PubRank

Kyung-A Lee

Author PubWeight™ 48.39‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Whole-genome sequencing and intensive analysis of the undomesticated soybean (Glycine soja Sieb. and Zucc.) genome. Proc Natl Acad Sci U S A 2010 2.15
2 Delta neutrophil index: a promising diagnostic and prognostic marker for sepsis. Shock 2012 1.31
3 CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia. Cancer Genet Cytogenet 2009 1.05
4 Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis. Cancer Genet Cytogenet 2009 0.99
5 Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean population. Clin Chem 2003 0.97
6 Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits. Cancer Genet Cytogenet 2009 0.94
7 Complete sequencing of a genetic polymorphism in NAT2 in the Korean population. Clin Chem 2002 0.93
8 Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts. Cancer Genet Cytogenet 2009 0.93
9 JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature. Cancer Genet Cytogenet 2009 0.92
10 Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy. Yonsei Med J 2011 0.86
11 TP53BP2 locus is associated with gastric cancer susceptibility. Int J Cancer 2005 0.86
12 LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD. Ann Dermatol 2011 0.85
13 The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis. J Korean Med Sci 2009 0.85
14 Profiling the dysregulated genes of keratinocytes in atopic dermatitis patients: cDNA microarray and interactomic analyses. J Dermatol Sci 2009 0.85
15 Cataloging coding sequence variations in human genome databases. PLoS One 2008 0.85
16 Novel in-frame deletion mutation in FLCN gene in a Korean family with recurrent primary spontaneous pneumothorax. Gene 2012 0.84
17 A novel PTEN mutation in a Korean patient with Cowden syndrome and vascular anomalies. Acta Derm Venereol 2011 0.84
18 CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations. Ann Lab Med 2011 0.84
19 Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics. Cancer Genet Cytogenet 2009 0.83
20 Rare translocations involving chromosome band 8p11 in myeloid neoplasms. Cancer Genet Cytogenet 2008 0.83
21 Determination of SMN1 and SMN2 copy numbers in a Korean population using multiplex ligation-dependent probe amplification. Korean J Lab Med 2010 0.83
22 Cytochrome P450 2C19 polymorphism is associated with reduced clopidogrel response in cerebrovascular disease. Yonsei Med J 2011 0.83
23 A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature. Cancer Genet Cytogenet 2009 0.82
24 MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities. Cancer Genet Cytogenet 2008 0.82
25 PutidaNET: interactome database service and network analysis of Pseudomonas putida KT2440. BMC Genomics 2009 0.82
26 Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years. Ann Clin Lab Sci 2010 0.82
27 Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature. Cancer Genet Cytogenet 2008 0.81
28 Delta neutrophil index discriminates true bacteremia from blood culture contamination. Clin Chim Acta 2013 0.81
29 Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23). Cancer Genet Cytogenet 2010 0.81
30 Automated detection of malaria-associated pseudoeosinophilia and abnormal WBC scattergram by the Sysmex XE-2100 hematology analyzer: a clinical study with 1,801 patients and real-time quantitative PCR analysis in vivax malaria-endemic area. Am J Trop Med Hyg 2010 0.81
31 Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA). Thromb Res 2009 0.81
32 A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis. Blood Coagul Fibrinolysis 2013 0.80
33 Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2):a case study and review of the literature. Cancer Genet Cytogenet 2009 0.79
34 BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia. Cancer Genet Cytogenet 2009 0.79
35 A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets. Ann Clin Lab Sci 2009 0.79
36 Cytogenetic features of 5q deletion and 5q- syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization. Cancer Genet Cytogenet 2010 0.79
37 ALK-positive anaplastic large cell lymphoma with TPM3-ALK translocation. Leuk Res 2012 0.78
38 Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations. Laryngoscope 2013 0.78
39 Spectrum of EGFR gene copy number changes and KRAS gene mutation status in Korean triple negative breast cancer patients. PLoS One 2013 0.78
