A citation-based method for searching scientific literature

Nicholas U Schwartz. Neurobiol Dis 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
85

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
57

Mutations in HspB1 and hereditary neuropathies.
Lydia K Muranova, Maria V Sudnitsyna, Sergei V Strelkov, Nikolai B Gusev. Cell Stress Chaperones 2020
12
57

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.
S M Ismailov, V P Fedotov, E L Dadali, A V Polyakov, C Van Broeckhoven, V I Ivanov, P De Jonghe, V Timmerman, O V Evgrafov. Eur J Hum Genet 2001
41
42

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
20
42

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
42

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
42

Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.
Hajime Tanabe, Yujiro Higuchi, Jun-Hui Yuan, Akihiro Hashiguchi, Akiko Yoshimura, Satoshi Ishihara, Satoshi Nozuma, Yuji Okamoto, Eiji Matsuura, Hiroyuki Ishiura,[...]. J Peripher Nerv Syst 2018
9
42

Small heat shock proteins in neurodegenerative diseases.
Leen Vendredy, Elias Adriaenssens, Vincent Timmerman. Cell Stress Chaperones 2020
21
42

Small heat shock proteins: Role in cellular functions and pathology.
Raman Bakthisaran, Ramakrishna Tangirala, Ch Mohan Rao. Biochim Biophys Acta 2015
246
28

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
28

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
28

MRI findings, patterns of disease distribution, and muscle fat fraction calculation in five patients with Charcot-Marie-Tooth type 2 F disease.
Michele Gaeta, Achille Mileto, Anna Mazzeo, Fabio Minutoli, Rita Di Leo, Nicola Settineri, Rocco Donato, Giorgio Ascenti, Alfredo Blandino. Skeletal Radiol 2012
34
28

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
28

Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience.
Marco Luigetti, Gian Maria Fabrizi, Giulia Bisogni, Angela Romano, Federica Taioli, Moreno Ferrarini, Daniela Bernardo, Paolo Maria Rossini, Mario Sabatelli. Clin Neurol Neurosurg 2016
15
28

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
28

Sequence, structure, and dynamic determinants of Hsp27 (HspB1) equilibrium dissociation are encoded by the N-terminal domain.
Ezelle T McDonald, Marco Bortolus, Hanane A Koteiche, Hassane S Mchaourab. Biochemistry 2012
66
28

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
201
28

Small heat shock proteins in inherited peripheral neuropathies.
Ines Dierick, Joy Irobi, Peter De Jonghe, Vincent Timmerman. Ann Med 2005
46
28



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
33
28

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
28

Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy.
Paolo Solla, Alessandro Vannelli, Alessandra Bolino, Giovanni Marrosu, Silvia Coviello, Maria Rita Murru, Stefania Tranquilli, Daniela Corongiu, Sara Benedetti, Maria Giovanna Marrosu. J Neurol Neurosurg Psychiatry 2010
27
28

HDAC6 regulates mitochondrial transport in hippocampal neurons.
Sigeng Chen, Geoffrey C Owens, Helen Makarenkova, David B Edelman. PLoS One 2010
179
14

Difference Tracker: ImageJ plugins for fully automated analysis of multiple axonal transport parameters.
Simon Andrews, Jonathan Gilley, Michael P Coleman. J Neurosci Methods 2010
41
14

Tau reduction prevents Abeta-induced defects in axonal transport.
Keith A Vossel, Kai Zhang, Jens Brodbeck, Aaron C Daub, Punita Sharma, Steven Finkbeiner, Bianxiao Cui, Lennart Mucke. Science 2010
361
14

Preclinical activity, pharmacodynamic, and pharmacokinetic properties of a selective HDAC6 inhibitor, ACY-1215, in combination with bortezomib in multiple myeloma.
Loredana Santo, Teru Hideshima, Andrew L Kung, Jen-Chieh Tseng, David Tamang, Min Yang, Matthew Jarpe, John H van Duzer, Ralph Mazitschek, Walter C Ogier,[...]. Blood 2012
437
14

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
Evan Reid, Mark Kloos, Allison Ashley-Koch, Lori Hughes, Simon Bevan, Ingrid K Svenson, Felicia Lennon Graham, Perry C Gaskell, Andrew Dearlove, Margaret A Pericak-Vance,[...]. Am J Hum Genet 2002
365
14


Development of Improved HDAC6 Inhibitors as Pharmacological Therapy for Axonal Charcot-Marie-Tooth Disease.
Veronick Benoy, Pieter Vanden Berghe, Matthew Jarpe, Philip Van Damme, Wim Robberecht, Ludo Van Den Bosch. Neurotherapeutics 2017
49
14

