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Audiology & Neuro-Otology|December 14, 2007
Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilitiesChen-Chi Wu, Pei-Jer Chen, Yu-Hsun Chiu, et al.
The Laryngoscope|September 1, 2009
Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairmentChen-Chi Wu, Ying-Chang Lu, Pei-Jer Chen, et al.
Audiology & Neuro-Otology|August 4, 2009
Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndromeChen-Chi Wu, Ying-Chang Lu, Pei-Jer Chen, et al.
Plos One|March 2, 2013
Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairmentChen-Chi Wu, Yin-Hung Lin, Ying-Chang Lu, et al.
Audiology & Neuro-Otology|March 13, 2010
Mutations in the OTOF gene in Taiwanese patients with auditory neuropathyYu-Hsun Chiu, Chen-Chi Wu, Ying-Chang Lu, et al.
JASA Express Letters|September 26, 2022
Low intensity ultrasound enhances cisplatin uptake in vitro by cochlear hair cellsYa-Cherng Chu, Yen-Hui Chan, Jormay Lim, et al.
Biochemical and Biophysical Research Communications|September 12, 2020
Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutationYen-Fu Cheng, Yi-Hsiu Tsai, Chun-Ying Huang, et al.
The Journal of Molecular Diagnostics : JMD|October 1, 2018
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular AqueductYin-Hung Lin, Chen-Chi Wu, Yi-Hsin Lin, et al.
The Laryngoscope|March 27, 2012
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndromeShih-Hao Wang, Chen-Chi Wu, Ying-Chang Lu, et al.
Scientific Reports|August 10, 2017
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing lossYin-Hung Lin, Yi-Hsin Lin, Ying-Chang Lu, et al.
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