A citation-based method for searching scientific literature

Emma F Smith, Pamela J Shaw, Kurt J De Vos. Neurosci Lett 2019
Times Cited: 192







List of co-cited articles
1695 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
19

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
19

Amyotrophic Lateral Sclerosis.
Robert H Brown, Ammar Al-Chalabi. N Engl J Med 2017
718
17

Decoding ALS: from genes to mechanism.
J Paul Taylor, Robert H Brown, Don W Cleveland. Nature 2016
998
15

The inhibition of TDP-43 mitochondrial localization blocks its neuronal toxicity.
Wenzhang Wang, Luwen Wang, Junjie Lu, Sandra L Siedlak, Hisashi Fujioka, Jingjing Liang, Sirui Jiang, Xiaopin Ma, Zhen Jiang, Edroaldo Lummertz da Rocha,[...]. Nat Med 2016
187
15

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Tetsuaki Arai, Masato Hasegawa, Haruhiko Akiyama, Kenji Ikeda, Takashi Nonaka, Hiroshi Mori, David Mann, Kuniaki Tsuchiya, Mari Yoshida, Yoshio Hashizume,[...]. Biochem Biophys Res Commun 2006
14

Amyotrophic lateral sclerosis.
Orla Hardiman, Ammar Al-Chalabi, Adriano Chio, Emma M Corr, Giancarlo Logroscino, Wim Robberecht, Pamela J Shaw, Zachary Simmons, Leonard H van den Berg. Nat Rev Dis Primers 2017
487
14

Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients.
Falk R Wiedemann, Giovanni Manfredi, Christian Mawrin, M Flint Beal, Eric A Schon. J Neurochem 2002
234
14

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
14


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
13

FUS Interacts with HSP60 to Promote Mitochondrial Damage.
Jianwen Deng, Mengxue Yang, Yanbo Chen, Xiaoping Chen, Jianghong Liu, Shufeng Sun, Haipeng Cheng, Yang Li, Eileen H Bigio, Marsel Mesulam,[...]. PLoS Genet 2015
102
13

The ALS disease-associated mutant TDP-43 impairs mitochondrial dynamics and function in motor neurons.
Wenzhang Wang, Li Li, Wen-Lang Lin, Dennis W Dickson, Leonard Petrucelli, Teng Zhang, Xinglong Wang. Hum Mol Genet 2013
173
13

Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models.
Jordi Magrané, Czrina Cortez, Wen-Biao Gan, Giovanni Manfredi. Hum Mol Genet 2014
193
12

Oxidative stress in ALS: key role in motor neuron injury and therapeutic target.
Siân C Barber, Pamela J Shaw. Free Radic Biol Med 2010
377
12

ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Rita Mejzini, Loren L Flynn, Ianthe L Pitout, Sue Fletcher, Steve D Wilton, P Anthony Akkari. Front Neurosci 2019
215
12

TDP-43 induces mitochondrial damage and activates the mitochondrial unfolded protein response.
Peng Wang, Jianwen Deng, Jie Dong, Jianghong Liu, Eileen H Bigio, Marsel Mesulam, Tao Wang, Lei Sun, Li Wang, Alan Yueh-Luen Lee,[...]. PLoS Genet 2019
82
14

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
Axel Freischmidt, Thomas Wieland, Benjamin Richter, Wolfgang Ruf, Veronique Schaeffer, Kathrin Müller, Nicolai Marroquin, Frida Nordin, Annemarie Hübers, Patrick Weydt,[...]. Nat Neurosci 2015
507
11

Amyotrophic lateral sclerosis.
Michael A van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R Jeroen Pasterkamp, Jan H Veldink, Leonard H van den Berg. Lancet 2017
495
11

Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts.
Elisa Onesto, Claudia Colombrita, Valentina Gumina, Maria Orietta Borghi, Sabrina Dusi, Alberto Doretti, Gigliola Fagiolari, Federica Invernizzi, Maurizio Moggio, Valeria Tiranti,[...]. Acta Neuropathol Commun 2016
95
11

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
10

TBK1: a new player in ALS linking autophagy and neuroinflammation.
James A Oakes, Maria C Davies, Mark O Collins. Mol Brain 2017
147
10


Impaired glucose tolerance in patients with amyotrophic lateral sclerosis.
Pierre-Francois Pradat, Gaelle Bruneteau, Paul H Gordon, Luc Dupuis, Dominique Bonnefont-Rousselot, Dominique Simon, Francois Salachas, Philippe Corcia, Vincent Frochot, Jean-Marc Lacorte,[...]. Amyotroph Lateral Scler 2010
116
9

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
9

Misfolded mutant SOD1 directly inhibits VDAC1 conductance in a mouse model of inherited ALS.
Adrian Israelson, Nir Arbel, Sandrine Da Cruz, Hristelina Ilieva, Koji Yamanaka, Varda Shoshan-Barmatz, Don W Cleveland. Neuron 2010
218
9

Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.
Shuo-Chien Ling, Magdalini Polymenidou, Don W Cleveland. Neuron 2013
985
9

Molecular Mechanisms of TDP-43 Misfolding and Pathology in Amyotrophic Lateral Sclerosis.
Archana Prasad, Vidhya Bharathi, Vishwanath Sivalingam, Amandeep Girdhar, Basant K Patel. Front Mol Neurosci 2019
229
9

State of play in amyotrophic lateral sclerosis genetics.
Alan E Renton, Adriano Chiò, Bryan J Traynor. Nat Neurosci 2014
959
9

