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Heonjong Han

Observed name: Han, Heonjong
ORCID: 0000-0001-9821-9294
Observed ORCID: 0000-0001-9821-9294
OpenAlex ID: A5079229114
TRRUST v2: an expanded reference database of human and mouse transcriptional regulatory interactions
2017 · Heonjong Han, Jae-Won Cho, et al. · Nucleic Acids Research · 2,041
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TRRUST: a reference database of human transcriptional regulatory interactions
2015 · Heonjong Han, Hongseok Shim, et al. · Scientific Reports · 474
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Prostaglandin E 2 receptor PTGER4-expressing macrophages promote intestinal epithelial barrier regeneration upon inflammation
2021 · Yi Rang Na, Daun Jung, et al. · Gut · 97
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Dysregulation of TFH-B-TRM lymphocyte cooperation is associated with unfavorable anti-PD-1 responses in EGFR-mutant lung cancer
2021 · Jae-Won Cho, Seyeon Park, et al. · Nature Communications · 68
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TRIM40 is a pathogenic driver of inflammatory bowel disease subverting intestinal barrier integrity
2023 · Sujin Kang, Jaekyung Kim, et al. · Nature Communications · 60
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NGSEA: network-based gene set enrichment analysis for interpreting gene expression phenotypes with functional gene sets
2019 · Heonjong Han, Sangyoung Lee, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 37
Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay
2022 · Go Hun Seo, Hane Lee, et al. · Molecular Medicine · 34
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The nucleolus is the site for inflammatory RNA decay during infection
2022 · Taeyun A. Lee, Heonjong Han, et al. · Nature Communications · 31
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Generation of Integration-free Induced Neural Stem Cells from Mouse Fibroblasts
2016 · Sung Min Kim, Jong-Wan Kim, et al. · Journal of Biological Chemistry · 29
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An integrated systems biology approach identifies positive cofactor 4 as a factor that increases reprogramming efficiency
2016 · Junghyun Jo, Sohyun Hwang, et al. · Nucleic Acids Research · 19
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Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders
2025 · Heonjong Han, Go Hun Seo, et al. · npj Genomic Medicine · 16
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Direct Conversion of Mouse Fibroblasts into Cholangiocyte Progenitor Cells
2018 · Kyung Tae Lim, Jonghun Kim, et al. · Stem Cell Reports · 14
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Clinical utility of genome sequencing in rare diseases: lessons from a single-center study of 1,452 Korean families
2025 · Seungbok Lee, Go Hun Seo, et al. · npj Genomic Medicine · 12
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High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight
2022 · Bruna Lucheze Freire, Thais Kataoka Homma, et al. · American Journal of Medical Genetics Part A · 11
Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program
2025 · Rin Khang, Hane Lee, et al. · Human Mutation · 6
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Secondary findings in 443 exome sequencing data
2024 · Marija Branković, Heonjong Han, et al. · Annals of Human Genetics · 4
Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family
2024 · Seung Woo Ryu, Ji‐Hee Yoon, et al. · Molecular Genetics & Genomic Medicine · 3
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A variant prioritization tool leveraging multiple instance learning for rare Mendelian disease genomic testing
2024 · Ho Heon Kim, Ju Yeop Baek, et al. · medRxiv · 2
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Cancer Gene Discovery by Network Analysis of Somatic Mutations Using the MUFFINN Server
2018 · Heonjong Han, Ben Lehner, et al. · Methods in molecular biology · 2
P661: A database of high allele frequency variants from exome sequencing data of 20,455 patients enriched with Asian population
2023 · Kisang Kwon, Seong-in Hyun, et al. · Genetics in Medicine Open · 1
eP239: Diagnostic performance of automated streamlined, daily updated, exome analysis in patients with delayed development
2022 · Go Hun Seo, Jungsul Lee, et al. · Genetics in Medicine · 1
P660: Accelerating novel gene discovery utilizing a constraint-based method on exome sequencing data of 23,670 patients
2023 · Won Chan Jeong, Kisang Kwon, et al. · Genetics in Medicine Open
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Additional file 2 of Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay
2022 · Seo, Go Hun, Lee, Hane, et al. · Figshare
Additional file 3 of Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay
2022 · Seo, Go Hun, Lee, Hane, et al. · Figshare
Additional file 4 of Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay
2022 · Seo, Go Hun, Lee, Hane, et al. · Figshare
Works count: 27
Citation count: 2,962
H-index: 12
I10-index: 14
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