Jung-Min Ko, Ph.D. - Publications

2001 University of Texas at Austin, Austin, Texas, U.S.A. 
Bilingual and Multicultural Education, Speech Communication, Adult and Continuing Education

166 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Lee Y, Choi Y, Seo GH, Kim GH, Choi IH, Keum C, Ko JM, Cheon CK, Jeon J, Choi JH, Yoo HW, Lee BH. Clinical and molecular spectra of BRAF-associated RASopathy. Journal of Human Genetics. PMID 33040082 DOI: 10.1038/s10038-020-00852-3  0.8
2020 Lee JS, Kim HY, Lee YA, Lee SY, Cho TJ, Ko JM. Clinical and Genetic Characteristics of 23 Korean Patients with Haploinsufficiency of the Short-stature Homeobox-containing Gene. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. PMID 32932528 DOI: 10.1055/a-1247-4863  0.64
2020 Lee JS, Jin HY, Ko JM, Kim SH, Han N, Park BK, Park M, Park HJ, Lee JA. Hyperammonemic Encephalopathy Mimicking Ornithine Transcarbamylase Deficiency in Fibrolamellar Hepatocellular Carcinoma: Successful Treatment with Continuous Venovenous Hemofiltration and Ammonia Scavengers. Cancer Research and Treatment : Official Journal of Korean Cancer Association. PMID 32898940 DOI: 10.4143/crt.2020.575  0.6
2020 Park HJ, Shin CH, Yoo WJ, Cho TJ, Kim MJ, Seong MW, Park SS, Lee JH, Sim NS, Ko JM. Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations. Orphanet Journal of Rare Diseases. 15: 205. PMID 32778138 DOI: 10.1186/s13023-020-01480-y  0.68
2020 Shin S, Suh DI, Ko JM, Park JD, Lee JM, Yi NJ, Kim YT, Park S, Lee S, Koh J, Choi YH. Combined lung and liver transplantation for noncirrhotic portal hypertension with severe hepatopulmonary syndrome in a patient with dyskeratosis congenital. Pediatric Transplantation. e13802. PMID 32777145 DOI: 10.1111/petr.13802  0.68
2020 Lee SH, Ko JM, Song MK, Song J, Park KS. A Korean child diagnosed with malonic aciduria harboring a novel start codon mutation following presentation with dilated cardiomyopathy. Molecular Genetics & Genomic Medicine. e1379. PMID 32602666 DOI: 10.1002/mgg3.1379  0.68
2020 Bang E, Kim YE, Ko JM, Kim MJ, Park SS, Seong MW, Mun JH. Lentigo Maligna in a Patient with Xeroderma Pigmentosum, Variant type: A case report with dermoscopic findings and review of the literature. Photodermatology, Photoimmunology & Photomedicine. PMID 32379927 DOI: 10.1111/phpp.12568  0.68
2020 Lee Y, Park S, Lee JS, Kim SY, Cho J, Yoo Y, Lee S, Yoo T, Lee M, Seo J, Lee J, Kneissl J, Lee J, Jeon H, Jeon EY, ... ... Ko JM, et al. Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population. Scientific Reports. 10: 1413. PMID 31996704 DOI: 10.1038/s41598-020-58101-8  0.68
2019 Lim C, Jung ST, Shin CH, Park MS, Yoo WJ, Chung CY, Choi IH, Ko JM, Cho TJ. Diagnosis and Management of Hip Dislocation in Patients with Kabuki Syndrome. Clinics in Orthopedic Surgery. 11: 474-481. PMID 31788172 DOI: 10.4055/cios.2019.11.4.474  0.52
2019 Ryu J, Ko JM, Shin CH. A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-up. Bmc Medical Genetics. 20: 188. PMID 31775791 DOI: 10.1186/s12881-019-0921-9  0.4
2019 Kim BY, Ko JM, Park MH, Koo SK. Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation. Stem Cell Research. 41: 101622. PMID 31715426 DOI: 10.1016/j.scr.2019.101622  0.44
2019 Park HJ, Ko JM, Lim J, Hong JH. American consumers' perception and acceptance of an ethnic food with strong flavor: A case study of Kimchi with varying levels of red pepper and fish sauce. Journal of the Science of Food and Agriculture. PMID 31646649 DOI: 10.1002/jsfa.10106  0.44
2019 Fiordaliso SK, Iwata-Otsubo A, Ritter AL, Quesnel-Vallières M, Fujiki K, Nishi E, Hancarova M, Miyake N, Morton JEV, Lee S, Hackmann K, Bando M, Masuda K, Nakato R, Arakawa M, ... ... Ko JM, et al. Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment. American Journal of Human Genetics. PMID 31587868 DOI: 10.1016/j.ajhg.2019.09.009  0.52
2019 Han SR, Lee YA, Shin CH, Yang SW, Lim BC, Cho TJ, Ko JM. Clinical and Molecular Characteristics of GNAS Inactivation Disorders Observed in 18 Korean Patients. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. PMID 31546270 DOI: 10.1055/a-1001-3575  0.52
2019 Choi N, Ko JM, Shin SH, Kim EK, Kim HS, Song MK, Choi CW. Phenotypic and Genetic Characteristics of Five Korean Patients with Costello Syndrome. Cytogenetic and Genome Research. PMID 31394527 DOI: 10.1159/000502045  0.48
2019 Sohn YB, Ko JM, Jang JY, Seong MW, Park SS, Suh DI, Ko JS, Shin CH. Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis. European Journal of Medical Genetics. 103681. PMID 31136843 DOI: 10.1016/j.ejmg.2019.103681  0.64
2019 Ko JM, Kim WJ, Kim SY, Lee JH, Chae JH, Kim KJ, Lim BC. Hyperammonemia in a case of herpes simplex and anti-N-methyl-d-aspartate receptor encephalitis. Brain & Development. PMID 30961960 DOI: 10.1016/j.braindev.2019.03.013  0.56
2019 Kim SY, Lim BC, Lee JS, Kim WJ, Kim H, Ko JM, Kim KJ, Choi SA, Kim H, Hwang H, Choi JE, Cho A, Moon J, Seong MW, Park SS, et al. The Korean undiagnosed diseases program: lessons from a one-year pilot project. Orphanet Journal of Rare Diseases. 14: 68. PMID 30894207 DOI: 10.1186/s13023-019-1041-5  0.64
2018 Heo YJ, Ko JM, Lee YA, Shin CH, Yang SW, Kim MJ, Park SS. Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy. Annals of Pediatric Endocrinology & Metabolism. 23: 220-225. PMID 30599484 DOI: 10.6065/apem.2018.23.4.220  0.68
