• 1046 Citations
  • 17 h-Index
20052019
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Fingerprint Dive into the research topics where Moon-Woo Seong is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 9 Similar Profiles
Mutation Medicine & Life Sciences
Korea Medicine & Life Sciences
Genes Medicine & Life Sciences
Republic of Korea Medicine & Life Sciences
Exons Medicine & Life Sciences
Polymerase Chain Reaction Medicine & Life Sciences
Disease Outbreaks Medicine & Life Sciences
Assays Chemical Compounds

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Research Output 2005 2019

  • 1046 Citations
  • 17 h-Index
  • 109 Article
  • 9 Letter
  • 2 Review article

Evaluation of the new Abbott Real-Time EBV assay: fully automated quantification of EBV in whole blood by targeting BLLF1

Lee, J. S., Yoon, M., Kim, M. J., Cho, S. I., Seong, M-W., Park, S. S. & Kim, J. Y., 1 Jun 2019, In : Diagnostic Microbiology and Infectious Disease. 94, 2, p. 135-139 5 p.

Research output: Contribution to journalArticleResearchpeer-review

DNA Viruses
Viruses
Virus Diseases
Viral Load
Limit of Detection

Genetic mutation profiles in Korean patients with inherited retinal diseases

Kim, M. S., Joo, K., Seong, M-W., Kim, M. J., Park, K., Park, S. S. & Woo, S. J., 1 Jun 2019, In : Journal of Korean Medical Science. 34, 21

Research output: Contribution to journalArticleResearchpeer-review

Open Access
Retinal Diseases
Mutation
Genes
Korea
Choroideremia

The Korean undiagnosed diseases program: Lessons from a one-year pilot project

Kim, S. Y., Lim, B. C., Lee, J. S., Kim, W. J., Kim, H., Ko, J. M., Kim, K., Choi, S. A., Kim, H., Hwang, H., Choi, J., Cho, A., Moon, J., Seong, M-W., Park, S. S., Lee, Y. J., Kim, Y. O., Kim, J. S., Kim, W. S., Kwon, Y. S. & 7 othersPark, J. D., Ahn, Y., Hwang, J. Y., Park, H. Y., Lee, Y., Choi, M. & Chae, J. H., 20 Mar 2019, In : Orphanet Journal of Rare Diseases. 14, 1, 68.

Research output: Contribution to journalArticleResearchpeer-review

Open Access
Rare Diseases
Workflow
Molecular Biology
Exome
Process Assessment (Health Care)

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

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 Jan 2019, In : European Journal of Medical Genetics. 103681.

Research output: Contribution to journalArticleResearchpeer-review

Cystic Fibrosis Transmembrane Conductance Regulator
Cystic Fibrosis
Exons
Early Diagnosis
Alleles