A citation-based method for searching scientific literature

Oliver Stehling, Hans-Peter Elsässer, Bernd Brückel, Ulrich Mühlenhoff, Roland Lill. Hum Mol Genet 2004
Times Cited: 146







List of co-cited articles
1159 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
55

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
46

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
45


The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins.
Ulrich Mühlenhoff, Nadine Richhardt, Michael Ristow, Gyula Kispal, Roland Lill. Hum Mol Genet 2002
265
30

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
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
28

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
27

Bacterial frataxin CyaY is the gatekeeper of iron-sulfur cluster formation catalyzed by IscS.
Salvatore Adinolfi, Clara Iannuzzi, Filippo Prischi, Chiara Pastore, Stefania Iametti, Stephen R Martin, Franco Bonomi, Annalisa Pastore. Nat Struct Mol Biol 2009
189
27

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
26



The Nfs1 interacting protein Isd11 has an essential role in Fe/S cluster biogenesis in mitochondria.
Alexander C Adam, Carsten Bornhövd, Holger Prokisch, Walter Neupert, Kai Hell. EMBO J 2006
168
24

Structure, function, and formation of biological iron-sulfur clusters.
Deborah C Johnson, Dennis R Dean, Archer D Smith, Michael K Johnson. Annu Rev Biochem 2005
911
24


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
24

Role of human mitochondrial Nfs1 in cytosolic iron-sulfur protein biogenesis and iron regulation.
Annette Biederbick, Oliver Stehling, Ralf Rösser, Brigitte Niggemeyer, Yumi Nakai, Hans-Peter Elsässer, Roland Lill. Mol Cell Biol 2006
130
23


Frataxin is essential for extramitochondrial Fe-S cluster proteins in mammalian tissues.
Alain Martelli, Marie Wattenhofer-Donzé, Stéphane Schmucker, Samuel Bouvet, Laurence Reutenauer, Hélène Puccio. Hum Mol Genet 2007
98
22


Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation.
M Cossée, H Puccio, A Gansmuller, H Koutnikova, A Dierich, M LeMeur, K Fischbeck, P Dollé, M Koenig. Hum Mol Genet 2000
265
21

Essential role of Isd11 in mitochondrial iron-sulfur cluster synthesis on Isu scaffold proteins.
Nils Wiedemann, Eugen Urzica, Bernard Guiard, Hanne Müller, Christiane Lohaus, Helmut E Meyer, Michael T Ryan, Chris Meisinger, Ulrich Mühlenhoff, Roland Lill,[...]. EMBO J 2006
171
21


RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload.
Patrizia Cavadini, Giorgio Biasiotto, Maura Poli, Sonia Levi, Rosanna Verardi, Isabella Zanella, Manuela Derosas, Rosaria Ingrassia, Marcella Corrado, Paolo Arosio. Blood 2007
129
19


The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron-sulfur cluster biogenesis.
Corinne Pondarré, Brendan B Antiochos, Dean R Campagna, Stephen L Clarke, Eric L Greer, Kathryn M Deck, Alice McDonald, An-Ping Han, Amy Medlock, Jeffery L Kutok,[...]. Hum Mol Genet 2006
152
19


Components involved in assembly and dislocation of iron-sulfur clusters on the scaffold protein Isu1p.
Ulrich Mühlenhoff, Jana Gerber, Nadine Richhardt, Roland Lill. EMBO J 2003
305
19

Iron-sulfur cluster biogenesis and human disease.
Tracey A Rouault, Wing Hang Tong. Trends Genet 2008
261
19

Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cells.
Robert A Schoenfeld, Eleonora Napoli, Alice Wong, Shan Zhan, Laurence Reutenauer, Dexter Morin, Alan R Buckpitt, Franco Taroni, Bo Lonnerdal, Michael Ristow,[...]. Hum Mol Genet 2005
90
20



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
17

The structure and function of frataxin.
Krisztina Z Bencze, Kalyan C Kondapalli, Jeremy D Cook, Stephen McMahon, César Millán-Pacheco, Nina Pastor, Timothy L Stemmler. Crit Rev Biochem Mol Biol 2006
107
17

Human ISD11 is essential for both iron-sulfur cluster assembly and maintenance of normal cellular iron homeostasis.
Yanbo Shi, Manik C Ghosh, Wing-Hang Tong, Tracey A Rouault. Hum Mol Genet 2009
113
17

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
M Cossée, A Dürr, M Schmitt, N Dahl, P Trouillas, P Allinson, M Kostrzewa, A Nivelon-Chevallier, K H Gustavson, A Kohlschütter,[...]. Ann Neurol 1999
262
16

Assembly and iron-binding properties of human frataxin, the protein deficient in Friedreich ataxia.
Patrizia Cavadini, Heather A O'Neill, Oldrich Benada, Grazia Isaya. Hum Mol Genet 2002
163
16

Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia.
R Lodi, J M Cooper, J L Bradley, D Manners, P Styles, D J Taylor, A H Schapira. Proc Natl Acad Sci U S A 1999
265
16

Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in mice.
René Thierbach, Tim J Schulz, Frank Isken, Anja Voigt, Brun Mietzner, Gunnar Drewes, Jürgen-Christoph von Kleist-Retzow, Rudolf J Wiesner, Mark A Magnuson, Hélène Puccio,[...]. Hum Mol Genet 2005
98
16

Iron-dependent self-assembly of recombinant yeast frataxin: implications for Friedreich ataxia.
J Adamec, F Rusnak, W G Owen, S Naylor, L M Benson, A M Gacy, G Isaya. Am J Hum Genet 2000
211
16


Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis.
Rebecca A Wingert, Jenna L Galloway, Bruce Barut, Helen Foott, Paula Fraenkel, Jennifer L Axe, Gerhard J Weber, Kimberly Dooley, Alan J Davidson, Bettina Schmid,[...]. Nature 2005
284
16



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
16

Mitochondrial iron detoxification is a primary function of frataxin that limits oxidative damage and preserves cell longevity.
Oleksandr Gakh, Sungjo Park, Gang Liu, Lee Macomber, James A Imlay, Gloria C Ferreira, Grazia Isaya. Hum Mol Genet 2006
161
15

Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin.
H Koutnikova, V Campuzano, F Foury, P Dollé, O Cazzalini, M Koenig. Nat Genet 1997
378
15

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
15



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.