2018 Kim SY, Ko JM, Choi SA, Cho A, Lee JS, Lim BC, Kim KJ, Chae JH. A 3-Month-Old Boy With Progressive Weakness. Brain Pathology (Zurich, Switzerland). 28: 773-774. PMID 30375113 DOI: 10.1111/bpa.12651  0.52
2018 Park PG, Park E, Hyun HS, Kang HG, Ha IS, Cho TJ, Ko JM, Cheong HI. Cutaneous Skeletal Hypophosphatemia Syndrome in Association with a Mosaic Mutation. Annals of Clinical and Laboratory Science. 48: 665-669. PMID 30373874  0.52
2018 Kang Y, Nam SH, Park KS, Kim Y, Kim JW, Lee E, Ko JM, Lee KA, Park I. DeviCNV: detection and visualization of exon-level copy number variants in targeted next-generation sequencing data. Bmc Bioinformatics. 19: 381. PMID 30326846 DOI: 10.1186/s12859-018-2409-6  0.68
2018 Kim YJ, Ko JM, Song J, Lee KA. Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases. Annals of Laboratory Medicine. 38: 616-618. PMID 30027710 DOI: 10.3343/alm.2018.38.6.616  0.68
2018 Ko JM, Park KS, Kang Y, Nam SH, Kim Y, Park I, Chae HW, Lee SM, Lee KA, Kim JW. A New Integrated Newborn Screening Workflow Can Provide a Shortcut to Differential Diagnosis and Confirmation of Inherited Metabolic Diseases. Yonsei Medical Journal. 59: 652-661. PMID 29869463 DOI: 10.3349/ymj.2018.59.5.652  0.68
2018 Kim D, Ko JM, Kim YM, Seo GH, Kim GH, Lee BH, Yoo HW. Low prevalence of argininosuccinate lyase deficiency among inherited urea cycle disorders in Korea. Journal of Human Genetics. PMID 29773863 DOI: 10.1038/s10038-018-0467-2  0.8
2018 Kim YM, Seo GH, Kim GH, Ko JM, Choi JH, Yoo HW. A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing. Bmc Medical Genetics. 19: 35. PMID 29506479 DOI: 10.1186/s12881-018-0546-4  0.8
2017 Kim KY, Kim JW, Lee KJ, Park E, Kang GH, Choi YH, Kim WS, Ko JM, Moon JS, Ko JS. A Novel Homozygous LIPA Mutation in a Korean Child with Lysosomal Acid Lipase Deficiency. Pediatric Gastroenterology, Hepatology & Nutrition. 20: 263-267. PMID 29302509 DOI: 10.5223/pghn.2017.20.4.263  0.6
2017 Kang HG, Lee M, Lee KB, Hughes M, Kwon BS, Lee S, McNagny KM, Ahn YH, Ko JM, Ha IS, Choi M, Cheong HI. Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome. Experimental & Molecular Medicine. 49: e414. PMID 29244787 DOI: 10.1038/emm.2017.227  0.52
2017 Choi JH, Lee BH, Heo SH, Kim GH, Kim YM, Kim DS, Ko JM, Sohn YB, Hong YH, Lee DH, Kook H, Lim HH, Kim KH, Kim WS, Hong GR, et al. Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype. Medicine. 96: e7387. PMID 28723748 DOI: 10.1097/MD.0000000000007387  0.8
2017 Kim SJ, Ko JM, Shin SH, Kim EK, Kim HS, Lee KA. Korean Monozygotic Twins with Lethal Acantholytic Epidermolysis Bullosa Caused by Two Novel DSP Mutations. Annals of Clinical and Laboratory Science. 47: 213-216. PMID 28442525  0.68
2017 An S, Cha HJ, Ko JM, Han H, Kim SY, Kim KS, Lee SJ, An IS, Kim S, Youn HJ, Ahn KJ, Kim SY. Kinetin Improves Barrier Function of the Skin by Modulating Keratinocyte Differentiation Markers. Annals of Dermatology. 29: 6-12. PMID 28223740 DOI: 10.5021/ad.2017.29.1.6  0.56
2016 Ko JM, Cho JS, Yoo Y, Seo J, Choi M, Chae JH, Lee HR, Cho TJ. Wiedemann-Steiner Syndrome With 2 Novel KMT2A Mutations: Variable Severity in Psychomotor Development and Musculoskeletal Manifestation. Journal of Child Neurology. PMID 27777327 DOI: 10.1177/0883073816674095  0.6
2016 Yoo H, Ko JM, Lim BC, Cheong HI. First Korean Patients with Craniofrontonasal Syndrome Confirmed by EFNB1 Analysis. Annals of Clinical and Laboratory Science. 46: 544-548. PMID 27650623  0.52
2016 Choe Y, Park E, Hyun HS, Ko JM, Kang HG, Kim JH, Park SH, Cheong HI. A 7-year-old girl presenting with a Bartter-like phenotype: Answers. Pediatric Nephrology (Berlin, Germany). PMID 27534763 DOI: 10.1007/s00467-016-3480-8  0.6
2016 Choe Y, Park E, Hyun HS, Ko JM, Kang HG, Kim JH, Park SH, Cheong HI. A 7-year-old girl presenting with a Bartter-like phenotype: Questions. Pediatric Nephrology (Berlin, Germany). PMID 27534762 DOI: 10.1007/s00467-016-3473-7  0.44
2016 Kang HG, Lee HK, Ahn YH, Joung JG, Nam J, Kim NK, Ko JM, Cho MH, Shin JI, Kim J, Park HW, Park YS, Ha IS, Chung WY, Lee DY, et al. Targeted exome sequencing resolves allelic and the genetic heterogeneity in the genetic diagnosis of nephronophthisis-related ciliopathy. Experimental & Molecular Medicine. 48: e251. PMID 27491411 DOI: 10.1038/emm.2016.63  0.44
2016 Kim YM, Cheon CK, Park KH, Park S, Kim GH, Yoo HW, Lee KA, Ko JM. Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency. Annals of Clinical and Laboratory Science. 46: 360-6. PMID 27466294  0.8
2016 Shin S, Kim K, Lee MJ, Lee J, Choi S, Kim KS, Ko JM, Han H, Kim SY, Youn HJ, Ahn KJ, An IS, An S, Cha HJ. Epigallocatechin Gallate-Mediated Alteration of the MicroRNA Expression Profile in 5α-Dihydrotestosterone-Treated Human Dermal Papilla Cells. Annals of Dermatology. 28: 327-334. PMID 27274631 DOI: 10.5021/ad.2016.28.3.327  0.56
2016 Ko JM. Genetic Syndromes Associated with Craniosynostosis. Journal of Korean Neurosurgical Society. 59: 187-91. PMID 27226847 DOI: 10.3340/jkns.2016.59.3.187  0.6
2016 Jeon I, Cicchetti F, Cisbani G, Lee S, Li E, Bae J, Lee N, Li L, Im W, Kim M, Kim HS, Oh SH, Kim TA, Ko JJ, Aubé B, et al. Human-to-mouse prion-like propagation of mutant huntingtin protein. Acta Neuropathologica. PMID 27221146 DOI: 10.1007/s00401-016-1582-9  0.52
