A citation-based method for searching scientific literature

Xiangtian Zhou, Yaping Qian, Juanjuan Zhang, Yi Tong, Pingping Jiang, Min Liang, Xianning Dai, Huihui Zhou, Fuxin Zhao, Yanchun Ji, Jun Qin Mo, Jia Qu, Min-Xin Guan. Invest Ophthalmol Vis Sci 2012
Times Cited: 30







List of co-cited articles
234 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
R M Andrews, I Kubacka, P F Chinnery, R N Lightowlers, D M Turnbull, N Howell. Nat Genet 1999
66

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
D C Wallace, G Singh, M T Lott, J A Hodge, T G Schurr, A M Lezza, L J Elsas, E K Nikoskelainen. Science 1988
60

An enhanced MITOMAP with a global mtDNA mutational phylogeny.
Eduardo Ruiz-Pesini, Marie T Lott, Vincent Procaccio, Jason C Poole, Marty C Brandon, Dan Mishmar, Christina Yi, James Kreuziger, Pierre Baldi, Douglas C Wallace. Nucleic Acids Res 2007
428
60

Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
Min Liang, Pingping Jiang, Feng Li, Juanjuan Zhang, Yanchun Ji, Yiqun He, Meifen Xu, Jinping Zhu, Xiangjuan Meng, Fuxin Zhao,[...]. Invest Ophthalmol Vis Sci 2014
37
60


Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
D A Mackey, R J Oostra, T Rosenberg, E Nikoskelainen, J Bronte-Stewart, J Poulton, A E Harding, G Govan, P A Bolhuis, S Norby. Am J Hum Genet 1996
259
53

Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families.
Juanjuan Zhang, Pingping Jiang, Xiaofen Jin, Xiaoling Liu, Minglian Zhang, Shipeng Xie, Min Gao, Sai Zhang, Yan-Hong Sun, Jinping Zhu,[...]. Mitochondrion 2014
28
57



A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.
Shasha Gong, Yanyan Peng, Pingping Jiang, Meng Wang, Mingjie Fan, Xinjian Wang, Hong Zhou, Huawei Li, Qingfeng Yan, Taosheng Huang,[...]. Nucleic Acids Res 2014
82
50

Inherited mitochondrial optic neuropathies.
P Yu-Wai-Man, P G Griffiths, G Hudson, P F Chinnery. J Med Genet 2009
265
46


The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Jia Qu, Ronghua Li, Xiangtian Zhou, Yi Tong, Fan Lu, Yaping Qian, Yongwu Hu, Jun Qin Mo, Constance E West, Min-Xin Guan. Invest Ophthalmol Vis Sci 2006
105
46


Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Pingping Jiang, Min Liang, Juanjuan Zhang, Yinglong Gao, Zheyun He, Han Yu, Fuxin Zhao, Yanchun Ji, Xiaoling Liu, Minglian Zhang,[...]. Invest Ophthalmol Vis Sci 2015
37
46

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Piero Barboni, Fred N Ross-Cisneros, Alfredo A Sadun. Biochim Biophys Acta 2009
160
43

Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations.
Qing-Peng Kong, Hans-Jürgen Bandelt, Chang Sun, Yong-Gang Yao, Antonio Salas, Alessandro Achilli, Cheng-Ye Wang, Li Zhong, Chun-Ling Zhu, Shi-Fang Wu,[...]. Hum Mol Genet 2006
314
43

Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Yanchun Ji, Min Liang, Juanjuan Zhang, Ling Zhu, Zengjun Zhang, Runing Fu, Xiaoling Liu, Minglian Zhang, Qun Fu, Fuxin Zhao,[...]. Invest Ophthalmol Vis Sci 2016
32
43



Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.
Juanjuan Zhang, Fuxin Zhao, Qun Fu, Min Liang, Yi Tong, Xiaoling Liu, Bei Lin, Hui Mi, Minglian Zhang, Qi-Ping Wei,[...]. Mitochondrion 2013
19
63


Assessing bioenergetic function in response to oxidative stress by metabolic profiling.
Brian P Dranka, Gloria A Benavides, Anne R Diers, Samantha Giordano, Blake R Zelickson, Colin Reily, Luyun Zou, John C Chatham, Bradford G Hill, Jianhua Zhang,[...]. Free Radic Biol Med 2011
316
36

