Hee-yeon Cho - Publications


33 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 Seo GH, Kim T, Choi IH, Park JY, Lee J, Kim S, Won DG, Oh A, Lee Y, Choi J, Lee H, Kang HG, Cho HY, Cho MH, Kim YJ, et al. Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE. Clinical Genetics. PMID 32901917 DOI: 10.1111/cge.13848  0.44
2015 Yang EM, Lee ST, Choi HJ, Cho HY, Lee JH, Kang HG, Park YS, Cheong HI, Ha IS. Tacrolimus for children with refractory nephrotic syndrome: a one-year prospective, multicenter, and open-label study of Tacrobell(®), a generic formula. World Journal of Pediatrics : Wjp. PMID 26684309 DOI: 10.1007/s12519-015-0062-y  0.44
2015 Lee JM, Park YS, Lee JH, Park SJ, Shin JI, Park YH, Yoo KH, Cho MH, Kim SY, Kim SH, Namgoong MK, Lee SJ, Lee JH, Cho HY, Han KH, et al. Atypical hemolytic uremic syndrome: Korean pediatric series. Pediatrics International : Official Journal of the Japan Pediatric Society. 57: 431-8. PMID 25443527 DOI: 10.1111/ped.12549  0.44
2014 Park E, Choi HJ, Lee JM, Ahn YH, Kang HG, Choi YM, Park SJ, Cho HY, Park YH, Lee SJ, Ha IS, Cheong HI. Muscle involvement in Dent disease 2. Pediatric Nephrology (Berlin, Germany). 29: 2127-32. PMID 24912603 DOI: 10.1007/s00467-014-2841-4  0.44
2013 Cho HY, Lee BH, Cheong HI. Translational read-through of a nonsense mutation causing Bartter syndrome. Journal of Korean Medical Science. 28: 821-6. PMID 23772144 DOI: 10.3346/jkms.2013.28.6.821  0.44
2013 Cho HY, Hyun HS, Kang HG, Ha IS, Cheong HI. Prevalence of 25(OH) vitamin D insufficiency and deficiency in pediatric patients on chronic dialysis. Peritoneal Dialysis International : Journal of the International Society For Peritoneal Dialysis. 33: 398-404. PMID 23209039 DOI: 10.3747/pdi.2011.00246  0.44
2012 Park KS, Hwang YJ, Cho MH, Ko CW, Ha IS, Kang HG, Cheong HI, Park YS, Lee YJ, Lee JH, Cho HY. Quality of life in children with end-stage renal disease based on a PedsQL ESRD module. Pediatric Nephrology (Berlin, Germany). 27: 2293-300. PMID 22832667 DOI: 10.1007/s00467-012-2262-1  0.44
2012 Park KS, Cho MH, Ha IS, Kang HG, Cheong HI, Park YS, Lee YJ, Lee JH, Cho HY. Validity and reliability of the Korean version of the pediatric quality of life ESRD module. Health and Quality of Life Outcomes. 10: 59. PMID 22672783 DOI: 10.1186/1477-7525-10-59  0.44
2012 Lee BH, Cho HY, Lee H, Han KH, Kang HG, Ha IS, Lee JH, Park YS, Shin JI, Lee DY, Kim SY, Choi Y, Cheong HI. Genetic basis of Bartter syndrome in Korea. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 27: 1516-21. PMID 21865213 DOI: 10.1093/ndt/gfr475  0.44
2011 Choi HJ, Cho HY, Ro H, Lee SH, Han KH, Lee H, Kang HG, Ha IS, Choi Y, Cheong HI. Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome. Pediatric Nephrology (Berlin, Germany). 26: 1981-8. PMID 21553324 DOI: 10.1007/s00467-011-1903-0  0.44
2010 Li A, Choi YS, Dziema H, Cao R, Cho HY, Jung YJ, Obrietan K. Proteomic profiling of the epileptic dentate gyrus. Brain Pathology (Zurich, Switzerland). 20: 1077-89. PMID 20608933 DOI: 10.1111/j.1750-3639.2010.00414.x  0.8
2010 Cao R, Li A, Cho HY, Lee B, Obrietan K. Mammalian target of rapamycin signaling modulates photic entrainment of the suprachiasmatic circadian clock. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 6302-14. PMID 20445056 DOI: 10.1523/JNEUROSCI.5482-09.2010  0.8
2009 Cao R, Li A, Cho HY. mTOR signaling in epileptogenesis: too much of a good thing? The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 12372-3. PMID 19812312 DOI: 10.1523/JNEUROSCI.3486-09.2009  0.8
2009 Choi YS, Lee B, Cho HY, Reyes IB, Pu XA, Saido TC, Hoyt KR, Obrietan K. CREB is a key regulator of striatal vulnerability in chemical and genetic models of Huntington's disease. Neurobiology of Disease. 36: 259-68. PMID 19632326 DOI: 10.1016/j.nbd.2009.07.014  0.8
2009 Lee B, Cao R, Choi YS, Cho HY, Rhee AD, Hah CK, Hoyt KR, Obrietan K. The CREB/CRE transcriptional pathway: protection against oxidative stress-mediated neuronal cell death. Journal of Neurochemistry. 108: 1251-65. PMID 19141071 DOI: 10.1111/j.1471-4159.2008.05864.x  0.8
2008 Mahler KL, Fleming JL, Dworkin AM, Gladman N, Cho HY, Mao JH, Balmain A, Toland AE. Sequence divergence of Mus spretus and Mus musculus across a skin cancer susceptibility locus Bmc Genomics. 9. PMID 19105829 DOI: 10.1186/1471-2164-9-626  0.8