2016 Bae H, Lee D, Kim YW, Choi J, Lee HJ, Kim SW, Kim T, Noh YH, Ko JH, Bang H, Lim I. Effects of hydrogen peroxide on voltage-dependent K(+) currents in human cardiac fibroblasts through protein kinase pathways. The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology. 20: 315-24. PMID 27162486 DOI: 10.4196/kjpp.2016.20.3.315  0.32
2016 Cho SH, Chung KW, Kim JO, Jang H, Yoo JK, Choi Y, Ko JJ, Kim JH, Nishi Y, Yanase T, Lee WS, Kim NK. Association of miR-146aC>G, miR-149C>T, miR-196a2T>C, and miR-499A>G polymorphisms with risk of recurrent implantation failure in Korean women. European Journal of Obstetrics, Gynecology, and Reproductive Biology. 202: 14-19. PMID 27156151 DOI: 10.1016/j.ejogrb.2016.04.009  0.64
2016 Jo SJ, Ko JA, Park JS, Yim HW, Lee KM, Lee MS. Psychosocial Factors Associated with Suicide Re-attempts in Persons with Chronic Mental Disabilities in Korea. Community Mental Health Journal. PMID 27154333 DOI: 10.1007/s10597-016-0010-x  0.36
2016 Myeong J, Ko J, Hong C, Yang D, Lee KP, Jeon JH, So I. The interaction domains of transient receptor potential canonical (TRPC)1/4 and TRPC1/5 heteromultimeric channels. Biochemical and Biophysical Research Communications. PMID 27131740 DOI: 10.1016/j.bbrc.2016.04.138  0.44
2016 Choi IY, Lee WH, Lee JJ, Park MJ, Ko JA, Choi JR, Shin HD. Characterization of a Septobasidium sp. Associated with Felt Disease of Schisandra chinensis. Mycobiology. 44: 58-62. PMID 27103856 DOI: 10.5941/MYCO.2016.44.1.58  0.32
2016 Nielsen SR, Quaranta V, Linford A, Emeagi P, Rainer C, Santos A, Ireland L, Sakai T, Sakai K, Kim YS, Engle D, Campbell F, Palmer D, Ko JH, Tuveson DA, et al. Macrophage-secreted granulin supports pancreatic cancer metastasis by inducing liver fibrosis. Nature Cell Biology. PMID 27088855 DOI: 10.1038/ncb3340  0.52
2016 Choi JS, Yoo HW, Lee KJ, Ko JM, Moon JS, Ko JS. Novel Mutations in the CPT1A Gene Identified in the Patient Presenting Jaundice as the First Manifestation of Carnitine Palmitoyltransferase 1A Deficiency. Pediatric Gastroenterology, Hepatology & Nutrition. 19: 76-81. PMID 27066452 DOI: 10.5223/pghn.2016.19.1.76  0.6
2016 Lee KJ, Choi SJ, Kim WS, Park SS, Moon JS, Ko JS. Esophageal Stricture Secondary to Candidiasis in a Child with Glycogen Storage Disease 1b. Pediatric Gastroenterology, Hepatology & Nutrition. 19: 71-75. PMID 27066451 DOI: 10.5223/pghn.2016.19.1.71  0.6
2016 Choi SJ, Lee KJ, Choi JS, Yang HR, Moon JS, Chang JY, Ko JS. Poor Prognostic Factors in Patients with Parenteral Nutrition-Dependent Pediatric Intestinal Failure. Pediatric Gastroenterology, Hepatology & Nutrition. 19: 44-53. PMID 27066448 DOI: 10.5223/pghn.2016.19.1.44  0.6
2016 Lee KJ, Choi SJ, Yang HR, Chang JY, Kang HJ, Shin HY, Kang GH, Ko JS, Moon JS. Stepwise Endoscopy Based on Sigmoidoscopy in Evaluating Pediatric Graft-versus-Host Disease. Pediatric Gastroenterology, Hepatology & Nutrition. 19: 29-37. PMID 27066447 DOI: 10.5223/pghn.2016.19.1.29  0.6
2016 Lee MR, Tsai CJ, Hu JY, Lee SW, Ko JC, Wang HC, Yu CJ, Lee LN, Hsueh PR. Acquisition of Mycobacterium abscessus among ventilator-dependent patients in Taiwan chronic respiratory care facilities. Future Microbiology. PMID 27064349 DOI: 10.2217/fmb.16.6  0.64
2016 Baek SH, Ko JH, Lee H, Jung J, Kong M, Lee JW, Lee J, Chinnathambi A, Zayed ME, Alharbi SA, Lee SG, Shim BS, Sethi G, Kim SH, Yang WM, et al. Resveratrol inhibits STAT3 signaling pathway through the induction of SOCS-1: Role in apoptosis induction and radiosensitization in head and neck tumor cells. Phytomedicine : International Journal of Phytotherapy and Phytopharmacology. 23: 566-77. PMID 27064016 DOI: 10.1016/j.phymed.2016.02.011  0.36
2016 Nguyen VP, Cho JS, Choi YI, Lee SW, Han KH, Ko JH. Evaluation of a novel promoter from Populus trichocarpa for mature xylem tissue specific gene delivery. Plant Physiology and Biochemistry : Ppb / Societe Francaise De Physiologie Vegetale. 104: 226-233. PMID 27038601 DOI: 10.1016/j.plaphy.2016.03.033  0.6
2016 Yi NJ, Lee JM, Kim H, Choi Y, Lee HW, Kim HY, Jin US, Ko JS, Moon JS, Jung CW, Lee KW, Suh KS. Simple ellipsoid reconstruction technique for a hypoplastic portal vein during pediatric liver transplantation. Liver Transplantation : Official Publication of the American Association For the Study of Liver Diseases and the International Liver Transplantation Society. PMID 27028426 DOI: 10.1002/lt.24445  0.6
2016 Jung LY, Lee SR, Jung JM, Kim YS, Lee SH, Rhee KS, Chae JK, Lee DH, Kim DS, Kim WH, Ko JK. Rosuvastatin Reduces Blood Viscosity in Patients with Acute Coronary Syndrome. Korean Circulation Journal. 46: 147-53. PMID 27014344 DOI: 10.4070/kcj.2016.46.2.147  0.48
2016 Ko JK, Um Y, Woo HM, Kim KH, Lee SM. Ethanol production from lignocellulosic hydrolysates using engineered Saccharomyces cerevisiae harboring xylose isomerase-based pathway. Bioresource Technology. 209: 290-296. PMID 26990396 DOI: 10.1016/j.biortech.2016.02.124  0.44
2016 Kim SH, Lee NE, Lee JS, Shin JH, Lee JY, Ko JH, Chang CL, Kim YS. Identification of mycobacterial antigens in human urine using immunoglobulin G isolated from sera of patients with active pulmonary tuberculosis. Journal of Clinical Microbiology. PMID 26984972 DOI: 10.1128/JCM.00236-16  0.36
