A citation-based method for searching scientific literature

Alessandra Maresca, Chiara la Morgia, Leonardo Caporali, Maria Lucia Valentino, Valerio Carelli. Mol Cell Neurosci 2013
Times Cited: 63







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



Times Cited
  Times     Co-cited
Similarity


Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.
Patrick Yu-Wai-Man, Philip G Griffiths, Patrick F Chinnery. Prog Retin Eye Res 2011
362
23

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy.
C Delettre, G Lenaers, J M Griffoin, N Gigarel, C Lorenzo, P Belenguer, L Pelloquin, J Grosgeorge, C Turc-Carel, E Perret,[...]. Nat Genet 2000
22

Multi-system neurological disease is common in patients with OPA1 mutations.
P Yu-Wai-Man, P G Griffiths, G S Gorman, C M Lourenco, A F Wright, M Auer-Grumbach, A Toscano, O Musumeci, M L Valentino, L Caporali,[...]. Brain 2010
275
22

Mitochondrial dysfunction as a cause of optic neuropathies.
Valerio Carelli, Fred N Ross-Cisneros, Alfredo A Sadun. Prog Retin Eye Res 2004
534
20

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
C Alexander, M Votruba, U E Pesch, D L Thiselton, S Mayer, A Moore, M Rodriguez, U Kellner, B Leo-Kottler, G Auburger,[...]. Nat Genet 2000
942
20

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
Valerio Carelli, Chiara La Morgia, Maria Lucia Valentino, Piero Barboni, Fred N Ross-Cisneros, Alfredo A Sadun. Biochim Biophys Acta 2009
149
19

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.
Patrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, Maria Esther Gallardo, Belén Bornstein, Anne Boissière, Yolanda Campos, Henry Rivera, Jesús González de la Aleja, Rosanna Carroccia,[...]. Brain 2008
360
17

Dominant optic atrophy.
Guy Lenaers, Christian Hamel, Cécile Delettre, Patrizia Amati-Bonneau, Vincent Procaccio, Dominique Bonneau, Pascal Reynier, Dan Milea. Orphanet J Rare Dis 2012
139
17

Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
C La Morgia, P Barboni, G Rizzo, M Carbonelli, G Savini, C Scaglione, S Capellari, S Bonazza, M P Giannoccaro, G Calandra-Buonaura,[...]. Eur J Neurol 2013
78
15

OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.
P Reynier, P Amati-Bonneau, C Verny, A Olichon, G Simard, A Guichet, C Bonnemains, F Malecaze, M C Malinge, J B Pelletier,[...]. J Med Genet 2004
109
15

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
14

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion.
Claudia Zanna, Anna Ghelli, Anna Maria Porcelli, Mariusz Karbowski, Richard J Youle, Simone Schimpf, Bernd Wissinger, Marcello Pinti, Andrea Cossarizza, Sara Vidoni,[...]. Brain 2008
238
14

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
Carla Giordano, Monica Montopoli, Elena Perli, Maurizia Orlandi, Marianna Fantin, Fred N Ross-Cisneros, Laura Caparrotta, Andrea Martinuzzi, Eugenio Ragazzi, Anna Ghelli,[...]. Brain 2011
153
12

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
132
12

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.
Gavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, Joanna D Stewart, Langping He, Andrew M Schaefer, Philip G Griffiths, Kati Ahlqvist, Anu Suomalainen, Pascal Reynier,[...]. Brain 2008
287
12

A neurodegenerative perspective on mitochondrial optic neuropathies.
Patrick Yu-Wai-Man, Marcela Votruba, Florence Burté, Chiara La Morgia, Piero Barboni, Valerio Carelli. Acta Neuropathol 2016
82
12

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
267
11

The retina in Parkinson's disease.
Neil K Archibald, Michael P Clarke, Urs P Mosimann, David J Burn. Brain 2009
221
11

Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy.
Metodi Dimitrov Metodiev, Sylvie Gerber, Laurence Hubert, Agnès Delahodde, Dominique Chretien, Xavier Gérard, Patrizia Amati-Bonneau, Marie-Christine Giacomotto, Nathalie Boddaert, Anna Kaminska,[...]. J Med Genet 2014
61
11

