AFD7A0-A3C8-497D-9DFC-E1007FCD1857Q28593424-B7EB82CB-093A-4D3A-96C6-4650C49E3563Q28770097-A0333CF5-5BF8-41F1-976E-DCFE7D58B161Q28822408-C90741EE-9336-48C0-9FE2-B2770A2916CEQ30276950-78D5990E-29B0-46B5-B42B-8F5C824BC09CQ30371907-EA7CDCE1-6FDC-4269-937A-387F67835F95Q30413835-FC901219-6F3E-4ED2-B5F5-910800895707Q30418487-95D6A421-9A1F-4B79-85BC-AA1BDA00946BQ30422039-7FC5CADB-2075-4AD8-89EA-6A32A57CAE8BQ30422958-CEDDD594-2CFF-4818-BA50-3F47F8FED3B6Q30431821-A9538E32-1A28-45A4-AEA0-606FDC308034Q30432771-129DDAA2-3A3A-43B6-9A39-AFCD8DB0AFF0Q30435297-174E3038-C2A8-492A-BCC5-D176D78B157AQ30583329-4ACA0186-7AFC-46CF-BD4F-4DAEDDB7A2DDQ30587068-2E162D48-60E6-47A7-891C-E2F824EC04B3Q30653340-2237AE6A-BE63-405A-AC08-BC653F20B261Q30671349-87B077E8-3B4F-4303-8FD4-9E24C9A6C78BQ30681290-8CB3EB80-9168-4773-8F14-55C8D225A93AQ30840823-2B1F1C5D-E657-433F-A247-5691FA5F96BCQ30865659-9DEC3EEF-DBDE-4D56-888F-9F2662F2B71CQ30908816-D7D630CE-2B27-45D0-9A13-646FB71A3A2AQ31094471-5E38BC27-4B7F-4ED6-B7A7-75F49F46DAEEQ31138145-4295D105-48D2-4319-93A0-35BC96AC5289Q31138389-22828450-FED4-46EB-AB38-E335E9329110Q33244586-7B1A8908-564C-4C03-8FB7-CB9CC51C9D66Q33358669-54DE6F15-C5E4-4F7A-84FA-CB4E17FC676FQ33419808-CC322DF6-737C-43E6-B46D-B2628683CF85Q33432685-492AECB5-FB9B-403F-A59F-77DA7FEEC67FQ33568411-60FF76C1-01E1-4C23-90A2-C53E46BF7542Q33597308-449125F3-3E70-4C83-A163-EE165119D47DQ33698614-996A8819-DE25-4CD6-A193-41E3F3A1429DQ33742044-E269BCDC-5330-43CD-98A8-8504A6F5F40BQ33760332-1A3E6E9B-D23D-4296-8B0F-1317F13CABBE
P50
description
computer scientist and geneticist
@en
wetenschapper
@nl
հետազոտող
@hy
name
Eleazar Eskin
@ast
Eleazar Eskin
@en
Eleazar Eskin
@es
Eleazar Eskin
@nl
type
label
Eleazar Eskin
@ast
Eleazar Eskin
@en
Eleazar Eskin
@es
Eleazar Eskin
@nl
prefLabel
Eleazar Eskin
@ast
Eleazar Eskin
@en
Eleazar Eskin
@es
Eleazar Eskin
@nl
P106
P21
P31
P496
0000-0003-1149-4758