A citation-based method for searching scientific literature

Elsa Fritz, Pamela Izaurieta, Alexandra Weiss, Franco R Mir, Patricio Rojas, David Gonzalez, Fabiola Rojas, Robert H Brown, Rodolfo Madrid, Brigitte van Zundert. J Neurophysiol 2013
Times Cited: 69







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



Times Cited
  Times     Co-cited
Similarity


Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons.
Makiko Nagai, Diane B Re, Tetsuya Nagata, Alcmène Chalazonitis, Thomas M Jessell, Hynek Wichterle, Serge Przedborski. Nat Neurosci 2007
862
53

Astrocytes from familial and sporadic ALS patients are toxic to motor neurons.
Amanda M Haidet-Phillips, Mark E Hester, Carlos J Miranda, Kathrin Meyer, Lyndsey Braun, Ashley Frakes, SungWon Song, Shibi Likhite, Matthew J Murtha, Kevin D Foust,[...]. Nat Biotechnol 2011
529
46

Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model.
Francesco Paolo Di Giorgio, Monica A Carrasco, Michelle C Siao, Tom Maniatis, Kevin Eggan. Nat Neurosci 2007
585
37

Astrocytes expressing mutant SOD1 and TDP43 trigger motoneuron death that is mediated via sodium channels and nitroxidative stress.
Fabiola Rojas, Nicole Cortes, Sebastian Abarzua, Agnieszka Dyrda, Brigitte van Zundert. Front Cell Neurosci 2014
75
33

Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons.
Brian J Wainger, Evangelos Kiskinis, Cassidy Mellin, Ole Wiskow, Steve S W Han, Jackson Sandoe, Numa P Perez, Luis A Williams, Seungkyu Lee, Gabriella Boulting,[...]. Cell Rep 2014
393
30

Non-cell-autonomous effect of human SOD1 G37R astrocytes on motor neurons derived from human embryonic stem cells.
Maria C N Marchetto, Alysson R Muotri, Yangling Mu, Alan M Smith, Gabriela G Cezar, Fred H Gage. Cell Stem Cell 2008
322
28

Direct conversion of patient fibroblasts demonstrates non-cell autonomous toxicity of astrocytes to motor neurons in familial and sporadic ALS.
Kathrin Meyer, Laura Ferraiuolo, Carlos J Miranda, Shibi Likhite, Sohyun McElroy, Samantha Renusch, Dara Ditsworth, Clotilde Lagier-Tourenne, Richard A Smith, John Ravits,[...]. Proc Natl Acad Sci U S A 2014
220
28

Necroptosis drives motor neuron death in models of both sporadic and familial ALS.
Diane B Re, Virginia Le Verche, Changhao Yu, Mackenzie W Amoroso, Kristin A Politi, Sudarshan Phani, Burcin Ikiz, Lucas Hoffmann, Martijn Koolen, Tetsuya Nagata,[...]. Neuron 2014
268
28

Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis.
Koji Yamanaka, Seung Joo Chun, Severine Boillee, Noriko Fujimori-Tonou, Hirofumi Yamashita, David H Gutmann, Ryosuke Takahashi, Hidemi Misawa, Don W Cleveland. Nat Neurosci 2008
795
26

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.
M E Gurney, H Pu, A Y Chiu, M C Dal Canto, C Y Polchow, D D Alexander, J Caliendo, A Hentati, Y W Kwon, H X Deng. Science 1994
26

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
24

Neonatal neuronal circuitry shows hyperexcitable disturbance in a mouse model of the adult-onset neurodegenerative disease amyotrophic lateral sclerosis.
Brigitte van Zundert, Marieke H Peuscher, Meri Hynynen, Adam Chen, Rachael L Neve, Robert H Brown, Martha Constantine-Paton, Mark C Bellingham. J Neurosci 2008
174
24


Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
D R Rosen, T Siddique, D Patterson, D A Figlewicz, P Sapp, A Hentati, D Donaldson, J Goto, J P O'Regan, H X Deng. Nature 1993
24

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond.
Hristelina Ilieva, Magdalini Polymenidou, Don W Cleveland. J Cell Biol 2009
742
21

