A citation-based method for searching scientific literature

R Ohara, K Imamura, F Morii, N Egawa, K Tsukita, T Enami, R Shibukawa, T Mizuno, M Nakagawa, H Inoue. Clin Pharmacol Ther 2017
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


Next-generation sequencing in Charcot-Marie-Tooth disease: opportunities and challenges.
Menelaos Pipis, Alexander M Rossor, Matilde Laura, Mary M Reilly. Nat Rev Neurol 2019
78
6

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
140
6


The kinesin-3, unc-104 regulates dendrite morphogenesis and synaptic development in Drosophila.
Jeannine V Kern, Yao V Zhang, Stella Kramer, Jay E Brenman, Tobias M Rasse. Genetics 2013
23
6

Charcot-Marie-Tooth disease: genetic and clinical spectrum in a Spanish clinical series.
Rafael Sivera, Teresa Sevilla, Juan Jesús Vílchez, Dolores Martínez-Rubio, María José Chumillas, Juan Francisco Vázquez, Nuria Muelas, Luis Bataller, José María Millán, Fancesc Palau,[...]. Neurology 2013
101
6


Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population.
Fiore Manganelli, Stefano Tozza, Chiara Pisciotta, Emilia Bellone, Rosa Iodice, Maria Nolano, Alessandro Geroldi, Simona Capponi, Paola Mandich, Lucio Santoro. J Peripher Nerv Syst 2014
58
6

Diagnosis, natural history, and management of Charcot-Marie-Tooth disease.
Davide Pareyson, Chiara Marchesi. Lancet Neurol 2009
341
6

A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease.
Philippe Latour, Christel Thauvin-Robinet, Chantal Baudelet-Méry, Pierre Soichot, Veronica Cusin, Laurence Faivre, Marie-Claire Locatelli, Martine Mayençon, Annie Sarcey, Emmanuel Broussolle,[...]. Am J Hum Genet 2010
165
6

HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease.
Constantin d'Ydewalle, Jyothsna Krishnan, Driss M Chiheb, Philip Van Damme, Joy Irobi, Alan P Kozikowski, Pieter Vanden Berghe, Vincent Timmerman, Wim Robberecht, Ludo Van Den Bosch. Nat Med 2011
308
6

A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24.
H-J Kim, S H Hong, C-S Ki, B-J Kim, J-S Shim, S-H Cho, J-H Park, J-W Kim. Neurology 2005
18
6

Identification of CR43467 encoding a long non-coding RNA as a novel genetic interactant with dFIG4, a CMT-causing gene.
Saki Shimada, Yuuka Muraoka, Kimihide Ibaraki, Toshiyuki Takano-Shimizu-Kouno, Hideki Yoshida, Masamitsu Yamaguchi. Exp Cell Res 2020
4
25

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta.
C Zhao, J Takita, Y Tanaka, M Setou, T Nakagawa, S Takeda, H W Yang, S Terada, T Nakata, Y Takei,[...]. Cell 2001
547
6


Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes.
Meriem Tazir, Mounia Bellatache, Sonia Nouioua, Jean-Michel Vallat. J Peripher Nerv Syst 2013
40
6

CMT1X phenotypes represent loss of GJB1 gene function.
M E Shy, C Siskind, E R Swan, K M Krajewski, T Doherty, D R Fuerst, P J Ainsworth, R A Lewis, S S Scherer, A F Hahn. Neurology 2007
122
6

Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice.
Zhuo Li, Yanyan Peng, Robert B Hufnagel, Yueh-Chiang Hu, Chuntao Zhao, Luis F Queme, Zaza Khuchua, Ashley M Driver, Fei Dong, Q Richard Lu,[...]. Hum Mol Genet 2017
29
6