2016 Kim YS, Khazaei Z, Ko J, Afarideh H, Ghergherehchi M. Estimation of photoneutron yield in linear accelerator with different collimation systems by Geant4 and MCNPX simulation codes. Physics in Medicine and Biology. 61: 2762-2779. PMID 26975304 DOI: 10.1088/0031-9155/61/7/2762  0.52
2016 Gul R, Park DR, Shawl AI, Im SY, Nam TS, Lee SH, Ko JK, Jang KY, Kim D, Kim UH. Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) and Cyclic ADP-Ribose (cADPR) Mediate Ca2+ Signaling in Cardiac Hypertrophy Induced by β-Adrenergic Stimulation. Plos One. 11: e0149125. PMID 26959359 DOI: 10.1371/journal.pone.0149125  0.36
2016 Ko JW, Park JW, Shin NR, Kim JH, Cho YK, Shin DH, Kim JC, Lee IC, Oh SR, Ahn KS, Shin IS. Copper oxide nanoparticle induces inflammatory response and mucus production via MAPK signaling in human bronchial epithelial cells. Environmental Toxicology and Pharmacology. 43: 21-26. PMID 26934431 DOI: 10.1016/j.etap.2016.02.008  0.6
2016 Ko JM, Seo J, Choi M, Song J, Lee KA, Shin CH. Rare Korean Cases of Very-long-chain Acyl-CoA Dehydrogenase Deficiency with a Novel Recurrent Mutation. Annals of Clinical and Laboratory Science. 46: 97-101. PMID 26927351  0.68
2016 Ko YJ, Kim DY, Won SS, Ahn CW, Kim IW, Kingon AI, Kim S, Ko JH, Jung J. Flexible Pb(Zr0.52Ti0.48)O3 Films for a Hybrid Piezoelectric-Pyroelectric Nanogenerator under Harsh Environments. Acs Applied Materials & Interfaces. PMID 26923080 DOI: 10.1021/acsami.6b00054  0.6
2016 Ko J, Kim IY, Kim C, Kim DT, Huang JY, Shin S. Analysis and control of the photon beam position at PLS-II. Journal of Synchrotron Radiation. 23: 448-54. PMID 26917132 DOI: 10.1107/S1600577516001338  0.6
2016 Ko JA, Nam SH, Kim D, Lee JH, Kim YM. Identification of catalytic amino acid residues by chemical modification in dextranase. Journal of Microbiology and Biotechnology. PMID 26907761 DOI: 10.4014/jmb.1601.01014  0.48
2016 Oh JY, Ko JH, Ryu JS, Lee HJ, Kim MK, Wee WR. Transcription Profiling of NOD-like Receptors in the Human Cornea with Disease. Ocular Immunology and Inflammation. 1-6. PMID 26902715 DOI: 10.3109/09273948.2015.1130844  0.6
2016 Yeon Kim D, Young Park E, Chang E, Kang HG, Koo Y, Ji Lee E, Yeong Ko J, Kyung Kong H, Chun KH, Hoon Park J. A novel miR-34a target, protein kinase D1, stimulates cancer stemness and drug resistance through GSK3/β-catenin signaling in breast cancer. Oncotarget. PMID 26895471 DOI: 10.18632/oncotarget.7443  0.48
2016 Park JH, Ko J, Park YS, Park J, Hwang J, Koh HC. Clearance of Damaged Mitochondria Through PINK1 Stabilization by JNK and ERK MAPK Signaling in Chlorpyrifos-Treated Neuroblastoma Cells. Molecular Neurobiology. PMID 26892626 DOI: 10.1007/s12035-016-9753-1  0.48
2016 Jang H, Lee OH, Lee Y, Yoon H, Chang EM, Park M, Lee JW, Hong K, Kim JO, Kim NK, Ko JJ, Lee DR, Yoon TK, Lee WS, Choi Y. Melatonin prevents cisplatin-induced primordial follicle loss via suppression of PTEN/AKT/FOXO3a pathway activation in the mouse ovary. Journal of Pineal Research. PMID 26882203 DOI: 10.1111/jpi.12316  0.4
2016 Kim IG, Ko J, Lee HR, Do SH, Park K. Mesenchymal cells condensation-inducible mesh scaffolds for cartilage tissue engineering. Biomaterials. 85: 18-29. PMID 26854388 DOI: 10.1016/j.biomaterials.2016.01.048  0.48
2016 Kim K, Yoo D, Choi H, Tamang S, Ko JH, Kim S, Kim YH, Jeong S. Halide-Amine Co-Passivated Indium Phosphide Colloidal Quantum Dots in Tetrahedral Shape. Angewandte Chemie (International Ed. in English). PMID 26849683 DOI: 10.1002/anie.201600289  0.4
2016 Kim YJ, Ryu JS, Park SY, Lee HJ, Ko JH, Kim MK, Wee WR, Oh JY. Comparison of Topical Application of TSG-6, Cyclosporine, and Prednisolone for Treating Dry Eye. Cornea. PMID 26807900 DOI: 10.1097/ICO.0000000000000756  0.4
2016 Kim JE, Shin JM, Ko JY, Ro YS. Importance of concomitant topical therapy in moderate-to-severe atopic dermatitis treated with cyclosporine. Dermatologic Therapy. PMID 26799345 DOI: 10.1111/dth.12333  0.52
2016 Min Ko J, Jung S, Seo J, Ho Shin C, Il Cheong H, Choi M, Kim OH, Cho TJ. SOFT syndrome caused by compound heterozygous mutations of POC1A and its skeletal manifestation. Journal of Human Genetics. PMID 26791357 DOI: 10.1038/jhg.2015.174  0.32
2016 Lee HS, Kim KH, Kim EY, Lee SY, Ko JJ, Lee KA. Obox4-silencing activated STAT3 and MPF/MAPK signaling accelerate GVBD in mouse oocytes. Reproduction (Cambridge, England). PMID 26762402 DOI: 10.1530/REP-15-0020  0.64
2016 In S, Hong YJ, Yeom H, Ko J, Kim H, Park SJ. Thermal and structural analysis of a cryogenic conduction cooling system for a HTS NMR magnet Progress in Superconductivity and Cryogenics (Psac). 18: 59-63. DOI: 10.9714/psac.2016.18.1.059  0.36
2016 Ko JM, Kim J, Park SA, Jin KN, Ahn MI, Kim SC, Han DH. Depth of pleural effusion in thoracentesis: Comparison of lateral, posterolateral and posterior approaches in the supine position Iranian Journal of Radiology. 13. DOI: 10.5812/iranjradiol.20919  0.4
2016 Kim KM, Lee YG, Park JH, Ko JM. Supercapacitive Properties of Composite Electrode Consisting of Activated Carbon and Di(1-aminopyrene)quinone Etri Journal. 38: 252-259. DOI: 10.4218/etrij.16.2515.0018  0.48
2016 Ko JM, Kim YC. Algebraic and topological structures on factorizations of fuzzy sets 1 Journal of Intelligent and Fuzzy Systems. 30: 1709-1718. DOI: 10.3233/IFS-151881  0.88
2016 Ko JM, Kim YC. Upper M-approximate operators and M -closed sets 1 Journal of Intelligent and Fuzzy Systems. 30: 1697-1708. DOI: 10.3233/IFS-151880  0.96
