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List of co-cited articles
1742 articles co-cited >1



Times Cited
  Times     Co-cited
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Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.
Oleg V Evgrafov, Irena Mersiyanova, Joy Irobi, Ludo Van Den Bosch, Ines Dierick, Conrad L Leung, Olga Schagina, Nathalie Verpoorten, Katrien Van Impe, Valeriy Fedotov,[...]. Nat Genet 2004
437
81

Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.
Joy Irobi, Katrien Van Impe, Pavel Seeman, Albena Jordanova, Ines Dierick, Nathalie Verpoorten, Andrej Michalik, Els De Vriendt, An Jacobs, Veerle Van Gerwen,[...]. Nat Genet 2004
314
46


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
302
38

Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2.
H Houlden, M Laura, F Wavrant-De Vrièze, J Blake, N Wood, M M Reilly. Neurology 2008
139
33

Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy.
Kazuki Kijima, Chikahiko Numakura, Tomohide Goto, Takao Takahashi, Tesshu Otagiri, Kazuo Umetsu, Kiyoshi Hayasaka. J Hum Genet 2005
69
40

Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study.
Ines Dierick, Jonathan Baets, Joy Irobi, An Jacobs, Els De Vriendt, Tine Deconinck, Luciano Merlini, Peter Van den Bergh, Vedrana Milic Rasic, Wim Robberecht,[...]. Brain 2008
98
25

Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy.
Leonardo Almeida-Souza, Sofie Goethals, Vicky de Winter, Ines Dierick, Rodrigo Gallardo, Joost Van Durme, Joy Irobi, Jan Gettemans, Frederic Rousseau, Joost Schymkowitz,[...]. J Biol Chem 2010
75
33

Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy.
Leonardo Almeida-Souza, Bob Asselbergh, Constantin d'Ydewalle, Kristof Moonens, Sofie Goethals, Vicky de Winter, Abdelkrim Azmi, Joy Irobi, Jean-Pierre Timmermans, Kris Gevaert,[...]. J Neurosci 2011
71
35

The human genome encodes 10 alpha-crystallin-related small heat shock proteins: HspB1-10.
Guido Kappé, Erik Franck, Pauline Verschuure, Wilbert C Boelens, Jack A M Leunissen, Wilfried W de Jong. Cell Stress Chaperones 2003
313
24

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.
Bei-sha Tang, Guo-hua Zhao, Wei Luo, Kun Xia, Fang Cai, Qian Pan, Ru-xu Zhang, Fu-feng Zhang, Xiao-min Liu, Biao Chen,[...]. Hum Genet 2005
129
24

Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.
Beisha Tang, Xiaomin Liu, Guohua Zhao, Wei Luo, Kun Xia, Qian Pan, Fang Cai, Zhengmao Hu, Cheng Zhang, Biao Chen,[...]. Arch Neurol 2005
56
39

Mutant HSPB8 causes motor neuron-specific neurite degeneration.
Joy Irobi, Leonardo Almeida-Souza, Bob Asselbergh, Vicky De Winter, Sofie Goethals, Ines Dierick, Jyothsna Krishnan, Jean-Pierre Timmermans, Wim Robberecht, Peter De Jonghe,[...]. Hum Mol Genet 2010
67
32

Abnormal small heat shock protein interactions involving neuropathy-associated HSP22 (HSPB8) mutants.
Jean-Marc Fontaine, Xiankui Sun, Adam D Hoppe, Stephanie Simon, Patrick Vicart, Michael J Welsh, Rainer Benndorf. FASEB J 2006
64
32

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy.
P Vicart, A Caron, P Guicheney, Z Li, M C Prévost, A Faure, D Chateau, F Chapon, F Tomé, J M Dupret,[...]. Nat Genet 1998
861
21


Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approach.
S J Kolb, P J Snyder, E J Poi, E A Renard, A Bartlett, S Gu, S Sutton, W D Arnold, M L Freimer, V H Lawson,[...]. Neurology 2010
74
28

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
315
20

A clinical phenotype of distal hereditary motor neuronopathy type II with a novel HSPB1 mutation.
Yoshihisa Ikeda, Akiko Abe, Chiho Ishida, Kazuya Takahashi, Kiyoshi Hayasaka, Masahito Yamada. J Neurol Sci 2009
37
54

A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype.
M Luigetti, G M Fabrizi, F Madia, M Ferrarini, A Conte, A Del Grande, G Tasca, P A Tonali, M Sabatelli. J Neurol Sci 2010
35
57

HspB8, a small heat shock protein mutated in human neuromuscular disorders, has in vivo chaperone activity in cultured cells.
Serena Carra, Mitchel Sivilotti, Aura T Chávez Zobel, Herman Lambert, Jacques Landry. Hum Mol Genet 2005
131
18

