Author

He Li

University of California San DiegoORCID 0000-0002-1766-5311Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

He Li10 papers · Binzhou Medical University

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Assay:DNA methylation· 1 Research Focus:fine-mapping· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1

Frequent Co-Authors

Agnieszka D’Antonio‐ChronowskaiD· 2 shared Erin N. SmithiD· 2 shared Hiroko Matsui· 2 shared Kelly A. FrazeriD· 2 shared Margaret K. R. DonovaniD· 2 shared Matteo D’AntonioiD· 2 shared Paola Benaglio· 2 shared William W. Young GreenwaldiD· 2 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenomics

Agnieszka D’Antonio‐ChronowskaORCID

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2 papers

Recent·Most cited

GenomicsNature GeneticsPeer-reviewedSep 30, 2019

Allele-specific NKX2-5 binding underlies multiple genetic associations with human EKG traits

Paola Benaglio, Agnieszka D’Antonio‐Chronowska, Wubin Ma…·Kelly A. Frazer

The paper identifies allele-specific NKX2-5 binding variants associated with EKG traits by integrating iPSC-CM data and GWAS, showing their role in heart rate loci and cardiac enhancer activity.

43 citations

humanDNA methylation

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GenomicsCell ReportsPeer-reviewedJul 1, 2018

Insights into the mutational burden of human induced pluripotent stem cells using an integrative omics approach

Matteo D’Antonio, Paola Benaglio, David A. Jakubosky…·Kelly A. Frazer

This study analyzes the mutational burden in human iPSCs using whole genome sequencing and integrates transcriptome and epigenome data to identify mutation patterns and their impact on gene expression.

88 citations

humanwhole-genome sequencing

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