A citation-based method for searching scientific literature

Kristien Verhoeven, Kristl G Claeys, Stephan Züchner, J Michael Schröder, Joachim Weis, Chantal Ceuterick, Albena Jordanova, Eva Nelis, Els De Vriendt, Matthias Van Hul, Pavel Seeman, Radim Mazanec, Gulam Mustafa Saifi, Kinga Szigeti, Pedro Mancias, Ian J Butler, Andrzej Kochanski, Barbara Ryniewicz, Jan De Bleecker, Peter Van den Bergh, Christine Verellen, Rudy Van Coster, Nathalie Goemans, Michaela Auer-Grumbach, Wim Robberecht, Vedrana Milic Rasic, Yoram Nevo, Ivajlo Tournev, Velina Guergueltcheva, Filip Roelens, Peter Vieregge, Paolo Vinci, Maria Teresa Moreno, H-J Christen, Michael E Shy, James R Lupski, Jeffery M Vance, Peter De Jonghe, Vincent Timmerman. Brain 2006
Times Cited: 256







List of co-cited articles
1239 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
52

MFN2 mutations cause severe phenotypes in most patients with CMT2A.
S M E Feely, M Laura, C E Siskind, S Sottile, M Davis, V S Gibbons, M M Reilly, M E Shy. Neurology 2011
119
36

Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations.
K W Chung, S B Kim, K D Park, K G Choi, J H Lee, H W Eun, J S Suh, J H Hwang, W K Kim, B C Seo,[...]. Brain 2006
185
33

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
32

Mitofusin 2 tethers endoplasmic reticulum to mitochondria.
Olga Martins de Brito, Luca Scorrano. Nature 2008
31

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
Stephan Züchner, Peter De Jonghe, Albena Jordanova, Kristl G Claeys, Velina Guergueltcheva, Sylvia Cherninkova, Steven R Hamilton, Greg Van Stavern, Karen M Krajewski, Jeffery Stajich,[...]. Ann Neurol 2006
241
30

Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex.
Albert Misko, Sirui Jiang, Iga Wegorzewska, Jeffrey Milbrandt, Robert H Baloh. J Neurosci 2010
384
28

Charcot-Marie-Tooth disease type 2A: from typical to rare phenotypic and genotypic features.
Francesco Bombelli, Tanya Stojkovic, Odile Dubourg, Andoni Echaniz-Laguna, Sandrine Tardieu, Kathy Larcher, Patrizia Amati-Bonneau, Philippe Latour, Odile Vignal, Cécile Cazeneuve,[...]. JAMA Neurol 2014
66
40

Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations.
Robert H Baloh, Robert E Schmidt, Alan Pestronk, Jeffrey Milbrandt. J Neurosci 2007
300
24


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
20

Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.
Judith Calvo, Benoît Funalot, Robert A Ouvrier, Leila Lazaro, Annick Toutain, Philippe De Mas, Pierre Bouche, Brigitte Gilbert-Dussardier, Marie-Christine Arne-Bes, Jean-Pierre Carrière,[...]. Arch Neurol 2009
83
24

Charcot-Marie-Tooth disease subtypes and genetic testing strategies.
Anita S D Saporta, Stephanie L Sottile, Lindsey J Miller, Shawna M E Feely, Carly E Siskind, Michael E Shy. Ann Neurol 2011
312
20

Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degeneration.
Albert L Misko, Yo Sasaki, Elizabeth Tuck, Jeffrey Milbrandt, Robert H Baloh. J Neurosci 2012
120
19


MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.
Giulia Stuppia, Federica Rizzo, Giulietta Riboldi, Roberto Del Bo, Monica Nizzardo, Chiara Simone, Giacomo P Comi, Nereo Bresolin, Stefania Corti. J Neurol Sci 2015
64
29

Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing.
Sinead M Murphy, Matilde Laura, Katherine Fawcett, Amelie Pandraud, Yo-Tsen Liu, Gabrielle L Davidson, Alexander M Rossor, James M Polke, Victoria Castleman, Hadi Manji,[...]. J Neurol Neurosurg Psychiatry 2012
209
18

Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations.
J M Polke, M Laurá, D Pareyson, F Taroni, M Milani, G Bergamin, V S Gibbons, H Houlden, S C Chamley, J Blake,[...]. Neurology 2011
55
32

Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations.
Jean-Michel Vallat, Robert A Ouvrier, John D Pollard, Corinne Magdelaine, Danqing Zhu, Garth A Nicholson, Simon Grew, Monique M Ryan, Benoît Funalot. J Neuropathol Exp Neurol 2008
68
25

Clinical implications of genetic advances in Charcot-Marie-Tooth disease.
Alexander M Rossor, James M Polke, Henry Houlden, Mary M Reilly. Nat Rev Neurol 2013
202
16

Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene.
Victoria H Lawson, Brad V Graham, Kevin M Flanigan. Neurology 2005
128
16

Structural basis of mitochondrial tethering by mitofusin complexes.
Takumi Koshiba, Scott A Detmer, Jens T Kaiser, Hsiuchen Chen, J Michael McCaffery, David C Chan. Science 2004
581
16

Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutations.
G A Nicholson, C Magdelaine, D Zhu, S Grew, M M Ryan, F Sturtz, J-M Vallat, R A Ouvrier. Neurology 2008
74
21



Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.
Romain Cartoni, Estelle Arnaud, Jean-Jacques Médard, Olivier Poirot, Delphine S Courvoisier, Roman Chrast, Jean-Claude Martinou. Brain 2010
67
22

Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of Charcot-Marie-Tooth type 2A.
Scott A Detmer, Christine Vande Velde, Don W Cleveland, David C Chan. Hum Mol Genet 2008
92
16

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

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
15


Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties.
Mario A Saporta, Vu Dang, Dmitri Volfson, Bende Zou, Xinmin Simon Xie, Adijat Adebola, Ronald K Liem, Michael Shy, John T Dimos. Exp Neurol 2015
65
21

MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.
Agostinho G Rocha, Antonietta Franco, Andrzej M Krezel, Jeanne M Rumsey, Justin M Alberti, William C Knight, Nikolaos Biris, Emmanouil Zacharioudakis, James W Janetka, Robert H Baloh,[...]. Science 2018
83
16

Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.
R Del Bo, M Moggio, M Rango, S Bonato, M G D'Angelo, S Ghezzi, G Airoldi, M T Bassi, M Guglieri, L Napoli,[...]. Neurology 2008
68
19

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
13

A cohort study of MFN2 mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients.
B-O Choi, K Nakhro, H J Park, Y S Hyun, J H Lee, S Kanwal, S-C Jung, K W Chung. Clin Genet 2015
24
54

CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis.
V Fridman, B Bundy, M M Reilly, D Pareyson, C Bacon, J Burns, J Day, S Feely, R S Finkel, T Grider,[...]. J Neurol Neurosurg Psychiatry 2015
151
13

Mitofusin 2 is necessary for striatal axonal projections of midbrain dopamine neurons.
Seungmin Lee, Fredrik H Sterky, Arnaud Mourier, Mügen Terzioglu, Staffan Cullheim, Lars Olson, Nils-Göran Larsson. Hum Mol Genet 2012
113
12


Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity.
Naotada Ishihara, Yuka Eura, Katsuyoshi Mihara. J Cell Sci 2004
448
12

Correcting mitochondrial fusion by manipulating mitofusin conformations.
Antonietta Franco, Richard N Kitsis, Julie A Fleischer, Evripidis Gavathiotis, Opher S Kornfeld, Guohua Gong, Nikolaos Biris, Ann Benz, Nir Qvit, Sara K Donnelly,[...]. Nature 2016
110
12


Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.
Hsiuchen Chen, Marc Vermulst, Yun E Wang, Anne Chomyn, Tomas A Prolla, J Michael McCaffery, David C Chan. Cell 2010
689
11

Axonal Transport Defects in a Mitofusin 2 Loss of Function Model of Charcot-Marie-Tooth Disease in Zebrafish.
Anna L Chapman, Ellen J Bennett, Tennore M Ramesh, Kurt J De Vos, Andrew J Grierson. PLoS One 2013
37
29

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.
Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, Virginie Guillet, Naïg Gueguen, Marie-Anne Pou de Crescenzo, Marc Ferré, Marie-Claire Malinge, Agnès Guichet, Guillaume Nicolas,[...]. Ann Neurol 2007
108
11

Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin.
Atsushi Tanaka, Megan M Cleland, Shan Xu, Derek P Narendra, Der-Fen Suen, Mariusz Karbowski, Richard J Youle. J Cell Biol 2010
868
11

Mitochondrial GTPase mitofusin 2 mutation in Charcot-Marie-Tooth neuropathy type 2A.
Kazuki Kijima, Chikahiko Numakura, Hiroko Izumino, Kazuo Umetsu, Atsuo Nezu, Toshihide Shiiki, Masafumi Ogawa, Yoshito Ishizaki, Takeshi Kitamura, Yasunobu Shozawa,[...]. Hum Genet 2005
188
11

Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutations.
Giuseppe Piscosquito, Paola Saveri, Stefania Magri, Claudia Ciano, Daniela Di Bella, Micaela Milani, Franco Taroni, Davide Pareyson. J Peripher Nerv Syst 2015
16
68

Mitochondrial fission, fusion, and stress.
Richard J Youle, Alexander M van der Bliek. Science 2012
10

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
10

GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance.
Axel Niemann, Konstanze Marion Wagner, Marcel Ruegg, Ueli Suter. Neurobiol Dis 2009
96
10


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.