Mutant dynactin in motor neuron disease.
Imke Puls, Catherine Jonnakuty, Bernadette H LaMonte, Erika L F Holzbaur, Mariko Tokito, Eric Mann, Mary Kay Floeter, Kimberly Bidus, Dennis Drayna, Shin J Oh,[...]. Nat Genet 2003
707
18

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
18

HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients.
Simona Capponi, Alessandro Geroldi, Paola Fossa, Marina Grandis, Paola Ciotti, Rossella Gulli, Angelo Schenone, Paola Mandich, Emilia Bellone. J Peripher Nerv Syst 2011
46
39

Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments.
Anne Holmgren, Delphine Bouhy, Vicky De Winter, Bob Asselbergh, Jean-Pierre Timmermans, Joy Irobi, Vincent Timmerman. Acta Neuropathol 2013
31
58

Charcot-Marie-Tooth disease neurofilament mutations disrupt neurofilament assembly and axonal transport.
Janet Brownlees, Steven Ackerley, Andrew J Grierson, Nick J O Jacobsen, Kerry Shea, Brian H Anderton, P Nigel Leigh, Christopher E Shaw, Christopher C J Miller. Hum Mol Genet 2002
147
17

Intermediate filament interactions can be altered by HSP27 and alphaB-crystallin.
M D Perng, L Cairns, P van den IJssel, A Prescott, A M Hutcheson, R A Quinlan. J Cell Sci 1999
239
17

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene.
I V Mersiyanova, A V Perepelov, A V Polyakov, V F Sitnikov, E L Dadali, R B Oparin, A N Petrin, O V Evgrafov. Am J Hum Genet 2000
315
17



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
403
16

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
544
15

Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease.
A Jordanova, P De Jonghe, C F Boerkoel, H Takashima, E De Vriendt, C Ceuterick, J-J Martin, I J Butler, P Mancias, S Ch Papasozomenos,[...]. Brain 2003
199
15

Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival.
Susanna C Benn, Daniel Perrelet, Ann C Kato, Joachim Scholz, Isabelle Decosterd, Richard J Mannion, Joanna C Bakowska, Clifford J Woolf. Neuron 2002
200
14

Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 gene.
Paola Mandich, Marina Grandis, Alessandra Varese, Alessandro Geroldi, Massimo Acquaviva, Paola Ciotti, Rossella Gulli, Laura Doria-Lamba, Gian Maria Fabrizi, Gaia Giribaldi,[...]. J Child Neurol 2010
24
58

Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases.
Serena Carra, Alessandra Boncoraglio, Bart Kanon, Jeanette F Brunsting, Melania Minoia, Anil Rana, Michel J Vos, Kay Seidel, Ody C M Sibon, Harm H Kampinga. J Biol Chem 2010
65
21


Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport.
Raül Pérez-Ollé, Miguel A López-Toledano, Dmitry Goryunov, Noemi Cabrera-Poch, Leonidas Stefanis, Kristy Brown, Ronald K H Liem. J Neurochem 2005
86
15

Regulation of Hsp27 oligomerization, chaperone function, and protective activity against oxidative stress/tumor necrosis factor alpha by phosphorylation.
T Rogalla, M Ehrnsperger, X Preville, A Kotlyarov, G Lutsch, C Ducasse, C Paul, M Wieske, A P Arrigo, J Buchner,[...]. J Biol Chem 1999
582
13

Structure and properties of K141E mutant of small heat shock protein HSP22 (HspB8, H11) that is expressed in human neuromuscular disorders.
Maria V Kim, Alexei S Kasakov, Alim S Seit-Nebi, Steven B Marston, Nikolai B Gusev. Arch Biochem Biophys 2006
33
39

HspB8 and Bag3: a new chaperone complex targeting misfolded proteins to macroautophagy.
Serena Carra, Samuel J Seguin, Jacques Landry. Autophagy 2008
164
13

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
100
13

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
182
13

Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis.
Sara Benedetti, Stefano Carlo Previtali, Silvia Coviello, Marina Scarlato, Federica Cerri, Emanuela Di Pierri, Lara Piantoni, Ivana Spiga, Raffaella Fazio, Nilo Riva,[...]. Arch Neurol 2010
42
30


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
402
12

Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation.
Ki Wha Chung, Sang-Beom Kim, Sun Young Cho, Su Jin Hwang, Sun Wha Park, Sung Hee Kang, Joonki Kim, Jeong Hyun Yoo, Byung-Ok Choi. Exp Mol Med 2008
30
40


Mitofusin 2 tethers endoplasmic reticulum to mitochondria.
Olga Martins de Brito, Luca Scorrano. Nature 2008
12

Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3).
Xiankui Sun, Jean-Marc Fontaine, Adam D Hoppe, Serena Carra, Cheryl DeGuzman, Jody L Martin, Stephanie Simon, Patrick Vicart, Michael J Welsh, Jacques Landry,[...]. Cell Stress Chaperones 2010
27
44


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.