2016 Kim HN, Park YJ, Kim JM, Lee JW, Ko JW, Kim HD, Lee SJ, Baek SS, Seo IS. The catalytic role of additive components for the nitridation of silicon/additive mixture Nippon Seramikkusu Kyokai Gakujutsu Ronbunshi/Journal of the Ceramic Society of Japan. 124: 192-196. DOI: 10.2109/jcersj2.15276  0.44
2016 Lee SY, Lee JK, Ko JJ. Implementation of system model applied to wearable device platform for the user's gesture recognition in vehicular environment Proceedings - 9th International Conference On Future Generation Communication and Networking, Fgcn 2015. 33-36. DOI: 10.1109/FGCN.2015.14  0.56
2016 Sim J, Lee H, Song K, Biswas S, Sharma A, Sharma GD, Ko J. Solution processed bulk heterojunction solar cells based on A-D-A small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups Journal of Materials Chemistry C. 4: 3508-3516. DOI: 10.1039/c6tc00323k  0.32
2016 Ryu J, Ko J, Lee H, Shin TG, Sohn D. Structural Response of Imogolite-Poly(acrylic acid) Hydrogel under Deformation Macromolecules. 49: 1873-1881. DOI: 10.1021/acs.macromol.5b02713  0.32
2016 Ko J, Kim BK, Han JW. Density Functional Theory Study for Catalytic Activation and Dissociation of CO2 on Bimetallic Alloy Surfaces Journal of Physical Chemistry C. 120: 3438-3447. DOI: 10.1021/acs.jpcc.6b00221  0.4
2016 Lee J, Han C, Lee TG, Chin J, Choi H, Lee W, Paik MJ, Won DH, Jeong G, Ko J, Yoon YJ, Nam SJ, Fenical W, Kang H. Marinopyrones A-D, α-pyrones from marine-derived actinomycetes of the family Nocardiopsaceae Tetrahedron Letters. 57: 1997-2000. DOI: 10.1016/j.tetlet.2016.03.084  0.4
2016 Lee HS, Latifatu M, Kim BC, Park JH, Lee YG, Kim KM, Park J, Baek YG, Ko JM. Supercapacitive properties of composite electrodes consisting of activated carbon and 1,4-dihydroxynaphthalene derivatives Synthetic Metals. 217: 29-36. DOI: 10.1016/j.synthmet.2016.03.012  0.48
2016 Sim J, Do K, Song K, Sharma A, Biswas S, Sharma GD, Ko J. D-A-D-A-D push pull organic small molecules based on 5,10-dihydroindolo[3,2-b]indole (DINI) central core donor for solution processed bulk heterojunction solar cells Organic Electronics: Physics, Materials, Applications. 30: 122-130. DOI: 10.1016/j.orgel.2015.11.036  0.32
2016 Kim KM, Lee YG, Shin DO, Ko JM. Supercapacitive properties of layered electrodes composed of electrodeposited RuO2 and polyaniline Electrochimica Acta. 196: 309-315. DOI: 10.1016/j.electacta.2016.02.194  0.48
2016 Cho HH, Kim WS, Choi YH, Cheon JE, Lee SM, Kim IO, Shin SM, Ko JS, Moon JS. Ultrasonography evaluation of infants with Alagille syndrome: In comparison with biliary atresia and neonatal hepatitis European Journal of Radiology. 85: 1045-1052. DOI: 10.1016/j.ejrad.2016.03.023  0.6
2016 Lee H, Jo H, Kim D, Biswas S, Sharma GD, Ko J. The effect of acceptor end groups on the physical and photovoltaic properties of A-π-D-π-A type oligomers with same S, N-heteropentacene central electron donor unit for solution processed organic solar cells Dyes and Pigments. 129: 209-219. DOI: 10.1016/j.dyepig.2016.02.029  0.32
2016 Choi H, Ko HM, Ko J. Stable and efficient star-shaped hole transporting materials with EDOT moiety as side arm for perovskite solar cells Dyes and Pigments. 126: 179-185. DOI: 10.1016/j.dyepig.2015.11.025  0.32
2016 Hamenu L, Lee HS, Latifatu M, Kim KM, Park J, Baek YG, Ko JM, Kaner RB. Lithium-silica nanosalt as a low-temperature electrolyte additive for lithium-ion batteries Current Applied Physics. 16: 611-617. DOI: 10.1016/j.cap.2016.03.012  0.48
2016 Lee JM, Jung KK, Ko JS. Formation of nickel microcones by using an electrodeposition solution containing H3BO3 Current Applied Physics. 16: 261-266. DOI: 10.1016/j.cap.2015.12.010  0.68
2016 Lee JM, Jung KK, Lee SH, Ko JS. One-step fabrication of nickel nanocones by electrodeposition using CaCl2·2H2O as capping reagent Applied Surface Science. 369: 163-169. DOI: 10.1016/j.apsusc.2016.02.006  0.68
2016 Park DJ, Sekhon SS, Ahn JY, Yoon H, Ko JH, Lee L, Kim YH, Min J. Proteomic analysis of lysosomal proteins in melanocyte B16F10 exposed to melanin Toxicology and Environmental Health Sciences. 8: 7-11. DOI: 10.1007/s13530-016-0256-2  0.48
2016 Le QAV, Sekhon SS, Lee L, Ko JH, Min J. Daphnia in water quality biomonitoring - “omic” approaches Toxicology and Environmental Health Sciences. 8. DOI: 10.1007/s13530-016-0255-3  0.48
2016 Lee JM, Jang CU, Choi CJ, Kwon KB, Han JS, Kwon NY, Ko JS. High-shock silicon accelerometer with an over-range stopper Journal of Mechanical Science and Technology. 30: 1817-1824. DOI: 10.1007/s12206-016-0338-8  0.68
2016 Kim KM, Lee YG, Shin DO, Ko JM. Supercapacitive properties of activated carbon electrode in potassium-polyacrylate hydrogel electrolytes Journal of Applied Electrochemistry. 1-7. DOI: 10.1007/s10800-016-0927-3  0.36
2016 Baek SH, Lee JH, Ko JH, Lee H, Nam D, Lee SG, Yang WM, Um JY, Lee J, Kim SH, Shim BS, Ahn KS. Ginkgetin Blocks Constitutive STAT3 Activation and Induces Apoptosis through Induction of SHP-1 and PTEN Tyrosine Phosphatases Phytotherapy Research. DOI: 10.1002/ptr.5557  0.36
2016 Ko J, Lee S, Shon T. Towards a novel quantification approach based on smart grid network vulnerability score International Journal of Energy Research. 40: 298-312. DOI: 10.1002/er.3356  0.52
