A citation-based method for searching scientific literature

Sylvie Gerber, Majida Charif, Arnaud Chevrollier, Tanguy Chaumette, Claire Angebault, Mariame Selma Kane, Aurélien Paris, Jennifer Alban, Mélanie Quiles, Cécile Delettre, Dominique Bonneau, Vincent Procaccio, Patrizia Amati-Bonneau, Pascal Reynier, Stéphanie Leruez, Raphael Calmon, Nathalie Boddaert, Benoit Funalot, Marlène Rio, Didier Bouccara, Isabelle Meunier, Hiromi Sesaki, Josseline Kaplan, Christian P Hamel, Jean-Michel Rozet, Guy Lenaers. Brain 2017
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


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
512
60

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
48

A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
Jill A Fahrner, Raymond Liu, Michael Scott Perry, Jessica Klein, David C Chan. Am J Med Genet A 2016
74
45

DNM1L-related mitochondrial fission defect presenting as refractory epilepsy.
Jason R Vanstone, Amanda M Smith, Skye McBride, Turaya Naas, Martin Holcik, Ghadi Antoun, Mary-Ellen Harper, Jean Michaud, Erick Sell, Pranesh Chakraborty,[...]. Eur J Hum Genet 2016
79
41

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
40

Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.
Ruth Sheffer, Liza Douiev, Simon Edvardson, Avraham Shaag, Khaled Tamimi, Devorah Soiferman, Vardiella Meiner, Ann Saada. Am J Med Genet A 2016
57
42

Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy.
Johannes Koch, René G Feichtinger, Peter Freisinger, Mechthild Pies, Falk Schrödl, Arcangela Iuso, Wolfgang Sperl, Johannes A Mayr, Holger Prokisch, Tobias B Haack. J Med Genet 2016
64
35

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
919
35

Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells.
E Smirnova, L Griparic, D L Shurland, A M van der Bliek. Mol Biol Cell 2001
31

Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy.
Alessia Nasca, Andrea Legati, Enrico Baruffini, Cecilia Nolli, Isabella Moroni, Anna Ardissone, Paola Goffrini, Daniele Ghezzi. Hum Mutat 2016
44
40

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
259
28

Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes.
Hanan E Shamseldin, Muneera Alshammari, Tarfa Al-Sheddi, Mustafa A Salih, Hisham Alkhalidi, Amal Kentab, Gabriela M Repetto, Mais Hashem, Fowzan S Alkuraya. J Med Genet 2012
110
28

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development.
Hsiuchen Chen, Scott A Detmer, Andrew J Ewald, Erik E Griffin, Scott E Fraser, David C Chan. J Cell Biol 2003
26

Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila.
Yu-Hsin Chao, Laurie A Robak, Fan Xia, Mary K Koenig, Adekunle Adesina, Carlos A Bacino, Fernando Scaglia, Hugo J Bellen, Michael F Wangler. Hum Mol Genet 2016
39
41

Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L.
Grace Yoon, Zeenat Malam, Tara Paton, Christian R Marshall, Ella Hyatt, Zhenya Ivakine, Stephen W Scherer, Kyong-Soon Lee, Cynthia Hawkins, Ronald D Cohn. J Pediatr 2016
44
36

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
342
26

Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice.
Naotada Ishihara, Masatoshi Nomura, Akihiro Jofuku, Hiroki Kato, Satoshi O Suzuki, Keiji Masuda, Hidenori Otera, Yae Nakanishi, Ikuya Nonaka, Yu-Ichi Goto,[...]. Nat Cell Biol 2009
663
25

Mitofusin 2 tethers endoplasmic reticulum to mitochondria.
Olga Martins de Brito, Luca Scorrano. Nature 2008
23

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
147
23

The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice.
Junko Wakabayashi, Zhongyan Zhang, Nobunao Wakabayashi, Yasushi Tamura, Masahiro Fukaya, Thomas W Kensler, Miho Iijima, Hiromi Sesaki. J Cell Biol 2009
409
23

DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
K Zaha, H Matsumoto, M Itoh, H Saitsu, K Kato, M Kato, S Ogata, K Murayama, Y Kishita, Y Mizuno,[...]. Clin Genet 2016
20
65

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
129
21

Syndromic parkinsonism and dementia associated with OPA1 missense mutations.
Valerio Carelli, Olimpia Musumeci, Leonardo Caporali, Claudia Zanna, Chiara La Morgia, Valentina Del Dotto, Anna Maria Porcelli, Michela Rugolo, Maria Lucia Valentino, Luisa Iommarini,[...]. Ann Neurol 2015
98
21

Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy.
Daniela Verrigni, Michela Di Nottia, Anna Ardissone, Enrico Baruffini, Alessia Nasca, Andrea Legati, Emanuele Bellacchio, Gigliola Fagiolari, Diego Martinelli, Lucia Fusco,[...]. Hum Mutat 2019
20
65

Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells.
Hidenori Otera, Chunxin Wang, Megan M Cleland, Kiyoko Setoguchi, Sadaki Yokota, Richard J Youle, Katsuyoshi Mihara. J Cell Biol 2010
612
20

During autophagy mitochondria elongate, are spared from degradation and sustain cell viability.
Ligia C Gomes, Giulietta Di Benedetto, Luca Scorrano. Nat Cell Biol 2011
20

