A citation-based method for searching scientific literature

Juanjuan Zhang, Pingping Jiang, Xiaofen Jin, Xiaoling Liu, Minglian Zhang, Shipeng Xie, Min Gao, Sai Zhang, Yan-Hong Sun, Jinping Zhu, Yanchun Ji, Qi-Ping Wei, Yi Tong, Min-Xin Guan. Mitochondrion 2014
Times Cited: 28







List of co-cited articles
271 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
57

Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.
Xiangtian Zhou, Yaping Qian, Juanjuan Zhang, Yi Tong, Pingping Jiang, Min Liang, Xianning Dai, Huihui Zhou, Fuxin Zhao, Yanchun Ji,[...]. Invest Ophthalmol Vis Sci 2012
30
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
57

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
53

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
53




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

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
46


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
46

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
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
42

Inherited mitochondrial optic neuropathies.
P Yu-Wai-Man, P G Griffiths, G Hudson, P F Chinnery. J Med Genet 2009
265
39


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
35

Oxidative stress in inherited mitochondrial diseases.
Genki Hayashi, Gino Cortopassi. Free Radic Biol Med 2015
95
35

Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
Tsutomu Suzuki, Asuteka Nagao, Takeo Suzuki. Annu Rev Genet 2011
355
35

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
35

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
47

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
32



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
32


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
32

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
28


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
28

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
28

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
28




Mitochondria-mediated transformation of human rho(0) cells.
M P King, G Attadi. Methods Enzymol 1996
68
28


Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
Yanli Ji, A-Mei Zhang, Xiaoyun Jia, Ya-Ping Zhang, Xueshan Xiao, Shiqiang Li, Xiangming Guo, Hans-Jürgen Bandelt, Qingjiong Zhang, Yong-Gang Yao. Am J Hum Genet 2008
113
25

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray, Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, Chiara La Morgia,[...]. Am J Hum Genet 2007
269
25

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
25


Mitochondrial tRNA mutations associated with deafness.
Jing Zheng, Yanchun Ji, Min-Xin Guan. Mitochondrion 2012
44
25

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
21

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
21

LHON: Mitochondrial Mutations and More.
E Kirches. Curr Genomics 2011
64
21


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
21

Analysis of aminoacylation of human mitochondrial tRNAs.
J A Enríquez, G Attardi. Methods Enzymol 1996
53
21

Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
Min-Xin Guan, Qingfeng Yan, Xiaoming Li, Yelena Bykhovskaya, Jaime Gallo-Teran, Petr Hajek, Noriko Umeda, Hui Zhao, Gema Garrido, Emebet Mengesha,[...]. Am J Hum Genet 2006
178
21


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.