Changhoon Kim

Seoul, Republic of Korea

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 18 publications

Machine Learning Reveals the Contribution of Rare Genetic Variants and Enhances Risk Prediction for Coronary Artery Disease in the Japanese Population.

Machine Learning Reveals the Contribution of Rare Genetic Variants and Enhances Risk Prediction for Coronary Artery Disease in the Japanese Population.

Journal: Circulation. Genomic and precision medicine

Published: June 04, 2026

Whole-genome sequencing of 3135 individuals representing the genetic diversity of the Japanese population.

Whole-genome sequencing of 3135 individuals representing the genetic diversity of the Japanese population.

Journal: Journal of human genetics

Published: November 29, 2024

A whole-genome reference panel of 14,393 individuals for East Asian populations accelerates discovery of rare functional variants.

A whole-genome reference panel of 14,393 individuals for East Asian populations accelerates discovery of rare functional variants.

Journal: Science advances

Published: August 09, 2023

ClinPharmSeq: A targeted sequencing panel for clinical pharmacogenetics implementation.

ClinPharmSeq: A targeted sequencing panel for clinical pharmacogenetics implementation.

Journal: PloS one

Published: February 03, 2022

Indigenous Ancestry and Admixture in the Uruguayan Population.

Indigenous Ancestry and Admixture in the Uruguayan Population.

Journal: Frontiers in genetics

Published: June 30, 2021

Genome assembly of the popular Korean soybean cultivar Hwangkeum.

Genome assembly of the popular Korean soybean cultivar Hwangkeum.

Journal: G3 (Bethesda, Md.)

Published: April 18, 2021

Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease.

Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease.

Journal: Human genomics

Published: March 08, 2021

A High Quality Asian Genome Assembly Identifies Features of Common Missing Regions.

A High Quality Asian Genome Assembly Identifies Features of Common Missing Regions.

Journal: Genes

Published: October 09, 2020

Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.

Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.

Journal: Nature genetics

Published: November 01, 2019

Legacy Data Confound Genomics Studies.

Legacy Data Confound Genomics Studies.

Journal: Molecular biology and evolution

Published: September 11, 2019

Systematic evaluation of library preparation methods and sequencing platforms for high-throughput whole genome bisulfite sequencing.

Systematic evaluation of library preparation methods and sequencing platforms for high-throughput whole genome bisulfite sequencing.

Journal: Scientific reports

Published: July 05, 2019

Whole Genome Sequencing and Re-sequencing of the Sable Antelope (Hippotragus niger): A Resource for Monitoring Diversity in ex Situ and in Situ Populations.

Whole Genome Sequencing and Re-sequencing of the Sable Antelope (Hippotragus niger): A Resource for Monitoring Diversity in ex Situ and in Situ Populations.

Journal: G3 (Bethesda, Md.)

Published: April 20, 2019

Showing 1-12 of 18

Last Updated: 09/26/2026