Chong Kun Cheon

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Venues

Human genomics

Yonsei medical journal

American journal of medical genetics. Part A

Journal of Korean medical science

Pusan National University School of Medicine

University of Ulsan College of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Pusan National University School of Medicine Mar 02 2009

South Korea

Associate Professor :: Pediatrics

Education History

University of Ulsan College of Medicine

South Korea

PHD :: Pediatrics

Publications

Sukdong Yoo, Chong Kun Cheon
NANS-CDG: Expanding clinical insights with a novel patient with novel variants. American journal of medical genetics. Part A (2024)
Unbeom Shin, Yeonsong Choi, Hwa Soo Ko, Kyungjae Myung, Semin Lee, Chong Kun Cheon, Yoonsung Lee
A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish. Human genomics 17 (1) (2023)
Unbeom Shin, Yeonsong Choi, Hwa Soo Ko, Kyungjae Myung, Semin Lee, Chong Kun Cheon, Yoonsung Lee
A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish. Human genomics 17 (1) (2023)
Unbeom Shin, Yeonsong Choi, Hwa Soo Ko, Kyungjae Myung, Semin Lee, Chong Kun Cheon, Yoonsung Lee
A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish. Human genomics 17 (1) (2023)
Unbeom Shin, Yeonsong Choi, Hwa Soo Ko, Kyungjae Myung, Semin Lee, Chong Kun Cheon, Yoonsung Lee
A heterozygous mutation in UBE2H in a patient with developmental delay leads to an aberrant brain development in zebrafish. Human genomics 17 (1) (2023)
Gilyazetdinov Kamil, Ju Young Yoon, Sukdong Yoo, Chong Kun Cheon
Clinical relevance of targeted exome sequencing in patients with rare syndromic short stature. Orphanet journal of rare diseases 16 (1) (2021)
Joo Young Lee, Ji Hye Lee, Chong Kun Cheon
Functional Characterization of Gomisin N in High-Fat-Induced Drosophila Obesity Models. International journal of molecular sciences 21 (19) (2020)
Chong Kun Cheon, Yeoun Joo Lee, Sukdong Yoo, Jung Hee Lee, Jeong Eun Lee, Hyun Ji Kim, Im Jeong Choi, Yeonsong Choi, Semin Lee, Ju Young Yoon
Delineation of the genetic and clinical spectrum, including candidate genes, of monogenic diabetes: a multicenter study in South Korea. Journal of pediatric endocrinology & metabolism : JPEM 33 (12) (2020)
Chong Kun Cheon
Association of Obesity or Overweight with Bone Health in Childhood and Adolescence: Another Health Risk Never to Be Underestimated. Journal of Korean medical science 32 (10) (2019)
Young A Kim, Seong Heon Kim, Chong Kun Cheon, Yoo-Mi Kim
A Rare Cause of Life-Threatening Ketoacidosis: Novel Compound Heterozygous OXCT1 Mutations Causing Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. Yonsei medical journal 60 (3) (2019)

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Publication Activity (10 Years)

Top Topics

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Chong Kun Cheon