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1) Zhang Q, Zhang L, Chen D, He X, Yao S, Zhang Z, *Chen Y, *Guan MX, Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function, Nucleic Acids Research, 2018 Nov, 46, 20, 10930-10945, SCI, 11.147, ,
2) Ying Z, Zheng J, Cai Z, Liu L, Dai Y, Yao J, Wang H, Gao Y, Zheng B, Tang X, Zhu Y, Guan MX, *Chen Y, Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation, Protein & Cell, 2015 Nov, 6, 11, 844-8, SCI, 7.575, 4,
3) Chen C, *Chen Y, Guan MX, A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation, Protein & Cell, 2015 Dec, 6, 12, 862-70, SCI, 7.575, 14,
4) Zheng J, Ying Z, Cai Z, Sun D, He Z, Gao Y, Zhang T, Zhu Y, *Chen Y, Guan MX, GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss, PLoS One, 2015 Jun, 10, 6, e0128691-, SCI, 3.337, 13,
5) Hu X, Mei S, Meng W, Xue S, Jiang L, Yang Y, Hui L,*Chen Y , Guan MX, CXCR4-mediated signaling regulates autophagy and influences acute myeloid leukemia cell survival and drug resistance, Cancer Letter, 2018 Jul, 425, , 1-12, SCI, 6.508, 9,
6) Li Q, Gao Z, *Chen Y, Guan MX, The role of mitochondria in osteogenic, adipogenic and chondrogenic differentiation of mesenchymal stem cells, Protein & Cell, 2017 Jun , 8, 6, 439-445, SCI, 7.575, 21,
7) Chen D, Li F, Yang Q, Tian M, Zhang Z, Zhang Q, *Chen Y, *Guan MX, The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish, The International Journal of Biochemistry & Cell Biology, 2016 May, 77, Pt A, 1-9, SCI, 3.654, ,
8) Hui L, *Chen Y, Tumor microenvironment: sanctuary of the devil, Cancer Letter, 2015 Nov , 368, 1, 7-13, SCI, 6.508, 77,
9) Zheng J, Meng WF, Zhang CF, Liu HQ, Yao J, Wang H, *Chen Y, Guan MX., New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population., J Zhejiang Univ Sci B, 2019 Feb, 20, 2, 164-169, SCI, 1.973, 1,
10) Zhang LW, Cang XH, *Chen Y, Guan MX., In vitro culture of mammalian inner ear hair cells., Journal of Zhejiang University SCIENCE B�, 2019 Feb, 20, 2, 170-179, SCI, 1.973, ,
11) Gao Z, *Chen Y, Guan MX, Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity, Journal of Otology, 2017 Mar , 12, 1, 1-8, , , ,
12) Meng W, Xue S, *Chen Y, The role of CXCL12 in tumor microenvironment, Gene, 2018 Jan , 641, , 105-110, SCI, 2.638, 17,
13) Chen X, Wang F, Maerhaba A, Li Q, Wang J, Liu X, Zheng J, Chen Y, *Guo Y, Novel mitochondrial gene variants in Northwestern Chinese probands with non-syndromic hearing loss by whole mitochondrial genome screening, Gene, 2018 Apr , 652, , 59-65, SCI, 2.638, ,
14) Tang X, Zheng J, Ying Z, Cai Z, Gao Y, He Z, Yu H, Yao J, Yang Y, Wang H, Chen Y, *Guan MX, Mitochondrial tRNASer(UCN) variants in 2651 Han Chinese subjects with hearing loss, Mitochondrion, 2015 May, 23, , 17-24, SCI, 3.226, 2,
15) Yu J, Zheng J, Zhao X, Liu J, Mao Z, Ling Y, Chen D, Chen C, Hui L, Cui L, Chen Y, Jiang P, *Guan MX, Aminoglycoside Stress Together with the 12S rRNA 1494C>T Mutation Leads to Mitophagy, PLoS One, 2014 Dec , 9, 12, e114650-, SCI, 2.776, 2,
16) Zhang W, Borthakur G, Gao C, Chen Y, Mu H, Ruvolo V, Nomoto K, Zhao N, Konopleva M, *Andreeff M, The Dual MEK/FLT3 Inhibitor E6201 Exerts Cytotoxic Activity against Acute Myeloid Leukemia Cells Harboring Resistance-Conferring FLT3 Mutations., Cancer Research, 2016 Mar, 76, 6, 1528-1537, SCI, 8.378, 13,
17) Jiang P, Wang M, Xue L, Xiao Y, Yu J, Wang H, Yao J, Liu H, Peng Y, Liu H, Li H, Chen Y, *Guan MX, A hypertension-associated tRNAAla mutation alters the tRNA metabolism and mitochondrial function, Molecular and Cellular Biology, 2016 May , 36, 14, 1920-1930, SCI, 3.735, 7,
18) Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, Ji Y, Liang M, Zhao F, Sun Y, Zhang M, Zhou X, Chen Y, Mo J, Huang T, Qu J, *Guan MX, The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber’s hereditary optic neuropathy-associated mitochondrial DNA mutation, Human Molecular Genetics, 2016 Feb , 25, 3, 584-96, SCI, 4.544, 20,
19) Su X, Wang W, Ruan G, Liang M, Zheng J, Chen Y, Wu H, Fahey TJ, Guan M, *Teng L, A Comprehensive Characterization of Mitochondrial Genome in Papillary Thyroid Cancer, International Journal of Molecular Sciences, 2016 Oct, 17, 10, E1594-, SCI, 4.183, 7,
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