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
Gavin Hudson, Valerio Carelli, Liesbeth Spruijt, Mike Gerards, Catherine Mowbray, Alessandro Achilli, Angela Pyle, Joanna Elson, Neil Howell, Chiara La Morgia,[...]. Am J Hum Genet 2007
268
9

Mitochondria: the next (neurode)generation.
Eric A Schon, Serge Przedborski. Neuron 2011
395
9

Detection of retinal changes in Parkinson's disease with spectral-domain optical coherence tomography.
Grant D Aaker, Jane S Myung, Joshua R Ehrlich, Mujtaba Mohammed, Claire Henchcliffe, Szilárd Kiss. Clin Ophthalmol 2010
86
9

Ability and reproducibility of Fourier-domain optical coherence tomography to detect retinal nerve fiber layer atrophy in Parkinson's disease.
Elena Garcia-Martin, Maria Satue, Isabel Fuertes, Sofia Otin, Raquel Alarcia, Raquel Herrero, Maria P Bambo, Javier Fernandez, Luis E Pablo. Ophthalmology 2012
90
9

Correlation between retinal morphological and functional findings and clinical severity in Parkinson's disease.
Ozgül Altintaş, Pervin Işeri, Berna Ozkan, Yusuf Cağlar. Doc Ophthalmol 2008
154
9

Optical coherence tomography in parkinsonian syndromes.
Philipp Albrecht, Ann-Kristin Müller, Martin Südmeyer, Stefano Ferrea, Marius Ringelstein, Eva Cohn, Orhan Aktas, Thomas Dietlein, Alexandra Lappas, Andreas Foerster,[...]. PLoS One 2012
116
9

The neuro-ophthalmology of mitochondrial disease.
J Alexander Fraser, Valérie Biousse, Nancy J Newman. Surv Ophthalmol 2010
153
9

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.
Valerio Carelli, Alessandro Achilli, Maria Lucia Valentino, Chiara Rengo, Ornella Semino, Maria Pala, Anna Olivieri, Marina Mattiazzi, Francesco Pallotti, Franco Carrara,[...]. Am J Hum Genet 2006
144
9

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy.
Stephan Klebe, Christel Depienne, Sylvie Gerber, Georges Challe, Mathieu Anheim, Perrine Charles, Estelle Fedirko, Elodie Lejeune, Julien Cottineau, Alfredo Brusco,[...]. Brain 2012
111
9

Retinal nerve fiber layer thinning in Parkinson disease.
Rivka Inzelberg, Jose Antonio Ramirez, Puiu Nisipeanu, Avinoam Ophir. Vision Res 2004
224
9

The prevalence and natural history of dominant optic atrophy due to OPA1 mutations.
Patrick Yu-Wai-Man, Philip G Griffiths, Ailbhe Burke, Peter W Sellar, Michael P Clarke, Lawrence Gnanaraj, Desiree Ah-Kine, Gavin Hudson, Birgit Czermin, Robert W Taylor,[...]. Ophthalmology 2010
112
9

Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies.
Patrick Yu-Wai-Man, Suma P Shankar, Valérie Biousse, Neil R Miller, Lora J H Bean, Bradford Coffee, Madhuri Hegde, Nancy J Newman. Ophthalmology 2011
35
17

Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data.
Marc Ferré, Angélique Caignard, Dan Milea, Stéphanie Leruez, Julien Cassereau, Arnaud Chevrollier, Patrizia Amati-Bonneau, Christophe Verny, Dominique Bonneau, Vincent Procaccio,[...]. Hum Mutat 2015
35
17

Effect of EPI-743 on the clinical course of the mitochondrial disease Leber hereditary optic neuropathy.
Alfredo A Sadun, Carlos Filipe Chicani, Fred N Ross-Cisneros, Piero Barboni, Martin Thoolen, William D Shrader, Kenneth Kubis, Valerio Carelli, Guy Miller. Arch Neurol 2012
110
7

