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Heasoo Koo

Observed names: H. Koo, HEASOO KOO, Hea-Soo Koo
Observed institutions: Ewha Womans University, Kongju National University, Ewha Womans University Medical Center, Ewha Womans University Mokdong Hospital, Ewha Womans University Seoul Hospital, Case Western Reserve University
ORCID: 0000-0002-3240-1410
Observed ORCID: 0000-0002-3240-1410
OpenAlex ID: A5110103403
SET binding factor 1 ( SBF1 ) mutation causes Charcot-Marie-Tooth disease type 4B3
2013 · Khriezhanuo Nakhro, Jin-Mo Park, et al. · Neurology · 88
Tumors of the Central Nervous System in Korea A Multicenter Study of 3221 Cases.
2002 · Yeon-Lim Suh, Heasoo Koo, et al. · Journal of Neuro-Oncology · 73
A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14
2011 · Byung-Ok Choi, Sung Hee Kang, et al. · Human Mutation · 67
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Prognostic value of p16INK4a and p14ARF gene hypermethylation in human colon cancer
2006 · Minjin Lee, Woon Sup Han, et al. · Pathology - Research and Practice · 60
A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy
2016 · Young Bin Hong, Jaesoon Joo, et al. · PLoS Genetics · 54
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A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot–Marie–Tooth disease type 2L
2013 · Khriezhanuo Nakhro, Jin-Mo Park, et al. · Neuromuscular Disorders · 51
DGAT2Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease
2016 · Young Bin Hong, Junghee Kang, et al. · Human Mutation · 50
Proximal Dominant Hereditary Motor and Sensory Neuropathy With Proximal Dominance Association With Mutation in the TRK-Fused Gene
2013 · Sang-Soo Lee, Hye Jin Lee, et al. · JAMA Neurology · 47
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Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease
2013 · Hyeon Jin Kim, Young Bin Hong, et al. · Orphanet Journal of Rare Diseases · 41
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Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot–Marie–Tooth disease family
2005 · K. W. Chung, I. N. Sunwoo, et al. · Neurogenetics · 41
Zonal Difference and Prognostic Significance of Foxp3 Regulatory T Cell Infiltration in Breast Cancer
2014 · Sewha Kim, Anbok Lee, et al. · Journal of Breast Cancer · 37
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A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease
2013 · Young Bin Hong, Ja Hyun Lee, et al. · BMC Medical Genetics · 30
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Bimodal upregulation of glial cell line‐derived neurotrophic factor (GDNF) in the neonatal rat brain following ischemic/hypoxic injury
2002 · Tomoaki Ikeda, Heasoo Koo, et al. · International Journal of Developmental Neuroscience · 30
Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2
2012 · B.-O. Choi, M.-H. Park, et al. · Neurogenetics · 29
Expression of glial cell line‐derived neurotrophic factor (GDNF) in the developing human fetal brain
2001 · H. Koo, B.H. Choi · International Journal of Developmental Neuroscience · 28
Immunoglobulin G4–associated inflammatory pseudotumor of urinary bladder: a case report
2013 · Sanghui Park, Jae Y. Ro, et al. · Annals of Diagnostic Pathology · 26
A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy
2015 · Yu-Ri Choi, Young Bin Hong, et al. · BMC Neurology · 23
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Electron Microscopy Pathology of ADSSL1 Myopathy
2017 · Hyung Jun Park, Jee Eun Lee, et al. · Journal of Clinical Neurology · 19
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A family with axonal sensorimotor polyneuropathy with TUBB3 mutation
2014 · YOUNG BIN HONG, JA HYUN LEE, et al. · Molecular Medicine Reports · 19
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A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement
2013 · Jin-Mo Park, Ye Jin Kim, et al. · Neuromuscular Disorders · 19
Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1
2016 · JINHO LEE, SUNG-CHUL JUNG, et al. · Molecular Medicine Reports · 17
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Ectopic Hamartomatous Thymoma: A Case Report Showing CD99+ Lymphocytes and a Low Proliferation Index
2003 · Shi Nae Lee, Min Sun Cho, et al. · Archives of Pathology & Laboratory Medicine · 17
Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy
2014 · Mi-Hyun Park, Hae-Mi Woo, et al. · Neurogenetics · 16
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Two recessive intermediate Charcot‐Marie‐Tooth patients with GDAP1 mutations
2011 · Ki W. Chung, Young S. Hyun, et al. · Journal of the Peripheral Nervous System · 15
Myotonic dystrophy type I combined with X-linked dominant Charcot–Marie–Tooth neuropathy
2010 · Hyun Sook Kim, Ki Wha Chung, et al. · Neurogenetics · 14
Works count: 78
Citation count: 1,044
H-index: 19
I10-index: 28
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