A citation-based method for searching scientific literature

Salvatore DiMauro, Eric A Schon, Valerio Carelli, Michio Hirano. Nat Rev Neurol 2013
Times Cited: 199







List of co-cited articles
1242 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mitochondrial diseases.
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, Michio Hirano, Yasutoshi Koga, Robert McFarland, Anu Suomalainen, David R Thorburn, Massimo Zeviani, Douglass M Turnbull. Nat Rev Dis Primers 2016
431
19

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
15

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery,[...]. Ann Neurol 2015
389
14

A mitochondrial protein compendium elucidates complex I disease biology.
David J Pagliarini, Sarah E Calvo, Betty Chang, Sunil A Sheth, Scott B Vafai, Shao-En Ong, Geoffrey A Walford, Canny Sugiana, Avihu Boneh, William K Chen,[...]. Cell 2008
12

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
160
11

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins.
Sarah E Calvo, Karl R Clauser, Vamsi K Mootha. Nucleic Acids Res 2016
734
11

Mitochondria: in sickness and in health.
Jodi Nunnari, Anu Suomalainen. Cell 2012
10

Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation.
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Valerio Carelli, Giacomo Pietro Comi, Carlo Minetti, Maurizio Moggio, Tiziana Mongini, Serenella Servidei,[...]. Neurology 2013
110
10


MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
Ayman W El-Hattab, Adekunle M Adesina, Jeremy Jones, Fernando Scaglia. Mol Genet Metab 2015
216
10

Sequence and organization of the human mitochondrial genome.
S Anderson, A T Bankier, B G Barrell, M H de Bruijn, A R Coulson, J Drouin, I C Eperon, D P Nierlich, B A Roe, F Sanger,[...]. Nature 1981
10

Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, Fernando Scaglia, Gregory M Enns, Russell Saneto, Irina Anselm, Bruce H Cohen, Marni J Falk, Carol Greene,[...]. Genet Med 2015
193
8

Human mitochondrial DNA: roles of inherited and somatic mutations.
Eric A Schon, Salvatore DiMauro, Michio Hirano. Nat Rev Genet 2012
409
8

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy.
Thomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, Jacinthe Rouleau, Suzette Heck, Maura Bailie, Alaa Atawan, Sandip Chattopadhyay, Marion Schubert, Aylin Garip,[...]. Brain 2011
253
8

Mitochondrial disorders as windows into an ancient organelle.
Scott B Vafai, Vamsi K Mootha. Nature 2012
395
8

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
I J Holt, A E Harding, R K Petty, J A Morgan-Hughes. Am J Hum Genet 1990
793
8

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.
Sarah E Calvo, Alison G Compton, Steven G Hershman, Sze Chern Lim, Daniel S Lieber, Elena J Tucker, Adrienne Laskowski, Caterina Garone, Shangtao Liu, David B Jaffe,[...]. Sci Transl Med 2012
301
7

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Valerio Carelli, Giacomo Pietro Comi, Alice Donati, Carlo Minetti, Maurizio Moggio, Tiziana Mongini,[...]. J Neurol 2014
68
10

Diagnostic criteria for respiratory chain disorders in adults and children.
F P Bernier, A Boneh, X Dennett, C W Chow, M A Cleary, D R Thorburn. Neurology 2002
408
7

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
J M Shoffner, M T Lott, A M Lezza, P Seibel, S W Ballinger, D C Wallace. Cell 1990
7

Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3.
Nahid A Khan, Mari Auranen, Ilse Paetau, Eija Pirinen, Liliya Euro, Saara Forsström, Lotta Pasila, Vidya Velagapudi, Christopher J Carroll, Johan Auwerx,[...]. EMBO Mol Med 2014
225
7

The in-depth evaluation of suspected mitochondrial disease.
Richard H Haas, Sumit Parikh, Marni J Falk, Russell P Saneto, Nicole I Wolf, Niklas Darin, Lee-Jun Wong, Bruce H Cohen, Robert K Naviaux. Mol Genet Metab 2008
227
7

The genetics and pathology of mitochondrial disease.
Charlotte L Alston, Mariana C Rocha, Nichola Z Lax, Doug M Turnbull, Robert W Taylor. J Pathol 2017
169
7

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
201
7

Leigh syndrome: One disorder, more than 75 monogenic causes.
Nicole J Lake, Alison G Compton, Shamima Rahman, David R Thorburn. Ann Neurol 2016
192
7