40 Effectiveness of in silico tagSNP selection methods: virtual analysis of the genotypes of pharmacogenetic genes. Pharmacogenomics 2007 0.78
41 Ambras syndrome in a Korean patient with balanced pericentric inversion (8)(p11.2q24.2). J Dermatol Sci 2010 0.78
42 Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality. Cancer Genet Cytogenet 2008 0.78
43 Homozygous SMN2 deletion is a major risk factor among twenty-five Korean sporadic amyotrophic lateral sclerosis patients. Yonsei Med J 2012 0.78
44 Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia. Cancer Genet Cytogenet 2010 0.78
45 Copy number variation and gene rearrangements in CYP2D6 genotyping using multiplex ligation-dependent probe amplification in Koreans. Pharmacogenomics 2012 0.78
46 Tetrasomy 8 in a patient with acute monoblastic leukemia. Korean J Lab Med 2008 0.77
47 A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome. BMC Med Genet 2008 0.77
48 Efficacy of imatinib mesylate (STI571) in chronic neutrophilic leukemia with t(15;19): case report. Am J Hematol 2004 0.77
49 Differential association of RANTES-403 and IL-1B-1464 polymorphisms on histological subtypes in male Korean patients with gastric cancer. Tumour Biol 2013 0.77
50 Korean adolescents' perceptions of nutrition and health towards fast foods in Busan area. Nutr Res Pract 2008 0.77
51 A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal-dominant hereditary spastic paraplegia. J Hum Genet 2002 0.77
52 Interleukin 10 polymorphisms differentially influence the risk of gastric cancer in East Asians and Caucasians. Cytokine 2010 0.77
53 A case of late-onset Li-Fraumeni-like syndrome with unilateral breast cancer. Ann Lab Med 2013 0.77
54 A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing loss. Biochem Biophys Res Commun 2012 0.76
55 Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer. Cancer Genet Cytogenet 2009 0.76
56 Rapid identification of thrombocytopenia-associated multiple organ failure using red blood cell parameters and a volume/hemoglobin concentration cytogram. Yonsei Med J 2011 0.75
57 A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer. Cancer Genet Cytogenet 2008 0.75
58 t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma. Cancer Genet Cytogenet 2007 0.75
59 A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency. Ann Clin Lab Sci 2011 0.75
60 Refractory anemia with ring sideroblasts associated with marked thrombocytosis harboring cytogenetic abnormality dup(2)(p15p22) treated with decitabine. Leuk Lymphoma 2012 0.75
61 Comparison of VERSANT Hepatitis B virus DNA 3.0 Assay with Digene Hybrid Capture II Hepatitis B virus DNA test in relation to clinical status of Hepatitis B virus. Korean J Lab Med 2007 0.75
62 A novel three-way variant t(4;17;5)(p16;q23;q31) in a case of secondary plasma cell leukemia. Leuk Res 2012 0.75
63 Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine. Cancer Genet Cytogenet 2008 0.75
64 A Gly1609Arg missense mutation in the vWF gene in a Korean patient with von Willebrand disease type 2A. Ann Clin Lab Sci 2012 0.75
65 Acute promyelocytic leukemia with trisomy 8 and del(9)(q22) after treatment of cervical cancer with concurrent chemoradiotherapy: a case report. Onkologie 2011 0.75
66 An SRY-deleted XXY female resulting from a paternally inherited t(Y;22). Ann Clin Lab Sci 2010 0.75
67 Two case reports of 1q triplication in myeloproliferative neoplasms. Cancer Genet Cytogenet 2009 0.75
68 Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia. Cancer Genet Cytogenet 2009 0.75
69 Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis. Cancer Genet Cytogenet 2008 0.75
70 Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia. Cancer Genet Cytogenet 2008 0.75
71 A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia. Cancer Genet Cytogenet 2007 0.75
72 Analysis of mutations in the XPD gene in a patient with brittle hair. Ann Clin Lab Sci 2013 0.75
73 Assessment of real-time PCR method for detection of EGFR mutation using both supernatant and cell pellet of malignant pleural effusion samples from non-small-cell lung cancer patients. Clin Chem Lab Med 2017 0.75
74 Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21. Cancer Genet Cytogenet 2009 0.75
75 Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia. Cancer Genet Cytogenet 2009 0.75
76 Analytical Performance of Multiplex Real-Time PCR for Six Sexually Transmitted Pathogens. Clin Lab 2015 0.75