A citation-based method for searching scientific literature

Hervé Tricoire, Amandine Palandri, Arthur Bourdais, Jean-Michel Camadro, Véronique Monnier. Hum Mol Genet 2014
Times Cited: 28







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



Times Cited
  Times     Co-cited
Similarity


Altered lipid metabolism in a Drosophila model of Friedreich's ataxia.
Juan A Navarro, Elisabeth Ohmann, Diego Sanchez, José A Botella, Gerhard Liebisch, María D Moltó, María D Ganfornina, Gerd Schmitz, Stephan Schneuwly. Hum Mol Genet 2010
71
46

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
46

Causative role of oxidative stress in a Drosophila model of Friedreich ataxia.
José V Llorens, Juan A Navarro, Maria J Martínez-Sebastián, Mary K Baylies, S Schneuwly, José A Botella, Maria D Moltó. FASEB J 2007
93
42

RNAi-mediated suppression of the mitochondrial iron chaperone, frataxin, in Drosophila.
Peter R Anderson, Kim Kirby, Arthur J Hilliker, John P Phillips. Hum Mol Genet 2005
107
42

Hydrogen peroxide scavenging rescues frataxin deficiency in a Drosophila model of Friedreich's ataxia.
Peter R Anderson, Kim Kirby, William C Orr, Arthur J Hilliker, John P Phillips. Proc Natl Acad Sci U S A 2008
84
42


Loss of Frataxin induces iron toxicity, sphingolipid synthesis, and Pdk1/Mef2 activation, leading to neurodegeneration.
Kuchuan Chen, Guang Lin, Nele A Haelterman, Tammy Szu-Yu Ho, Tongchao Li, Zhihong Li, Lita Duraine, Brett H Graham, Manish Jaiswal, Shinya Yamamoto,[...]. Elife 2016
45
32


Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin.
M Babcock, D de Silva, R Oaks, S Davis-Kaplan, S Jiralerspong, L Montermini, M Pandolfo, J Kaplan. Science 1997
726
28

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.
H Puccio, D Simon, M Cossée, P Criqui-Filipe, F Tiziano, J Melki, C Hindelang, R Matyas, P Rustin, M Koenig. Nat Genet 2001
536
28

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.
A Rötig, P de Lonlay, D Chretien, F Foury, M Koenig, D Sidi, A Munnich, P Rustin. Nat Genet 1997
774
28

Impaired nuclear Nrf2 translocation undermines the oxidative stress response in Friedreich ataxia.
Vincent Paupe, Emmanuel P Dassa, Sergio Goncalves, Françoise Auchère, Maria Lönn, Arne Holmgren, Pierre Rustin. PLoS One 2009
147
28

Deferiprone and idebenone rescue frataxin depletion phenotypes in a Drosophila model of Friedreich's ataxia.
Sirena Soriano, José V Llorens, Laura Blanco-Sobero, Lucía Gutiérrez, Pablo Calap-Quintana, M Puerto Morales, M Dolores Moltó, M José Martínez-Sebastián. Gene 2013
32
25

Mitoferrin modulates iron toxicity in a Drosophila model of Friedreich's ataxia.
Juan A Navarro, Jose A Botella, Christoph Metzendorf, Maria I Lind, Stephan Schneuwly. Free Radic Biol Med 2015
39
25

Loss of Frataxin activates the iron/sphingolipid/PDK1/Mef2 pathway in mammals.
Kuchuan Chen, Tammy Szu-Yu Ho, Guang Lin, Kai Li Tan, Matthew N Rasband, Hugo J Bellen. Elife 2016
39
25

Human frataxin activates Fe-S cluster biosynthesis by facilitating sulfur transfer chemistry.
Jennifer Bridwell-Rabb, Nicholas G Fox, Chi-Lin Tsai, Andrew M Winn, David P Barondeau. Biochemistry 2014
107
21


dfh is a Drosophila homolog of the Friedreich's ataxia disease gene.
J Cañizares, J M Blanca, J A Navarro, E Monrós, F Palau, M D Moltó. Gene 2000
31
21


GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology.
Sahar Al-Mahdawi, Ricardo Mouro Pinto, Dhaval Varshney, Lorraine Lawrence, Margaret B Lowrie, Sian Hughes, Zoe Webster, Julian Blake, J Mark Cooper, Rosalind King,[...]. Genomics 2006
163
21

