| Potential therapeutic agents for COVID-19 based on the analysis of protease and RNA polymerase docking YC Chang, YA Tung, KH Lee, TF Chen, YC Hsiao, HC Chang, TT Hsieh, ... MDPI AG, 2020 | 137 | 2020 |
| Newborn genetic screening for hearing impairment: a population-based longitudinal study CC Wu, CH Tsai, CC Hung, YH Lin, YH Lin, FL Huang, PN Tsao, YN Su, ... Genetics in Medicine 19 (1), 6-12, 2017 | 91 | 2017 |
| Identifying children with poor cochlear implantation outcomes using massively parallel sequencing CC Wu, YH Lin, TC Liu, KN Lin, WS Yang, CJ Hsu, PL Chen, CM Wu Medicine 94 (27), e1073, 2015 | 78 | 2015 |
| Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations CM Wu, HC Ko, YT Tsou, YH Lin, JL Lin, CK Chen, PL Chen, CC Wu PloS one 10 (9), e0138575, 2015 | 64 | 2015 |
| Etiologic and audiologic characteristics of patients with pediatric-onset unilateral and asymmetric sensorineural hearing loss PH Lin, CJ Hsu, YH Lin, YH Lin, HY Lee, CC Wu, TC Liu JAMA otolaryngology–head & neck surgery 143 (9), 912-919, 2017 | 45 | 2017 |
| Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment CC Wu, YH Lin, YC Lu, PJ Chen, WS Yang, CJ Hsu, PL Chen PloS one 8 (2), e57369, 2013 | 44 | 2013 |
| ABO genotyping with next‐generation sequencing to resolve heterogeneity in donors with serology discrepancies PC Wu, YH Lin, LF Tsai, MH Chen, PL Chen, SC Pai Transfusion 58 (9), 2232-2242, 2018 | 42 | 2018 |
| Concurrent hearing, genetic, and cytomegalovirus screening in newborns, Taiwan CY Lu, PN Tsao, YY Ke, YH Lin, YH Lin, CC Hung, YN Su, WC Hsu, ... The Journal of Pediatrics 199, 144-150. e1, 2018 | 35 | 2018 |
| Mutation screening of the EYA1, SIX1, and SIX5 genes in an east asian cohort with branchio‐oto‐renal syndrome SH Wang, CC Wu, YC Lu, YH Lin, YN Su, WL Hwu, IS Yu, CJ Hsu The Laryngoscope 122 (5), 1130-1136, 2012 | 35 | 2012 |
| Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese population CC Wu, CY Tsai, YH Lin, PY Chen, PH Lin, YF Cheng, CM Wu, YH Lin, ... Genes 10 (10), 772, 2019 | 34 | 2019 |
| Differences in the pathogenicity of the p. H723R mutation of the common deafness-associated SLC26A4 gene in humans and mice YC Lu, CC Wu, TH Yang, YH Lin, IS Yu, SW Lin, Q Chang, X Lin, ... PloS one 8 (6), e64906, 2013 | 28 | 2013 |
| Timing of cochlear implantation in auditory neuropathy patients with OTOF mutations: Our experience with 10 patients CC Wu, CJ Hsu, FL Huang, YH Lin, YH Lin, TC Liu, CM Wu Clinical Otolaryngology 43 (1), 352-357, 2018 | 26 | 2018 |
| A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss YH Lin, YH Lin, YC Lu, TC Liu, CY Chen, CJ Hsu, PL Chen, CC Wu Scientific reports 7 (1), 7551, 2017 | 24 | 2017 |
| Prediction model for audiological outcomes in patients with GJB2 mutations PY Chen, YH Lin, TC Liu, YH Lin, LH Tseng, TH Yang, PL Chen, CC Wu, ... Ear and hearing 41 (1), 143-149, 2020 | 23 | 2020 |
| Contribution of adiponectin and its type 1 receptor to age-related hearing impairment CC Wu, CH Tsai, YC Lu, HC Lin, JH Hwang, YH Lin, WS Yang, PJ Chen, ... Neurobiology of aging 36 (6), 2085-2093, 2015 | 20 | 2015 |
| Clinical heterogeneity of LRRK2 p. I2012T mutation TS Fan, RM Wu, PL Chen, TF Chen, HY Li, YH Lin, CY Chen, ML Chen, ... Parkinsonism & Related Disorders 33, 36-43, 2016 | 18 | 2016 |
| Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations J Erdenechuluun, YH Lin, K Ganbat, D Bataakhuu, Z Makhbal, CY Tsai, ... PLoS One 13 (12), e0209797, 2018 | 17 | 2018 |
| Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing YH Lin, CC Wu, TY Hsu, WY Chiu, CJ Hsu, PL Chen Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 771, 1-5, 2015 | 15 | 2015 |
| pubmedKB: an interactive web server for exploring biomedical entity relations in the biomedical literature PH Li, TF Chen, JY Yu, SH Shih, CH Su, YH Lin, HK Tsai, HF Juan, ... Nucleic Acids Research 50 (W1), W616-W622, 2022 | 14 | 2022 |
| Hearing impairment with monoallelic GJB2 variants: a GJB2 cause or non-GJB2 cause? YH Lin, PC Wu, CY Tsai, YH Lin, MY Lo, SJ Hsu, PH Lin, ... The Journal of Molecular Diagnostics 23 (10), 1279-1291, 2021 | 13 | 2021 |
