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Chong Kun Cheon

12PUBLICATIONS

31CO-AUTHORS

Performance artHealth surveillanceVeterinary pathologyGenomicsGene expression (incl. microarray and other genome-wide approaches)

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Publications (12)

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|Mar 06, 2026

<i>PRPS1</i> (p.V42L) Mutation in Arts Syndrome Induces Aberrant Neural Stem Cell Development and Neuronal Senescence-Like Phenotype: Rescue by Nicotinamide Mononucleotide Supplementation.

Ji-Hee Kim, Su-Jung Park, Jeong-A Lee

|Dec 03, 2025

[Achievements and Expectations of the Rare Disease Diagnostic Support Program in the Republic of Korea].

Ye Eun Lee, Jee Young Kim, Jun Kil Choi

|Jul 12, 2025

Multidisciplinary Care Model as a Center of Excellence for Fabry Disease: A Practical Guide to Diagnosis and Management by Clinical Specialty in South Korea.

Soo Yong Lee, Il Young Kim, Sung-Ho Ahn

|Apr 14, 2025

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

Rin Khang, Hane Lee, Jihye Kim

|Mar 19, 2025

Prader-Willi syndrome gene expression profiling of obese and non-obese patients reveals transcriptional changes in CLEC4D and ANXA3.

Ju Young Yoon, Choong Ho Shin, Murim Choi

|Jun 01, 2024

NANS-CDG: Expanding clinical insights with a novel patient with novel variants.

Sukdong Yoo, Chong Kun Cheon

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Frequent Collaborators

2 joint publications

Sukdong Yoo

1 joint publications

Young A Kim

1 joint publications

Seong Heon Kim

1 joint publications

Yoo Mi Kim

1 joint publications

Gilyazetdinov Kamil

1 joint publications

Ju Young Yoon

1 joint publications

Yun Hak Kim

1 joint publications

Rin Khang

1 joint publications

Hane Lee

1 joint publications

Jihye Kim

Frequent Collaborators

2 joint publications

Sukdong Yoo

1 joint publications

Young A Kim

1 joint publications

Seong Heon Kim

1 joint publications

Yoo Mi Kim

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