2016 Choi KM, Lee E, Ko J, Kim JY, Lee S, Seo WS, Choi SM, Lee KH, Kimk SJ. Thermoelectric property of Ag-doped ZnSb/few-layer-graphene composites Bulletin of the Korean Chemical Society. 37: 720-724. DOI: 10.1002/bkcs.10760  0.4
2016 Cook JB, Kim HS, Yan Y, Ko JS, Robbennolt S, Dunn B, Tolbert SH. Mesoporous MoS2 as a Transition Metal Dichalcogenide Exhibiting Pseudocapacitive Li and Na-Ion Charge Storage Advanced Energy Materials. DOI: 10.1002/aenm.201501937  0.48
2016 Jung E, Ko J, Kim H. Design of customized local information system based on big data analysis International Journal of Applied Engineering Research. 11: 766-769.  0.36
2015 Kwon HI, Paek JO, Kim JE, Ro YS, Ko JY. Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis. The International Journal of Lower Extremity Wounds. PMID 26711368 DOI: 10.1177/1534734615623432  0.68
2015 Song KJ, Ko JH, Choi BW. Relationship between magnetic resonance imaging findings and spinal cord injury in extension injury of the cervical spine. European Journal of Orthopaedic Surgery & Traumatology : Orthopedie Traumatologie. PMID 26695064 DOI: 10.1007/s00590-015-1731-1  0.44
2015 Park HK, Kim EJ, Ko JY. Alitretinoin: treatment for refractory palmoplantar keratoderma. The British Journal of Dermatology. PMID 26617313 DOI: 10.1111/bjd.14327  0.68
2015 Choi H, Jo H, Paek S, Ko K, Ko HM, Lee JK, Ko J. Efficient Hole Transporting Materials with Triazole Core for High Efficiency Perovskite Solar Cells. Chemistry, An Asian Journal. PMID 26573775 DOI: 10.1002/asia.201501178  0.32
2015 Sohn YB, Ko JM, Shin CH, Yang SW, Chae JH, Lee KA. Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients. Journal of Human Genetics. PMID 26538304 DOI: 10.1038/jhg.2015.135  0.44
2015 Cheon CK, Ko JM. Kabuki syndrome: clinical and molecular characteristics. Korean Journal of Pediatrics. 58: 317-24. PMID 26512256 DOI: 10.3345/kjp.2015.58.9.317  0.68
2015 Paek S, Rub MA, Choi H, Kosa SA, Alamry KA, Cho JW, Gao P, Ko J, Asiri AM, Nazeeruddin MK. A dual-functional asymmetric squaraine-based low band gap hole transporting material for efficient perovskite solar cells. Nanoscale. PMID 26511537 DOI: 10.1039/c5nr05697g  0.32
2015 Jeon HW, Cho JS, Park EJ, Han KH, Choi YI, Ko JH. Developing xylem-preferential expression of PdGA20ox1, a gibberellin 20-oxidase 1 from Pinus densiflora, improves woody biomass production in a hybrid poplar. Plant Biotechnology Journal. PMID 26503830 DOI: 10.1111/pbi.12484  0.6
2015 Park JW, Lee IC, Shin NR, Jeon CM, Kwon OK, Ko JW, Kim JC, Oh SR, Shin IS, Ahn KS. Copper oxide nanoparticles aggravate airway inflammation and mucus production in asthmatic mice via MAPK signaling. Nanotoxicology. 1-8. PMID 26472121 DOI: 10.3109/17435390.2015.1078851  0.6
2015 Ko JM. Genetic Syndromes associated with Congenital Heart Disease. Korean Circulation Journal. 45: 357-61. PMID 26413101 DOI: 10.4070/kcj.2015.45.5.357  0.44
2015 Choi JH, Lee BH, Ko JM, Sohn YB, Lee JS, Kim GH, Heo SH, Park JY, Kim YM, Kim JH, Yoo HW. Erratum: A Phase 2 Multi-center, Open-label, Switch-over Trial to Evaluate the Safety and Efficacy of Abcertin® in Patients with Type 1 Gaucher Disease. Journal of Korean Medical Science. 30: 1373. PMID 26339182 DOI: 10.3346/jkms.2015.30.9.1373  0.8
2015 Yoon JK, Ahn KJ, Kwon BS, Kim GB, Bae EJ, Noh CI, Ko JM. The strong association of left-side heart anomalies with Kabuki syndrome. Korean Journal of Pediatrics. 58: 256-62. PMID 26300940 DOI: 10.3345/kjp.2015.58.7.256  0.32
2015 Choi JH, Lee BH, Kim JH, Kim GH, Kim YM, Cho J, Cheon CK, Ko JM, Lee JH, Yoo HW. Clinical outcomes and the mutation spectrum of the OTC gene in patients with ornithine transcarbamylase deficiency. Journal of Human Genetics. PMID 25994866 DOI: 10.1038/jhg.2015.54  0.8
2015 Choi JH, Lee BH, Ko JM, Sohn YB, Lee JS, Kim GH, Heo SH, Park JY, Kim YM, Kim JH, Yoo HW. A phase 2 multi-center, open-label, switch-over trial to evaluate the safety and efficacy of Abcertin® in patients with type 1 Gaucher disease. Journal of Korean Medical Science. 30: 378-84. PMID 25829804 DOI: 10.3346/jkms.2015.30.4.378  0.8
2015 Ko JM, Bae JS, Choi JS, Miura K, Lee HR, Kim OH, Kim NK, Oh SK, Ozono K, Lee CK, Choi IH, Park WY, Cho TJ. Skeletal overgrowth syndrome caused by overexpression of C-type natriuretic peptide in a girl with balanced chromosomal translocation, t(1;2)(q41;q37.1). American Journal of Medical Genetics. Part A. 167: 1033-8. PMID 25728306 DOI: 10.1002/ajmg.a.36884  0.44
2015 Han MS, Ko JM, Cho TJ, Park WY, Cheong HI. A novel NOTCH2 mutation identified in a Korean family with Hajdu-Cheney syndrome showing phenotypic diversity. Annals of Clinical and Laboratory Science. 45: 110-4. PMID 25696021  0.44
2015 Ko JK, Choi CH, Lee SW, Lee TH. Emergency placement of stent-graft for symptomatic acute carotid artery occlusion after endarterectomy. Journal of Neurointerventional Surgery. PMID 25653229 DOI: 10.1136/neurintsurg-2014-011553.rep  0.64
2015 Seo J, Choi IH, Lee JS, Yoo Y, Kim NK, Choi M, Ko JM, Shin YB. Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations. Journal of Human Genetics. 60: 213-5. PMID 25608830 DOI: 10.1038/jhg.2015.2  0.44
2015 Ko JY, Kang N, Lee JH, Kim JS, Kim WS, Park SJ, Kim YT, Jeon YJ. Angiotensin I-converting enzyme inhibitory peptides from an enzymatic hydrolysate of flounder fish (Paralichthys olivaceus) muscle as a potent anti-hypertensive agent Process Biochemistry. DOI: 10.1016/j.procbio.2016.01.009  0.36
