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


Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease.
Michael N Weedon, Robert Hastings, Richard Caswell, Weijia Xie, Konrad Paszkiewicz, Thalia Antoniadi, Maggie Williams, Cath King, Lynn Greenhalgh, Ruth Newbury-Ecob,[...]. Am J Hum Genet 2011
185
6

Sorbitol dehydrogenase: structure, function and ligand design.
O El-Kabbani, C Darmanin, R P-T Chung. Curr Med Chem 2004
43
6

Sorbitol dehydrogenase of Drosophila. Gene, protein, and expression data show a two-gene system.
T Luque, L Hjelmqvist, G Marfany, O Danielsson, M El-Ahmad, B Persson, H Jörnvall, R González-Duarte. J Biol Chem 1998
15
6

Knockdown of the Drosophila FIG4 induces deficient locomotive behavior, shortening of motor neuron, axonal targeting aberration, reduction of life span and defects in eye development.
Akane Kyotani, Yumiko Azuma, Itaru Yamamoto, Hideki Yoshida, Ikuko Mizuta, Toshiki Mizuno, Masanori Nakagawa, Takahiko Tokuda, Masamitsu Yamaguchi. Exp Neurol 2016
24
6

Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway.
Kojiro Suda, Yuuka Muraoka, Andrea Ortega-Yáñez, Hideki Yoshida, Fuma Kizu, Teruhisa Hochin, Hiroshi Kimura, Masamitsu Yamaguchi. Exp Cell Res 2019
5
20

Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons.
Jean-Michel Cioni, Julie Qiaojin Lin, Anne V Holtermann, Max Koppers, Maximilian A H Jakobs, Afnan Azizi, Benita Turner-Bridger, Toshiaki Shigeoka, Kristian Franze, William A Harris,[...]. Cell 2019
184
6

Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease.
Henry L Paulson, James Y Garbern, Timothy F Hoban, Karen M Krajewski, Richard A Lewis, Kenneth H Fischbeck, Robert I Grossman, Robert Lenkinski, John A Kamholz, Michael E Shy. Ann Neurol 2002
124
6

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
332
6

Peripheral neuropathy in complex inherited diseases: an approach to diagnosis.
Alexander M Rossor, Aisling S Carr, Helen Devine, Hoskote Chandrashekar, Ana Lara Pelayo-Negro, Davide Pareyson, Michael E Shy, Steven S Scherer, Mary M Reilly. J Neurol Neurosurg Psychiatry 2017
38
6

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.
Albena Jordanova, Joy Irobi, Florian P Thomas, Patrick Van Dijck, Kris Meerschaert, Maarten Dewil, Ines Dierick, An Jacobs, Els De Vriendt, Velina Guergueltcheva,[...]. Nat Genet 2006
277
6

Neuropathology of Charcot-Marie-Tooth and related disorders.
J Michael Schröder. Neuromolecular Med 2006
36
6

Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A.
A M Robertson, J Perea, A McGuigan, R H M King, J R Muddle, A A Gabreëls-Festen, P K Thomas, C Huxley. J Anat 2002
66
6

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
6

Phosphatidylinositol 3,5-bisphosphate: low abundance, high significance.
Amber J McCartney, Yanling Zhang, Lois S Weisman. Bioessays 2014
140
6

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32.
P Anzini, D H Neuberg, M Schachner, E Nelles, K Willecke, J Zielasek, K V Toyka, U Suter, R Martini. J Neurosci 1997
251
6

Mitochondrial defects and neuromuscular degeneration caused by altered expression of Drosophila Gdap1: implications for the Charcot-Marie-Tooth neuropathy.
Víctor López Del Amo, Marta Seco-Cervera, José Luís García-Giménez, Alexander J Whitworth, Federico V Pallardó, Máximo Ibo Galindo. Hum Mol Genet 2015
30
6

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.
K Hayasaka, M Himoro, W Sato, G Takada, K Uyemura, N Shimizu, T D Bird, P M Conneally, P F Chance. Nat Genet 1993
329
6

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.
C Huxley, E Passage, A Manson, G Putzu, D Figarella-Branger, J F Pellissier, M Fontés. Hum Mol Genet 1996
182
6

Charcot-Marie-Tooth disease: frequency of genetic subtypes in a German neuromuscular center population.
Burkhard Gess, Anja Schirmacher, Matthias Boentert, Peter Young. Neuromuscul Disord 2013
56
6

Endosomal phosphoinositides and human diseases.
Anne-Sophie Nicot, Jocelyn Laporte. Traffic 2008
112
6

Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS.
Clement Y Chow, John E Landers, Sarah K Bergren, Peter C Sapp, Adrienne E Grant, Julie M Jones, Lesley Everett, Guy M Lenk, Diane M McKenna-Yasek, Lois S Weisman,[...]. Am J Hum Genet 2009
287
6

Unique clinical and neurophysiologic profile of a cohort of children with CMTX3.
Manoj Kanhangad, Kayla Cornett, Megan H Brewer, Garth A Nicholson, Monique M Ryan, Robert L Smith, Gopinath M Subramanian, Helen K Young, Stephan Züchner, Marina L Kennerson,[...]. Neurology 2018
2
50

Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2.
Michael Gonzalez, Heather McLaughlin, Henry Houlden, Min Guo, Liu Yo-Tsen, Marios Hadjivassilious, Fiorella Speziani, Xiang-Lei Yang, Anthony Antonellis, Mary M Reilly,[...]. J Neurol Neurosurg Psychiatry 2013
99
6

