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Young Ik Koh

Yonsei University

9H指数
20论文数
208被引数
收录论文 10
发表时间
HAP1 interaction with KCNQ4 attenuates channel surface expression and functionHAP1与KCNQ4的相互作用减弱通道的表面表达和功能
err2026-02-01
err0
errOAAI
errKim, Jung Ah; Oh, Kyung Seok; Roh, Jae Won; Koh, Young Ik; Lin, Haiyue; Jung, Jinsei; Gee, Heon Yung
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MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss
err2024-11-01
err0
errOAAI
errJung, Jinsei; Joo, Sun Young; Min, Hyehyun; Roh, Jae Won; Kim, Kyung Ah; Ma, Ji-Hyun; Rim, John Hoon; Kim, Jung Ah; Kim, Se Jin; Jang, Seung Hyun; Koh, Young Ik; Kim, Hye-Youn; Lee, Ho; Kim, Byoung Choul; Gee, Heon Yung; Bok, Jinwoong; Choi, Jae Young; Seong, Je Kyung
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Overlooked KCNQ4 variants augment the risk of hearing loss
err2023-04-03
err5
errOAAI
errOh, Kyung Seok; Roh, Jae Won; Joo, Sun Young; Ryu, Kunhi; Kim, Jung Ah; Kim, Se Jin; Jang, Seung Hyun; Koh, Young Ik; Kim, Da Hye; Kim, Hye-Youn; Choi, Murim; Jung, Jinsei; Namkung, Wan; Nam, Joo Hyun; Choi, Jae Young; Gee, Heon Yung
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OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin
errAUTOPHAGY
IF14.3
err2022-03-06
err15
errOAAI
errKoh, Young Ik; Oh, Kyung Seok; Kim, Jung Ah; Noh, Byunghwa; Choi, Hye Ji; Joo, Sun Young; Rim, John Hoon; Kim, Hye-Youn; Kim, Dong Yun; Yu, Seyoung; Kim, Da Hye; Lee, Sang-Guk; Jung, Jinsei; Choi, Jae Young; Gee, Heon Yung
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COCH-related autosomal dominant nonsyndromic hearing loss: a phenotype-genotype studyCOCH相关常染色体显性非综合征性耳聋: 一项表型-基因型研究
err2021-09-16
err12
errOAAI
errOh, Kyung Seok; Walls, Daniel; Joo, Sun Young; Kim, Jung Ah; Yoo, Jee Eun; Koh, Young Ik; Kim, Da Hye; Rim, John Hoon; Choi, Hye Ji; Kim, Hye-Youn; Yu, Seyoung; Smith, Richard J.; Choi, Jae Young; Gee, Heon Yung; Jung, Jinsei
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Differential genetic diagnoses of adult post-lingual hearing loss according to the audiogram pattern and novel candidate gene evaluation
err2021-09-14
err15
errOAAI
errRim, John Hoon; Noh, Byunghwa; Koh, Young Ik; Joo, Sun Young; Oh, Kyung Seok; Kim, Kyumin; Kim, Jung Ah; Kim, Da Hye; Kim, Hye-Youn; Yoo, Jee Eun; Lee, Seung-Tae; Bok, Jin Woong; Lee, Min Goo; Jung, Jinsei; Choi, Jae Young; Gee, Heon Yung
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Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss
err2021-07-28
err17
errOAAI
errLee, Sang-Yeon; Choi, Hyun Been; Park, Mina; Choi, Il Soon; An, Jieun; Kim, Ami; Kim, Eunku; Kim, Nahyun; Han, Jin Hee; Kim, Min Young; Lee, Seung Min; Oh, Doo-Yi; Kim, Bong Jik; Yi, Nayoung; Nayoung, K. D. Kim; Lee, Chung; Park, Woong-Yang; Koh, Young Ik; Gee, Heon Yung; Cho, Hyun Sung; Kang, Tong Mook; Choi, Byung Yoon
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Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment
err2019-08-21
err7
errOAAI
errJung, Jinsei; Lin, Haiyue; Koh, Young Ik; Ryu, Kunhi; Lee, Joon Suk; Rim, John Hoon; Choi, Hye Ji; Lee, Hak Joon; Kim, Hye-Youn; Yu, Seyoung; Jin, Hyunsoo; Lee, Ji Hyun; Lee, Min Goo; Namkung, Wan; Choi, Jae Young; Gee, Heon Yung
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A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators
err2018-12-17
err16
errOAAI
errShin, Dong Hoon; Jung, Jinsei; Koh, Young Ik; Rim, John Hoon; Lee, Joon Suk; Choi, Hye Ji; Joo, Sun Young; Yu, Seyoung; Cha, Do Hyeon; Lee, Seung Yeon; Lee, Ji Hyun; Lee, Min Goo; Choi, Jae Young; Gee, Heon Yung
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Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss
err2018-11-09
err22
errOAAI
errJung, Jinsei; Choi, Hyun Been; Koh, Young Ik; Rim, John Hoon; Choi, Hye Ji; Kim, Sung Huhn; Lee, Jae Hyun; An, Jieun; Kim, Ami; Lee, Joon Suk; Joo, Sun Young; Yu, Seyoung; Choi, Jae Young; Kang, Tong Mook; Gee, Heon Yung
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