A citation-based method for searching scientific literature

Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M Remes, Alice Kaganovich, Sonja W Scholz, Jamie Duckworth, Jinhui Ding, Daniel W Harmer, Dena G Hernandez, Janel O Johnson, Kin Mok, Mina Ryten, Danyah Trabzuni, Rita J Guerreiro, Richard W Orrell, James Neal, Alex Murray, Justin Pearson, Iris E Jansen, David Sondervan, Harro Seelaar, Derek Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alex Gerhard, Julie Snowden, David Mann, David Neary, Michael A Nalls, Terhi Peuralinna, Lilja Jansson, Veli-Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä-Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chiò, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D Rothstein, Michael Sendtner, Carsten Drepper, Evan E Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana D Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel M Williams, Peter Heutink, Stuart Pickering-Brown, Huw R Morris, Pentti J Tienari, Bryan J Traynor. Neuron 2011
Times Cited: 2587







List of co-cited articles
1201 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Learning and memory: consolidation of fear.
Darran Yates. Nat Rev Neurosci 2014
80
1

What do we really know about the ubiquitin-proteasome pathway in muscle atrophy?
R T Jagoe, A L Goldberg. Curr Opin Clin Nutr Metab Care 2001
294
1




Amyotrophic lateral sclerosis: macro-EMG and twitch forces of single motor units.
R Dengler, A Konstanzer, G Küther, S Hesse, W Wolf, A Struppler. Muscle Nerve 1990
109
1

Cu/Zn superoxide dismutase-like immunoreactivity in Lewy body-like inclusions of sporadic amyotrophic lateral sclerosis.
N Shibata, A Hirano, M Kobayashi, S Sasaki, T Kato, S Matsumoto, Z Shiozawa, T Komori, A Ikemoto, T Umahara. Neurosci Lett 1994
118
1


Abnormalities of satellite cells function in amyotrophic lateral sclerosis.
Pierre-François Pradat, Aude Barani, Julia Wanschitz, Odile Dubourg, Anne Lombès, Anne Bigot, Vincent Mouly, Gaelle Bruneteau, François Salachas, Timothée Lenglet,[...]. Amyotroph Lateral Scler 2011
40
2

A polarizing question: do M1 and M2 microglia exist?
Richard M Ransohoff. Nat Neurosci 2016
663
1

HGFA Is an Injury-Regulated Systemic Factor that Induces the Transition of Stem Cells into GAlert.
Joseph T Rodgers, Matthew D Schroeder, Chanthia Ma, Thomas A Rando. Cell Rep 2017
53
1

The anti-inflammatory effect of exercise.
Anne Marie W Petersen, Bente Klarlund Pedersen. J Appl Physiol (1985) 2005
1

The role of semaphorin3A in myogenic regeneration and the formation of functional neuromuscular junctions on new fibres.
Judy E Anderson, Mai-Khoi Q Do, Nasibeh Daneshvar, Takahiro Suzuki, Junio Dort, Wataru Mizunoya, Ryuichi Tatsumi. Biol Rev Camb Philos Soc 2017
15
6


Neuregulin-1 promotes functional improvement by enhancing collateral sprouting in SOD1(G93A) ALS mice and after partial muscle denervation.
Renzo Mancuso, Anna Martínez-Muriana, Tatiana Leiva, David Gregorio, Lorena Ariza, Marta Morell, Jesús Esteban-Pérez, Alberto García-Redondo, Ana C Calvo, Gabriela Atencia-Cibreiro,[...]. Neurobiol Dis 2016
32
3

Decreased circulating ErbB4 ectodomain fragments as a read-out of impaired signaling function in amyotrophic lateral sclerosis.
Inmaculada Lopez-Font, Aitana Sogorb-Esteve, Míriam Javier-Torrent, Gunnar Brinkmalm, Mireia Herrando-Grabulosa, Belen García-Lareu, Janina Turon-Sans, Ricardo Rojas-García, Alberto Lleó, Carlos A Saura,[...]. Neurobiol Dis 2019
6
16