Treatment of hereditary optic neuropathies.
Nancy J Newman. Nat Rev Neurol 2012
40
12

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner, Irina V Mersiyanova, Maria Muglia, Nisrine Bissar-Tadmouri, Julie Rochelle, Elena L Dadali, Mario Zappia, Eva Nelis, Alessandra Patitucci, Jan Senderek,[...]. Nat Genet 2004
7

OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution.
Ghizlane Elachouri, Sara Vidoni, Claudia Zanna, Alexandre Pattyn, Hassan Boukhaddaoui, Karen Gaget, Patrick Yu-Wai-Man, Giuseppe Gasparre, Emmanuelle Sarzi, Cécile Delettre,[...]. Genome Res 2011
151
7

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype.
Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, Arnaud Chevrollier, Annie Verschueren, Nathalie Bonello-Palot, Konstantina Fragaki, Aline Cano, Jean Pouget, Jean-François Pellissier,[...]. Brain 2012
156
7


A lethal defect of mitochondrial and peroxisomal fission.
Hans R Waterham, Janet Koster, Carlo W T van Roermund, Petra A W Mooyer, Ronald J A Wanders, James V Leonard. N Engl J Med 2007
528
7

Inner retinal layer thinning in Parkinson disease.
Mohammedyusuf E Hajee, Wayne F March, Douglas R Lazzaro, Arthur H Wolintz, Eric M Shrier, Sofya Glazman, Ivan G Bodis-Wollner. Arch Ophthalmol 2009
180
7


TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophy.
Sylvain Hanein, Isabelle Perrault, Olivier Roche, Sylvie Gerber, Noman Khadom, Marlene Rio, Nathalie Boddaert, Marc Jean-Pierre, Nora Brahimi, Valérie Serre,[...]. Am J Hum Genet 2009
64
7

eOPA1: an online database for OPA1 mutations.
Marc Ferré, Patrizia Amati-Bonneau, Yves Tourmen, Yves Malthièry, Pascal Reynier. Hum Mutat 2005
102
7

Visual symptoms in Parkinson's disease and Parkinson's disease dementia.
Neil K Archibald, Mike P Clarke, Urs P Mosimann, David J Burn. Mov Disord 2011
119
7

OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria.
Marjan Huizing, Heidi Dorward, Lien Ly, Enriko Klootwijk, Robert Kleta, Flemming Skovby, Wuhong Pei, Benjamin Feldman, William A Gahl, Yair Anikster. Mol Genet Metab 2010
22
22

OPA1 mutations associated with dominant optic atrophy influence optic nerve head size.
Piero Barboni, Michele Carbonelli, Giacomo Savini, Beatrice Foscarini, Vincenzo Parisi, Maria L Valentino, Arturo Carta, Annamaria De Negri, Federico Sadun, Massimo Zeviani,[...]. Ophthalmology 2010
42
11

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
168
7

Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation.
Piero Barboni, Giacomo Savini, Maria Lucia Cascavilla, Leonardo Caporali, Jacopo Milesi, Enrico Borrelli, Chiara La Morgia, Maria Lucia Valentino, Giacinto Triolo, Andrea Lembo,[...]. Am J Ophthalmol 2014
37
13

The human dynamin-related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter-membrane space.
Aurélien Olichon, Laurent J Emorine, Eric Descoins, Laetitia Pelloquin, Laetitia Brichese, Nicole Gas, Emmanuelle Guillou, Cécile Delettre, Annie Valette, Christian P Hamel,[...]. FEBS Lett 2002
303
7

The retina as an early biomarker of neurodegeneration in a rotenone-induced model of Parkinson's disease: evidence for a neuroprotective effect of rosiglitazone in the eye and brain.
Eduardo Maria Normando, Benjamin Michael Davis, Lies De Groef, Shereen Nizari, Lisa A Turner, Nivedita Ravindran, Milena Pahlitzsch, Jonathan Brenton, Giulia Malaguarnera, Li Guo,[...]. Acta Neuropathol Commun 2016
59
8


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.