ScholarWorks@Hanyang University: Kim, Young Eun

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Kim, Young Eun (김영은)

서울 의과대학 (DEPARTMENT OF LABORATORY MEDICINE)

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Tel 02-2290-8974
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Amyotrophic lateral sclerosis:6||Frontotemporal dementia:3||amyotrophic lateral sclerosis:3||OXTR:2||Gerotarget:2||FADS2:2||common variation:2||preterm:2||Nextgeneration sequencing:2||frontotemporal dementia:2||COMT:2||ALS:2||imaging genetics:2||NOTCH3:2||ANXA11:2||CADASIL:2||MCRIBS:2||Exome sequencing:1||FUS:1||Fused in sarcoma:1||GNPTAB:1||GRN:1||Gene:1||Helminths:1||Human cell models:1||ITM2B gene:1||Induced neuron:1||Korea:1||Korean:1||Lysosomal storage disease:1||MAPT:1||Mendelian disorder:1||Microglia:1||Microtubule:1||Mitochondria:1||Mortality:1||Mucolipidosis:1||Mucopolysaccharidosis IIIB:1||Multigene panel:1||Mutation:1||NA:1||NAGLU:1||NCKAP1:1||NEK1:1||NGS:1||Neuronal cytoplasmic inclusion:1||Novel mutation:1||Nuclear localization signal:1||PRNP:1||Parasites:1||Pathogenic:1||Phagocytosis:1||Prenatal diagnosis:1||Primary cilia:1||Prognosis:1||Protozoa:1||RNA sequencing:1||Spinocerebellar ataxia type 2:1||Stress granules:1||Subcortical vascular cognitive impairment (SVCI):1||TBK1:1||TERT promoter:1||Telomere:1||Thyroid cancer:1||Trichuris:1||Variant:1||Variant interpretation:1||behavioral variant frontotemporal dementia:1||betagalactosylceramidase:1||c.800G>:1||case report:1||cerebral amyloid angiopathy:1||cerebral microbleed:1||cerebrotendinous xanthomatosis:1||dementia:1||dilysine motif:1||globoid cell leukodystrophy:1||heterogeneity:1||induced neuron:1||krabbe disease:1||lacune:1||lowcomplexity domain:1||mass cytometry:1||motor neuron disease:1||neurogenetics:1||nextgeneration sequencing:1||novel likely pathogenic variant:1||peripheral blood mononuclear cells:1||psychosine:1||s disease:1||semantic variant primary progressive aphasia:1||silver nanoparticles:1||single cells:1||stress granule:1||subcortical vascular cognitive impairment:1||white matter hyperintensity:1||AARS2:1||wholeexome sequencing:1||APOE epsilon 4 noncarriers:1||ATXN2:1||Alzheimer’s disease:1||American College of Medical Genetics (ACMG):1||Amyotrophic Lateral Sclerosis:1||BRAF:1||C:1||Ctype lectin:1||CAG repeat expansion:1||CSF1R:1||CYP27A1 gene mutation:1||Cell cycle:1||DNA damage response:1||De novo mutation:1||ER retention:1||Earlyonset Alzheimer&apos:1||

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222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1366

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