Mitochondria-mediated transformation of human rho(0) cells.
M P King, G Attadi. Methods Enzymol 1996
68
36


Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
Jia Qu, Xiangtian Zhou, Juanjuan Zhang, Fuxin Zhao, Yan-Hong Sun, Yi Tong, Qi-Ping Wei, Wansi Cai, Li Yang, Constance E West,[...]. Ophthalmology 2009
45
33

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy.
Xiaoyun Jia, Shiqiang Li, Xueshan Xiao, Xiangming Guo, Qingjiong Zhang. J Hum Genet 2006
71
33

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy.
Y Mashima, K Yamada, M Wakakura, K Kigasawa, J Kudoh, N Shimizu, Y Oguchi. Curr Eye Res 1998
102
33

An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria.
Youfen Li, Marilena D'Aurelio, Jian-Hong Deng, Jeong-Soon Park, Giovanni Manfredi, Peiqing Hu, Jianxin Lu, Yidong Bai. J Biol Chem 2007
88
33

Oxidative stress in inherited mitochondrial diseases.
Genki Hayashi, Gino Cortopassi. Free Radic Biol Med 2015
95
33


The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation.
P Riordan-Eva, M D Sanders, G G Govan, M G Sweeney, J Da Costa, A E Harding. Brain 1995
375
30




A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.
Pingping Jiang, Meng Wang, Ling Xue, Yun Xiao, Jialing Yu, Hui Wang, Juan Yao, Hao Liu, Yanyan Peng, Hanqing Liu,[...]. Mol Cell Biol 2016
42
30

Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
Pingping Jiang, Min Liang, Chaofan Zhang, Xiaoxu Zhao, Qiufen He, Limei Cui, Xiaoling Liu, Yan-Hong Sun, Qun Fu, Yanchun Ji,[...]. Hum Mol Genet 2016
27
33

Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
Xiangtian Zhou, Hongxing Zhang, Fuxin Zhao, Yanchun Ji, Yi Tong, Juanjuan Zhang, Yu Zhang, Li Yang, Yaping Qian, Fan Lu,[...]. Mol Genet Metab 2010
33
26

Mitochondrial genome variation in eastern Asia and the peopling of Japan.
Masashi Tanaka, Vicente M Cabrera, Ana M González, José M Larruga, Takeshi Takeyasu, Noriyuki Fuku, Li-Jun Guo, Raita Hirose, Yasunori Fujita, Miyuki Kurata,[...]. Genome Res 2004
345
26

Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells.
Alice Wong, Lucia Cavelier, Heather E Collins-Schramm, Michael F Seldin, Michael McGrogan, Marja-Liisa Savontaus, Gino A Cortopassi. Hum Mol Genet 2002
147
26


LHON: Mitochondrial Mutations and More.
E Kirches. Curr Genomics 2011
64
26

The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.
Ronghua Li, Jia Qu, Xiangtian Zhou, Yi Tong, Yongwu Hu, Yaping Qian, Fan Lu, Jun Qin Mo, Constance E West, Min-Xin Guan. Gene 2006
57
23

Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
Tsutomu Suzuki, Asuteka Nagao, Takeo Suzuki. Annu Rev Genet 2011
355
23

Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium.
Anna Ghelli, Claudia Zanna, Anna Maria Porcelli, Anthony H V Schapira, Andrea Martinuzzi, Valerio Carelli, Michela Rugolo. J Biol Chem 2003
152
23

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.
Rosa Pello, Miguel A Martín, Valerio Carelli, Leo G Nijtmans, Alessandro Achilli, Maria Pala, Antonio Torroni, Aurora Gómez-Durán, Eduardo Ruiz-Pesini, Andrea Martinuzzi,[...]. Hum Mol Genet 2008
126
23

Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.
Douglas C Wallace, Marie T Lott. Handb Exp Pharmacol 2017
35
23

Mitochondrial tRNA mutations associated with deafness.
Jing Zheng, Yanchun Ji, Min-Xin Guan. Mitochondrion 2012
44
20




Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.