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Yuanyuan Lu, Ph.D.

Affiliations: 
2014 Mechanical Engineering University of North Carolina, Charlotte, Charlotte, NC, United States 
Area:
Mechanical Engineering, Materials Science Engineering
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"Yuanyuan Lu"
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Qiuming Wei grad student 2014 UNC Charlotte
 (A comprehensive study of the microstructure and mechanical behavior of HCP-based multilayered nanofilms.)

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Publications

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Lu YJ, Yao J, Wei QJ, et al. (2015) Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis. Medicine. 94: e2248
Li D, Lv P, Zhu J, et al. (2015) NiCu Alloy Nanoparticle-Loaded Carbon Nanofibers for Phenolic Biosensor Applications. Sensors (Basel, Switzerland). 15: 29419-29433
Liu Z, Xiao Y, Tang L, et al. (2015) Apolipoprotein A1 -75 G/A and +83 C/T polymorphisms and renal cancer risk. Lipids in Health and Disease. 14: 143
Jiang Q, Huang H, Liu Q, et al. (2015) Continuous IV infusion of MESNA can prevent hemorrhagic cystitis in HSCT and retain MESNA concentration in urine. Bone Marrow Transplantation
Li-Yang MN, Shen XF, Wei QJ, et al. (2015) IVS8+1 DelG, a Novel Splice Site Mutation Causing DFNA5 Deafness in a Chinese Family. Chinese Medical Journal. 128: 2510-2515
Yao J, Qian X, Bao J, et al. (2015) Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations. Scientific Reports. 5: 10831
Xing G, Yao J, Wu B, et al. (2015) Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 210-8
Lu Y, Yao J, Yu J, et al. (2014) The association between abnormal microRNA-10b expression and cancer risk: a meta-analysis. Scientific Reports. 4: 7498
Wei Q, Zhu H, Qian X, et al. (2014) Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of Translational Medicine. 12: 311
Tan M, Shen X, Yao J, et al. (2014) Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non‑syndromic hearing loss. International Journal of Molecular Medicine. 34: 1467-72
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