A citation-based method for searching scientific literature

Jiro Fukae, Yoshikuni Mizuno, Nobutaka Hattori. Mitochondrion 2007
Times Cited: 68







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



Times Cited
  Times     Co-cited
Similarity



Oxidative damage in nucleic acids and Parkinson's disease.
Yusaku Nakabeppu, Daisuke Tsuchimoto, Hiroo Yamaguchi, Kunihiko Sakumi. J Neurosci Res 2007
183
13

Hereditary early-onset Parkinson's disease caused by mutations in PINK1.
Enza Maria Valente, Patrick M Abou-Sleiman, Viviana Caputo, Miratul M K Muqit, Kirsten Harvey, Suzana Gispert, Zeeshan Ali, Domenico Del Turco, Anna Rita Bentivoglio, Daniel G Healy,[...]. Science 2004
13

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.
Andreas Bender, Kim J Krishnan, Christopher M Morris, Geoffrey A Taylor, Amy K Reeve, Robert H Perry, Evelyn Jaros, Joshua S Hersheson, Joanne Betts, Thomas Klopstock,[...]. Nat Genet 2006
10

Oxidative DNA damage in the parkinsonian brain: an apparent selective increase in 8-hydroxyguanine levels in substantia nigra.
Z I Alam, A Jenner, S E Daniel, A J Lees, N Cairns, C D Marsden, P Jenner, B Halliwell. J Neurochem 1997
601
10

Chronic systemic pesticide exposure reproduces features of Parkinson's disease.
R Betarbet, T B Sherer, G MacKenzie, M Garcia-Osuna, A V Panov, J T Greenamyre. Nat Neurosci 2000
10


Oxidative stress in Parkinson's disease.
Peter Jenner. Ann Neurol 2003
10

Mitochondrial biology and oxidative stress in Parkinson disease pathogenesis.
Claire Henchcliffe, M Flint Beal. Nat Clin Pract Neurol 2008
511
10

Mitochondrial dysfunction and oxidative damage in parkin-deficient mice.
James J Palacino, Dijana Sagi, Matthew S Goldberg, Stefan Krauss, Claudia Motz, Maik Wacker, Joachim Klose, Jie Shen. J Biol Chem 2004
725
8


Premature ageing in mice expressing defective mitochondrial DNA polymerase.
Aleksandra Trifunovic, Anna Wredenberg, Maria Falkenberg, Johannes N Spelbrink, Anja T Rovio, Carl E Bruder, Mohammad Bohlooly-Y, Sebastian Gidlöf, Anders Oldfors, Rolf Wibom,[...]. Nature 2004
8

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
T Kitada, S Asakawa, N Hattori, H Matsumine, Y Yamamura, S Minoshima, M Yokochi, Y Mizuno, N Shimizu. Nature 1998
8

8-Oxoguanine causes neurodegeneration during MUTYH-mediated DNA base excision repair.
Zijing Sheng, Sugako Oka, Daisuke Tsuchimoto, Nona Abolhassani, Hiroko Nomaru, Kunihiko Sakumi, Hidetaka Yamada, Yusaku Nakabeppu. J Clin Invest 2012
89
8

Early-onset familial parkinsonism due to POLG mutations.
Guido Davidzon, Paul Greene, Michelangelo Mancuso, Kevin J Klos, J Eric Ahlskog, Michio Hirano, Salvatore DiMauro. Ann Neurol 2006
170
7

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
Petri Luoma, Atle Melberg, Juha O Rinne, Jyrki A Kaukonen, Nina N Nupponen, Richard M Chalmers, Anders Oldfors, Ilkka Rautakorpi, Leena Peltonen, Kari Majamaa,[...]. Lancet 2004
402
7


Parkinson's disease: mechanisms and models.
William Dauer, Serge Przedborski. Neuron 2003
7

Alpha-synuclein in Lewy bodies.
M G Spillantini, M L Schmidt, V M Lee, J Q Trojanowski, R Jakes, M Goedert. Nature 1997
7

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
M H Polymeropoulos, C Lavedan, E Leroy, S E Ide, A Dehejia, A Dutra, B Pike, H Root, J Rubenstein, R Boyer,[...]. Science 1997
7

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy.
Derek Narendra, Atsushi Tanaka, Der-Fen Suen, Richard J Youle. J Cell Biol 2008
7

A generalised increase in protein carbonyls in the brain in Parkinson's but not incidental Lewy body disease.
Z I Alam, S E Daniel, A J Lees, D C Marsden, P Jenner, B Halliwell. J Neurochem 1997
419
7

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Vincenzo Bonifati, Patrizia Rizzu, Marijke J van Baren, Onno Schaap, Guido J Breedveld, Elmar Krieger, Marieke C J Dekker, Ferdinando Squitieri, Pablo Ibanez, Marijke Joosse,[...]. Science 2003
7

Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.
Nada Al-Tassan, Nikolas H Chmiel, Julie Maynard, Nick Fleming, Alison L Livingston, Geraint T Williams, Angela K Hodges, D Rhodri Davies, Sheila S David, Julian R Sampson,[...]. Nat Genet 2002
927
7


Increased 8-oxo-dGTPase in the mitochondria of substantia nigral neurons in Parkinson's disease.
H Shimura-Miura, N Hattori, D Kang, K Miyako, Y Nakabeppu, Y Mizuno. Ann Neurol 1999
119
5

