Author details

Full Name

Eleazar Eskin

Affiliation

ORCID

Career Start Year

2000

Papers

210

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37481717	Genetic pathways regulating the longitudinal acquisition of cocaine self-administration in a panel of inbred and recombinant inbred mice.	Cell Rep	2023
36126104	Ensemble neural network model for detecting thyroid eye disease using external photographs.	Br J Ophthalmol	2023
36711635	Leveraging family data to design Mendelian Randomization that is provably robust to population stratification.	bioRxiv	2023
37197991	Leveraging family data to design Mendelian randomization that is provably robust to population stratification.	Genome Res	2023
36810591	3D Printing as an Effective Quality Assurance Implementation in Massive-Scale SARS-CoV-2 Testing at aÂ SwabSeq Next-Generation Sequencing Laboratory.		2023
36999049	RNA-seq data science: From raw data to effective interpretation.	Front Genet	2023
35232963	Robust Mendelian randomization in the presence of residual population stratification, batch effects and horizontal pleiotropy.	Nat Commun	2022
36250793	Accurate modeling of replication rates in genome-wide association studies by accounting for Winner's Curse and study-specific heterogeneity.	G3: Genes, Genomes, Genetics	2022
35753701	A comprehensive benchmarking of WGS-based deletion structural variant callers.	Brief Bioinform	2022
35379194	Genomic epidemiology of the Los Angeles COVID-19 outbreak and the early history of the B.1.43 strain in the USA.	BMC Genomics	2022
36342933	Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations.	PLoS Genetics	2022
35622842	Bruins-in-Genomics: Evaluation of the impact of a UCLA undergraduate summer program in computational biology on participating students.	PLoS ONE	2022
34543273	Identifying causal variants by fine mapping across multiple studies.	PLoS Genet	2021
34211145	Massively scaled-up testing for SARS-CoV-2 RNA via next-generation sequencing of pooled and barcoded nasal and saliva samples.	Nat Biomed Eng	2021
33931127	MARS: leveraging allelic heterogeneity to increase power of association testing.	Genome Biol	2021
33352115	PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics.	Am J Hum Genet	2021
33050709	Genetic determinants of ammonia-induced acute lung injury in mice.	American Journal of Physiology - Lung Cellular and Molecular Physiology	2021
32723395	Correction to: Improving the usability and comprehensiveness of microbial databases.	BMC Biol	2020
32264902	Improving the usability and comprehensiveness of microbial databases.	BMC Biol	2020
32183840	Benchmarking of computational error-correction methods for next-generation sequencing data.	Genome Biol	2020
32053016	A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies.	Journal of Computational Biology	2020
32296059	Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma.	Nat Commun	2020
32887888	Author Correction: Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing.	Nat Commun	2020
32913072	The impact of sex on gene expression across human tissues.	Science	2020
32912225	Metalign: efficient alignment-based metagenomic profiling via containment min hash.	Genome Biol	2020
32561710	Profiling immunoglobulin repertoires across multiple human tissues using RNA sequencing.	Nat Commun	2020
30833765	How bioinformatics and open data can boost basic science in countries and universities with limited resources.	Nat Biotechnol	2019
31834882	Leveraging allelic imbalance to refine fine-mapping for eQTL studies.	PLoS Genet	2019
31869344	A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity.	PLoS Genet	2019
30383443	Word and Sentence Embedding Tools to Measure Semantic Similarity of Gene Ontology Terms by Their Definitions.	J Comput Biol	2019
30272994	Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.	Journal of Computational Biology	2019
30918265	Systematic benchmarking of omics computational tools.	Nat Commun	2019
30813962	Improving the usability and archival stability of bioinformatics software.	Genome Biol	2019
31455884	Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage.	Nat Neurosci	2019
31420589	A linear mixed model approach to gene expression-tumor aneuploidy association studies.	Scientific Reports	2019
31220077	Challenges and recommendations to improve the installability and archival stability of omics computational tools.	PLoS Biol	2019
31167634	MiCoP: microbial community profiling method for detecting viral and fungal organisms in metagenomic samples.	BMC Genomics	2019
31366909	Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology.	Nature Communications	2019
29548336	ROP: dumpster diving in RNA-sequencing to find the source of 1 trillion reads across diverse adult human tissues.	Genome Biol	2018
30589851	Population structure in genetic studies: Confounding factors and mixed models.	PLoS Genetics	2018
29914364	An integrated -omics analysis of the epigenetic landscape of gene expression in human blood cells.	BMC Genomics	2018
30241486	BayesCCE: a Bayesian framework for estimating cell-type composition from DNA methylation without the need for methylation reference.		2018
29955180	Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.	Nat Genet	2018
29949991	Finding associated variants in genome-wide association studies on multiple traits.		2018
29942083	Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits.	Nat Genet	2018
29621227	Involving undergraduates in genomics research to narrow the education-research gap.	Nat Biotechnol	2018
29752291	An Association Mapping Framework To Account for Potential Sex Difference in Genetic Architectures.	Genetics	2018
29743478	Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia.	Transl Psychiatry	2018
29114909	An ancestry-based approach for detecting interactions.	Genet Epidemiol	2018
27663501	Improved methods for multi-trait fine mapping of pleiotropic risk loci.	Bioinformatics	2017