2008 Park HW, Oh D, Kim N, Cho HY, Moon KC, Chae JH, Ahn HS, Choi Y, Cheong HI. Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease. Pediatric Nephrology (Berlin, Germany). 23: 1555-8. PMID 18481107 DOI: 10.1007/s00467-008-0847-5  0.44
2008 Cao R, Lee B, Cho HY, Saklayen S, Obrietan K. Photic regulation of the mTOR signaling pathway in the suprachiasmatic circadian clock. Molecular and Cellular Neurosciences. 38: 312-24. PMID 18468454 DOI: 10.1016/j.mcn.2008.03.005  0.8
2008 Choi HJ, Lee BH, Cho HY, Moon KC, Ha IS, Nagata M, Choi Y, Cheong HI. Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 51: 834-8. PMID 18436095 DOI: 10.1053/j.ajkd.2008.01.018  0.44
2008 Choi YS, Cho HY, Hoyt KR, Naegele JR, Obrietan K. IGF-1 receptor-mediated ERK/MAPK signaling couples status epilepticus to progenitor cell proliferation in the subgranular layer of the dentate gyrus. Glia. 56: 791-800. PMID 18338791 DOI: 10.1002/glia.20653  0.8
2008 Cho HY, Lee BH, Choi HJ, Ha IS, Choi Y, Cheong HI. Renal manifestations of Dent disease and Lowe syndrome. Pediatric Nephrology (Berlin, Germany). 23: 243-9. PMID 18038239 DOI: 10.1007/s00467-007-0686-9  0.44
2008 Cho HY, Lee JH, Choi HJ, Lee BH, Ha IS, Choi Y, Cheong HI. WT1 and NPHS2 mutations in Korean children with steroid-resistant nephrotic syndrome. Pediatric Nephrology (Berlin, Germany). 23: 63-70. PMID 17934764 DOI: 10.1007/s00467-007-0620-1  0.44
2007 Cheong HI, Cho HY, Kim JH, Yu YS, Ha IS, Choi Y. A clinico-genetic study of renal coloboma syndrome in children. Pediatric Nephrology (Berlin, Germany). 22: 1283-9. PMID 17541647 DOI: 10.1007/s00467-007-0525-z  0.44
2007 Cheong HI, Cho HY, Park HW, Ha IS, Choi Y. Molecular genetic study of congenital nephrogenic diabetes insipidus and rescue of mutant vasopressin V2 receptor by chemical chaperones. Nephrology (Carlton, Vic.). 12: 113-7. PMID 17371330 DOI: 10.1111/j.1440-1797.2006.00759.x  0.44
2007 Choi YS, Lin SL, Lee B, Kurup P, Cho HY, Naegele JR, Lombroso PJ, Obrietan K. Status epilepticus-induced somatostatinergic hilar interneuron degeneration is regulated by striatal enriched protein tyrosine phosphatase. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 2999-3009. PMID 17360923 DOI: 10.1523/JNEUROSCI.4913-06.2007  0.8
2007 Cho HY, Lee BS, Moon KC, Ha IS, Cheong HI, Choi Y. Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate. Pediatric Nephrology (Berlin, Germany). 22: 874-80. PMID 17295030 DOI: 10.1007/s00467-007-0438-x  0.44
2007 Lee BS, Cho HY, Kim EJ, Kang HG, Ha IS, Cheong HI, Kim JG, Lee HS, Choi Y. Clinical outcomes of childhood lupus nephritis: a single center's experience. Pediatric Nephrology (Berlin, Germany). 22: 222-31. PMID 17131162 DOI: 10.1007/s00467-006-0286-0  0.44
2007 Cheong HI, Cho HY, Moon KC, Ha IS, Choi Y. Pattern of double glomerulopathy in children. Pediatric Nephrology (Berlin, Germany). 22: 521-7. PMID 17109138 DOI: 10.1007/s00467-006-0342-9  0.44
2007 Paik KH, Lee BH, Cho HY, Kang HG, Ha IS, Cheong HI, Jin DK, Moon KC, Choi Y. Primary focal segmental glomerular sclerosis in children: clinical course and prognosis. Pediatric Nephrology (Berlin, Germany). 22: 389-95. PMID 17058050 DOI: 10.1007/s00467-006-0301-5  0.44
2006 Lee BH, Cho HY, Kang HG, Ha IS, Cheong HI, Moon KC, Lim IS, Choi Y. Idiopathic membranous nephropathy in children. Pediatric Nephrology (Berlin, Germany). 21: 1707-15. PMID 16951933 DOI: 10.1007/s00467-006-0246-8  0.44
2006 Cho HY, Lee BS, Kang CH, Kim WH, Ha IS, Cheong HI, Choi Y. Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect. Pediatric Nephrology (Berlin, Germany). 21: 1909-12. PMID 16932893 DOI: 10.1007/s00467-006-0273-5  0.44
2005 Cheong HI, Cho SJ, Zheng SH, Cho HY, Ha IS, Choi Y. Two novel mutations in the aquaporin 2 gene in a girl with congenital nephrogenic diabetes insipidus. Journal of Korean Medical Science. 20: 1076-8. PMID 16361827  0.44
2005 Kang JH, Choi HJ, Cho HY, Lee JH, Ha IS, Cheong HI, Choi Y. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations. Pediatric Nephrology (Berlin, Germany). 20: 1490-3. PMID 16047219 DOI: 10.1007/s00467-005-1969-7  0.44
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