Imaging axonal transport of mitochondria in vivo.
Thomas Misgeld, Martin Kerschensteiner, Florence M Bareyre, Robert W Burgess, Jeff W Lichtman. Nat Methods 2007
288
14

Tubastatin A, an HDAC6 inhibitor, alleviates stroke-induced brain infarction and functional deficits: potential roles of α-tubulin acetylation and FGF-21 up-regulation.
Zhifei Wang, Yan Leng, Junyu Wang, Hsiao-Mei Liao, Joel Bergman, Peter Leeds, Alan Kozikowski, De-Maw Chuang. Sci Rep 2016
71
14

KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction.
Jessica Duis, Shannon Dean, Carolyn Applegate, Amy Harper, Rui Xiao, Weimin He, James D Dollar, Lisa R Sun, Marta Biderman Waberski, Thomas O Crawford,[...]. Ann Neurol 2016
31
14

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
14

In vivo imaging of axonal transport in murine motor and sensory neurons.
Katherine L Gibbs, Bernadett Kalmar, James N Sleigh, Linda Greensmith, Giampietro Schiavo. J Neurosci Methods 2016
33
14

Axonal transport declines with age in two distinct phases separated by a period of relative stability.
Stefan Milde, Robert Adalbert, M Handan Elaman, Michael P Coleman. Neurobiol Aging 2015
55
14

Axonopathy and transport deficits early in the pathogenesis of Alzheimer's disease.
Gorazd B Stokin, Concepción Lillo, Tomás L Falzone, Richard G Brusch, Edward Rockenstein, Stephanie L Mount, Rema Raman, Peter Davies, Eliezer Masliah, David S Williams,[...]. Science 2005
855
14



Differential regulation of dynein and kinesin motor proteins by tau.
Ram Dixit, Jennifer L Ross, Yale E Goldman, Erika L F Holzbaur. Science 2008
631
14

HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patients.
Wenting Guo, Maximilian Naujock, Laura Fumagalli, Tijs Vandoorne, Pieter Baatsen, Ruben Boon, Laura Ordovás, Abdulsamie Patel, Marc Welters, Thomas Vanwelden,[...]. Nat Commun 2017
169
14

Hydroxamates: relationships between structure and plasma stability.
Marion Flipo, Julie Charton, Akila Hocine, Sandrine Dassonneville, Benoit Deprez, Rebecca Deprez-Poulain. J Med Chem 2009
79
14

Characterization of New Transgenic Mouse Models for Two Charcot-Marie-Tooth-Causing HspB1 Mutations using the Rosa26 Locus.
Delphine Bouhy, Thomas Geuens, Vicky De Winter, Leonardo Almeida-Souza, Istvan Katona, Joachim Weis, Tino Hochepied, Steven Goossens, Jody J Haigh, Sophie Janssens,[...]. J Neuromuscul Dis 2016
9
14

Releasing Syntaphilin Removes Stressed Mitochondria from Axons Independent of Mitophagy under Pathophysiological Conditions.
Mei-Yao Lin, Xiu-Tang Cheng, Prasad Tammineni, Yuxiang Xie, Bing Zhou, Qian Cai, Zu-Hang Sheng. Neuron 2017
97
14

Overexpression of mutant HSP27 causes axonal neuropathy in mice.
Jinho Lee, Sung-Chul Jung, Jaesoon Joo, Yu-Ri Choi, Hyo Won Moon, Geon Kwak, Ha Kyung Yeo, Ji-Su Lee, Hye-Jee Ahn, Namhee Jung,[...]. J Biomed Sci 2015
27
14

Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development.
Manisha Juneja, Joshua Burns, Mario A Saporta, Vincent Timmerman. J Neurol Neurosurg Psychiatry 2019
44
14

Rational design and simple chemistry yield a superior, neuroprotective HDAC6 inhibitor, tubastatin A.
Kyle V Butler, Jay Kalin, Camille Brochier, Guilio Vistoli, Brett Langley, Alan P Kozikowski. J Am Chem Soc 2010
495
14

Tubulin acetylation protects long-lived microtubules against mechanical ageing.
Didier Portran, Laura Schaedel, Zhenjie Xu, Manuel Théry, Maxence V Nachury. Nat Cell Biol 2017
230
14

HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth disease.
Veronick Benoy, Lawrence Van Helleputte, Robert Prior, Constantin d'Ydewalle, Wanda Haeck, Natasja Geens, Wendy Scheveneels, Begga Schevenels, M Zameel Cader, Kevin Talbot,[...]. Brain 2018
70
14


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.