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Cell Reports. Medicine|July 1, 2025
Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approachSang-Yeon Lee, Seungbok Lee, Seongyeol Park, et al.
Molecular Therapy. Nucleic Acids|August 6, 2024
Discovery of novel disease-causing mutation in <i>SSBP1</i> and its correction using adenine base editor to improve mitochondrial functionJu Hyuen Cha, Seok-Hoon Lee, Yejin Yun, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2020
Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approachBong Jik Kim, Doo-Yi Oh, Jin Hee Han, et al.
Sensors (Basel, Switzerland)|December 11, 2025
Wide-Dynamic-Range Lead-Free SWIR Image Sensors Based on InAs Thin-Film Quantum-Dot Photodiodes <sup>†</sup>Myonglae Chu, Wenya Song, Joo Hyoung Kim, et al.
Experimental & Molecular Medicine|July 28, 2021
Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing lossSang-Yeon Lee, Hyun Been Choi, Mina Park, et al.
Nature Communications|August 5, 2025
PAM-flexible adenine base editing rescues hearing loss in a humanized MPZL2 mouse model harboring an East Asian founder mutationShao Wei Hu, Sohyang Jeong, Luoying Jiang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2021
A nonsense <i>TMEM43</i> variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorderMinwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi, et al.
Med (New York, N.Y.)|October 24, 2025
International expert consensus on gene therapy for hereditary hearing loss: Based on clinical trialsXintai Fan, Ziwen Gao, Jiake Zhong, et al.
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