2015 Park J, Ko J, Cha J, Jeong S. Stirling-type pulse tube refrigerator (PTR) with cold compression: Cold compressor, colder expander Cryogenics. DOI: 10.1016/j.cryogenics.2015.08.001  0.36
2015 Lee JM, Jung KK, Ko JS. Effect of NaCl in a nickel electrodeposition on the formation of nickel nanostructure Journal of Materials Science. 1-9. DOI: 10.1007/s10853-015-9614-8  0.68
2014 Rhie YJ, Lee KH, Ko JM, Lee WJ, Kim JH, Kim HS. KISS1 gene polymorphisms in Korean girls with central precocious puberty. Journal of Korean Medical Science. 29: 1120-5. PMID 25120323 DOI: 10.3346/jkms.2014.29.8.1120  0.68
2014 Park GH, Lee SJ, Yim H, Han JH, Kim HJ, Sohn YB, Ko JM, Jeong SY. TAGLN expression is upregulated in NF1-associated malignant peripheral nerve sheath tumors by hypomethylation in its promoter and subpromoter regions. Oncology Reports. 32: 1347-54. PMID 25109740 DOI: 10.3892/or.2014.3379  0.64
2014 Lee GM, Ko JM, Shin CH, Yang SW. A Korean boy with 46,XX testicular disorder of sex development caused by SOX9 duplication. Annals of Pediatric Endocrinology & Metabolism. 19: 108-12. PMID 25077096 DOI: 10.6065/apem.2014.19.2.108  0.4
2014 Park SH, Lee JE, Sohn YB, Ko JM. First identified Korean family with Sotos syndrome caused by a novel intragenic mutation in NSD1. Annals of Clinical and Laboratory Science. 44: 228-31. PMID 24795065  0.48
2014 Cheon CK, Sohn YB, Ko JM, Lee YJ, Song JS, Moon JW, Yang BK, Ha IS, Bae EJ, Jin HS, Jeong SY. Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome. Journal of Human Genetics. 59: 321-5. PMID 24739679 DOI: 10.1038/jhg.2014.25  0.44
2014 Lee HJ, Yoon SC, Ko JM, Seong MW, Park SS, Choi JS, Oh SK. Monochorionic dizygotic twins with discordant sex and confined blood chimerism. European Journal of Pediatrics. 173: 1249-52. PMID 24706113 DOI: 10.1007/s00431-014-2312-8  0.64
2014 Choi Y, Yi NJ, Ko JS, Ko JM, Jin US, Kim HS, Lee KH, Cho TJ, Suh SW, Yoo T, Lee KW, Suh KS. Living donor liver transplantation for an infant with osteogenesis imperfecta and intrahepatic cholestasis: report of a case. Journal of Korean Medical Science. 29: 441-4. PMID 24616597 DOI: 10.3346/jkms.2014.29.3.441  0.36
2014 Kim JH, Ko JM, Tchah H. Fuchs Endothelial Corneal Dystrophy in a Heterozygous Carrier of Congenital Hereditary Endothelial Dystrophy Type 2 with a Novel Mutation in SLC4A11. Ophthalmic Genetics. PMID 24502824 DOI: 10.3109/13816810.2014.881510  0.68
2014 Kang YH, Jeong S, Ko JM, Lee JY, Choi Y, Lee C, Cho SY. Two-component solution processing of oxide semiconductors for thin-film transistors via self-combustion reaction Journal of Materials Chemistry C. 2: 4247-4256. DOI: 10.1039/c4tc00139g  0.4
2013 Lee CG, Park SJ, Yun JN, Ko JM, Kim HJ, Yim SY, Sohn YB. Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center study. Yonsei Medical Journal. 54: 1463-70. PMID 24142652 DOI: 10.3349/ymj.2013.54.6.1463  0.64
2013 Min BJ, Ko JM, Seo ME, Choi JS, Oh SK, Jeon J, Kim E, Moon JE, Choi IH, Lee C, Kim OH, Cho TJ, Park WY. An interstitial, apparently-balanced chromosomal insertion in the etiology of Langer-Giedion syndrome in an Asian family. European Journal of Medical Genetics. 56: 561-5. PMID 23832104 DOI: 10.1016/j.ejmg.2013.06.011  0.6
2013 Ko JM, Choi IH, Baek GH, Kim KW. First Korean family with a mutation in TPM2 associated with Sheldon-Hall syndrome. Journal of Korean Medical Science. 28: 780-3. PMID 23678273 DOI: 10.3346/jkms.2013.28.5.780  0.48
2013 Ko JM, Sohn YB, Jeong SY, Kim HJ, Messiaen LM. Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1. Pediatric Neurology. 48: 447-53. PMID 23668869 DOI: 10.1016/j.pediatrneurol.2013.02.004  0.64
2013 Choi SA, Ko JM, Shin CH, Yang SW, Choi JS, Oh SK. Monozygotic twin discordant for Down syndrome: mos 47,XX,+21/46,XX and 46,XX. European Journal of Pediatrics. 172: 1117-20. PMID 23559333 DOI: 10.1007/s00431-013-1998-3  0.44
2013 Ko JM, Lim BC, Kim KJ, Hwang YS, Ryu HW, Lee JH, Kim JS, Chae JH. Distinct neurological features in a patient with Schinzel-Giedion syndrome caused by a recurrent SETBP1 mutation. Child's Nervous System : Chns : Official Journal of the International Society For Pediatric Neurosurgery. 29: 525-9. PMID 23400866 DOI: 10.1007/s00381-013-2047-2  0.56
2013 Sohn YB, Lee CG, Ko JM, Yang JA, Yun JN, Jung EJ, Jin HS, Park SJ, Jeong SY. Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations. Journal of Human Genetics. 58: 73-7. PMID 23190751 DOI: 10.1038/jhg.2012.135  0.48
2012 Ko JM, Shin CH, Yang SW, Seong MW, Park SS, Song J. The first Korean case of lysinuric protein intolerance: presented with short stature and increased somnolence. Journal of Korean Medical Science. 27: 961-4. PMID 22876067 DOI: 10.3346/jkms.2012.27.8.961  0.64
2012 Ko JM, Park HK, Yang S, Hwang IT. Influence of catch-up growth on IGFBP-2 levels and association between IGFBP-2 and cardiovascular risk factors in Korean children born SGA. Endocrine Journal. 59: 725-33. PMID 22673199 DOI: DN/JST.JSTAGE/endocrj/EJ12-0080  0.44
2012 Ko JM, Yang S, Kim SY, Lee HS, Hwang JS, Hwang IT. E23K polymorphism of the KCNJ11 gene in Korean children with type 1 diabetes. World Journal of Pediatrics : Wjp. 8: 169-72. PMID 22573428 DOI: 10.1007/s12519-012-0355-3  0.64
