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Dong Hwan Lee
Observed name:
D. ‐H. Lee
Institution:
Korea University
Observed institutions:
Seoul National University,
Korea University,
Soonchunhyang University,
Soonchunhyang University Hospital Seoul,
Ajou University,
Jeonbuk National University
show all 6
ORCID:
0000-0002-0153-1458
Observed ORCID:
0000-0002-0153-1458
OpenAlex ID:
A5100700014
Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening
2018
·
Naoaki Shibata
, Yuki Hasegawa
, et al.
·
Molecular Genetics and Metabolism Reports
·
125
PDF
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency
2005
·
Yao Bang Lu
, Keiko Kobayashi
, et al.
·
Journal of Human Genetics
·
117
Physical water treatment using RF electric fields for the mitigation of CaCO3 fouling in cooling water
2010
·
Leonard D. Tijing
, Hang Young Kim
, et al.
·
International Journal of Heat and Mass Transfer
·
80
Screening of newborns and high-risk group of children for inborn metabolic disorders using tandem mass spectrometry in South Korea: a three-year report
2005
·
Hye-Ran Yoon
, Kyung Ryul Lee
, et al.
·
Clinica Chimica Acta
·
80
Regulation of the Vibrio vulnificus hupA Gene by Temperature Alteration and Cyclic AMP Receptor Protein and Evaluation of Its Role in Virulence
2009
·
Man Hwan Oh
, Sung Min Lee
, et al.
·
Infection and Immunity
·
69
Pilot study of mass screening for Wilson's disease in Korea
2002
·
Si Houn Hahn
, Soo Young Lee
, et al.
·
Molecular Genetics and Metabolism
·
62
Hydride and borohydride derivatives of (pentamethylcyclopentadienyl)(tertiary phosphine)ruthenium
1987
·
Hiroharu Suzuki
, Dong Hwan Lee
, et al.
·
Organometallics
·
60
A Consensus Sequence for Binding of SmcR, a Vibrio vulnificus LuxR Homologue, and Genome-wide Identification of the SmcR Regulon
2008
·
Dong Hwan Lee
, Hye Sook Jeong
, et al.
·
Journal of Biological Chemistry
·
51
PDF
Mutation analysis of PAH gene and characterization of a recurrent deletion mutation in Korean patients with phenylketonuria
2008
·
Yong-Wha Lee
, Dong Hwan Lee
, et al.
·
Experimental & Molecular Medicine
·
42
PDF
Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations
2012
·
Yen-Hui Chiu
, Ying-Chen Chang
, et al.
·
Journal of Human Genetics
·
40
Congenital Hypothyroidism: Analysis of Discordant US and Scintigraphic Findings
2011
·
Yun-Woo Chang
, Dong Hwan Lee
, et al.
·
Radiology
·
34
Molecular screening of the TSH receptor (TSHR) and thyroid peroxidase (TPO) genes in Korean patients with nonsyndromic congenital hypothyroidism
2011
·
Seung-Tae Lee
, Dong Hwan Lee
, et al.
·
Clinical Endocrinology
·
33
Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia
2007
·
Yong-Wha Lee
, Dong Hwan Lee
, et al.
·
Molecular Genetics and Metabolism
·
33
Evidence that the Vibrio vulnificus flagellar regulator FlhF is regulated by a quorum sensing master regulator SmcR
2012
·
Seung Min Kim
, Dong Hwan Lee
, et al.
·
Microbiology
·
32
Novel SLC37A4 Mutations in Korean Patients With Glycogen Storage Disease Ib
2017
·
Rihwa Choi
, Hyung-Doo Park
, et al.
·
Annals of Laboratory Medicine
·
26
Newborn screening of inherited metabolic disease in Korea
2006
·
Dong Hwan Lee
·
Korean Journal of Pediatrics
·
20
The molecular basis of UDP-galactose-4-epimerase (GALE) deficiency galactosemia in Korean patients
2005
·
Hyung-Doo Park
, Kyung Un Park
, et al.
·
Genetics in Medicine
·
17
PDF
Clinical, Biochemical and Genetic Analyses in Two Korean Patients with Medium-chain Acyl-CoA Dehydrogenase Deficiency
2011
·
Hye In Woo
, Hyung-Doo Park
, et al.
·
Annals of Laboratory Medicine
·
16
Determination of phenylalanine in blood by high-performance anion-exchange chromatography–pulsed amperometric detection to diagnose phenylketonuria
2009
·
Ji-Seon Jeong
, Hee-Jung Sim
, et al.
·
Journal of Chromatography A
·
16
Enzyme replacement therapy improves joint motion and outcome of the 12‐min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation
2012
·
Young Bae Sohn
, Sung Won Park
, et al.
·
American Journal of Medical Genetics Part A
·
15
Tandem mass spectrometric analysis for disorders in amino, organic and fatty acid metabolism: two year experience in South Korea.
2003
·
Hye-Ran Yoon
, Kyung Ryul Lee
, et al.
·
PubMed
·
15
Novel GALTvariations and mutation spectrum in the Korean population with decreased galactose-1-phosphate uridyltransferase activity
2014
·
Rihwa Choi
, Kyoung Il Jo
, et al.
·
BMC Medical Genetics
·
13
PDF
Identification of a Novel Splicing Mutation in the ARSA Gene in a Patient with Late-infantile Form of Metachromatic Leukodystrophy
2010
·
Dong-Hee Kang
, Dong Hwan Lee
, et al.
·
Annals of Laboratory Medicine
·
12
Molecular and population genetics of phenylketonuria in Orientals: Correlation between phenotype and genotype
1994
·
Y. Okano
, Y. Hase
, et al.
·
Journal of Inherited Metabolic Disease
·
12
Reassessing the significance of the PAH c.158G>A (p.Arg53His) variant in patients with hyperphenylalaninemia
2017
·
Rihwa Choi
, Jeongho Lee
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
11
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Works count:
75
Citation count:
1,146
H-index:
17
I10-index:
27
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