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
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,[...]. Neuron 2011
21

Onset and progression in inherited ALS determined by motor neurons and microglia.
Séverine Boillée, Koji Yamanaka, Christian S Lobsiger, Neal G Copeland, Nancy A Jenkins, George Kassiotis, George Kollias, Don W Cleveland. Science 2006
20

Human embryonic stem cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation.
Francesco Paolo Di Giorgio, Gabriella L Boulting, Samuel Bobrowicz, Kevin C Eggan. Cell Stem Cell 2008
339
20

Mitochondrial dysfunction in SOD1G93A-bearing astrocytes promotes motor neuron degeneration: prevention by mitochondrial-targeted antioxidants.
Patricia Cassina, Adriana Cassina, Mariana Pehar, Raquel Castellanos, Mandi Gandelman, Andrés de León, Kristine M Robinson, Ronald P Mason, Joseph S Beckman, Luis Barbeito,[...]. J Neurosci 2008
223
20

Astrocytes carrying the superoxide dismutase 1 (SOD1G93A) mutation induce wild-type motor neuron degeneration in vivo.
Sophia T Papadeas, Sarah E Kraig, Colin O'Banion, Angelo C Lepore, Nicholas J Maragakis. Proc Natl Acad Sci U S A 2011
135
20

Reactive oxygen species trigger motoneuron death in non-cell-autonomous models of ALS through activation of c-Abl signaling.
Fabiola Rojas, David Gonzalez, Nicole Cortes, Estibaliz Ampuero, Diego E Hernández, Elsa Fritz, Sebastián Abarzua, Alexis Martinez, Alvaro A Elorza, Alejandra Alvarez,[...]. Front Cell Neurosci 2015
54
25

Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
A M Clement, M D Nguyen, E A Roberts, M L Garcia, S Boillée, M Rule, A P McMahon, W Doucette, D Siwek, R J Ferrante,[...]. Science 2003
805
18

Astrocyte pathology and the absence of non-cell autonomy in an induced pluripotent stem cell model of TDP-43 proteinopathy.
Andrea Serio, Bilada Bilican, Sami J Barmada, Dale Michael Ando, Chen Zhao, Rick Siller, Karen Burr, Ghazal Haghi, David Story, Agnes Lumi Nishimura,[...]. Proc Natl Acad Sci U S A 2013
236
18


Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival.
Smita Saxena, Francesco Roselli, Katyayani Singh, Kerstin Leptien, Jean-Pierre Julien, Francois Gros-Louis, Pico Caroni. Neuron 2013
179
18

Phenotypically aberrant astrocytes that promote motoneuron damage in a model of inherited amyotrophic lateral sclerosis.
Pablo Díaz-Amarilla, Silvia Olivera-Bravo, Emiliano Trias, Andrea Cragnolini, Laura Martínez-Palma, Patricia Cassina, Joseph Beckman, Luis Barbeito. Proc Natl Acad Sci U S A 2011
119
18

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Manuela Neumann, Deepak M Sampathu, Linda K Kwong, Adam C Truax, Matthew C Micsenyi, Thomas T Chou, Jennifer Bruce, Theresa Schuck, Murray Grossman, Christopher M Clark,[...]. Science 2006
17

Molecular biology of amyotrophic lateral sclerosis: insights from genetics.
Piera Pasinelli, Robert H Brown. Nat Rev Neurosci 2006
823
17

Targeting RNA foci in iPSC-derived motor neurons from ALS patients with a C9ORF72 repeat expansion.
Dhruv Sareen, Jacqueline G O'Rourke, Pratap Meera, A K M G Muhammad, Sharday Grant, Megan Simpkinson, Shaughn Bell, Sharon Carmona, Loren Ornelas, Anais Sahabian,[...]. Sci Transl Med 2013
467
17


Early pathogenesis in the adult-onset neurodegenerative disease amyotrophic lateral sclerosis.
Brigitte van Zundert, Pamela Izaurieta, Elsa Fritz, Francisco J Alvarez. J Cell Biochem 2012
55
20

RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention.
Christopher J Donnelly, Ping-Wu Zhang, Jacqueline T Pham, Aaron R Haeusler, Nipun A Mistry, Svetlana Vidensky, Elizabeth L Daley, Erin M Poth, Benjamin Hoover, Daniel M Fines,[...]. Neuron 2013
614
15

Decoding ALS: from genes to mechanism.
J Paul Taylor, Robert H Brown, Don W Cleveland. Nature 2016
15

ALS: a disease of motor neurons and their nonneuronal neighbors.
Séverine Boillée, Christine Vande Velde, Don W Cleveland. Neuron 2006
14

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
Caroline Vance, Boris Rogelj, Tibor Hortobágyi, Kurt J De Vos, Agnes Lumi Nishimura, Jemeen Sreedharan, Xun Hu, Bradley Smith, Deborah Ruddy, Paul Wright,[...]. Science 2009
14

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
Jemeen Sreedharan, Ian P Blair, Vineeta B Tripathi, Xun Hu, Caroline Vance, Boris Rogelj, Steven Ackerley, Jennifer C Durnall, Kelly L Williams, Emanuele Buratti,[...]. Science 2008
14

Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS mice.
Jason J Kuo, Martijn Schonewille, Teepu Siddique, Annet N A Schults, Ronggen Fu, Peter R Bär, Roberta Anelli, C J Heckman, Alfons B A Kroese. J Neurophysiol 2004
137
14


Upregulation of persistent sodium conductances in familial ALS.
Steve Vucic, Matthew C Kiernan. J Neurol Neurosurg Psychiatry 2010
58
17

State of play in amyotrophic lateral sclerosis genetics.
Alan E Renton, Adriano Chiò, Bryan J Traynor. Nat Neurosci 2014
965
14

Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity.
Philip Van Damme, Elke Bogaert, Maarten Dewil, Nicole Hersmus, Dora Kiraly, Wendy Scheveneels, Ilse Bockx, Dries Braeken, Nathalie Verpoorten, Kristien Verhoeven,[...]. Proc Natl Acad Sci U S A 2007
147
14

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.
L I Bruijn, M W Becher, M K Lee, K L Anderson, N A Jenkins, N G Copeland, S S Sisodia, J D Rothstein, D R Borchelt, D L Price,[...]. Neuron 1997
14

Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability.
Anna-Claire Devlin, Karen Burr, Shyamanga Borooah, Joshua D Foster, Elaine M Cleary, Imbisaat Geti, Ludovic Vallier, Christopher E Shaw, Siddharthan Chandran, Gareth B Miles. Nat Commun 2015
180
14

Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS.
Daryl A Bosco, Gerardo Morfini, N Murat Karabacak, Yuyu Song, Francois Gros-Louis, Piera Pasinelli, Holly Goolsby, Benjamin A Fontaine, Nathan Lemay, Diane McKenna-Yasek,[...]. Nat Neurosci 2010
480
13

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
T J Kwiatkowski, D A Bosco, A L Leclerc, E Tamrazian, C R Vanderburg, C Russ, A Davis, J Gilchrist, E J Kasarskis, T Munsat,[...]. Science 2009
13

Early electrophysiological abnormalities in lumbar motoneurons in a transgenic mouse model of amyotrophic lateral sclerosis.
Cyril Bories, Julien Amendola, Boris Lamotte d'Incamps, Jacques Durand. Eur J Neurosci 2007
95
13

Trehalose delays the progression of amyotrophic lateral sclerosis by enhancing autophagy in motoneurons.
Karen Castillo, Melissa Nassif, Vicente Valenzuela, Fabiola Rojas, Soledad Matus, Gabriela Mercado, Felipe A Court, Brigitte van Zundert, Claudio Hetz. Autophagy 2013
233
13


Early excitability changes in lumbar motoneurons of transgenic SOD1G85R and SOD1G(93A-Low) mice.
Arnaud Pambo-Pambo, Jacques Durand, Jean-Patrick Gueritaud. J Neurophysiol 2009
75
13

Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.
Shuo-Chien Ling, Magdalini Polymenidou, Don W Cleveland. Neuron 2013
986
13


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.