2012 Ko JM, Jeong SY, Yang JA, Park DH, Yoon SH. Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations. Plastic and Reconstructive Surgery. 129: 814e-21e. PMID 22544111 DOI: 10.1097/PRS.0b013e31824a2dda  0.36
2012 Ko JM, Yang JA, Jeong SY, Kim HJ. Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism. Molecular Medicine Reports. 5: 943-8. PMID 22294196 DOI: 10.3892/mmr.2012.764  0.64
2012 Ko JM, Park HK, Yang S, Kim EY, Chung SC, Hwang IT. Association between insulin-like growth factor binding protein-2 levels and cardiovascular risk factors in Korean children. Endocrine Journal. 59: 335-43. PMID 22293585 DOI: JST.JSTAGE/endocrj/EJ11-0358  0.64
2011 Kim JH, Ko JM, Lee I, Kim JY, Kim MJ, Tchah H. A novel mutation of the decorin gene identified in a Korean family with congenital hereditary stromal dystrophy. Cornea. 30: 1473-7. PMID 21993463 DOI: 10.1097/ICO.0b013e3182137788  0.68
2011 Park SJ, Jung EH, Ryu RS, Kang HW, Ko JM, Kim HJ, Cheon CK, Hwang SH, Kang HY. Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases. Molecular Cytogenetics. 4: 12. PMID 21549014 DOI: 10.1186/1755-8166-4-12  0.44
2010 Kang SH, Choi SH, Seong NJ, Ko JM, Cho ES, Ko KP. Comparative study of lumbar magnetic resonance imaging and myelography in young soldiers with herniated lumbar disc. Journal of Korean Neurosurgical Society. 48: 501-5. PMID 21430976 DOI: 10.3340/jkns.2010.48.6.501  0.28
2010 Ko JM, Kim JB, Pai KS, Yun JN, Park SJ. Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome. Journal of Korean Medical Science. 25: 1798-801. PMID 21165297 DOI: 10.3346/jkms.2010.25.12.1798  0.48
2010 Ko JM, Kim SH. Clinical features and outcomes of holoprosencephaly in Korea. Pediatric Neurology. 43: 245-52. PMID 20837302 DOI: 10.1016/j.pediatrneurol.2010.05.001  0.6
2010 Park KB, Han KR, Lee JW, Kim SH, Kim do W, Kim C, Ko JM. Early diagnosis of fabry disease in a patient with toe tip pain. The Korean Journal of Pain. 23: 207-10. PMID 20830268 DOI: 10.3344/kjp.2010.23.3.207  0.6
2010 Ko JM, Lee HS, Hwang JS. KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect. Endocrine Journal. 57: 701-9. PMID 20631455 DOI: JST.JSTAGE/endocrj/K10E-073  0.64
2010 Cheon CK, Lee BH, Ko JM, Kim HJ, Yoo HW. Novel mutation in SLC6A19 causing late-onset seizures in Hartnup disorder. Pediatric Neurology. 42: 369-71. PMID 20399395 DOI: 10.1016/j.pediatrneurol.2010.01.009  0.8
2010 Ko JM, Cheon CK, Kim GH, Kim SH, Kim KS, Yoo HW. Clinical characterization and analysis of the SRD5A2 gene in six Korean patients with 5alpha-reductase type 2 deficiency. Hormone Research in PæDiatrics. 73: 41-8. PMID 20190539 DOI: 10.1159/000271915  0.8
2010 Ko JM, Kim JM, Kim GH, Lee BH, Yoo HW. Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome. Clinical Endocrinology. 73: 66-71. PMID 20148908 DOI: 10.1111/j.1365-2265.2010.03782.x  0.8
2010 Ko JM, Kim JM, Cheon CK, Kim DH, Lee DY, Cheong WY, Kim EY, Park MJ, Yoo HW. The common exon 3 polymorphism of the growth hormone receptor gene and the effect of growth hormone therapy on growth in Korean patients with Turner syndrome. Clinical Endocrinology. 72: 196-202. PMID 19681916 DOI: 10.1111/j.1365-2265.2009.03681.x  0.76
2009 Park JY, Kim GH, Kim SS, Ko JM, Lee JJ, Yoo HW. Effects of a chemical chaperone on genetic mutations in alpha-galactosidase A in Korean patients with Fabry disease. Experimental & Molecular Medicine. 41: 1-7. PMID 19287194 DOI: 10.3858/emm.2009.41.1.001  0.8
2009 Ko JM, Cheon CK, Kim GH, Yoo HW. A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase gene. European Journal of Pediatrics. 168: 877-80. PMID 18853185 DOI: 10.1007/s00431-008-0849-0  0.8
2009 Ko JM, Park JY, Yoo HW. Common exon 3 polymorphism of the GH receptor (GHR) gene and effect of GH therapy on growth in Korean children with idiopathic short stature (ISS). Clinical Endocrinology. 70: 82-7. PMID 18793346 DOI: 10.1111/j.1365-2265.2008.03418.x  0.8
2008 Nguyen HD, Ko JM, Kim HJ, Kim SK, Cho SH, Nam JD, Lee JY. Electrochemical properties of poly(3,4-ethylenedioxythiophene) nanofiber non-woven web formed by electrospinning. Journal of Nanoscience and Nanotechnology. 8: 4718-21. PMID 19049093 DOI: 10.1166/JNN.2008.IC39  0.64
2008 Ko JM, Kim JM, Kim GH, Yoo HW. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome. Journal of Human Genetics. 53: 999-1006. PMID 19020799 DOI: 10.1007/s10038-008-0343-6  0.8
2008 Ko JM, Kim GH, Kim KM, Hong SJ, Yoo HW. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis. Journal of Korean Medical Science. 23: 912-5. PMID 18955805 DOI: 10.3346/jkms.2008.23.5.912  0.8
2008 Choi JH, Cho YM, Suh KS, Yoon HR, Kim GH, Kim SS, Ko JM, Lee JH, Park YS, Yoo HW. Short-term efficacy of enzyme replacement therapy in Korean patients with Fabry disease. Journal of Korean Medical Science. 23: 243-50. PMID 18437007 DOI: 10.3346/jkms.2008.23.2.243  0.8
2007 Ko JM, Kim GH, Kim JH, Kim JY, Choi JH, Ushikai M, Saheki T, Kobayashi K, Yoo HW. Six cases of citrin deficiency in Korea. International Journal of Molecular Medicine. 20: 809-15. PMID 17982687  0.8
2007 Ko JM, Lee JH, Kim GH, Kim AR, Yoo HW. A case of a Korean newborn with IMAGe association presenting with hyperpigmented skin at birth. European Journal of Pediatrics. 166: 879-80. PMID 17120039 DOI: 10.1007/s00431-006-0321-y  0.8
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