Author

Sung Eun Hong

Seoul National UniversityORCID 0000-0003-3437-8936Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Murim ChoiiD· 2 shared Taekyeong Yoo· 2 shared Anna ChoiD· 1 shared Byung Chan LimiD· 1 shared Eun Young JeoniD· 1 shared Eunha KimiD· 1 shared Hyoungseok Jeon· 1 shared Hyuna KimiD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Murim ChoiORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintSep 20, 2024

Identification of genes conferring individual-level variation responsible for metabolic dysfunction-associated steatohepatitis using single-cell eQTL analysis

Sung Eun Hong, Seon Ju Mun, Young Ju Lee…·Murim Choi

The paper identifies genes responsible for metabolic dysfunction-associated steatohepatitis using single-cell eQTL analysis in liver biopsies from MASLD patients and controls.

1 citation

humanscRNA-seq

𝕏 PostBluesky

GeneticsScientific ReportsPeer-reviewedJan 29, 2020

Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population

Youngha Lee, Soojin Park, Jin Sook Lee…·Jong‐Hee Chae

The paper identifies pathogenic variants in 57.5% of 553 undiagnosed neurodevelopmental patients, revealing a high proportion of recessive variants and their potential for carrier screening.

6 citations

humanwhole-exome sequencing

𝕏 PostBluesky