연구실적
<2015년 SCI 연구논문>
Lee SJ1, Chae JH2, Lee JA1, Cho SI1, Seo SH1, Park H1, Seong MW1, Park SS1. Non-homologous end joining repair mechanism-mediated deletion of CHD7 gene in a patient with typical CHARGE syndrome. Ann Lab Med. 2015 Jan;35(1):141-5. Epub 2014 Dec 8. PMID: 25553296
Roh EY1, In JW2, Shin S1, Yoon JH1, Park KU2, Song EY3. Performance of LIFECODES HLA-DQB1 typing kit using Luminex platform in Koreans. Ann Lab Med. 2015 Jan;35(1):123-7. Epub 2014 Dec 8. PMID: 25553292
Park H1, Rho EY2, In JW2, Kim I3, Yoon SS3, Park S3, Shin S2, Park KU2, Song EY2. The impact of HLA and KIR ligand mismatching on unrelated allogeneic hematopoietic stem cell transplantation in Korean adult patients. Ann Lab Med. 2015 Jan;35(1):111-7. Epub 2014 Dec 8. PMID: 25553290
In JW1, Roh EY1, Oh S2, Shin S1, Park KU1, Song EY3. Allele and Haplotype Frequencies of Human Leukocyte Antigen-A, -B, -C, -DRB1, and -DQB1 From Sequence-Based DNA Typing Data in Koreans. Ann Lab Med. 2015 Jul;35(4):429-35. Epub 2015 May 21. PMID: 26131415
Hwang JM1, Seong MW, Kim JH, Park SS. Absence of CHN1 in two patients with a bilateral absence of cranial nerves IV and VI. Graefes Arch Clin Exp Ophthalmol. 2015 Mar;253(3):491-2. Epub 2014 Oct 22. PMID: 25331612
Seo SH1, Hwang SM2, Ko JM3, Ko JS3, Hyun YJ1, Cho SI1, Park H1, Kim SY4, Seong MW1, Park SS1. Identification of novel mutations in the VPS33B gene involved in arthrogryposis, renal dysfunction, and cholestasis syndrome. Clin Genet. 2015 Jul;88(1):80-4. Epub 2014 Aug 7. PMID: 24917129
Park H1, Hong S1, Cho SI1, Cho TJ2, Choi IH2, Jin DK3, Sohn YB4, Park SW3, Cho HH5, Cheon JE5, Kim SY6, Kim JY7, Park SS8, Seong MW9. Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene. Eur J Med Genet. 2015 Mar;58(3):175-9. Epub 2014 Dec 24. PMID: 25542771
Park H1, Kang SH2, Park S3, Kim SY4, Seo SH5, Lee SJ5, Lee JA5, Cho SI5, Sung JJ6, Lee KW6, Kim JY7, Park SS8, Seong MW9. Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia. J Neurol Sci. 2015 Oct 15;357(1-2):167-72. Epub 2015 Jul 17. PMID: 26208798
Seong MW1, Seo SH1, Yu YS2, Hwang JM3, Cho SI1, Ra EK1, Park H1, Lee SJ1, Kim JY4, Park SS5. Diagnostic application of an extensive gene panel for Leber congenital amaurosis with severe genetic heterogeneity. J Mol Diagn. 2015 Jan;17(1):100-5. Epub 2014 Oct 24. PMID: 25445212
Oh EJ1, Park H2, Park KU3, Kang ES4, Kim HS5, Song EY6. Interlaboratory Comparison of the Results of Lifecodes LSA Class I and Class II Single Antigen Kits for Human Leukocyte Antigen Antibody Detection. Ann Lab Med. 2015 May;35(3):321-8. Epub 2015 Apr 1. PMID: 25932440
Kim JA1, Im KO2, Park SN2, Kwon JS2, Kim SY1, Oh K3, Lee DS3, Kim MK4, Kim SW4, Jang M5, Lee G5, Oh YM6, Lee SD6, Lee DS7. Cytogenetic heterogeneity and their serial dynamic changes during acquisition of cytogenetic aberrations in cultured mesenchymal stem cells. Mutat Res. 2015 Jul;777:60-8. Epub 2015 Apr 18. PMID: 25974687
Kim SY1, Im K, Park SN, Kwon J, Kim JA, Choi Q, Hwang SM, Han SH, Kwon S, Oh IH, Lee DS. Asymmetric aneuploidy in mesenchymal stromal cells detected by in situ karyotyping and fluorescence in situ hybridization: suggestions for reference values for stem cells. Stem Cells Dev. 2015 Jan 1;24(1):77-92. PMID: 25019198
Kim M1, Hwang S2, Park K2, Kim SY3, Lee YK4, Lee DS5. Increased expression of interferon signaling genes in the bone marrow microenvironment of myelodysplastic syndromes. PLoS One. 2015 Mar 24;10(3):e0120602. eCollection 2015. PMID: 25803272
Lee JS1, Im K2, Park SN2, Park HS1, Kim JA1, Choi Q1, Kim SY1, Cha CH3, Oh HS4, Kim IH5, Lee DS6. A challenging diagnosis: crystal-storing histiocytosis in plasma cell myeloma. Am J Clin Pathol. 2015 Feb;143(2):300-4. PMID: 25596257
Kim SY1, Im K2, Park SN2, Kwon J2, Kim JA1, Lee DS3. CALR, JAK2, and MPL mutation profiles in patients with four different subtypes of myeloproliferative neoplasms: primary myelofibrosis, essential thrombocythemia, polycythemia vera, and myeloproliferative neoplasm, unclassifiable. Am J Clin Pathol. 2015 May;143(5):635-44. PMID: 25873496
Lee SJ1, Tien HF2, Park HJ3, Kim JA1, Lee DS1,4. Gradual increase of chronic lymphocytic leukemia incidence in Korea, 1999-2010: comparison to plasma cell myeloma. Leuk Lymphoma. 2016;57(3):585-9. PMID: 26133722
<2016년 SCI 연구논문>
Kim SY, Park SJ, Cho SY, Cha RH, Jee HG, Kim G, Shin HS, Kim Y, Jung YM, Yang JS, Kim SS, Cho SI, Kim MJ, Lee JS, Lee SJ, Seo SH, Park SS, Seong MW. Viral RNA in Blood as Indicator of Severe Outcome in Middle East Respiratory Syndrome Coronavirus Infection. Emerg Infect Dis. 2016 Oct;22(10):1813-6. Epub 2016 Oct 15.
