A citation-based method for searching scientific literature

Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Piero Barboni, Fred N Ross-Cisneros, Alfredo A Sadun. Biochim Biophys Acta 2009
Times Cited: 160







List of co-cited articles
1039 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
37

Mitochondrial dysfunction as a cause of optic neuropathies.
Valerio Carelli, Fred N Ross-Cisneros, Alfredo A Sadun. Prog Retin Eye Res 2004
564
34

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.
Patrick Yu-Wai-Man, Philip G Griffiths, Patrick F Chinnery. Prog Retin Eye Res 2011
386
33

Inherited mitochondrial optic neuropathies.
P Yu-Wai-Man, P G Griffiths, G Hudson, P F Chinnery. J Med Genet 2009
265
27


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
20

The epidemiology of Leber hereditary optic neuropathy in the North East of England.
P Yu-Wai-Man, P G Griffiths, D T Brown, N Howell, D M Turnbull, P F Chinnery. Am J Hum Genet 2003
303
18


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
15


Mouse mtDNA mutant model of Leber hereditary optic neuropathy.
Chun Shi Lin, Mark S Sharpley, Weiwei Fan, Katrina G Waymire, Alfredo A Sadun, Valerio Carelli, Fred N Ross-Cisneros, Peter Baciu, Eric Sung, Meagan J McManus,[...]. Proc Natl Acad Sci U S A 2012
136
14

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.
Carla Giordano, Luisa Iommarini, Luca Giordano, Alessandra Maresca, Annalinda Pisano, Maria Lucia Valentino, Leonardo Caporali, Rocco Liguori, Stefania Deceglie, Marina Roberti,[...]. Brain 2014
183
14


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
13


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
13

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy.
C Delettre, G Lenaers, J M Griffoin, N Gigarel, C Lorenzo, P Belenguer, L Pelloquin, J Grosgeorge, C Turc-Carel, E Perret,[...]. Nat Genet 2000
13

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
35

Mathematically modeling the involvement of axons in Leber's hereditary optic neuropathy.
Billy X Pan, Fred N Ross-Cisneros, Valerio Carelli, Kelly S Rue, Solange R Salomao, Milton N Moraes-Filho, Milton N Moraes, Adriana Berezovsky, Rubens Belfort, Alfredo A Sadun. Invest Ophthalmol Vis Sci 2012
79
16

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
35


The neuro-ophthalmology of mitochondrial disease.
J Alexander Fraser, Valérie Biousse, Nancy J Newman. Surv Ophthalmol 2010
161
12

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
40

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
16

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
12

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
12

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
12

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
12

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion.
Claudia Zanna, Anna Ghelli, Anna Maria Porcelli, Mariusz Karbowski, Richard J Youle, Simone Schimpf, Bernd Wissinger, Marcello Pinti, Andrea Cossarizza, Sara Vidoni,[...]. Brain 2008
242
12

Natural history of Leber's hereditary optic neuropathy: longitudinal analysis of the retinal nerve fiber layer by optical coherence tomography.
Piero Barboni, Michele Carbonelli, Giacomo Savini, Carolina do V F Ramos, Arturo Carta, Adriana Berezovsky, Solange R Salomao, Valerio Carelli, Alfredo A Sadun. Ophthalmology 2010
138
12



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
33

Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.
A E Harding, M G Sweeney, G G Govan, P Riordan-Eva. Am J Hum Genet 1995
215
11

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
C Alexander, M Votruba, U E Pesch, D L Thiselton, S Mayer, A Moore, M Rodriguez, U Kellner, B Leo-Kottler, G Auburger,[...]. Nat Genet 2000
964
11

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
Carla Giordano, Monica Montopoli, Elena Perli, Maurizia Orlandi, Marianna Fantin, Fred N Ross-Cisneros, Laura Caparrotta, Andrea Martinuzzi, Eugenio Ragazzi, Anna Ghelli,[...]. Brain 2011
163
11


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
13

Macular nerve fibre and ganglion cell layer changes in acute Leber's hereditary optic neuropathy.
Nicole Balducci, Giacomo Savini, Maria Lucia Cascavilla, Chiara La Morgia, Giacinto Triolo, Rosa Giglio, Michele Carbonelli, Vincenzo Parisi, Alfredo A Sadun, Francesco Bandello,[...]. Br J Ophthalmol 2016
50
22


LHON: Mitochondrial Mutations and More.
E Kirches. Curr Genomics 2011
64
15

Multi-system neurological disease is common in patients with OPA1 mutations.
P Yu-Wai-Man, P G Griffiths, G S Gorman, C M Lourenco, A F Wright, M Auer-Grumbach, A Toscano, O Musumeci, M L Valentino, L Caporali,[...]. Brain 2010
289
10

OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion.
Christian Frezza, Sara Cipolat, Olga Martins de Brito, Massimo Micaroni, Galina V Beznoussenko, Tomasz Rudka, Davide Bartoli, Roman S Polishuck, Nika N Danial, Bart De Strooper,[...]. Cell 2006
10

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
10

Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids.
Alessandra Baracca, Giancarlo Solaini, Gianluca Sgarbi, Giorgio Lenaz, Agostino Baruzzi, Anthony H V Schapira, Andrea Martinuzzi, Valerio Carelli. Arch Neurol 2005
124
10

Leber's Hereditary Optic Neuropathy.
Alfredo A Sadun, Chiara La Morgia, Valerio Carelli. Curr Treat Options Neurol 2011
86
11

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
9

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
15

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
9

Gene-environment interactions in Leber hereditary optic neuropathy.
Matthew Anthony Kirkman, Patrick Yu-Wai-Man, Alex Korsten, Miriam Leonhardt, Konstantin Dimitriadis, Ireneaus F De Coo, Thomas Klopstock, Patrick Francis Chinnery. Brain 2009
219
9


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.