公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2022 | Gene therapy with a synthetic adeno-associated viral vector improves audiovestibular phenotypes in Pjvk-mutant mice | Lu, Ying-Chang; Tsai, Yi-Hsiu; Chan, Yen-Huei; Hu, Chin-Ju; Huang, Chun-Ying; Xiao, Ru; Hsu, Chuan-Jen; Vandenberghe, Luk H; CHEN-CHI WU ; Cheng, Yen-Fu | JCI insight | 4 | 3 | |
2020 | Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutation | Cheng Y.-F.; Tsai Y.-H.; Huang C.-Y.; Lee Y.-S.; Chang P.-C.; Lu Y.-C.; Hsu C.-J.; Chen-Chi Wu | Biochemical and Biophysical Research Communications | 6 | 7 | |
2019 | Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutation | Cheng Y.-F.; Chan Y.-H.; Hu C.-J.; Lu Y.-C.; Saeki T.; Hosoya M.; Saegusa C.; Fujioka M.; Okano H.; Weng S.-M.; Hsu C.-J.; Chang K.-H.; Chen-Chi Wu | Stem Cell Research | 5 | 4 | |
2023 | Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant | Chan, Yen-Hui; Tsai, Cheng-Yu; Ho, Chang-Han; Lu, Ying-Chang; PEI-HSUAN LIN ; TA-CHING CHEN ; YOU-TZUNG CHEN ; Huang, Cheng-Yen; TIEN-CHEN LIU ; Hsu, Chuan-Jen; CHEN-CHI WU | Stem Cell Research | 0 | 0 | |
2018 | Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation | Chan, Yen Hui; Cheng, Yen Fu; YOU-TZUNG CHEN ; Huang, Cheng Yen; CHIN-HSIEN LIN ; Hu, Chin Ju; Lu, Ying Chang; Chen-Chi Wu ; Hsu, Chuan Jen | Stem Cell Research | 3 | 2 | |
2022 | Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variant | Chan, Yen-Hui; Ho, Chang-Han; Tsai, Cheng-Yu; Lu, Ying-Chang; PEI-HSUAN LIN ; TA-CHING CHEN ; YOU-TZUNG CHEN ; Huang, Cheng-Yen; TIEN-CHEN LIU ; Hsu, Chuan-Jen; CHEN-CHI WU ; Hsu, Chuan-Jen | Stem Cell Research | 1 | 1 | |
2011 | Genetic characteristics in children with cochlear implants and the corresponding auditory performance | CHEN-CHI WU ; TIEN-CHEN LIU ; Wang S.-H.; Hsu C.-J.; Wu C.-M. | Laryngoscope | 42 | 37 | |
2019 | Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese population | CHEN-CHI WU ; Tsai, Cheng-Yu; Lin, Yi-Hsin; Chen, Pey-Yu; PEI-HSUAN LIN ; Cheng, Yen-Fu; Wu, Che-Ming; Lin, Yin-Hung; Lee, Chee-Yee; Erdenechuluun, Jargalkhuu; TIEN-CHEN LIU ; PEI-LUNG CHEN ; Hsu, Chuan-Jen | Genes | 31 | 27 | |
2023 | Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment | Chiang Yu-ting; PEI-HSUAN LIN ; Lo, Ming-Yu; HSIN-LIN CHEN ; Lee, Chen-Yu; Tsai, Cheng-Yu; Lin, Yin-Hung; Tsai, Shih-Feng; TIEN-CHEN LIU ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; Jacob Shujui Hsu ; CHEN-CHI WU | The Journal of molecular diagnostics : JMD | 0 | 0 | |
2023 | Genetic Underpinnings and Audiological Characteristics in Children With Unilateral Sensorineural Hearing Loss | Lee, Chen-Yu; PEI-HSUAN LIN ; Chiang Yu-ting; Tsai, Cheng-Yu; Yang, Shu-Yu; Chen, You-Mei; Li, Chao-Hsuan; CHUN-YI LU ; TIEN-CHEN LIU ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; Jacob Shujui Hsu ; CHEN-CHI WU | Otolaryngology - Head and Neck Surgery | 2 | 0 | |
