第 1 到 13 筆結果,共 13 筆。
公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 | |
---|---|---|---|---|---|---|---|
1 | 2020 | Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations | Chen P.-Y.; Lin Y.-H.; TIEN-CHEN LIU ; Lin Y.-H.; LI-HUI TSENG ; TING-HUA YANG ; PEI-LUNG CHEN ; Chen-Chi Wu ; Hsu C.-J. | Ear and hearing | 15 | 16 | |
2 | 2019 | Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct | Lin Y.-H.; Chen-Chi Wu ; Lin Y.-H.; Lu Y.-C.; Chen C.-S.; TIEN-CHEN LIU ; PEI-LUNG CHEN ; Hsu C.-J. | Journal of Molecular Diagnostics | 10 | 7 | |
3 | 2017 | Etiologic and audiologic characteristics of patients with pediatric-onset unilateral and asymmetric sensorineural hearing loss | PEI-HSUAN LIN ; Hsu C.-J.; Lin Y.-H.; Lin Y.-H.; Lee H.-Y.; Chen-Chi Wu ; TIEN-CHEN LIU | JAMA Otolaryngology - Head and Neck Surgery | 33 | 30 | |
4 | 2017 | Newborn genetic screening for hearing impairment: a population-based longitudinal study | Chen-Chi Wu ; Tsai C.-H.; Hung C.-C.; Lin Y.-H.; Lin Y.-H.; Huang F.-L.; PO-NIEN TSAO ; Su Y.-N.; Lee Y.L.; Hsieh W.-S.; Hsu C.-J. | Genetics in Medicine | 53 | 50 | |
5 | 2017 | A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss | Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; TIEN-CHEN LIU ; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN ; CHIEN-YU CHEN ; CHEN-CHI WU | Scientific Reports | 19 | 19 | |
6 | 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 | |
7 | 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 | |
8 | 2015 | Contribution of adiponectin and its type 1 receptor to age-related hearing impairment | Chen-Chi Wu ; Tsai C.-H.; Lu Y.-C.; Lin H.-C.; Hwang J.-H.; Lin Y.-H.; WEI-SHIUNG YANG ; PEI-JER CHEN ; WEI-CHIH LIAO ; Lee Y.L.; TIEN-CHEN LIU ; Hsu C.-J. | Neurobiology of Aging | 14 | 13 | |
9 | 2015 | Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutations | Wu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN ; Chen-Chi Wu | PLoS ONE | 39 | 36 | |
10 | 2013 | Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment | Chen-Chi Wu ; Lin Y.-H.; Lu Y.-C.; PEI-JER CHEN ; WEI-SHIUNG YANG ; Hsu C.-J.; PEI-LUNG CHEN | PLoS ONE | 33 | 47 | |
11 | 2013 | Differences in the Pathogenicity of the p.H723R Mutation of the Common Deafness-Associated SLC26A4 Gene in Humans and Mice | Lu Y.-C.; Chen-Chi Wu ; TING-HUA YANG ; Lin Y.-H.; Yu I.-S.; SHU-WHA LIN ; Chang Q.; Lin X.; Wong J.-M.; Hsu C.-J. | PLoS ONE | 23 | 17 | |
12 | 2012 | Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome | Wang S.-H.; Chen-Chi Wu ; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; WUH-LIANG HWU ; Yu I.-S.; Hsu C.-J. | Laryngoscope | 27 | 19 | |
13 | 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 |