Overexpression of human and fly frataxins in Drosophila provokes deleterious effects at biochemical, physiological and developmental levels.
Juan A Navarro, José V Llorens, Sirena Soriano, José A Botella, Stephan Schneuwly, María J Martínez-Sebastián, María D Moltó. PLoS One 2011
28
21

Alternative mitochondrial electron transfer as a novel strategy for neuroprotection.
Yi Wen, Wenjun Li, Ethan C Poteet, Luokun Xie, Cong Tan, Liang-Jun Yan, Xiaohua Ju, Ran Liu, Hai Qian, Marian A Marvin,[...]. J Biol Chem 2011
187
21

Metal Homeostasis Regulators Suppress FRDA Phenotypes in a Drosophila Model of the Disease.
Sirena Soriano, Pablo Calap-Quintana, José Vicente Llorens, Ismael Al-Ramahi, Lucía Gutiérrez, María José Martínez-Sebastián, Juan Botas, María Dolores Moltó. PLoS One 2016
20
30

Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.
V Campuzano, L Montermini, Y Lutz, L Cova, C Hindelang, S Jiralerspong, Y Trottier, S J Kish, B Faucheux, P Trouillas,[...]. Hum Mol Genet 1997
559
21

In vivo maturation of human frataxin.
Ivano Condò, Natascia Ventura, Florence Malisan, Alessandra Rufini, Barbara Tomassini, Roberto Testi. Hum Mol Genet 2007
90
21

Elucidation of the mechanism of mitochondrial iron loading in Friedreich's ataxia by analysis of a mouse mutant.
Michael Li-Hsuan Huang, Erika M Becker, Megan Whitnall, Yohan Suryo Rahmanto, Prem Ponka, Des R Richardson. Proc Natl Acad Sci U S A 2009
161
17

Mammalian frataxin: an essential function for cellular viability through an interaction with a preformed ISCU/NFS1/ISD11 iron-sulfur assembly complex.
Stéphane Schmucker, Alain Martelli, Florent Colin, Adeline Page, Marie Wattenhofer-Donzé, Laurence Reutenauer, Hélène Puccio. PLoS One 2011
176
17

Friedreich ataxia: the clinical picture.
Massimo Pandolfo. J Neurol 2009
262
17

Frataxin deficiency leads to defects in expression of antioxidants and Nrf2 expression in dorsal root ganglia of the Friedreich's ataxia YG8R mouse model.
Yuxi Shan, Robert A Schoenfeld, Genki Hayashi, Eleonora Napoli, Tasuku Akiyama, Mirela Iodi Carstens, Earl E Carstens, Mark A Pook, Gino A Cortopassi. Antioxid Redox Signal 2013
107
17

Drosophila frataxin: an iron chaperone during cellular Fe-S cluster bioassembly.
Kalyan C Kondapalli, Nicole M Kok, Andrew Dancis, Timothy L Stemmler. Biochemistry 2008
51
17

Prevention and reversal of severe mitochondrial cardiomyopathy by gene therapy in a mouse model of Friedreich's ataxia.
Morgane Perdomini, Brahim Belbellaa, Laurent Monassier, Laurence Reutenauer, Nadia Messaddeq, Nathalie Cartier, Ronald G Crystal, Patrick Aubourg, Hélène Puccio. Nat Med 2014
136
17


A new method for detection and quantification of heartbeat parameters in Drosophila, zebrafish, and embryonic mouse hearts.
Martin Fink, Carles Callol-Massot, Angela Chu, Pilar Ruiz-Lozano, Juan Carlos Izpisua Belmonte, Wayne Giles, Rolf Bodmer, Karen Ocorr. Biotechniques 2009
179
17

Frataxin acts as an iron chaperone protein to modulate mitochondrial aconitase activity.
Anne-Laure Bulteau, Heather A O'Neill, Mary Claire Kennedy, Masao Ikeda-Saito, Grazia Isaya, Luke I Szweda. Science 2004
292
17

Neuroprotective actions of methylene blue and its derivatives.
Ethan Poteet, Ali Winters, Liang-Jun Yan, Kyle Shufelt, Kayla N Green, James W Simpkins, Yi Wen, Shao-Hua Yang. PLoS One 2012
108
17

