Hae-Mi Woo

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

Hae-Mi Woo, Hong-Joon Park, Jeong‐In Baek et al. · BMC Medical Genetics · 2013 · 39 citations · Full text

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

Hae-Mi Woo, Hong-Joon Park, Mi‐Hyun Park et al. · BMC Medical Genetics · 2014 · 32 citations · Full text

Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2

B. O. Choi, M.‐H. Park, Ki Wha Chung et al. · Neurogenetics · 2012 · 28 citations

Novel S90w Mutation, Mendelian Disorder, Genetic Disorder +8

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

Mi‐Hyun Park, Hwanseok Rhee, Jung Hoon Park et al. · PLoS ONE · 2014 · 22 citations · Full text

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

Hyung Jin Kim, Hae-Mi Woo, Jihee Ryu et al. · PLoS ONE · 2013 · 15 citations · Full text

Organ Development, Pten Deficiency, Synaptic Signaling +25