Works by Jong-Keuk Lee
Results: 38
Are Genetic Variants Associated with the Location of Cerebral Arterial Lesions in Stroke Patients?
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- Cerebrovascular Diseases, 2020, v. 49, n. 3, p. 262, doi. 10.1159/000508301
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- Article
Porcine alveolar macrophage Mac-1 (CD11b/CD18) adhesion molecule expression.
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- Xenotransplantation, 1996, v. 3, n. 4, p. 304, doi. 10.1111/j.1399-3089.1996.tb00152.x
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- Article
Molecular cloning and characterization of the porcine CD 18 leukocyte adhesion molecule.
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- Xenotransplantation, 1996, v. 3, n. 2, p. 222, doi. 10.1111/j.1399-3089.1996.tb00141.x
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- Article
Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height.
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- Human Genetics, 2012, v. 131, n. 3, p. 471, doi. 10.1007/s00439-011-1096-4
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- Article
The CCR5 (−2135C/T) Polymorphism may be Associated with the Development of Kawasaki Disease in Korean Children.
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- Journal of Clinical Immunology, 2009, v. 29, n. 1, p. 22, doi. 10.1007/s10875-008-9218-z
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- Article
Associations between the neuron-specific glucocorticoid receptor (NR3C1) Bcl-1 polymorphisms and suicide in cancer patients within the first year of diagnosis.
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- Behavioral & Brain Functions, 2016, v. 12, p. 1, doi. 10.1186/s12993-016-0104-1
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- Article
Response to "Familial Intracranial Aneurysm Requires Not Only Whole-Exome Sequencing, But Also Mitochondrial DNA Sequencing".
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- Korean Journal of Radiology, 2022, v. 23, n. 5, p. 568, doi. 10.3348/kjr.2022.0084
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- Article
Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm.
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- Korean Journal of Radiology, 2022, v. 23, n. 1, p. 101, doi. 10.3348/kjr.2021.0467
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- Article
Rare Neurovascular Diseases in Korea: Classification and Related Genetic Variants.
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- Korean Journal of Radiology, 2021, v. 22, n. 8, p. 1379, doi. 10.3348/kjr.2020.1171
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- Article
Variations in the Number of CCL3L1 Gene Copies and Kawasaki Disease in Korean Children.
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- Pediatric Cardiology, 2012, v. 33, n. 8, p. 1259, doi. 10.1007/s00246-012-0289-5
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- Article
Assessment of Risk Factors for Korean Children with Kawasaki Disease.
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- Pediatric Cardiology, 2012, v. 33, n. 4, p. 513, doi. 10.1007/s00246-011-0143-1
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- Article
Genetic polymorphisms in the transforming growth factor beta-induced gene associated with BMI.
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- Human Mutation, 2005, v. 25, n. 3, p. 322, doi. 10.1002/humu.9315
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- Article
Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis.
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- Journal of Human Genetics, 2013, v. 58, n. 8, p. 521, doi. 10.1038/jhg.2013.43
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- Article
Identification of 15 loci influencing height in a Korean population.
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- Journal of Human Genetics, 2010, v. 55, n. 1, p. 27, doi. 10.1038/jhg.2009.116
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- Article
Polymorphisms in interleukin 8 and its receptors ( IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 781, doi. 10.1007/s10038-006-0021-5
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- Article
Polymorphisms in the leptin receptor (LEPR)—putative association with obesity and T2DM.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 85, doi. 10.1007/s10038-005-0327-8
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- Article
Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 112, doi. 10.1007/s10038-005-0331-z
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- Article
Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population.
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- Journal of Human Genetics, 2003, v. 48, n. 5, p. 213, doi. 10.1007/s10038-003-0011-9
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- Article
Mutations in DZIP1 and XYLT1 are associated with nonsyndromic early onset high myopia in the Korean population.
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- 2017
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- Letter to the Editor
Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis.