Mitochondrial ATP synthase: architecture, function and pathology.
An I Jonckheere, Jan A M Smeitink, Richard J T Rodenburg. J Inherit Metab Dis 2012
251
7

Mitochondrial respiratory-chain diseases.
Salvatore DiMauro, Eric A Schon. N Engl J Med 2003
7

Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.
A L Andreu, M G Hanna, H Reichmann, C Bruno, A S Penn, K Tanji, F Pallotti, S Iwata, E Bonilla, B Lach,[...]. N Engl J Med 1999
300
7

Pathogenic mitochondrial DNA mutations are common in the general population.
Hannah R Elliott, David C Samuels, James A Eden, Caroline L Relton, Patrick F Chinnery. Am J Hum Genet 2008
352
6

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
6

Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.
Judith Altmann, Boriana Büchner, Aleksandra Nadaj-Pakleza, Jochen Schäfer, Sandra Jackson, Diana Lehmann, Marcus Deschauer, Robert Kopajtich, Ronald Lautenschläger, Klaus A Kuhn,[...]. J Neurol 2016
48
12

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.
Matthew G D Bates, John P Bourke, Carla Giordano, Giulia d'Amati, Douglass M Turnbull, Robert W Taylor. Eur Heart J 2012
115
6

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.
Robert W Taylor, Angela Pyle, Helen Griffin, Emma L Blakely, Jennifer Duff, Langping He, Tania Smertenko, Charlotte L Alston, Vivienne C Neeve, Andrew Best,[...]. JAMA 2014
207
6

Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways.
L Giordano, S Deceglie, P d'Adamo, M L Valentino, C La Morgia, F Fracasso, M Roberti, M Cappellari, G Petrosillo, S Ciaravolo,[...]. Cell Death Dis 2015
63
9



Mitochondrial dysfunction as a cause of optic neuropathies.
Valerio Carelli, Fred N Ross-Cisneros, Alfredo A Sadun. Prog Retin Eye Res 2004
516
6

Mitochondrial complex I-linked disease.
Richard J Rodenburg. Biochim Biophys Acta 2016
82
7

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.
Patrick Yu-Wai-Man, Philip G Griffiths, Patrick F Chinnery. Prog Retin Eye Res 2011
342
6

mTOR inhibition alleviates mitochondrial disease in a mouse model of Leigh syndrome.
Simon C Johnson, Melana E Yanos, Ernst-Bernhard Kayser, Albert Quintana, Maya Sangesland, Anthony Castanza, Lauren Uhde, Jessica Hui, Valerie Z Wall, Arni Gagnidze,[...]. Science 2013
291
6


Respiratory active mitochondrial supercomplexes.
Rebeca Acín-Pérez, Patricio Fernández-Silva, Maria Luisa Peleato, Acisclo Pérez-Martos, Jose Antonio Enriquez. Mol Cell 2008
505
6

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Alexander J Abrams, Robert B Hufnagel, Adriana Rebelo, Claudia Zanna, Neville Patel, Michael A Gonzalez, Ion J Campeanu, Laurie B Griffin, Saskia Groenewald, Alleene V Strickland,[...]. Nat Genet 2015
105
6

Recent advances in understanding the molecular genetic basis of mitochondrial disease.
Kyle Thompson, Jack J Collier, Ruth I C Glasgow, Fiona M Robertson, Angela Pyle, Emma L Blakely, Charlotte L Alston, Monika Oláhová, Robert McFarland, Robert W Taylor. J Inherit Metab Dis 2020
51
11

Emerging concepts in the therapy of mitochondrial disease.
Carlo Viscomi, Emanuela Bottani, Massimo Zeviani. Biochim Biophys Acta 2015
65
7


Mutations causing mitochondrial disease: What is new and what challenges remain?
Robert N Lightowlers, Robert W Taylor, Doug M Turnbull. Science 2015
171
5

Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.
Maria Pia Giannoccaro, Chiara La Morgia, Giovanni Rizzo, Valerio Carelli. Mov Disord 2017
78
6

Idebenone treatment in Leber's hereditary optic neuropathy.
Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Giovanni Rizzo, Michele Carbonelli, Anna Maria De Negri, Federico Sadun, Arturo Carta, Silvana Guerriero, Francesca Simonelli,[...]. Brain 2011
128
5


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.