Transneuronal delivery of hyper-interleukin-6 enables functional recovery after severe spinal cord injury in mice.
Marco Leibinger, Charlotte Zeitler, Philipp Gobrecht, Anastasia Andreadaki, Günter Gisselmann, Dietmar Fischer. Nat Commun 2021
8
12

Markers of Accelerated Skeletal Muscle Regenerative Response in Murphy Roths Large Mice: Characteristics of Muscle Progenitor Cells and Circulating Factors.
Chieh Tseng, Krishna Sinha, Haiying Pan, Yan Cui, Ping Guo, Chih Yi Lin, Fan Yang, Zhenhan Deng, Holger K Eltzschig, Aiping Lu,[...]. Stem Cells 2019
5
20

Triathletes are over-represented in a population of patients with ALS.
Marc Gotkine, Yechiel Friedlander, Hagit Hochner. Amyotroph Lateral Scler Frontotemporal Degener 2014
21
4

Denervation-related alterations and biological activity of miRNAs contained in exosomes released by skeletal muscle fibers.
Rita De Gasperi, Sayyed Hamidi, Lauren M Harlow, Hanna Ksiezak-Reding, William A Bauman, Christopher P Cardozo. Sci Rep 2017
19
5


RNA targets of wild-type and mutant FET family proteins.
Jessica I Hoell, Erik Larsson, Simon Runge, Jeffrey D Nusbaum, Sujitha Duggimpudi, Thalia A Farazi, Markus Hafner, Arndt Borkhardt, Chris Sander, Thomas Tuschl. Nat Struct Mol Biol 2011
218
1


Investigating CCNF mutations in a Taiwanese cohort with amyotrophic lateral sclerosis.
Pei-Chien Tsai, Yi-Chu Liao, Po-Lin Chen, Yuh-Cherng Guo, Ying-Hao Chen, Kang-Yang Jih, Kon-Ping Lin, Bing-Wen Soong, Ching-Paio Tsai, Yi-Chung Lee. Neurobiol Aging 2018
6
16

Properties of Glial Cell at the Neuromuscular Junction Are Incompatible with Synaptic Repair in the SOD1G37R ALS Mouse Model.
Éric Martineau, Danielle Arbour, Joanne Vallée, Richard Robitaille. J Neurosci 2020
4
25

The serum lipid profiles of amyotrophic lateral sclerosis patients: A study from south-west China and a meta-analysis.
Rui Huang, Xiaoyan Guo, Xueping Chen, Zhenzhen Zheng, Qianqian Wei, Bei Cao, Yan Zeng, Huifang Shang. Amyotroph Lateral Scler Frontotemporal Degener 2015
34
2

Weight stability masks sarcopenia in elderly men and women.
D Gallagher, E Ruts, M Visser, S Heshka, R N Baumgartner, J Wang, R N Pierson, F X Pi-Sunyer, S B Heymsfield. Am J Physiol Endocrinol Metab 2000
279
1

Clinical care of patients with amyotrophic lateral sclerosis.
Aleksandar Radunović, Hiroshi Mitsumoto, P Nigel Leigh. Lancet Neurol 2007
86
1

Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patients.
Gaëlle Bruneteau, Stéphanie Bauché, Jose Luis Gonzalez de Aguilar, Guy Brochier, Nathalie Mandjee, Marie-Laure Tanguy, Ghulam Hussain, Anthony Behin, Frédéric Khiami, Elhadi Sariali,[...]. Ann Clin Transl Neurol 2015
34
2

Skeletal muscle satellite cells in amyotrophic lateral sclerosis.
Annarita Scaramozza, Valeria Marchese, Valentina Papa, Roberta Salaroli, Gianni Sorarù, Corrado Angelini, Giovanna Cenacchi. Ultrastruct Pathol 2014
23
4


Wildtype motoneurons, ALS-Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling.
Blandine Madji Hounoum, Sylvie Mavel, Emmanuelle Coque, Franck Patin, Patrick Vourc'h, Sylviane Marouillat, Lydie Nadal-Desbarats, Patrick Emond, Philippe Corcia, Christian R Andres,[...]. Glia 2017
29
3

