• 875 Citations
  • 16 h-Index
20012019
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Fingerprint Dive into the research topics where Jae Sung Ko is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 17 Similar Profiles
Mutation Medicine & Life Sciences
Pediatrics Medicine & Life Sciences
Liver Transplantation Medicine & Life Sciences
Korea Medicine & Life Sciences
Helicobacter pylori Medicine & Life Sciences
Liver Medicine & Life Sciences
Genes Medicine & Life Sciences
Cholestasis Medicine & Life Sciences

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Research Output 2001 2019

  • 875 Citations
  • 16 h-Index
  • 73 Article
  • 7 Review article
  • 2 Comment/debate

Deletion of exons 16–17b of CFTR is frequently identified in Korean patients with cystic fibrosis

Sohn, Y. B., Ko, J. M., Jang, J. Y., Seong, M-W., Park, S. S., Suh, D. I., Ko, J. S. & Shin, C. H., 1 Aug 2019, In : European Journal of Medical Genetics. 62, 8, 103681.

Research output: Contribution to journalArticleResearchpeer-review

Cystic Fibrosis Transmembrane Conductance Regulator
Cystic Fibrosis
Exons
Early Diagnosis
Alleles
1 Citation (Scopus)

Association between vitamin D deficiency and suspected nonalcoholic fatty liver disease in an adolescent population

Cho, Y. H., Kim, J. W., Shim, J. O., Yang, H., Chang, J. Y., Moon, J. S. & Ko, J. S., 1 May 2019, In : Pediatric Gastroenterology, Hepatology and Nutrition. 22, 3, p. 233-241 9 p.

Research output: Contribution to journalArticleResearchpeer-review

Vitamin D Deficiency
Population
Obesity
Nutrition Surveys
Waist Circumference

Benign recurrent intrahepatic cholestasis type 2 in siblings with novel ABCB11 mutations

Sohn, M. J., Woo, M. H., Seong, M-W., Park, S. S., Kang, G. H., Moon, J. S. & Ko, J. S., 1 Jan 2019, In : Pediatric Gastroenterology, Hepatology and Nutrition. 22, 2, p. 201-206 6 p.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
Jaundice
Siblings
Liver Function Tests
Cholestasis
Mutation
2 Citations (Scopus)
Epstein-Barr Virus Infections
Cytomegalovirus
Human Herpesvirus 4
Immunoglobulin M
Liver
1 Citation (Scopus)
Open Access
Hepatolenticular Degeneration
Multiplex Polymerase Chain Reaction
DNA Sequence Analysis
Phenotype
Mutation