Parkinson's disease is associated with oxidative damage to cytoplasmic DNA and RNA in substantia nigra neurons.
J Zhang, G Perry, M A Smith, D Robertson, S J Olson, D G Graham, T J Montine. Am J Pathol 1999
450
5

A selective increase in particulate superoxide dismutase activity in parkinsonian substantia nigra.
H Saggu, J Cooksey, D Dexter, F R Wells, A Lees, P Jenner, C D Marsden. J Neurochem 1989
395
5

Base excision repair capacity in mitochondria and nuclei: tissue-specific variations.
Bensu Karahalil, Barbara A Hogue, Nadja C de Souza-Pinto, Vilhelm A Bohr. FASEB J 2002
94
5

Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1.
Sherif F El-Khamisy, Gulam M Saifi, Michael Weinfeld, Fredrik Johansson, Thomas Helleday, James R Lupski, Keith W Caldecott. Nature 2005
331
5

The metabolic syndrome resulting from a knockout of the NEIL1 DNA glycosylase.
Vladimir Vartanian, Brian Lowell, Irina G Minko, Thomas G Wood, Jeffrey D Ceci, Shakeeta George, Scott W Ballinger, Christopher L Corless, Amanda K McCullough, R Stephen Lloyd. Proc Natl Acad Sci U S A 2006
176
5

Accumulation of premutagenic DNA lesions in mice defective in removal of oxidative base damage.
A Klungland, I Rosewell, S Hollenbach, E Larsen, G Daly, B Epe, E Seeberg, T Lindahl, D E Barnes. Proc Natl Acad Sci U S A 1999
677
5

DNA repair, mitochondria, and neurodegeneration.
L Weissman, N C de Souza-Pinto, T Stevnsner, V A Bohr. Neuroscience 2007
116
5

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease.
R Krüger, W Kuhn, T Müller, D Woitalla, M Graeber, S Kösel, H Przuntek, J T Epplen, L Schöls, O Riess. Nat Genet 1998
5

Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism.
Laura Silvestri, Viviana Caputo, Emanuele Bellacchio, Luigia Atorino, Bruno Dallapiccola, Enza Maria Valente, Giorgio Casari. Hum Mol Genet 2005
348
5

alpha-Synuclein locus triplication causes Parkinson's disease.
A B Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, M Hulihan, T Peuralinna, A Dutra, R Nussbaum,[...]. Science 2003
5

Mitochondrial alterations of retinal pigment epithelium in age-related macular degeneration.
Janos Feher, Illes Kovacs, Marco Artico, Carlo Cavallotti, Antonio Papale, Corrado Balacco Gabrieli. Neurobiol Aging 2006
248
5

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease.
P T Luoma, J Eerola, S Ahola, A H Hakonen, O Hellström, K T Kivistö, P J Tienari, A Suomalainen. Neurology 2007
108
5

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin.
Ira E Clark, Mark W Dodson, Changan Jiang, Joseph H Cao, Jun R Huh, Jae Hong Seol, Soon Ji Yoo, Bruce A Hay, Ming Guo. Nature 2006
5

Inducible nitric oxide synthase stimulates dopaminergic neurodegeneration in the MPTP model of Parkinson disease.
G T Liberatore, V Jackson-Lewis, S Vukosavic, A S Mandir, M Vila, W G McAuliffe, V L Dawson, T M Dawson, S Przedborski. Nat Med 1999
835
5

Staging of brain pathology related to sporadic Parkinson's disease.
Heiko Braak, Kelly Del Tredici, Udo Rüb, Rob A I de Vos, Ernst N H Jansen Steur, Eva Braak. Neurobiol Aging 2003
5

Parkinson's disease.
Bobby Thomas, M Flint Beal. Hum Mol Genet 2007
561
5

Immunohistochemical detection of 4-hydroxynonenal protein adducts in Parkinson disease.
A Yoritaka, N Hattori, K Uchida, M Tanaka, E R Stadtman, Y Mizuno. Proc Natl Acad Sci U S A 1996
792
5


Basal lipid peroxidation in substantia nigra is increased in Parkinson's disease.
D T Dexter, C J Carter, F R Wells, F Javoy-Agid, Y Agid, A Lees, P Jenner, C D Marsden. J Neurochem 1989
5

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase.
H Shimura, N Hattori, S i Kubo, Y Mizuno, S Asakawa, S Minoshima, N Shimizu, K Iwai, T Chiba, K Tanaka,[...]. Nat Genet 2000
5


Proanthocyanidin-rich fraction from Croton celtidifolius Baill confers neuroprotection in the intranasal 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine rat model of Parkinson's disease.
Eduardo L G Moreira, Daniel Rial, Aderbal S Aguiar, Cláudia P Figueiredo, Jarbas M Siqueira, Silvia DalBó, Heros Horst, Jade de Oliveira, Gianni Mancini, Tiago S dos Santos,[...]. J Neural Transm (Vienna) 2010
47
8


Neuroprotective and neurorescue effect of black tea extract in 6-hydroxydopamine-lesioned rat model of Parkinson's disease.
R K Chaturvedi, S Shukla, K Seth, S Chauhan, C Sinha, Y Shukla, A K Agrawal. Neurobiol Dis 2006
65
6


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.