第 1 到 21 筆結果,共 21 筆。
公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 | |
---|---|---|---|---|---|---|---|
1 | 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 | |
2 | 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 | |
3 | 2023 | Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population | Lee, Yen-Hui; Tsai, Cheng-Yu; Lu, Yue-Sheng; PEI-HSUAN LIN ; Chiang Yu-ting; TING-HUA YANG ; Jacob Shujui Hsu ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; TIEN-CHEN LIU ; CHEN-CHI WU | Genes | 0 | 0 | |
4 | 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 | |
5 | 2022 | Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications | Lee, Chee-Yee; PEI-HSUAN LIN ; Tsai, Cheng-Yu; Chiang Yu-ting; Chiou, Hong-Ping; Chiang, Ko-Yin; PEI-LUNG CHEN ; Jacob Shujui Hsu ; TIEN-CHEN LIU ; Wu, Hung-Pin; CHEN-CHI WU ; Hsu, Chuan-Jen | Biomedicines | 4 | 5 | |
6 | 2022 | Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study | PEI-HSUAN LIN ; Wu, Hung-Pin; Wu, Che-Ming; Chiang, Yu-ting; Jacob Shujui Hsu ; Tsai, Cheng-Yu; Wang, Han; Tseng, Li-Hui; Chen, Pey-Yu; TING-HUA YANG ; Hsu, Chuan-Jen; PEI-LUNG CHEN ; CHEN-CHI WU ; TIEN-CHEN LIU | Biomedicines | 10 | 5 | |
7 | 2022 | Cochlear implantation in LEOPARD syndrome: Our experience with three patients | Wu, Ping-Che; Tsai, Cheng-Yu; PEI-HSUAN LIN ; Chou, Pao-Hsuan; Huang, Fang-Lih; PEI-LUNG CHEN ; Shiao, Jiun-Yih; TIEN-CHEN LIU ; Hsu, Chuan-Jen; Huang, Chang-Wei; CHEN-CHI WU | Clinical Otolaryngology | 0 | 0 | |
8 | 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 | |
9 | 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 | |
10 | 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 | |
11 | 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 | |
12 | 2020 | An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response | PEI-HSUAN LIN ; Hsu, Chuan-Jen; Lin, Yin-Hung; Lin, Yi-Hsin; Yang, Shu-Yu; TING-HUA YANG ; PEI-LUNG CHEN ; Chen-Chi Wu ; TIEN-CHEN LIU | Scientific Reports | 6 | 3 | |
13 | 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 | |
14 | 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 | |
15 | 2018 | Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations | Erdenechuluun, Jargalkhuu; Lin, Yin-Hung; Ganbat, Khongorzul; Bataakhuu, Delgermaa; Makhbal, Zaya; Tsai, Cheng-Yu; Lin, Yi-Hsin; Chan, Yen-Hui; Hsu, Chuan-Jen; WEI-CHUNG HSU ; PEI-LUNG CHEN ; CHEN-CHI WU | PLoS ONE | 11 | 11 | |
16 | 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 | 20 | 19 | |
17 | 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 | |
18 | 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 | |
19 | 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 | |
20 | 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 | |
21 | 2012 | Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas | CHENG-PING WANG ; TSENG-CHENG CHEN ; YIH-LEONG CHANG ; JENG-YUH KO ; TSUNG-LIN YANG ; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN ; Chen-Chi Wu ; PEI-JEN LOU | Oral Oncology | 10 | 9 |