Skeletal Muscle Satellite Cells, Mitochondria, and MicroRNAs: Their Involvement in the Pathogenesis of ALS.
Stavroula Tsitkanou, Paul A Della Gatta, Aaron P Russell. Front Physiol 2016
25
4

Impaired expression of insulin-like growth factor-1 system in skeletal muscle of amyotrophic lateral sclerosis patients.
Christian Lunetta, Massimo Serafini, Alessandro Prelle, Paolo Magni, Elena Dozio, Massimiliano Ruscica, Jenny Sassone, Clarissa Colciago, Maurizio Moggio, Massimo Corbo,[...]. Muscle Nerve 2012
29
3

Association of paraspinal and diaphragm denervation in ALS.
Mamede de Carvalho, Susana Pinto, Michael Swash. Amyotroph Lateral Scler 2010
28
3


Human aging, muscle mass, and fiber type composition.
J Lexell. J Gerontol A Biol Sci Med Sci 1995
786
1


Nogo-A regulates myogenesis via interacting with Filamin-C.
SunYoung Park, Ji-Hwan Park, Un-Beom Kang, Seong-Kyoon Choi, Ahmed Elfadl, H M Arif Ullah, Myung-Jin Chung, Ji-Yoon Son, Hyun Ho Yun, Jae-Min Park,[...]. Cell Death Discov 2021
2
50

CuZnSOD gene deletion targeted to skeletal muscle leads to loss of contractile force but does not cause muscle atrophy in adult mice.
Yiqiang Zhang, Carol Davis, George K Sakellariou, Yun Shi, Anna C Kayani, Daniel Pulliam, Arunabh Bhattacharya, Arlan Richardson, Malcolm J Jackson, Anne McArdle,[...]. FASEB J 2013
42
2


The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors.
Trevor N Stitt, Doreen Drujan, Brian A Clarke, Frank Panaro, Yekatarina Timofeyva, William O Kline, Michael Gonzalez, George D Yancopoulos, David J Glass. Mol Cell 2004
1

Neocortical glial cell numbers in human brains.
D P Pelvig, H Pakkenberg, A K Stark, B Pakkenberg. Neurobiol Aging 2008
279
1

Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.
Chun-Hong Xia, Elizabeth A Roberts, Lu-Shiun Her, Xinran Liu, David S Williams, Don W Cleveland, Lawrence S B Goldstein. J Cell Biol 2003
228
1



Terminal Schwann cells participate in neuromuscular synapse remodeling during reinnervation following nerve injury.
Hyuno Kang, Le Tian, Michelle Mikesh, Jeff W Lichtman, Wesley J Thompson. J Neurosci 2014
70
1

Potential therapeutic targets for ALS: MIR206, MIR208b and MIR499 are modulated during disease progression in the skeletal muscle of patients.
Lorena Di Pietro, Mirko Baranzini, Maria Grazia Berardinelli, Wanda Lattanzi, Mauro Monforte, Giorgio Tasca, Amelia Conte, Giandomenico Logroscino, Fabrizio Michetti, Enzo Ricci,[...]. Sci Rep 2017
27
3

Non-neuronal cells in amyotrophic lateral sclerosis - from pathogenesis to biomarkers.
Björn F Vahsen, Elizabeth Gray, Alexander G Thompson, Olaf Ansorge, Daniel C Anthony, Sally A Cowley, Kevin Talbot, Martin R Turner. Nat Rev Neurol 2021
3
33

The truncated C-terminal RNA recognition motif of TDP-43 protein plays a key role in forming proteinaceous aggregates.
Yi-Ting Wang, Pan-Hsien Kuo, Chien-Hao Chiang, Jhe-Ruei Liang, Yun-Ru Chen, Shuying Wang, James C K Shen, Hanna S Yuan. J Biol Chem 2013
63
1


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.