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Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene.
Patrizia Formichi, Elena Radi, Eleonora Giorgi, Gian Nicola Gallus, Jlenia Brunetti, Carla Battisti, Alessandra Rufa, Maria Teresa Dotti, Rossella Franceschini, Luisa Bracci, Antonio Federico. J Neurol Sci 2015
Times Cited: 8






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



Times Cited
  Times     Co-cited
Similarity


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
4
50

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
4
50

Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis.
Aurélien Olichon, Laurent Baricault, Nicole Gas, Emmanuelle Guillou, Annie Valette, Pascale Belenguer, Guy Lenaers. J Biol Chem 2003
812
4
50

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
3
37

Treatment strategies for inherited optic neuropathies: past, present and future.
P Yu-Wai-Man, M Votruba, A T Moore, P F Chinnery. Eye (Lond) 2014
86
3
37

Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations.
Virginie Agier, Patricia Oliviero, Jeanne Lainé, Caroline L'Hermitte-Stead, Samantha Girard, Sandrine Fillaut, Claude Jardel, Frédéric Bouillaud, Anne Laure Bulteau, Anne Lombès. Biochim Biophys Acta 2012
40
3
37

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
3
37

Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics.
Marcel V Alavi, Nico Fuhrmann. Mol Neurodegener 2013
76
3
37

Changes in Mitochondrial Morphology and Bioenergetics in Human Lymphoblastoid Cells With Four Novel OPA1 Mutations.
Shu-Huei Kao, May-Yung Yen, An-Guor Wang, Yi-Ling Yeh, An-Lo Lin. Invest Ophthalmol Vis Sci 2015
19
3
37

Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates.
Patrick Yu-Wai-Man, Patrick F Chinnery. Ophthalmology 2013
40
3
37

Dominant optic atrophy: correlation between clinical and molecular genetic studies.
Anu Puomila, Kirsi Huoponen, Maija Mäntyjärvi, Petra Hämäläinen, Reetta Paananen, Eeva-Marja Sankila, Marja-Liisa Savontaus, Mirja Somer, Eeva Nikoskelainen. Acta Ophthalmol Scand 2005
48
3
37

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
3
37

Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families.
P KJER. Acta Ophthalmol Suppl 1959
121
3
37

OPA1-associated disorders: phenotypes and pathophysiology.
Patrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, Arnaud Chevrollier, Marc Ferré, Virginie Guillet, Naïg Gueguen, Dominique Loiseau, Marie-Anne Pou de Crescenzo, Christophe Verny,[...]. Int J Biochem Cell Biol 2009
101
3
37

Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations.
Amy C Cohn, Carmel Toomes, Catherine Potter, Katherine V Towns, Alex W Hewitt, Chris F Inglehearn, Jamie E Craig, David A Mackey. Am J Ophthalmol 2007
84
3
37

Inherited mitochondrial optic neuropathies.
P Yu-Wai-Man, P G Griffiths, G Hudson, P F Chinnery. J Med Genet 2009
250
3
37

Dominant optic atrophy: updates on the pathophysiology and clinical manifestations of the optic atrophy 1 mutation.
Bo Y Chun, Joseph F Rizzo. Curr Opin Ophthalmol 2016
28
3
37

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
2
25

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
1043
2
25

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
2
25

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
2
25

Idebenone protects against retinal damage and loss of vision in a mouse model of Leber's hereditary optic neuropathy.
Fabrice D Heitz, Michael Erb, Corinne Anklin, Dimitri Robay, Vincent Pernet, Nuri Gueven. PLoS One 2012
70
2
25

Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesis.
Aurélien Olichon, Thomas Landes, Laetitia Arnauné-Pelloquin, Laurent J Emorine, Valérie Mils, Agnès Guichet, Cécile Delettre, Christian Hamel, Patrizia Amati-Bonneau, Dominique Bonneau,[...]. J Cell Physiol 2007
103
2
25

Opa1 deficiency in a mouse model of dominant optic atrophy leads to retinal ganglion cell dendropathy.
Pete A Williams, James E Morgan, Marcela Votruba. Brain 2010
71
2
25

OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability.
Le Chen, Tingting Liu, Alice Tran, Xiyuan Lu, Alexey A Tomilov, Vanessa Davies, Gino Cortopassi, Nipavan Chiamvimonvat, Donald M Bers, Marcela Votruba,[...]. J Am Heart Assoc 2012
120
2
25

Down-regulation of OPA1 alters mouse mitochondrial morphology, PTP function, and cardiac adaptation to pressure overload.
Jerome Piquereau, Fanny Caffin, Marta Novotova, Alexandre Prola, Anne Garnier, Philippe Mateo, Dominique Fortin, Le Ha Huynh, Valérie Nicolas, Marcel V Alavi,[...]. Cardiovasc Res 2012
122
2
25

NQO1-dependent redox cycling of idebenone: effects on cellular redox potential and energy levels.
Roman H Haefeli, Michael Erb, Anja C Gemperli, Dimitri Robay, Isabelle Courdier Fruh, Corinne Anklin, Robert Dallmann, Nuri Gueven. PLoS One 2011
120
2
25

