Xiaomei Ouyang - Concepedia

Author

Xiaomei Ouyang

University of Miami

Also Known As

Ouyang Xiaomei, X Ouyang, Xiao-Mei Ouyang, Xiao-mei Ouyang, Xiaomei OUYANG, Xiaomei Ouyang, Xiao‐Mei Ouyang

Publications

842

Citations

H-Index

Concepts

All Affiliations

University of Miami Imperial College London Xiamen University Charing Cross Hospital Chinese PLA General Hospital

About

Xiaomei Ouyang is an author at University of Miami specializing in medicine, genetics, and cell signaling.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	415
2	Cell Biology	4	4	116
3	Arts	2	2	84
4	Public Health	1	1	10
5	Biostatistics	1	1	10

Xiaomei Ouyang

Publications

771

Citations

H-Index

Page 1

	Year	Citations
Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2 Xue Zhong Liu, Dongyi Han, Jianzhong Li, The American Journal of Human Genetics Developmental BiologyGenetic DisorderPrps1 Gene CauseGeneticsMolecular Genetics	2009	123
Antioxidant enzymes, presbycusis, and ethnic variability Anthony Bared, Xiaomei Ouyang, Simón I. Angeli, Otolaryngology	2010	70
Proxy activation of protein ErbB2 by heterologous ligands implies a heterotetrameric mode of receptor tyrosine kinase interaction Guo Huang, Xiaomei Ouyang, Richard J. Epstein Biochemical Journal	1998	58
Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene Nele Hilgert, Matthew J. Huentelman, Ashley Q. Thorburn, European Journal of Human Genetics Genetic AnalysisAllelic VariantPhenotypic VariationGenetic DisorderGenetics	2008	53
Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population Rosemary I. Kabahuma, Xiaomei Ouyang, Li Du, International Journal of Pediatric Otorhinolaryngology Gjb6 DeletionGenetic DisorderGeneticsAudiologyArts	2011	48
Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II Denise Yan, Xiaomei Ouyang, Danielle Patterson, Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyLong Isoform	2009	43
Reduced ability of transforming growth factor-alpha to induce EGF receptor heterodimerization and downregulation suggests a mechanism of oncogenic synergy with ErbB2 Timothy Gulliford, Guo Huang, Xiaomei Ouyang, Oncogene Signal TransductionDevelopmental BiologySignaling PathwayReceptor Tyrosine KinaseEgf Receptor Heterodimerization	1997	43
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China Yi Sun, Jing Chen, Han-Jun Sun, Journal of Human Genetics Genetic DisorderGeneticsAudiologyHearing DisordersAuditory Research	2010	36
Transforming growth factor-alpha short-circuits downregulation of the epidermal growth factor receptor Xiaomei Ouyang, Timothy Gulliford, Guo-Cai Huang, Journal of Cellular Physiology Signal TransductionSignaling PathwayTumor MicroenvironmentHuman GrowthGrowth Hormone	1999	34
Mutation Analysis of <i>Slc26a4</i> in Mainland Chinese Patients with Enlarged Vestibular Aqueduct Samuel Reyes, Guojian Wang, Xiaomei Ouyang, Otolaryngology	2009	34

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