Hyun S. Cheong

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 91 publications

Single-Nucleotide Polymorphisms of BRCA1 and BRCA2 and Risk of Papillary Thyroid Carcinoma.

Single-Nucleotide Polymorphisms of BRCA1 and BRCA2 and Risk of Papillary Thyroid Carcinoma.

Journal: Cancers
Published: March 11, 2025

A novel variant of telomerase reverse transcriptase (TERT) associated with risk of glioma in a Korean population.

A novel variant of telomerase reverse transcriptase (TERT) associated with risk of glioma in a Korean population.

Journal: Scientific reports
Published: July 16, 2024

Reply to "Clinical Relevance of Genetic Variants in Juvenile Stroke Patients: A Plea for a Precise Classification".

Reply to "Clinical Relevance of Genetic Variants in Juvenile Stroke Patients: A Plea for a Precise Classification".

Journal: Annals of neurology
Published: June 20, 2023

TPX2 Amplification-Driven Aberrant Mitosis in Culture Adapted Human Embryonic Stem Cells with gain of 20q11.21.

TPX2 Amplification-Driven Aberrant Mitosis in Culture Adapted Human Embryonic Stem Cells with gain of 20q11.21.

Journal: Stem cell reviews and reports
Published: January 28, 2023

TPX2 prompts mitotic survival via the induction of BCL2L1 through YAP1 protein stabilization in human embryonic stem cells.

TPX2 prompts mitotic survival via the induction of BCL2L1 through YAP1 protein stabilization in human embryonic stem cells.

Journal: Experimental & molecular medicine
Published: May 03, 2022

Two independent variants of epidermal growth factor receptor associated with risk of glioma in a Korean population.

Two independent variants of epidermal growth factor receptor associated with risk of glioma in a Korean population.

Journal: Scientific reports
Published: April 22, 2022

Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients.

Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients.

Journal: Annals of neurology
Published: March 15, 2022

Asian-specific 3'UTR variant in CDKN2B associated with risk of pituitary adenoma.

Asian-specific 3'UTR variant in CDKN2B associated with risk of pituitary adenoma.

Journal: Molecular biology reports
Published: January 25, 2022

Difference of copy number variation in blood of patients with lung cancer.

Difference of copy number variation in blood of patients with lung cancer.

Journal: The International journal of biological markers
Published: December 14, 2020

A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population.

A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population.

Journal: BMC medical genetics
Published: July 24, 2020

Association of APOE genotype with lipid profiles and type 2 diabetes mellitus in a Korean population.

Association of APOE genotype with lipid profiles and type 2 diabetes mellitus in a Korean population.

Journal: Genes & genomics
Published: July 11, 2020

Genetic analysis of primary open-angle glaucoma-related risk alleles in a Korean population: the GLAU-GENDISK study.

Genetic analysis of primary open-angle glaucoma-related risk alleles in a Korean population: the GLAU-GENDISK study.

Journal: The British journal of ophthalmology
Published: February 17, 2020
Showing 1-12 of 91

Last Updated: 09/26/2026