Author

Hae-Mi Woo

Observed names: H.-M. Woo, H.‐M. Woo

Institution: Korea National Institute of Health

Observed institutions: National Institutes of Health, Korea National Institute of Health, National Institute of Health, National Institute of Health

OpenAlex ID: A5044490384

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

2013 · Hae-Mi Woo, Hong-Joon Park, et al. · BMC Medical Genetics · 38

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

2014 · Hae-Mi Woo, Hong-Joon Park, et al. · BMC Medical Genetics · 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

Comprehensive Analysis to Improve the Validation Rate for Single Nucleotide Variants Detected by Next-Generation Sequencing

2014 · Mi-Hyun Park, Hwanseok Rhee, et al. · PLoS ONE · 22

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

Conditional Deletion of Pten Leads to Defects in Nerve Innervation and Neuronal Survival in Inner Ear Development

2013 · Hyung Jin Kim, Hae-Mi Woo, et al. · PLoS ONE · 16

Patterns of Gene Expression Associated with Pten Deficiency in the Developing Inner Ear

2014 · Hyung Jin Kim, Jihee Ryu, et al. · PLoS ONE · 14

Application of whole‐exome sequencing for detecting copy number variants in CMT1A/HNPP

2015 · H.‐Y. Jo, M.‐H. Park, et al. · Clinical Genetics · 12

Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage

2011 · Mi-Hyun Park, Hong-Joon Park, et al. · Genes & Genetic Systems

Works count: 9

Citation count: 177

H-index: 8

I10-index: 8