A citation-based method for searching scientific literature

Mohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, Shahriar Nafissi, Barbara Scheiber-Mojdehkar, Mehri Khatami. Neurol Sci 2008
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Oxidative stress biomarkers in mitochondrial myopathies, basally and after cysteine donor supplementation.
Michelangelo Mancuso, Daniele Orsucci, Annalisa Logerfo, Anna Rocchi, Lucia Petrozzi, Claudia Nesti, Fabio Galetta, Gino Santoro, Luigi Murri, Gabriele Siciliano. J Neurol 2010
50
14

Regulation of ubiquinone metabolism.
G Dallner, P J Sindelar. Free Radic Biol Med 2000
152
14

Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.
Veronica Crugnola, Costanza Lamperti, Valeria Lucchini, Dario Ronchi, Lorenzo Peverelli, Alessandro Prelle, Monica Sciacco, Andreina Bordoni, Elisa Fassone, Francesco Fortunato,[...]. Arch Neurol 2010
89
14

Current and emerging treatment options in the management of Friedreich ataxia.
Michelangelo Mancuso, Daniele Orsucci, Anna Choub, Gabriele Siciliano. Neuropsychiatr Dis Treat 2010
16
14

Prevalence of mitochondrial DNA disease in adults.
Andrew M Schaefer, Robert McFarland, Emma L Blakely, Langping He, Roger G Whittaker, Robert W Taylor, Patrick F Chinnery, Douglass M Turnbull. Ann Neurol 2008
377
14

Coenzyme Q10.
Robert Alan Bonakdar, Erminia Guarneri. Am Fam Physician 2005
89
14

A phase 3, double-blind, placebo-controlled trial of idebenone in friedreich ataxia.
David R Lynch, Susan L Perlman, Thomas Meier. Arch Neurol 2010
120
14

Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III.
Petra Kaufmann, John L P Thompson, Gilberto Levy, Richard Buchsbaum, Jeremy Shefner, Lisa S Krivickas, Jonathan Katz, Yvonne Rollins, Richard J Barohn, Carlayne E Jackson,[...]. Ann Neurol 2009
138
14

Mutations in coenzyme Q10 biosynthetic genes.
Salvatore DiMauro, Catarina M Quinzii, Michio Hirano. J Clin Invest 2007
68
14

Tolerance of high-dose (3,000 mg/day) coenzyme Q10 in ALS.
K L Ferrante, J Shefner, H Zhang, R Betensky, M O'Brien, H Yu, M Fantasia, J Taft, M F Beal, B Traynor,[...]. Neurology 2005
114
14


Coenzyme Q as an antiadipogenic factor.
Sandy Bour, Maria-Carmen Carmona, Anne Galinier, Sylvie Caspar-Bauguil, Luc Van Gaal, Bart Staels, Luc Pénicaud, Louis Casteilla. Antioxid Redox Signal 2011
19
14

Role of mitochondria in neuronal cell death induced by oxidative stress; neuroprotection by Coenzyme Q10.
M Somayajulu, S McCarthy, M Hung, M Sikorska, H Borowy-Borowski, S Pandey. Neurobiol Dis 2005
121
14


ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency.
Clotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, Catarina M Quinzii, Mirna Assoum, Nathalie Drouot, Cleverson Busso, Samira Makri, Lamia Ali-Pacha, Traki Benhassine,[...]. Am J Hum Genet 2008
202
14



Oxidative stress induces degradation of mitochondrial DNA.
Inna Shokolenko, Natalia Venediktova, Alexandra Bochkareva, Glenn L Wilson, Mikhail F Alexeyev. Nucleic Acids Res 2009
283
14

Evaluation of coenzyme Q as an antioxidant strategy for Alzheimer's disease.
Teri L Wadsworth, James A Bishop, Anuradha S Pappu, Randall L Woltjer, Joseph F Quinn. J Alzheimers Dis 2008
60
14


Coenzyme Q10 modulates cognitive impairment against intracerebroventricular injection of streptozotocin in rats.
Tauheed Ishrat, M Badruzzaman Khan, Md Nasrul Hoda, Seema Yousuf, Muzamil Ahmad, Mubeen A Ansari, Abdullah S Ahmad, Fakhrul Islam. Behav Brain Res 2006
127
14

Huntington's disease and mitochondrial alterations: emphasis on experimental models.
Verónica Pérez-De la Cruz, Paul Carrillo-Mora, Abel Santamaría. J Bioenerg Biomembr 2010
6
16

CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures.
Julie Mollet, Agnès Delahodde, Valérie Serre, Dominique Chretien, Dimitri Schlemmer, Anne Lombes, Nathalie Boddaert, Isabelle Desguerre, Pascale de Lonlay, Hélène Ogier de Baulny,[...]. Am J Hum Genet 2008
190
14

Mutations in mitochondrial DNA polymerase-gamma promote breast tumorigenesis.
Keshav K Singh, Vanniarajan Ayyasamy, Kjerstin M Owens, Manika Sapru Koul, Marija Vujcic. J Hum Genet 2009
87
14

Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study.
Lisa A Carey, Charles M Perou, Chad A Livasy, Lynn G Dressler, David Cowan, Kathleen Conway, Gamze Karaca, Melissa A Troester, Chiu Kit Tse, Sharon Edmiston,[...]. JAMA 2006
14




Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1.
Janghoo Lim, Juan Crespo-Barreto, Paymaan Jafar-Nejad, Aaron B Bowman, Ronald Richman, David E Hill, Harry T Orr, Huda Y Zoghbi. Nature 2008
225
14

Association of the polymorphism of the CAG repeat in the mitochondrial DNA polymerase gamma gene (POLG) with testicular germ-cell cancer.
M Blomberg Jensen, H Leffers, J H Petersen, G Daugaard, N E Skakkebaek, E Rajpert-De Meyts. Ann Oncol 2008
16
14

POLG mutations in Alpers syndrome.
K V Nguyen, E Østergaard, S Holst Ravn, T Balslev, E Rubaek Danielsen, A Vardag, P J McKiernan, G Gray, R K Naviaux. Neurology 2005
101
14

Conducting Molecular Epidemiological Research in the Age of HIPAA: A Multi-Institutional Case-Control Study of Breast Cancer in African-American and European-American Women.
Christine B Ambrosone, Gregory L Ciupak, Elisa V Bandera, Lina Jandorf, Dana H Bovbjerg, Gary Zirpoli, Karen Pawlish, James Godbold, Helena Furberg, Anne Fatone,[...]. J Oncol 2009
91
14


Ten genes for inherited breast cancer.
Tom Walsh, Mary-Claire King. Cancer Cell 2007
311
14

Reduced mitochondrial DNA copy number is correlated with tumor progression and prognosis in Chinese breast cancer patients.
Man Yu, Yunli Zhou, Yurong Shi, Liansheng Ning, Yi Yang, Xiyin Wei, Ning Zhang, Xishan Hao, Ruifang Niu. IUBMB Life 2007
173
14


Y chromosome microdeletions in infertile men with varicocele.
E Moro, P Marin, A Rossi, A Garolla, A Ferlin. Mol Cell Endocrinol 2000
28
14


Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain.
R Del Bo, A Bordoni, M Sciacco, A Di Fonzo, S Galbiati, M Crimi, N Bresolin, G P Comi. Neurology 2003
51
14



Oxidative stress and sperm mitochondrial DNA mutation in idiopathic oligoasthenozoospermic men.
R Kumar, S Venkatesh, M Kumar, M Tanwar, M B Shasmsi, R Kumar, N P Gupta, R K Sharma, P Talwar, Rima Dada. Indian J Biochem Biophys 2009
56
14


The clinical significance of the POLG gene polymorphism in male infertility.
C Krausz, E Guarducci, L Becherini, S Degl'Innocenti, L Gerace, G Balercia, G Forti. J Clin Endocrinol Metab 2004
49
14

Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
Eleonora Lamantea, Valeria Tiranti, Andreina Bordoni, Antonio Toscano, Francesco Bono, Serena Servidei, Alex Papadimitriou, Hans Spelbrink, Laura Silvestri, Giorgio Casari,[...]. Ann Neurol 2002
200
14


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
14

Beneficial effect of microsurgical varicocelectomy on human sperm DNA integrity.
A Zini, A Blumenfeld, J Libman, J Willis. Hum Reprod 2005
109
14

A novel missense mutation C11994T in the mitochondrial ND4 gene as a cause of low sperm motility in the Indian subcontinent.
Deepa Selvi Rani, Ayyasamy Vanniarajan, Nalini J Gupta, Baidyanath Chakravarty, Lalji Singh, Kumarasamy Thangaraj. Fertil Steril 2006
48
14



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.