A citation-based method for searching scientific literature

Simona Capponi, Alessandro Geroldi, Paola Fossa, Marina Grandis, Paola Ciotti, Rossella Gulli, Angelo Schenone, Paola Mandich, Emilia Bellone. J Peripher Nerv Syst 2011
Times Cited: 47







List of co-cited articles
519 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
441
68

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
141
59

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
79
44

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

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
70
42

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
99
40

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
74
40

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
40


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
317
34

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
43


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
57
31


The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan.
Kon-Ping Lin, Bing-Wen Soong, Chih-Chao Yang, Li-Wen Huang, Ming-Hong Chang, I-Hui Lee, Anthony Antonellis, Yi-Chung Lee. PLoS One 2011
73
29

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
32
43

Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family.
Claudia Stancanelli, Gian Maria Fabrizi, Moreno Ferrarini, Tiziana Cavallaro, Federica Taioli, Rita Di Leo, Massimo Russo, Luca Gentile, Antonio Toscano, Giuseppe Vita,[...]. Neurol Sci 2015
18
77

Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations.
Andoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, Yann Péréon, Elias Adriaenssens, Mansour Haidar, Simona Capponi, Thierry Maisonobe, Emmanuel Fournier, Odile Dubourg,[...]. Hum Mutat 2017
36
38

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
54

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
75
27


Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress.
Emil Ylikallio, Svetlana Konovalova, Yogesh Dhungana, Taru Hilander, Nella Junna, Juhani V Partanen, Jussi P Toppila, Mari Auranen, Henna Tyynismaa. BBA Clin 2015
23
56

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
864
25

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
70
25

The distal hereditary motor neuropathies.
Alexander M Rossor, Bernadett Kalmar, Linda Greensmith, Mary M Reilly. J Neurol Neurosurg Psychiatry 2012
141
25


Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1.
Simona Capponi, Thomas Geuens, Alessandro Geroldi, Paola Origone, Simonetta Verdiani, Elena Cichero, Elias Adriaenssens, Vicky De Winter, Monica Bandettini di Poggio, Marco Barberis,[...]. Hum Mutat 2016
33
36

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
131
23

Small heat shock proteins HSP27 (HspB1), αB-crystallin (HspB5) and HSP22 (HspB8) as regulators of cell death.
Julie Acunzo, Maria Katsogiannou, Palma Rocchi. Int J Biochem Cell Biol 2012
205
23

Large potentials of small heat shock proteins.
Evgeny V Mymrikov, Alim S Seit-Nebi, Nikolai B Gusev. Physiol Rev 2011
293
23

A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2.
Alexander M Rossor, Gabrielle L Davidson, Julian Blake, James M Polke, Sinéad M Murphy, Henry Houlden, Amy Innes, Bernadett Kalmar, Linda Greensmith, Mary M Reilly. J Peripher Nerv Syst 2012
14
78

Neuropathy- and myopathy-associated mutations in human small heat shock proteins: Characteristics and evolutionary history of the mutation sites.
Rainer Benndorf, Jody L Martin, Sergei L Kosakovsky Pond, Joel O Wertheim. Mutat Res Rev Mutat Res 2014
43
25

HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomes.
Alice S Kwok, Kanchan Phadwal, Bradley J Turner, Peter L Oliver, Annie Raw, Anna Katharina Simon, Kevin Talbot, Vishwas R Agashe. J Neurochem 2011
41
24

Small heat shock proteins and α-crystallins: dynamic proteins with flexible functions.
Eman Basha, Heather O'Neill, Elizabeth Vierling. Trends Biochem Sci 2012
331
21

Three-dimensional structure of α-crystallin domain dimers of human small heat shock proteins HSPB1 and HSPB6.
E V Baranova, S D Weeks, S Beelen, O V Bukach, N B Gusev, S V Strelkov. J Mol Biol 2011
78
21

Structure and properties of G84R and L99M mutants of human small heat shock protein HspB1 correlating with motor neuropathy.
Victoria V Nefedova, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Arch Biochem Biophys 2013
20
50

Physico-chemical properties of R140G and K141Q mutants of human small heat shock protein HspB1 associated with hereditary peripheral neuropathies.
Victoria V Nefedova, Petr N Datskevich, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Biochimie 2013
25
40

The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy.
Christina DiVincenzo, Christopher D Elzinga, Adam C Medeiros, Izabela Karbassi, Jeremiah R Jones, Matthew C Evans, Corey D Braastad, Crystal M Bishop, Malgorzata Jaremko, Zhenyuan Wang,[...]. Mol Genet Genomic Med 2014
119
21

Biochemical characterization of small heat shock protein HspB8 (Hsp22)-Bag3 interaction.
Anton A Shemetov, Nikolai B Gusev. Arch Biochem Biophys 2011
40
22

A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L.
Khriezhanuo Nakhro, Jin-Mo Park, Ye Jin Kim, Bo Ram Yoon, Jeong Hyun Yoo, Heasoo Koo, Byung-Ok Choi, Ki Wha Chung. Neuromuscul Disord 2013
32
28

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
314
19

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
43
20

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
19


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
30

Late onset dHMN II caused by c.404C>G mutation in HSPB1 gene.
Moritz Oberstadt, Diana Mitter, Joseph Classen, Petra Baum. J Peripher Nerv Syst 2016
11
81

Novel HSPB1 mutation causes both motor neuronopathy and distal myopathy.
D J Lewis-Smith, J Duff, A Pyle, H Griffin, T Polvikoski, D Birchall, R Horvath, P F Chinnery. Neurol Genet 2016
19
47

Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene.
Alexander M Rossor, Jasper M Morrow, James M Polke, Sinead M Murphy, Henry Houlden, Matilde Laura, Hadi Manji, Julian Blake, Mary M Reilly. Neuromuscul Disord 2017
21
42

HspB8 and Bag3: a new chaperone complex targeting misfolded proteins to macroautophagy.
Serena Carra, Samuel J Seguin, Jacques Landry. Autophagy 2008
169
17

Effect of mutations in the beta5-beta7 loop on the structure and properties of human small heat shock protein HSP22 (HspB8, H11).
Alexei S Kasakov, Olesya V Bukach, Alim S Seit-Nebi, Steven B Marston, Nikolai B Gusev. FEBS J 2007
31
25


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.