PMID: 27479636
Lee JS1, Lee JH2, Lee KE3, Kim JH2, Hong JM1, Ra EK1, Seo SH1, Lee SJ1, Kim MJ1, Park SS1, Seong MW4. Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma. BMC Med Genet. 2016 Jul 20;17(1):48. PMID: 27439424
Seong MW1, Cho SI1, Park H1, Seo SH1, Lee SJ1, Kim EC1, Park SS2. Genotyping Influenza Virus by Next-Generation Deep Sequencing in Clinical Specimens. Ann Lab Med. 2016 May;36(3):255-8. PMID: 26915615
Seong MW, Kim SY, Corman VM, Kim TS, Cho SI, Kim MJ, Lee SJ, Lee JS, Seo SH, Ahn JS, Yu BS, Park N, Oh MD, Park WB, Lee JY, Kim G, Joh JS, Jeong I, Kim EC, Drosten C, Park SS. Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015. Emerg Infect Dis. 2016 Feb;22(2):327-30.
PMID: 26814649
Kim MJ1, Cho SI1, Chae JH2, Lim BC2, Lee JS1, Lee SJ1, Seo SH1, Park H3, Cho A4, Kim SY5, Kim JY6, Park SS1, Seong MW7. Pitfalls of Multiple Ligation-Dependent Probe Amplifications in Detecting DMD Exon Deletions or Duplications. J Mol Diagn. 2016 Mar;18(2):253-9. Epub 2015 Dec 29. PMID: 26743743
Seo SH, Lee SJ, Park S, Kim MJ, Song JY, Ra EK, Cho SI, Kim HK, Yang MG, Kim JY, Park SS, Seong MW. Performance of two commercially available BCR-ABL1 quantification assays that use an international reporting scale. Clin Chem Lab Med. 2016 Jul 1;54(7):1157-60. PMID: 26587743
Seong MW1, Cho A2, Park HW1, Seo SH1, Lim BC3, Seol D1, Cho SI1, Park SS1, Chae JH3. Clinical applications of next-generation sequencing-based gene panel in patients with muscular dystrophy: Korean experience. Clin Genet. 2015 Jun 8. doi: 10.1111/cge.12621. [Epub ahead of print]. PMID: 26060040
Park WB1, Cho JY2, Park SI2, Kim EJ1, Yoon S2, Yoon SH2, Lee JO1, Koh Y1, Song KH1, Choe PG1, Yu KS2, Kim ES1, Bang SM1, Kim NJ1, Kim I1, Oh MD1, Kim HB3, Song SH4. Effectiveness of increasing the frequency of posaconazole syrup administration to achieve optimal plasma concentrations in patients with haematological malignancy. Int J Antimicrob Agents. 2016 Jul;48(1):106-10. Epub 2016 May 12. PMID: 27234674
Hwang SM1,2, Kim SY3, Kim JA2, Park HS2, Park SN4, Im K4, Kim K4, Kim SM4, Lee DS5,6. Short telomere length and its correlation with gene mutations in myelodysplastic syndrome. J Hematol Oncol. 2016 Jul 28;9(1):62. PMID: 27465399
Kim JA1, Hwang B2, Park SN3, Huh S2, Im K3, Choi S4, Chung HY1, Huh J5, Seo EJ6, Lee JH7, Bang D2, Lee DS1,3. Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing. PLoS One. 2016 Dec 13;11(12):e0167641. eCollection 2016. PMID: 27959900
Lee N1, Jun JH1, Lee DS2. Decreased sensitivity of the automatic white precursor cell channel (WPC) for blast flagging in patients with leukopenia. Clin Biochem. 2016 Jun;49(9):675-81. Epub 2016 Jan 19. PMID: 26800779