Nayoung Yi

Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss

Sang‐Yeon Lee, Hyun Been Choi, Mina Park et al. · Experimental & Molecular Medicine · 2021 · 41 citations · Full text

Medicine, Molecular Genetics, Pharmacology +17

Novel genotype–phenotype correlation of functionally characterized <i>LMX1A</i> variants linked to sensorineural hearing loss

Sang‐Yeon Lee, Jin Hee Han, Marge Carandang et al. · Human Mutation · 2020 · 33 citations

Life Sciences, Genetics, Molecular Genetics +17

Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss

So Young Kim, Bong Jik Kim, Doo Yi Oh et al. · Scientific Reports · 2022 · 17 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Central auditory maturation and behavioral outcomes after cochlear implantation in prelingual auditory neuropathy spectrum disorder related to OTOF variants (DFNB9): Lessons from pilot study

Sang‐Yeon Lee, Jin Hee Han, Hoo-Kang Song et al. · PLoS ONE · 2021 · 13 citations · Full text

Health Professions, Audiology, Otolaryngology +17

Full etiologic spectrum of pediatric severe to profound hearing loss of consecutive 119 cases

Young Seok Kim, Yoonjoong Kim, Hyoung Won Jeon et al. · Scientific Reports · 2022 · 13 citations · Full text

Medicine, Otolaryngology, Pediatrics +17