Epidemiologic Study of Charcot-Marie-Tooth Disease: A Systematic Review.
Lidiane Carine Lima Santos Barreto, Fernanda Santos Oliveira, Paula Santos Nunes, Iandra Maria Pinheiro de França Costa, Catarina Andrade Garcez, Gabriel Mattos Goes, Eduardo Luis Aquino Neves, Jullyana de Souza Siqueira Quintans, Adriano Antunes de Souza Araújo. Neuroepidemiology 2016
114
6

Cerebral white matter abnormalities in patients with charcot-marie-tooth disease.
Mina Lee, Chang-Hyun Park, Hwa-Kyung Chung, Hyeon Jin Kim, Yunseo Choi, Jeong Hyun Yoo, Young Chul Yoon, Young Bin Hong, Ki Wha Chung, Byung-Ok Choi,[...]. Ann Neurol 2017
20
6


KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2.
Jean-Baptiste Rivière, Siriram Ramalingam, Valérie Lavastre, Masoud Shekarabi, Sébastien Holbert, Julie Lafontaine, Myriam Srour, Nancy Merner, Daniel Rochefort, Pascale Hince,[...]. Am J Hum Genet 2011
137
6

Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice.
C S Gillespie, D L Sherman, S M Fleetwood-Walker, D F Cottrell, S Tait, E M Garry, V C Wallace, J Ure, I R Griffiths, A Smith,[...]. Neuron 2000
151
6

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
P I Patel, B B Roa, A A Welcher, R Schoener-Scott, B J Trask, L Pentao, G J Snipes, C A Garcia, U Francke, E M Shooter,[...]. Nat Genet 1992
484
6

Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage.
J P Magyar, R Martini, T Ruelicke, A Aguzzi, K Adlkofer, Z Dembic, J Zielasek, K V Toyka, U Suter. J Neurosci 1996
188
6

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
131
6


Analysis of neural crest cells from Charcot-Marie-Tooth disease patients demonstrates disease-relevant molecular signature.
Fukiko Kitani-Morii, Keiko Imamura, Takayuki Kondo, Ryo Ohara, Takako Enami, Ran Shibukawa, Takuya Yamamoto, Kazuya Sekiguchi, Junya Toguchida, Toshiki Mizuno,[...]. Neuroreport 2017
7
14

Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease.
Marina Grandis, Massimo Leandri, Tiziana Vigo, Michele Cilli, Michael W Sereda, Gianfranco Gherardi, Luana Benedetti, Gianluigi Mancardi, Michele Abbruzzese, Klaus-Armin Nave,[...]. Exp Neurol 2004
15
6

Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathy.
Erik Storkebaum, Ricardo Leitão-Gonçalves, Tanja Godenschwege, Leslie Nangle, Monica Mejia, Inge Bosmans, Tinne Ooms, An Jacobs, Patrick Van Dijck, Xiang-Lei Yang,[...]. Proc Natl Acad Sci U S A 2009
77
6

A transgenic rat model of Charcot-Marie-Tooth disease.
M Sereda, I Griffiths, A Pühlhofer, H Stewart, M J Rossner, F Zimmerman, J P Magyar, A Schneider, E Hund, H M Meinck,[...]. Neuron 1996
290
6

A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration.
Víctor López Del Amo, Martina Palomino-Schätzlein, Marta Seco-Cervera, José Luis García-Giménez, Federico Vicente Pallardó, Antonio Pineda-Lucena, Máximo Ibo Galindo. Biochim Biophys Acta Mol Basis Dis 2017
12
8

Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy.
Ilaria Vaccari, Antonietta Carbone, Stefano Carlo Previtali, Yevgeniya A Mironova, Valeria Alberizzi, Roberta Noseda, Cristina Rivellini, Francesca Bianchi, Ubaldo Del Carro, Maurizio D'Antonio,[...]. Hum Mol Genet 2015
36
6

Mitofusin gain and loss of function drive pathogenesis in Drosophila models of CMT2A neuropathy.
Najla El Fissi, Manuel Rojo, Aїcha Aouane, Esra Karatas, Gabriela Poliacikova, Claudine David, Julien Royet, Thomas Rival. EMBO Rep 2018
43
6

Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies.
Gulam Mustafa Saifi, Kinga Szigeti, G Jackson Snipes, Carlos A Garcia, James R Lupski. J Investig Med 2003
52
6

Nerve Biopsy Is Still Useful in Some Inherited Neuropathies.
Mathilde Duchesne, Stéphane Mathis, Laurence Richard, Corinne Magdelaine, Philippe Corcia, Sonia Nouioua, Meriem Tazir, Laurent Magy, Jean-Michel Vallat. J Neuropathol Exp Neurol 2018
9
11

A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: A Simple System for Complex, Heterogeneous Diseases.
Weronika Rzepnikowska, Joanna Kaminska, Dagmara Kabzińska, Katarzyna Binięda, Andrzej Kochański. Int J Mol Sci 2020
9
11

Two rare human mitofusin 2 mutations alter mitochondrial dynamics and induce retinal and cardiac pathology in Drosophila.
William H Eschenbacher, Moshi Song, Yun Chen, Poonam Bhandari, Peter Zhao, Casey C Jowdy, John T Engelhard, Gerald W Dorn. PLoS One 2012
21
6

A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene.
Marina L Kennerson, Eppie M Yiu, David T Chuang, Aditi Kidambi, Shih-Chia Tso, Carolyn Ly, Rabia Chaudhry, Alexander P Drew, Gary Rance, Martin B Delatycki,[...]. Hum Mol Genet 2013
46
6

Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination.
Bo Hu, Megan McCollum, Vignesh Ravi, Sezgi Arpag, Daniel Moiseev, Ryan Castoro, Bret Mobley, Bryan Burnette, Carly Siskind, John Day,[...]. Ann Neurol 2018
23
6


Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E.
Florence Dequen, Mohammed Filali, Roxanne C Larivière, Rodolphe Perrot, Shin-Ichi Hisanaga, Jean-Pierre Julien. Hum Mol Genet 2010
37
6

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Andrea Cortese, Yi Zhu, Adriana P Rebelo, Sara Negri, Steve Courel, Lisa Abreu, Chelsea J Bacon, Yunhong Bai, Dana M Bis-Brewer, Enrico Bugiardini,[...]. Nat Genet 2020
45
6


The Protective Effects of Levetiracetam on a Human iPSCs-Derived Spinal Muscular Atrophy Model.
Shiori Ando, Michinori Funato, Kazuki Ohuchi, Satoshi Inagaki, Arisu Sato, Junko Seki, Chizuru Kawase, Toshio Saito, Hisahide Nishio, Shinsuke Nakamura,[...]. Neurochem Res 2019
12
8

On the origin of the extracellular action potential waveform: A modeling study.
Carl Gold, Darrell A Henze, Christof Koch, György Buzsáki. J Neurophysiol 2006
300
6

Levetiracetam: a review of its use in epilepsy.
Katherine A Lyseng-Williamson. Drugs 2011
122
6

High-resolution CMOS MEA platform to study neurons at subcellular, cellular, and network levels.
Jan Müller, Marco Ballini, Paolo Livi, Yihui Chen, Milos Radivojevic, Amir Shadmani, Vijay Viswam, Ian L Jones, Michele Fiscella, Roland Diggelmann,[...]. Lab Chip 2015
109
6

Human Mesenchymal Stromal Cells Unveil an Unexpected Differentiation Potential toward the Dopaminergic Neuronal Lineage.
Giulia Gaggi, Andrea Di Credico, Pascal Izzicupo, Francesco Alviano, Michele Di Mauro, Angela Di Baldassarre, Barbara Ghinassi. Int J Mol Sci 2020
5
20

Spare Parts from Discarded Materials: Fetal Annexes in Regenerative Medicine.
Giulia Gaggi, Pascal Izzicupo, Andrea Di Credico, Silvia Sancilio, Angela Di Baldassarre, Barbara Ghinassi. Int J Mol Sci 2019
11
9



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.