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Ki-O Lee

KIT D816 mutation associates with adverse outcomes in core binding factor acute myeloid leukemia, especially in the subgroup with RUNX1/RUNX1T1 rearrangement
2012 · on behalf of AML/MDS working party, Korean Society of Hematology, Hee-Jin Kim, et al. · Annals of Hematology · 66
Founder effects in two predominant intronic mutations of UNC13D, c.118-308C>T and c.754-1G>C underlie the unusual predominance of type 3 familial hemophagocytic lymphohistiocytosis (FHL3) in Korea
2012 · on behalf of the Korea Histiocytosis Working Party, Ja Young Seo, et al. · Annals of Hematology · 43
Gene mutation profiles and prognostic implications in Korean patients with T-lymphoblastic leukemia
2013 · Hee Jae Huh, Soo Hyun Lee, et al. · Annals of Hematology · 21
Clinical significance of SF3B1 mutations in Korean patients with myelodysplastic syndromes and myelodysplasia/myeloproliferative neoplasms with ring sideroblasts
2013 · Ja Young Seo, Ki-O Lee, et al. · Annals of Hematology · 17
Mutation spectrum and inhibitor risk in 100 K orean patients with severe haemophilia A
2012 · H.‐J. Kim, H.‐J. Kim, et al. · Haemophilia · 15
Molecular genetic analysis of Korean patients with coagulation factor XII deficiency
2010 · Min-Jung Kwon, Hee-Jin Kim, et al. · Blood Coagulation & Fibrinolysis · 15
Paternal Somatic Mosaicism of a Novel Frameshift Mutation in ELANE Causing Severe Congenital Neutropenia
2015 · Hee-Jung Kim, Hee-Jung Kim, et al. · Pediatric Blood & Cancer · 13
Hereditary gene mutations in Korean patients with isolated erythrocytosis
2014 · Ja-Hyun Jang, Ja Young Seo, et al. · Annals of Hematology · 13
Distinct genetic profile with recurrent population-specific missense variants in Korean adult atypical hemolytic uremic syndrome
2020 · Jae Won Yun, Jisu Oh, et al. · Thrombosis Research · 11
High frequency of JAK2 exon 12 mutations in Korean patients with polycythaemia vera: novel mutations and clinical significance
2016 · Chang-Hun Park, Ki-O Lee, et al. · Journal of Clinical Pathology · 11
A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case Report.
2015 · Mi-Ae Jang, Ji-Yoon Kim, et al. · PubMed · 10
Maternal low-level somatic mosaicism of Cys155Tyr of F9 in severe hemophilia B
2014 · Hee-Jung Kim, Ki-O Lee, et al. · Blood Coagulation & Fibrinolysis · 10
Molecular characterization of female hemophilia A by multiplex ligation-dependent probe amplification analysis and X-chromosome inactivation study
2011 · Min-Jung Song, Hee-Jin Kim, et al. · Blood Coagulation & Fibrinolysis · 10
Prevalence of type 5 familial hemophagocytic lymphohistiocytosis in Korea and novel mutations in STXBP2
2015 · J.Y. Seo, J.Y. Seo, et al. · Clinical Genetics · 9
Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes
2012 · Hye In Woo, In-Ae Park, et al. · Blood Coagulation & Fibrinolysis · 8
Novel and recurrent mutations in the F13A1 gene in unrelated Korean patients with congenital factor XIII deficiency
2014 · Mi-Ae Jang, Young Shil Park, et al. · Blood Coagulation & Fibrinolysis · 7
Recurrent mutations and genotype–phenotype correlations in hereditary factor VII deficiency in Korea
2011 · Min-Jung Kwon, Ki-Young Yoo, et al. · Blood Coagulation & Fibrinolysis · 7
Sequence variation data of F8 and F9 genes in functionally validated control individuals: implications on the molecular diagnosis of hemophilia
2013 · Ja Young Seo, Mi-Ae Jang, et al. · Blood Research · 6
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Congenital factor V deficiency from compound heterozygous mutations with a novel variant c.2426del (p.Pro809Hisfs∗2) in the F5 gene
2020 · Chang-Hun Park, Min-Seung Park, et al. · Medicine · 5
The genomic architecture of the PROS1 gene underlying large tandem duplication mutation that causes thrombophilia from hereditary protein S deficiency
2014 · Ja Young Seo, Ki-O Lee, et al. · Gene · 5
Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiency
2010 · Hee-Jung Kim, Hee-Jin Kim, et al. · Blood Coagulation & Fibrinolysis · 5
Myelodysplastic Syndrome/Myeloproliferative Neoplasm with Ring Sideroblasts and Thrombocytosis with Cooccurrent SF3B1 and MPL Gene Mutations: A Case Report and Brief Review of the Literature
2019 · Chang-Hun Park, Jae Won Yun, et al. · Laboratory Medicine · 3
Evaluation of Imprecision for Analysis of Short Tandem Repeats by Use of Mixed Blood Cells in Variable Concentrations
2004 · Sun-Young Kong, Chang-Seok Ki, et al. · Clinical Chemistry · 3
Frequently Delayed Diagnosis and Misdiagnosis in MYH9-related Disorders: Data from Genetically Confirmed Cases of Korean Patients
2019 · Chang-Hun Park, Young-Eun Kim, et al. · Laboratory Medicine Online · 2
Monocytosis and Clonal Hematopoiesis in Peripheral Blood as Indicators of Myeloid Neoplasm in Erdheim-Chester Disease
2026 · Chang-Hun Park, SooHo Yu, et al. · Clinical Laboratory
Works count: 27
Citation count: 315
H-index: 10
I10-index: 13
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