Xiaomei Ouyang

847 total citations
32 papers, 510 citations indexed

About

Xiaomei Ouyang is a scholar working on Molecular Biology, Sensory Systems and Oncology. According to data from OpenAlex, Xiaomei Ouyang has authored 32 papers receiving a total of 510 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Sensory Systems and 7 papers in Oncology. Recurrent topics in Xiaomei Ouyang's work include Hearing, Cochlea, Tinnitus, Genetics (11 papers), HER2/EGFR in Cancer Research (7 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Xiaomei Ouyang is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (11 papers), HER2/EGFR in Cancer Research (7 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Xiaomei Ouyang collaborates with scholars based in United States, United Kingdom and China. Xiaomei Ouyang's co-authors include Richard J. Epstein, Denise Yan, Guo Huang, Li Du, Simón I. Angeli, Hongyi Zhang, Xue-Zhong Liu, Anthony Bared, Xue Zhong Liu and Xue Zhong Liu and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Oncogene.

In The Last Decade

Xiaomei Ouyang

31 papers receiving 506 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Xiaomei Ouyang United States 14 259 190 131 95 87 32 510
M Lathrop France 8 105 0.4× 96 0.5× 21 0.2× 47 0.5× 27 0.3× 18 364
Ali Muhammad Waryah Pakistan 12 191 0.7× 150 0.8× 13 0.1× 69 0.7× 32 0.4× 39 412
Majida Charif Morocco 17 417 1.6× 167 0.9× 17 0.1× 105 1.1× 11 0.1× 51 617
Mounira Hmani‐Aifa Tunisia 14 274 1.1× 256 1.3× 28 0.2× 131 1.4× 39 0.4× 19 706
Vikas Malik United Kingdom 14 275 1.1× 40 0.2× 20 0.2× 24 0.3× 40 0.5× 48 527
Imad Ghazi France 10 618 2.4× 87 0.5× 26 0.2× 31 0.3× 93 1.1× 15 688
Shaked Shivatzki Israel 10 249 1.0× 162 0.9× 11 0.1× 46 0.5× 7 0.1× 16 462
Shoujun Gu United States 10 188 0.7× 151 0.8× 40 0.3× 58 0.6× 8 0.1× 18 356
Nataliya Di Donato Germany 18 463 1.8× 54 0.3× 25 0.2× 20 0.2× 19 0.2× 61 914

Countries citing papers authored by Xiaomei Ouyang

Since Specialization
Citations

This map shows the geographic impact of Xiaomei Ouyang's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Xiaomei Ouyang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xiaomei Ouyang more than expected).

Fields of papers citing papers by Xiaomei Ouyang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xiaomei Ouyang. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Xiaomei Ouyang. The network helps show where Xiaomei Ouyang may publish in the future.

Co-authorship network of co-authors of Xiaomei Ouyang

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaomei Ouyang. A scholar is included among the top collaborators of Xiaomei Ouyang based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Xiaomei Ouyang. Xiaomei Ouyang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ouyang, Xiaomei, et al.. (2025). Dietary succinate supplementation alleviates DSS-induced colitis via the IL-4Rα/Hif-1α Axis. International Immunopharmacology. 152. 114408–114408. 3 indexed citations
2.
Ouyang, Xiaomei, Ying Lin, Xiaodong Zhao, et al.. (2025). The SERPINB4 gene mutation identified in twin patients with Crohn’s disease impaires the intestinal epithelial cell functions. Scientific Reports. 15(1). 2638–2638.
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Su, Meng, Paul J. Benke, Güney Bademci, et al.. (2018). Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies. Molecular Cytogenetics. 11(1). 43–43. 2 indexed citations
6.
Zhang, Jian, Ziyi Liu, Jie Fang, et al.. (2016). Abnormal mRNA splicing but normal auditory brainstem response (ABR) in mice with the prestin (SLC26A5) IVS2-2A > G mutation. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 790. 1–7. 4 indexed citations
7.
Vivero, Richard J., Xiaomei Ouyang, Wendy Liu, et al.. (2013). Audiologic and Genetic Features of the A3243G mtDNA Mutation. Genetic Testing and Molecular Biomarkers. 17(5). 383–389. 5 indexed citations
8.
Fan, Yao‐Shan, Xiaomei Ouyang, Mustafa Tekin, et al.. (2013). Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray. Molecular Cytogenetics. 6(1). 38–38. 25 indexed citations
9.
Angeli, Simón I., Anthony Bared, Xiaomei Ouyang, et al.. (2012). Audioprofiles and antioxidant enzyme genotypes in presbycusis. The Laryngoscope. 122(11). 2539–2542. 12 indexed citations
10.
Vivero, Richard J., Xiaomei Ouyang, Denise Yan, et al.. (2012). Mitochondrial DNA Mutation Screening in an Ethnically Diverse Nonsyndromic Deafness Cohort. Genetic Testing and Molecular Biomarkers. 16(9). 1146–1148. 8 indexed citations
11.
Ouyang, Xiaomei, Li Du, Denise Yan, et al.. (2011). 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. International Journal of Pediatric Otorhinolaryngology. 75(5). 611–617. 44 indexed citations
12.
Ouyang, Xiaomei, et al.. (2011). Clinical comparison of hearing‐impaired patients with DFNB1 against heterozygote carriers of connexin 26 mutations. The Laryngoscope. 121(4). 811–814. 12 indexed citations
13.
Chen, Jing, Han-Jun Sun, Jing Cheng, et al.. (2010). Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China. Journal of Human Genetics. 56(1). 64–70. 30 indexed citations
14.
Yan, Denise, Xiaomei Ouyang, Danielle Patterson, et al.. (2009). Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II. Journal of Human Genetics. 54(12). 732–738. 31 indexed citations
15.
Ouyang, Xiaomei, et al.. (2001). Association of ErbB2 Ser1113 phosphorylation with epidermal growth factor receptor co-expression and poor prognosis in human breast cancer. Molecular and Cellular Biochemistry. 218(1-2). 47–54. 16 indexed citations
16.
Ouyang, Xiaomei, et al.. (1999). Transforming growth factor-alpha short-circuits downregulation of the epidermal growth factor receptor. Journal of Cellular Physiology. 179(1). 52–57. 22 indexed citations
17.
Ouyang, Xiaomei, et al.. (1998). Adjacent Carboxyterminal Tyrosine Phosphorylation Events Identify Functionally Distinct ErbB2 Receptor Subsets: Implications for Molecular Diagnostics. Experimental Cell Research. 241(2). 467–475. 11 indexed citations
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Ouyang, Xiaomei, T. Gulliford, Hongyi Zhang, Guo Huang, & Richard J. Epstein. (1996). Human Cancer Cells Exhibit Protein Kinase C-dependent c-erbB-2 Transmodulation That Correlates with Phosphatase Sensitivity and Kinase Activity. Journal of Biological Chemistry. 271(36). 21786–21792. 22 indexed citations
20.
Ouyang, Xiaomei, Hongyi Zhang, Trevor A. Bayston, & L. C. Archard. (1995). Detection of Coxsackievirus B3 RNA in mouse myocarditis by nested polymerase chain reaction. Clinical and Diagnostic Virology. 3(3). 233–245. 6 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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