An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2.
Farida Korobova, Vinay Ramabhadran, Henry N Higgs. Science 2013
426
20

ER tubules mark sites of mitochondrial division.
Jonathan R Friedman, Laura L Lackner, Matthew West, Jared R DiBenedetto, Jodi Nunnari, Gia K Voeltz. Science 2011
20

Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission.
Oliver C Losón, Zhiyin Song, Hsiuchen Chen, David C Chan. Mol Biol Cell 2013
557
18

MiD49 and MiD51, new components of the mitochondrial fission machinery.
Catherine S Palmer, Laura D Osellame, David Laine, Olga S Koutsopoulos, Ann E Frazier, Michael T Ryan. EMBO Rep 2011
368
18

Multiple dynamin family members collaborate to drive mitochondrial division.
Jason E Lee, Laura M Westrate, Haoxi Wu, Cynthia Page, Gia K Voeltz. Nature 2016
235
18

The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission.
Ruchika Anand, Timothy Wai, Michael J Baker, Nikolay Kladt, Astrid C Schauss, Elena Rugarli, Thomas Langer. J Cell Biol 2014
370
18

A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial division.
Chuang-Rung Chang, Cara Marie Manlandro, Damien Arnoult, Julia Stadler, Ammon E Posey, R Blake Hill, Craig Blackstone. J Biol Chem 2010
117
18

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
107
18

Structural basis of mitochondrial receptor binding and constriction by DRP1.
Raghav Kalia, Ray Yu-Ruei Wang, Ali Yusuf, Paul V Thomas, David A Agard, Janet M Shaw, Adam Frost. Nature 2018
86
18

Conformational changes in Dnm1 support a contractile mechanism for mitochondrial fission.
Jason A Mears, Laura L Lackner, Shunming Fang, Elena Ingerman, Jodi Nunnari, Jenny E Hinshaw. Nat Struct Mol Biol 2011
267
16

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy.
Gilad Twig, Alvaro Elorza, Anthony J A Molina, Hibo Mohamed, Jakob D Wikstrom, Gil Walzer, Linsey Stiles, Sarah E Haigh, Steve Katz, Guy Las,[...]. EMBO J 2008
16

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
278
16

Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation.
Ronen Spiegel, Ann Saada, Padraig J Flannery, Florence Burté, Devorah Soiferman, Morad Khayat, Verónica Eisner, Eugene Vladovski, Robert W Taylor, Laurence A Bindoff,[...]. J Med Genet 2016
54
18

Critical reappraisal confirms that Mitofusin 2 is an endoplasmic reticulum-mitochondria tether.
Deborah Naon, Marta Zaninello, Marta Giacomello, Tatiana Varanita, Francesca Grespi, Sowmya Lakshminaranayan, Annalisa Serafini, Martina Semenzato, Stephanie Herkenne, Maria Isabel Hernández-Alvarez,[...]. Proc Natl Acad Sci U S A 2016
250
16

De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity.
Emma Ladds, Andrea Whitney, Eszter Dombi, Monika Hofer, Geetha Anand, Victoria Harrison, Carl Fratter, Janet Carver, Ines A Barbosa, Michael Simpson,[...]. Neurol Genet 2018
16
62

Aberrant Drp1-mediated mitochondrial division presents in humans with variable outcomes.
Brittany N Whitley, Christina Lam, Hong Cui, Katrina Haude, Renkui Bai, Luis Escobar, Afifa Hamilton, Lauren Brady, Mark A Tarnopolsky, Lauren Dengle,[...]. Hum Mol Genet 2018
18
55

Cooperative and independent roles of the Drp1 adaptors Mff, MiD49 and MiD51 in mitochondrial fission.
Laura D Osellame, Abeer P Singh, David A Stroud, Catherine S Palmer, Diana Stojanovski, Rajesh Ramachandran, Michael T Ryan. J Cell Sci 2016
150
15

Mitochondrial fusion protects against neurodegeneration in the cerebellum.
Hsiuchen Chen, J Michael McCaffery, David C Chan. Cell 2007
603
15


Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.
Vanessa J Davies, Andrew J Hollins, Malgorzata J Piechota, Wanfen Yip, Jennifer R Davies, Kathryn E White, Phillip P Nicols, Michael E Boulton, Marcela Votruba. Hum Mol Genet 2007
281
15

Molecular basis of selective mitochondrial fusion by heterotypic action between OPA1 and cardiolipin.
Tadato Ban, Takaya Ishihara, Hiroto Kohno, Shotaro Saita, Ayaka Ichimura, Katsumi Maenaka, Toshihiko Oka, Katsuyoshi Mihara, Naotada Ishihara. Nat Cell Biol 2017
145
15

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
15

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy.
Marcel V Alavi, Stefanie Bette, Simone Schimpf, Frank Schuettauf, Ulrich Schraermeyer, Hans F Wehrl, Lukas Ruttiger, Susanne C Beck, Felix Tonagel, Bernd J Pichler,[...]. Brain 2007
178
15

Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation.
Bianca Hartmann, Timothy Wai, Hao Hu, Thomas MacVicar, Luciana Musante, Björn Fischer-Zirnsak, Werner Stenzel, Ralph Gräf, Lambert van den Heuvel, Hans-Hilger Ropers,[...]. Elife 2016
58
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.