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Rachel V Baxter, Kamel Ben Othmane, Julie M Rochelle, Jason E Stajich, Christine Hulette, Susan Dew-Knight, Faycal Hentati, Mongi Ben Hamida, S Bel, Judy E Stenger,[...]. Nat Genet 2002
271
6

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
Clement Y Chow, Yanling Zhang, James J Dowling, Natsuko Jin, Maja Adamska, Kensuke Shiga, Kinga Szigeti, Michael E Shy, Jun Li, Xuebao Zhang,[...]. Nature 2007
356
6

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.
Yuan-Yuan Lu, He Lyu, Su-Qin Jin, Yue-Huan Zuo, Jing Liu, Zhao-Xia Wang, Wei Zhang, Yun Yuan. Chin Med J (Engl) 2017
14
7

Connexin mutations in X-linked Charcot-Marie-Tooth disease.
J Bergoffen, S S Scherer, S Wang, M O Scott, L J Bone, D L Paul, K Chen, M W Lensch, P F Chance, K H Fischbeck. Science 1993
893
6

Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.
Violaine Plante-Bordeneuve, Gérard Said. Muscle Nerve 2002
23
6

Emerging technologies for gene manipulation in Drosophila melanogaster.
Koen J T Venken, Hugo J Bellen. Nat Rev Genet 2005
141
6


Enhancing folic acid metabolism suppresses defects associated with loss of Drosophila mitofusin.
Juan Garrido-Maraver, Ivana Celardo, Ana C Costa, Susann Lehmann, Samantha H Y Loh, L Miguel Martins. Cell Death Dis 2019
9
11

Rab GTPase Function in Endosome and Lysosome Biogenesis.
Lars Langemeyer, Florian Fröhlich, Christian Ungermann. Trends Cell Biol 2018
162
6

Genetic spectrum of hereditary neuropathies with onset in the first year of life.
Jonathan Baets, Tine Deconinck, Els De Vriendt, Magdalena Zimoń, Laetitia Yperzeele, Kim Van Hoorenbeeck, Kristien Peeters, Ronen Spiegel, Yesim Parman, Berten Ceulemans,[...]. Brain 2011
70
6

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
228
6


New developments in Charcot-Marie-Tooth neuropathy and related diseases.
Davide Pareyson, Paola Saveri, Chiara Pisciotta. Curr Opin Neurol 2017
99
6

Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locus.
M Auer-Grumbach, P De Jonghe, K Wagner, K Verhoeven, H P Hartung, V Timmerman. Neurology 2000
37
6


A rat model of Charcot-Marie-Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients.
Robert Fledrich, Beate Schlotter-Weigel, Tuuli J Schnizer, Sven P Wichert, Ruth M Stassart, Gerd Meyer zu Hörste, Axel Klink, Bernhard G Weiss, Uwe Haag, Maggie C Walter,[...]. Brain 2012
34
6

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.
Anthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, Imke Puls, Annette Abel, Shih-Queen Lee-Lin, Albena Jordanova, Ivo Kremensky, Kyproula Christodoulou, Lefkos T Middleton,[...]. Am J Hum Genet 2003
408
6

Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases.
Sven Niehues, Julia Bussmann, Georg Steffes, Ines Erdmann, Caroline Köhrer, Litao Sun, Marina Wagner, Kerstin Schäfer, Guangxia Wang, Sophia N Koerdt,[...]. Nat Commun 2015
68
6

Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
Ahmed Bouhouche, Nazha Birouk, Hamid Azzedine, Ali Benomar, Garry Durosier, Dorothée Ente, Marie-Paule Muriel, Merle Ruberg, Ilham Slassi, Mohamed Yahyaoui,[...]. Brain 2007
25
6

Dominant GDAP1 mutations cause predominantly mild CMT phenotypes.
M Zimoń, J Baets, G M Fabrizi, E Jaakkola, D Kabzińska, J Pilch, A B Schindler, D R Cornblath, K H Fischbeck, M Auer-Grumbach,[...]. Neurology 2011
64
6

A reconstituted mammalian APC-kinesin complex selectively transports defined packages of axonal mRNAs.
Sebastian Baumann, Artem Komissarov, Maria Gili, Verena Ruprecht, Stefan Wieser, Sebastian P Maurer. Sci Adv 2020
29
6

Prevalence, Mortality, and Cause of Death in Charcot-Marie-Tooth Disease in Korea: A Nationwide, Population-Based Study.
Hyung Jun Park, Young-Chul Choi, Ji Won Oh, Sang-Wook Yi. Neuroepidemiology 2020
4
25

Genetic epidemiology, demographic, and clinical characteristics of Charcot-Marie-tooth disease in the island of Gran Canaria (Spain).
Manuel Lousa, Carlos Vázquez-Huarte-Mendicoa, Antonio J Gutiérrez, Pedro Saavedra, Beatriz Navarro, Antonio Tugores. J Peripher Nerv Syst 2019
8
12

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
42
6

Genetic screening of the genes interacting with Drosophila FIG4 identified a novel link between CMT-causing gene and long noncoding RNAs.
Yuuka Muraoka, Aya Nakamura, Ryo Tanaka, Kojiro Suda, Yumiko Azuma, Yukie Kushimura, Luca Lo Piccolo, Hideki Yoshida, Ikuko Mizuta, Takahiko Tokuda,[...]. Exp Neurol 2018
20
6


X-linked Charcot-Marie-Tooth disease: phenotypic expression of a novel mutation Ile127Ser in the GJB1 (connexin 32) gene.
Petr Vondracek, Pavel Seeman, Marketa Hermanova, Lenka Fajkusova. Muscle Nerve 2005
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.