C9orf72 Hexanucleotide Expansions Are Associated with Altered Endoplasmic Reticulum Calcium Homeostasis and Stress Granule Formation in Induced Pluripotent Stem Cell-Derived Neurons from Patients with Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.
Ruxandra Dafinca, Jakub Scaber, Nida'a Ababneh, Tatjana Lalic, Gregory Weir, Helen Christian, Jane Vowles, Andrew G L Douglas, Alexandra Fletcher-Jones, Cathy Browne,[...]. Stem Cells 2016
135
9


Poly(GR) in C9ORF72-Related ALS/FTD Compromises Mitochondrial Function and Increases Oxidative Stress and DNA Damage in iPSC-Derived Motor Neurons.
Rodrigo Lopez-Gonzalez, Yubing Lu, Tania F Gendron, Anna Karydas, Helene Tran, Dejun Yang, Leonard Petrucelli, Bruce L Miller, Sandra Almeida, Fen-Biao Gao. Neuron 2016
210
9

C9ORF72-ALS/FTD-associated poly(GR) binds Atp5a1 and compromises mitochondrial function in vivo.
So Yoen Choi, Rodrigo Lopez-Gonzalez, Gopinath Krishnan, Hannah L Phillips, Alissa Nana Li, William W Seeley, Wei-Dong Yao, Sandra Almeida, Fen-Biao Gao. Nat Neurosci 2019
88
9

Dyslipidemia is a protective factor in amyotrophic lateral sclerosis.
L Dupuis, P Corcia, A Fergani, J-L Gonzalez De Aguilar, D Bonnefont-Rousselot, R Bittar, D Seilhean, J-J Hauw, L Lacomblez, J-P Loeffler,[...]. Neurology 2008
351
8

Amyotrophic lateral sclerosis.
Matthew C Kiernan, Steve Vucic, Benjamin C Cheah, Martin R Turner, Andrew Eisen, Orla Hardiman, James R Burrell, Margaret C Zoing. Lancet 2011
8

C9orf72-mediated ALS and FTD: multiple pathways to disease.
Rubika Balendra, Adrian M Isaacs. Nat Rev Neurol 2018
252
8

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
8

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.
Kohji Mori, Shih-Ming Weng, Thomas Arzberger, Stephanie May, Kristin Rentzsch, Elisabeth Kremmer, Bettina Schmid, Hans A Kretzschmar, Marc Cruts, Christine Van Broeckhoven,[...]. Science 2013
832
8

Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Elizabeth T Cirulli, Brittany N Lasseigne, Slavé Petrovski, Peter C Sapp, Patrick A Dion, Claire S Leblond, Julien Couthouis, Yi-Fan Lu, Quanli Wang, Brian J Krueger,[...]. Science 2015
613
8


Hypermetabolism in ALS patients: an early and persistent phenomenon.
C Bouteloup, J-C Desport, P Clavelou, N Guy, H Derumeaux-Burel, A Ferrier, P Couratier. J Neurol 2009
216
8

Energy metabolism in amyotrophic lateral sclerosis.
Luc Dupuis, Pierre-François Pradat, Albert C Ludolph, Jean-Philippe Loeffler. Lancet Neurol 2011
334
8

TDP-43 Triggers Mitochondrial DNA Release via mPTP to Activate cGAS/STING in ALS.
Chien-Hsiung Yu, Sophia Davidson, Cassandra R Harapas, James B Hilton, Michael J Mlodzianoski, Pawat Laohamonthonkul, Cynthia Louis, Ronnie Ren Jie Low, Jonas Moecking, Dominic De Nardo,[...]. Cell 2020
148
8

Inhibition of Drp1/Fis1 interaction slows progression of amyotrophic lateral sclerosis.
Amit U Joshi, Nay L Saw, Hannes Vogel, Anna D Cunnigham, Mehrdad Shamloo, Daria Mochly-Rosen. EMBO Mol Med 2018
76
10

ALS/FTD-associated FUS activates GSK-3β to disrupt the VAPB-PTPIP51 interaction and ER-mitochondria associations.
Radu Stoica, Sébastien Paillusson, Patricia Gomez-Suaga, Jacqueline C Mitchell, Dawn Hw Lau, Emma H Gray, Rosa M Sancho, Gema Vizcay-Barrena, Kurt J De Vos, Christopher E Shaw,[...]. EMBO Rep 2016
148
8

ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43.
Radu Stoica, Kurt J De Vos, Sébastien Paillusson, Sarah Mueller, Rosa M Sancho, Kwok-Fai Lau, Gema Vizcay-Barrena, Wen-Lang Lin, Ya-Fei Xu, Jada Lewis,[...]. Nat Commun 2014
338
8

Autophagy and mitophagy in ALS.
Chantell S Evans, Erika L F Holzbaur. Neurobiol Dis 2019
76
10

Decreased mRNA expression of PGC-1α and PGC-1α-regulated factors in the SOD1G93A ALS mouse model and in human sporadic ALS.
Nadine Thau, Sarah Knippenberg, Sonja Körner, Klaus Jan Rath, Reinhard Dengler, Susanne Petri. J Neuropathol Exp Neurol 2012
66
10

Hypermetabolism in ALS is associated with greater functional decline and shorter survival.
Frederik J Steyn, Zara A Ioannides, Ruben P A van Eijk, Susan Heggie, Kathryn A Thorpe, Amelia Ceslis, Saman Heshmat, Anjali K Henders, Naomi R Wray, Leonard H van den Berg,[...]. J Neurol Neurosurg Psychiatry 2018
93
7

Insulin resistance in amyotrophic lateral sclerosis.
E T Reyes, O H Perurena, B W Festoff, R Jorgensen, W V Moore. J Neurol Sci 1984
69
10


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.