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: 48



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
Times Cited: 311




List of shared articles



Times cited

Chaperonopathies: Spotlight on Hereditary Motor Neuropathies.
Vincenzo Lupo, Carmen Aguado, Erwin Knecht, Carmen Espinós. Front Mol Biosci 2016
17

Charcot-Marie-Tooth 2F (Hsp27 mutations): A review.
Nicholas U Schwartz. Neurobiol Dis 2019
7

Human HspB1, HspB3, HspB5 and HspB8: Shaping these disease factors during vertebrate evolution.
Rainer Benndorf, Ryan Velazquez, Jordan D Zehr, Sergei L Kosakovsky Pond, Jody L Martin, Alexander G Lucaci. Cell Stress Chaperones 2022
0

Mutations in HspB1 and hereditary neuropathies.
Lydia K Muranova, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Cell Stress Chaperones 2020
14

Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.
Jaakko Sarparanta, Per Harald Jonson, Sabita Kawan, Bjarne Udd. Int J Mol Sci 2020
25

Proline isomerization in the C-terminal region of HSP27.
T Reid Alderson, Justin L P Benesch, Andrew J Baldwin. Cell Stress Chaperones 2017
18

A novel p.T139M mutation in HSPB1 highlighting the phenotypic spectrum in a family.
Jakkrit Amornvit, Mehmet E Yalvac, Lei Chen, Zarife Sahenk. Brain Behav 2017
11

Mutations of small heat shock proteins and human congenital diseases.
P N Datskevich, V V Nefedova, M V Sudnitsyna, N B Gusev. Biochemistry (Mosc) 2012
32

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

Mitochondrial deficits and abnormal mitochondrial retrograde axonal transport play a role in the pathogenesis of mutant Hsp27-induced Charcot Marie Tooth Disease.
Bernadett Kalmar, Amy Innes, Klaus Wanisch, Alicia Koyen Kolaszynska, Amelie Pandraud, Gavin Kelly, Andrey Y Abramov, Mary M Reilly, Giampietro Schiavo, Linda Greensmith. Hum Mol Genet 2017
32

Small Heat Shock Proteins and Distal Hereditary Neuropathies.
V V Nefedova, L K Muranova, M V Sudnitsyna, A S Ryzhavskaya, N B Gusev. Biochemistry (Mosc) 2015
18

Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations.
Elena Abati, Stefania Magri, Megi Meneri, Giulia Manenti, Daniele Velardo, Francesca Balistreri, Chiara Pisciotta, Paola Saveri, Nereo Bresolin, Giacomo Pietro Comi,[...]. Ann Clin Transl Neurol 2021
3

Small heat shock proteins in neurodegenerative diseases.
Leen Vendredy, Elias Adriaenssens, Vincent Timmerman. Cell Stress Chaperones 2020
30

Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.
Delphine Bouhy, Vincent Timmerman. Ann Neurol 2013
23


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
38

Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series.
Matthew Katz, Mark Davis, Fleur C Garton, Robert Henderson, Vanda Bharti, Naomi Wray, Pamela McCombe. J Neurol Sci 2020
8

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

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