Heonjong Han

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 18 publications

Clinical utility of genome sequencing in rare diseases: lessons from a single-center study of 1,452 Korean families.

Clinical utility of genome sequencing in rare diseases: lessons from a single-center study of 1,452 Korean families.

Journal: NPJ genomic medicine
Published: July 17, 2025

Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program.

Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program.

Journal: Human mutation
Published: August 26, 2024

Secondary findings in 443 exome sequencing data.

Secondary findings in 443 exome sequencing data.

Journal: Annals of human genetics
Published: June 27, 2024

Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders.

Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders.

Journal: NPJ genomic medicine
Published: June 12, 2024

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.

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.

Journal: Molecular genetics & genomic medicine
Published: July 09, 2023

TRIM40 is a pathogenic driver of inflammatory bowel disease subverting intestinal barrier integrity.

TRIM40 is a pathogenic driver of inflammatory bowel disease subverting intestinal barrier integrity.

Journal: Nature communications
Published: April 18, 2022

High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight.

High frequency of genetic/epigenetic disorders in short stature children born with very low birth weight.

Journal: American journal of medical genetics. Part A
Published: February 04, 2022

Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay.

Diagnostic performance of automated, streamlined, daily updated exome analysis in patients with neurodevelopmental delay.

Journal: Molecular medicine (Cambridge, Mass.)
Published: December 23, 2021

The nucleolus is the site for inflammatory RNA decay during infection.

The nucleolus is the site for inflammatory RNA decay during infection.

Journal: Nature communications
Published: December 08, 2021

Dysregulation of TFH-B-TRM lymphocyte cooperation is associated with unfavorable anti-PD-1 responses in EGFR-mutant lung cancer.

Dysregulation of TFH-B-TRM lymphocyte cooperation is associated with unfavorable anti-PD-1 responses in EGFR-mutant lung cancer.

Journal: Nature communications
Published: December 12, 2020

Prostaglandin E2 receptor PTGER4-expressing macrophages promote intestinal epithelial barrier regeneration upon inflammation.

Prostaglandin E2 receptor PTGER4-expressing macrophages promote intestinal epithelial barrier regeneration upon inflammation.

Journal: Gut
Published: June 09, 2020

NGSEA: Network-Based Gene Set Enrichment Analysis for Interpreting Gene Expression Phenotypes with Functional Gene Sets.

NGSEA: Network-Based Gene Set Enrichment Analysis for Interpreting Gene Expression Phenotypes with Functional Gene Sets.

Journal: Molecules and cells
Published: April 08, 2019
Showing 1-12 of 18

Last Updated: 09/26/2026