Idebenone treatment in patients with OPA1-mutant dominant optic atrophy.
Piero Barboni, Maria Lucia Valentino, Chiara La Morgia, Michele Carbonelli, Giacomo Savini, Annamaria De Negri, Francesca Simonelli, Federico Sadun, Leonardo Caporali, Alessandra Maresca,[...]. Brain 2013
49
2
25

The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.
Emmanuelle Sarzi, Claire Angebault, Marie Seveno, Naïg Gueguen, Benjamin Chaix, Guy Bielicki, Nathalie Boddaert, Anne-Laure Mausset-Bonnefont, Chantal Cazevieille, Valérie Rigau,[...]. Brain 2012
70
2
25

OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L.
Zhiyin Song, Hsiuchen Chen, Maja Fiket, Christiane Alexander, David C Chan. J Cell Biol 2007
533
2
25

Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.
H Eiberg, B Kjer, P Kjer, T Rosenberg. Hum Mol Genet 1994
121
2
25

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
2
25

OPA1-dependent cristae modulation is essential for cellular adaptation to metabolic demand.
David A Patten, Jacob Wong, Mireille Khacho, Vincent Soubannier, Ryan J Mailloux, Karine Pilon-Larose, Jason G MacLaurin, David S Park, Heidi M McBride, Laura Trinkle-Mulcahy,[...]. EMBO J 2014
215
2
25

Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.
M Votruba, A T Moore, S S Bhattacharya. J Med Genet 1998
98
2
25

Mitochondrial dysfunction in optic neuropathies: animal models and therapeutic options.
Valerio Carelli, Chiara La Morgia, Alfredo A Sadun. Curr Opin Neurol 2013
29
2
25

Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy.
Raffaele Lodi, Caterina Tonon, Maria Lucia Valentino, Stefano Iotti, Valeria Clementi, Emil Malucelli, Piero Barboni, Lora Longanesi, Simone Schimpf, Bernd Wissinger,[...]. Ann Neurol 2004
107
2
25

Therapeutic Approaches to Inherited Optic Neuropathies.
Patrick Yu-Wai-Man. Semin Neurol 2015
14
2
25

Mitochondrial Ca2+ uptake correlates with the severity of the symptoms in autosomal dominant optic atrophy.
László Fülöp, Anikó Rajki, Erika Maka, Mária Judit Molnár, András Spät. Cell Calcium 2015
14
2
25

OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy.
Patrick Yu-Wai-Man, Michael I Trenell, Kieren G Hollingsworth, Philip G Griffiths, Patrick F Chinnery. Brain 2011
27
2
25

Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling.
Sara Cipolat, Tomasz Rudka, Dieter Hartmann, Veronica Costa, Lutgarde Serneels, Katleen Craessaerts, Kristine Metzger, Christian Frezza, Wim Annaert, Luciano D'Adamio,[...]. Cell 2006
532
2
25

OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion.
Christian Frezza, Sara Cipolat, Olga Martins de Brito, Massimo Micaroni, Galina V Beznoussenko, Tomasz Rudka, Davide Bartoli, Roman S Polishuck, Nika N Danial, Bart De Strooper,[...]. Cell 2006
1086
2
25

Mathematically modeling the involvement of axons in Leber's hereditary optic neuropathy.
Billy X Pan, Fred N Ross-Cisneros, Valerio Carelli, Kelly S Rue, Solange R Salomao, Milton N Moraes-Filho, Milton N Moraes, Adriana Berezovsky, Rubens Belfort, Alfredo A Sadun. Invest Ophthalmol Vis Sci 2012
74
2
25

Dominant optic atrophy in Denmark - report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%.
Gitte J Almind, Jakob Ek, Thomas Rosenberg, Hans Eiberg, Michael Larsen, Lucamp Lucamp, Karen Brøndum-Nielsen, Karen Grønskov. BMC Med Genet 2012
23
2
25

Optical coherence tomography shows early loss of the inferior temporal quadrant retinal nerve fiber layer in autosomal dominant optic atrophy.
Sung Wook Park, Jeong-Min Hwang. Graefes Arch Clin Exp Ophthalmol 2015
11
2
25

Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy.
P Kjer, O A Jensen, L Klinken. Acta Ophthalmol (Copenh) 1983
149
2
25

Dissociation of Pupillary Post-Illumination Responses from Visual Function in Confirmed OPA1 c.983A > G and c.2708_2711delTTAG Autosomal Dominant Optic Atrophy.
Claus Nissen, Cecilia Rönnbäck, Birgit Sander, Kristina Herbst, Dan Milea, Michael Larsen, Henrik Lund-Andersen. Front Neurol 2015
12
2
25

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.
Patrick Yu-Wai-Man, Philip G Griffiths, Patrick F Chinnery. Prog Retin Eye Res 2011
362
2
25

Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies.
Chiara La Morgia, Fred N Ross-Cisneros, Alfredo A Sadun, Jens Hannibal, Alessandra Munarini, Vilma Mantovani, Piero Barboni, Gaetano Cantalupo, Kevin R Tozer, Elisa Sancisi,[...]. Brain 2010
124
2
25

Superoxide generation explains common features of optic neuropathies associated with cecocentral scotomas.
Leonard A Levin. J Neuroophthalmol 2015
16
2
25

Imaging of the macula indicates early completion of structural deficit in autosomal-dominant optic atrophy.
Cecilia Rönnbäck, Dan Milea, Michael Larsen. Ophthalmology 2013
33
2
25


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.

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