2014 | Gradenigo syndrome caused by nontuberculous mycobacteria | Chen P.-Y.; Chen-Chi Wu ; TSUNG-LIN YANG ; Hsu C.-J.; YI-TSEN LIN ; Lin K.-N. | Audiology and Neurotology | 9 | 6 | |
2011 | The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese | Lin Y.-H.; CHEN-CHI WU ; Hsu C.-J.; Hwang J.-H.; TIEN-CHEN LIU | Laryngoscope | 35 | 21 | |
2023 | Health Utilities of Bilateral Severe-to-Profound Hearing Loss with Assistive Devices | Chen, Yi-Wen; PEI-HSUAN LIN ; Fang, Te-Yung; CHEN-CHI WU ; Wang, Pa-Chun; Wang, Han; Ko, Yu | Healthcare (Basel, Switzerland) | 0 | 0 | |
2022 | Hearing Features and Cochlear Implantation Outcomes in Patients With Pathogenic MYO15A Variants: a Multicenter Observational Study | Chen, Pey-Yu; Tsai, Cheng-Yu; Wu, Jiunn-Liang; Li, Yi-Lu; Wu, Che-Ming; Chen, Kuang-Chao; Hwang, Chung-Feng; Wu, Hung-Pin; Lin, Hung-Ching; Cheng, Yen-Fu; Lo, Ming-Yu; TIEN-CHEN LIU ; TING-HUA YANG ; PEI-LUNG CHEN ; Hsu, Chuan-Jen; CHEN-CHI WU | Ear and hearing | 1 | 1 | |
2021 | Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause? | Lin, Yi-Hsin; Wu, Ping-Che; Tsai, Cheng-Yu; Lin, Yin-Hung; Lo, Ming-Yu; Hsu, Shu-Jui; PEI-HSUAN LIN ; Erdenechuluun, Jargalkhuu; Wu, Hung-Pin; Hsu, Chuan-Jen; CHEN-CHI WU ; PEI-LUNG CHEN | Journal of Molecular Diagnostics | 8 | 4 | |
2022 | Helical structure motifs made searchable for functional peptide design | Tsai C.-Y.; Salawu E.O.; Li H.; Lin G.-Y.; Kuo T.-Y.; Voon L.; Sharma A.; Hu K.-D.; Cheng Y.-Y.; Sahoo S.; Stuart L.; Chen C.-W.; Chang Y.-Y.; Lu Y.-L.; Ke S.; Ortiz C.L.D.; Fang B.-S.; Chen-Chi Wu ; Lan C.-Y.; Fu H.-W.; Yang L.-W. | Nature Communications | 9 | 5 | |
2021 | Hereditary hearing impairment with cutaneous abnormalities | Lee, Tung-Lin; PEI-HSUAN LIN ; PEI-LUNG CHEN ; JIN-BON HONG ; CHEN-CHI WU | Genes | 4 | 2 | |
2015 | Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing | Lin Y.-H.; Chen-Chi Wu ; Hsu T.-Y.; WEI-YIH CHIU ; Hsu C.-J.; PEI-LUNG CHEN | Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis | 12 | 12 | |
2022 | Identification of nine novel variants across PAX3, SOX10, EDNRB, and MITF genes in Waardenburg syndrome with next-generation sequencing | Lee, Chen-Yu; Lo, Ming-Yu; Chen, You-Mei; PEI-HSUAN LIN ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; CHEN-CHI WU ; Jacob Shujui Hsu | Molecular Genetics & Genomic Medicine | 3 | 2 | |
2015 | Identifying children with poor cochlear implantation outcomes using massively parallel sequencing | Chen-Chi Wu ; Lin Y.-H.; TIEN-CHEN LIU ; Lin K.-N.; WEI-SHIUNG YANG ; Hsu C.-J.; PEI-LUNG CHEN ; Wu C.-M. | Medicine (United States) | 49 | 40 | |