Friedreich ataxia mouse models with progressive cerebellar and sensory ataxia reveal autophagic neurodegeneration in dorsal root ganglia.
Delphine Simon, Hervé Seznec, Anne Gansmuller, Nadège Carelle, Philipp Weber, Daniel Metzger, Pierre Rustin, Michel Koenig, Hélène Puccio. J Neurosci 2004
136
17


The dorsal root ganglion in Friedreich's ataxia.
Arnulf H Koeppen, Jennifer A Morral, Ashley N Davis, Jiang Qian, Simone V Petrocine, Mitchell D Knutson, Walter M Gibson, Matthew J Cusack, Danhong Li. Acta Neuropathol 2009
87
17

Friedreich ataxia: the oxidative stress paradox.
Hervé Seznec, Delphine Simon, Cécile Bouton, Laurence Reutenauer, Ariane Hertzog, Pawel Golik, Vincent Procaccio, Manisha Patel, Jean-Claude Drapier, Michel Koenig,[...]. Hum Mol Genet 2005
169
17

Frataxin inactivation leads to steroid deficiency in flies and human ovarian cells.
Amandine Palandri, David L'hôte, Joëlle Cohen-Tannoudji, Hervé Tricoire, Véronique Monnier. Hum Mol Genet 2015
22
22

Does oxidative stress contribute to the pathology of Friedreich's ataxia? A radical question.
Jeffrey S Armstrong, Omar Khdour, Sidney M Hecht. FASEB J 2010
82
17

Idebenone delays the onset of cardiac functional alteration without correction of Fe-S enzymes deficit in a mouse model for Friedreich ataxia.
Hervé Seznec, Delphine Simon, Laurent Monassier, Paola Criqui-Filipe, Anne Gansmuller, Pierre Rustin, Michel Koenig, Hélène Puccio. Hum Mol Genet 2004
92
14

Clinical and genetic abnormalities in patients with Friedreich's ataxia.
A Dürr, M Cossee, Y Agid, V Campuzano, C Mignard, C Penet, J L Mandel, A Brice, M Koenig. N Engl J Med 1996
739
14

The heart in Friedreich ataxia: definition of cardiomyopathy, disease severity, and correlation with neurological symptoms.
Frank Weidemann, Christian Rummey, Bart Bijnens, Stefan Störk, Ruta Jasaityte, Jan Dhooge, Aigul Baltabaeva, George Sutherland, Jörg B Schulz, Thomas Meier. Circulation 2012
80
14

Mortality in Friedreich ataxia.
Amy Y Tsou, Erin K Paulsen, Sarah J Lagedrost, Susan L Perlman, Katherine D Mathews, George R Wilmot, Bernard Ravina, Arnulf H Koeppen, David R Lynch. J Neurol Sci 2011
165
14

A systematic analysis of human disease-associated gene sequences in Drosophila melanogaster.
L T Reiter, L Potocki, S Chien, M Gribskov, E Bier. Genome Res 2001
531
14

A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila.
Georg Dietzl, Doris Chen, Frank Schnorrer, Kuan-Chung Su, Yulia Barinova, Michaela Fellner, Beate Gasser, Kaolin Kinsey, Silvia Oppel, Susanne Scheiblauer,[...]. Nature 2007
14

Near infrared muscle spectroscopy in patients with Friedreich's ataxia.
David R Lynch, Gwen Lech, Jennifer M Farmer, Laura J Balcer, William Bank, Britton Chance, Robert B Wilson. Muscle Nerve 2002
34
14

Glutathione-dependent redox status of frataxin-deficient cells in a yeast model of Friedreich's ataxia.
Françoise Auchère, Renata Santos, Sara Planamente, Emmanuel Lesuisse, Jean-Michel Camadro. Hum Mol Genet 2008
66
14

A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases.
Shinya Yamamoto, Manish Jaiswal, Wu-Lin Charng, Tomasz Gambin, Ender Karaca, Ghayda Mirzaa, Wojciech Wiszniewski, Hector Sandoval, Nele A Haelterman, Bo Xiong,[...]. Cell 2014
230
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.