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研究成果 
|
研究計畫
|
年度
|
研究名稱
|
擔任
工作
|
補助
金額
|
補助
單位
|
|
100
|
聽障基因TMPRSS3突變之功能分析(3/3)
|
主持人
|
1420,000
|
國科會
|
|
99
|
聽障基因TMPRSS3突變之功能分析(2/3)
|
主持人
|
1420,000
|
國科會
|
|
99
|
利用酵母菌sGASP系統來探討TMPRSS3突變後造成聽障的機轉
|
主持人
|
47,000
|
國科會大專生計畫
|
|
98
|
聽障基因TMPRSS3突變之功能分析(1/3)
|
主持人
|
1420,000
|
國科會
|
|
98
|
利用爪蟾卵母細胞(Xenopus oocyte)來探討Cx26基因突變造成的功能影響
|
主持人
|
47,000
|
國科會大專生計畫
|
|
97
|
Study of the etiology of nonsyndromic deafness: Analysis of the functional properties of CONNEXIN 29 (GJE1) and CLAUDIN 14 gene mu9tants in nonsyndromic deafness
|
主持人
|
1500,000
|
國科會
|
|
97
|
KCNQ4基因突變造成非症候群聽障之功能研究
|
主持人
|
47,000
|
國科會大專生計畫
|
論文發表
|
年度
|
著作
|
期刊
屬性
|
期刊最佳
百分比
|
|
99
|
Wang WH, Yang JJ, Lin YC, Yang JT, Li SY* (2010) Novel expression patterns of connexin 30.3 in adult rat cochlea. Hearing Research 265:77-82 (IF:2.428; 2010)
|
SCI
|
4.9% (2/41)
|
|
99
|
Yang JJ, Wang WH, Lin YC, Weng HH, Yang JT, Hwang CF, Wu CM, Li SY* (2010) Prospective variants screening of connexin genes in children with hearing impairment: Genotype/ Phenotype Correlation. Human Genetics 128:303-313 (IF:5.04; 2010) SCI
|
SCI
|
14.7%(23/156)
|
|
99
|
Yang JJ, Su MC, Chien KH, Hsin CH, Li SY* (2010) Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. International Journal of Pediatric Otorhinolaryngology 74:489-493 (IF:1.067; 2010) SCI
|
SCI
|
51.2%(21/41)
|
|
99
|
Hong HM1, Yang JJ 1, Shieh JC, Lin ML, Li SY* (2010) Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss. Human Genetics 127:545-551 (1: Co-first Author) (IF:5.047; 2010) SCI
|
SCI
|
14.7%(23/156)
|
|
99
|
Hong HM1, Yang JJ1, Su CC, Chang JY, Li TC, Li SY* (2010) A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss. Human Genetics 127: 191-199 (1: Co-first Author) (IF:5.047; 2010) SCI
|
SCI
|
14.7%(23/156)
|
|
99
|
Wang WH, Yang JJ, Lin YC, Yang JT, Chan CH, Li SY* (2010) Identification of novel variants in the Cx29 gene of nonsyndromic hearing loss patients using buccal cells and RFLP method. Audiology and Neur-otology 15:81-87 (IF:2.228; 2010) SCI
|
SCI
|
9.8% (4/41)
|
|
98
|
Su MC1, Yang JJ1, Su CC, Hsin CH, Li SY* (2009) Identification of novel variants in the Myosin VIIA gene of patients with nonsyndromic hearing loss from Taiwan. International Journal of Pediatric Otorhinolaryngology 73: 811-815 (1: Co-first Author) (IF:1.067; 2010) SCI
|
SCI
|
51.2%(21/41)
|
|
98
|
Lai YC, Wang WC, Yang JJ, Li SY* (2009) Expansion of CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene in idiopathic oligozoospermia patients. Journal of Assisted Reproduction and Genetics 26:257-261 (IF:1.253; 2010) SCI
|
SCI
|
69%(52/75)
|
|
97
|
Su MC, Yang JJ, Chou MY, Hsin CH, Su CC, Ku WC, Li SY* (2008) Expression and localization of Tmie in adult rat cochlea. Histochemistry and Cell Biology 130: 119-126 (IF:4.727; 2010) SCI
|
SCI
|
11.1%(1/9)
|
|
97
|
Yen YC1, Yang JJ1, Chou MC, Li SY* (2008) Absence of OPTINEURIN (OPTN) gene mutations in Taiwanese patients with Juvenile-Onset Open-Angle Glaucoma. Molecular Vision 14: 487-494 (1:Co-first Author) (IF:2.511; 2010) SCI
|
SCI
|
25.4%(14/55)
|
|
