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Xiao Mei Ouyang

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TOP 3
Xiao Mei Ouyang; Denise Yan; Idil Aslan; Li Lin Du; Mustafa Tekin; Xue Zhong Liu
Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairment.
Denise Yan; Kazusaku Kamiya; Xiao Mei Ouyang; Xue Zhong Liu
Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.
Xiao Mei Ouyang; Denise Yan; Hui Jun Yuan; Dai Pu; Li Lin Du; Don Yi Han; Xue Zhong Liu
The genetic bases for non-syndromic hearing loss among Chinese.

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All Publications

2011: Xiao Mei Ouyang; Denise Yan; Idil Aslan; Li Lin Du; Mustafa Tekin; Xue Zhong Liu
Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairment.
Genetic testing and molecular biomarkers 2011;15(5):333-6.
2011: Denise Yan; Kazusaku Kamiya; Xiao Mei Ouyang; Xue Zhong Liu
Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice.
International journal of experimental pathology 2011;92(1):66-71.
2009: Xiao Mei Ouyang; Denise Yan; Hui Jun Yuan; Dai Pu; Li Lin Du; Don Yi Han; Xue Zhong Liu
The genetic bases for non-syndromic hearing loss among Chinese.
Journal of human genetics 2009;54(3):131-40.
2009: Xue Zhong Liu; Yongyi Yuan; Denise Yan; Emilie Hong Ding; Xiao Mei Ouyang; Yu Fei; Wenxue Tang; Huijun Yuan; Qing Chang; Li Lin Du; Xin Zhang; Guojian Wang; Shoeb Ahmad; Dong Yang Kang; Xi Lin; Pu Dai
Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31.
Human genetics 2009;125(1):53-62.
2008: Xue Zhong Liu; Simon I Angeli; Xiao Mei Ouyang; W Liu; X M Ke; Y H Liu; S X Liu; Li Lin Du; X W Deng; H Yuan; Denise Yan
Audiological and genetic features of the mtDNA mutations.
Acta oto-laryngologica 2008;128(7):732-8.
2007: J Cheng; D Y Han; P Dai; H J Sun; R Tao; Q Sun; Denise Yan; W Qin; H Y Wang; Xiao Mei Ouyang; Shu-Zhi Yang; Ju-yang Cao; G Y Feng; Li Lin Du; Y Z Zhang; Suo-Qiang Zhai; W Y Yang; Xue Zhong Liu; L He; Hui-jun Yuan
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.
Clinical genetics 2007;72(5):471-7.
2007: Denise Yan; Xiao Mei Ouyang; Simon I Angeli; Li Lin Du; Xue Zhong Liu
Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss.
American journal of medical genetics. Part A 2007;143(4):385-6.
2006: Denise Yan; F Li; M L Hall; C Sage; W-H Hu; Cosmas Giallourakis; G Upadhyay; Xiao Mei Ouyang; Li Lin Du; John R Bethea; Zheng Yi Chen; V Yajnik; Xue Zhong Liu
An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C).
Journal of molecular biology 2006;357(3):755-64.
2006: Denise Yan; X Ke; S Blanton; Xiao Mei Ouyang; Arti Pandya; Li Lin Du; Walter E Nance; Xue Zhong Liu
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.
Journal of medical genetics 2006;43(2):170-4.
2005: Simon I Angeli; Denise Yan; Fred F Telischi; Thomas J Balkany; Xiao Mei Ouyang; Li Lin Du; Adrien A Eshraghi; Leslie Goodwin; Xue Zhong Liu
Etiologic diagnosis of sensorineural hearing loss in adults.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2005;132(6):890-5.
2005: Xiao Mei Ouyang; Denise Yan; Li Lin Du; J Fielding Hejtmancik; Samuel G Jacobson; Walter E Nance; An Ren Li; Simon I Angeli; Muriel Kaiser; Valerie Newton; Steve D M Brown; Thomas J Balkany; Xue Zhong Liu
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
Human genetics 2005;116(4):292-9.
2005: Denise Yan; Xiao Mei Ouyang; Xiaofeng Zhu; Li Lin Du; Zheng Yi Chen; Xue Zhong Liu
Refinement of the DFNA41 locus and candidate genes analysis.
Journal of human genetics 2005;50(10):516-22.
2005: Qing Yin Zheng; Denise Yan; Xiao Mei Ouyang; Li Lin Du; Heping Yu; Bo Chang; Kenneth R Johnson; Xue Zhong Liu
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans.
Human molecular genetics 2005;14(1):103-11.
2004: Xiao Mei Ouyang; Denise Yan; J Fielding Hejtmancik; S G Jacobson; A R Li; Li Lin Du; Simon I Angeli; M Kaiser; Thomas J Balkany; Xue Zhong Liu
Mutational spectrum in Usher syndrome type II.
Clinical genetics 2004;65(4):288-93.
2003: Denise Yan; Hong-Joon Park; Xiao Mei Ouyang; Arti Pandya; Katsumi Doi; Raadnabazar Erdenetungalag; Li Lin Du; Naoki Matsushiro; Walter E Nance; Andrew J Griffith; Xue Zhong Liu
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians.
Human genetics 2003;114(1):44-50.
2003: Xue Zhong Liu; Xiao Mei Ouyang; Xia Juan Xia; Jing Zheng; Arti Pandya; Fang Li; Li Lin Du; Katherine O Welch; Christine Petit; Richard J H Smith; Bradley T Webb; Denise Yan; Kathleen S Arnos; David Corey; Peter Dallos; Walter E Nance; Zheng Yi Chen
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.
Human molecular genetics 2003;12(10):1155-62.
2003: Xiao Mei Ouyang; J Fielding Hejtmancik; S G Jacobson; Xia Juan Xia; A Li; Li Lin Du; V Newton; M Kaiser; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian allele.
Clinical genetics 2003;63(2):150-3.
2002: Xue Zhong Liu; Xia Juan Xia; Xiao Mei Ke; Xiao Mei Ouyang; Li Lin Du; Yu He Liu; Simon I Angeli; Fred F Telischi; Walter E Nance; Thomas J Balkany; Li Rong Xu
The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
Human genetics 2002;111(4-5):394-7.
2002: Xiao Mei Ouyang; Xia Juan Xia; Elisabeth Verpy; Li Lin Du; Arti Pandya; Christine Petit; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
Human genetics 2002;111(1):26-30.
2001: Xue Zhong Liu; Xia Juan Xia; J Adams; Zheng Yi Chen; Katherine O Welch; Mustafa Tekin; Xiao Mei Ouyang; A Kristiansen; Arti Pandya; Thomas J Balkany; Kathleen S Arnos; Walter E Nance
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.
Human molecular genetics 2001;10(25):2945-51.