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- Rheumatology, 2022, v. 61, n. 3, p. 1204, doi. 10.1093/rheumatology/keab443
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- Article
The Association of a Single-Nucleotide Polymorphism of the IL-2 Inducible T-cell Kinase Gene with Asthma.
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- Annals of Human Genetics, 2011, v. 75, n. 3, p. 359, doi. 10.1111/j.1469-1809.2010.00637.x
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- Article
Joint Identification of Multiple Genetic Variants via Elastic-Net Variable Selection in a Genome-Wide Association Analysis.
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- Annals of Human Genetics, 2010, v. 74, n. 5, p. 416, doi. 10.1111/j.1469-1809.2010.00597.x
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- Article
Association of FLT3 Polymorphisms With Low BMD and Risk of Osteoporotic Fracture in Postmenopausal Women.
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- Journal of Bone & Mineral Research, 2007, v. 22, n. 11, p. 1752, doi. 10.1359/jbmr.070705
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- Article
Gene-Based Single Nucleotide Polymorphisms and Linkage Disequilibrium Patterns of 29 Asthma Candidate Genes in the Chromosome 5q31–33 Region in Koreans.
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- International Archives of Allergy & Immunology, 2006, v. 139, n. 3, p. 209, doi. 10.1159/000091166
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- Article
Large-scale identification and characterization of genetic variants in asthma candidate genes.
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- Immunogenetics, 2005, v. 57, n. 9, p. 636, doi. 10.1007/s00251-005-0024-y
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- Article
Identification of regulatory polymorphisms in the TNF–TNF receptor superfamily.
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- Immunogenetics, 2005, v. 57, n. 5, p. 297, doi. 10.1007/s00251-005-0800-8
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- Article
Development of SNP-based human identification system.
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- International Journal of Legal Medicine, 2010, v. 124, n. 2, p. 125, doi. 10.1007/s00414-009-0389-9
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- Article
Hygiene Hypothesis as the Etiology of Kawasaki Disease: Dysregulation of Early B Cell Development.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 22, p. 12334, doi. 10.3390/ijms222212334
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- Article
Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease?
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- Gut & Liver, 2015, v. 9, n. 6, p. 767, doi. 10.5009/gnl15176
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- Article
Preferential occurrence of spliceosome mutations in acute myeloid leukemia with preceding myelodysplastic syndrome and/or myelodysplasia morphology.
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- Leukemia & Lymphoma, 2015, v. 56, n. 8, p. 2301, doi. 10.3109/10428194.2014.995648
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- Article
Establishment of Kawasaki disease database based on metadata standard.
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- Database: The Journal of Biological Databases & Curation, 2016, v. 2016, p. 1, doi. 10.1093/database/baw109
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- Article
Frequency and Clinicopathologic Features of RUNX1 Mutations in Patients With Acute Myeloid Leukemia Not Otherwise Specified.
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- 2017
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- Publication type:
- journal article
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1241, doi. 10.1038/ng.981
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- Article
Identification of the TIFAB Gene as a Susceptibility Locus for Coronary Artery Aneurysm in Patients with Kawasaki Disease.
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- Pediatric Cardiology, 2019, v. 40, n. 3, p. 483, doi. 10.1007/s00246-018-1992-7
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- Article
Common Variants in the CRP Promoter are Associated with a High C-Reactive Protein Level in Kawasaki Disease.
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- Pediatric Cardiology, 2015, v. 36, n. 2, p. 438, doi. 10.1007/s00246-014-1032-1
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- Article
Replication and Meta-Analysis of GWAS Identified Susceptibility Loci in Kawasaki Disease Confirm the Importance of B Lymphoid Tyrosine Kinase (<i>BLK</i>) in Disease Susceptibility.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072037
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- Article
Frequent Amplification of CENPF, GMNN and CDK13 Genes in Hepatocellular Carcinomas.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043223
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- Article
Novel classification and pathogenetic analysis of hypoganglionosis and adult-onset Hirschsprung's disease.
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- 2011
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- Publication type:
- journal article