A citation-based method for searching scientific literature

Julie Smeyers, Elena-Gaia Banchi, Morwena Latouche. Front Cell Neurosci 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Mitochondrial dysfunction is a converging point of multiple pathological pathways in amyotrophic lateral sclerosis.
Ping Shi, Yanming Wei, Jiayu Zhang, Jozsef Gal, Haining Zhu. J Alzheimers Dis 2010
58
100

Amyotrophic Lateral Sclerosis: An Update for 2018.
Björn Oskarsson, Tania F Gendron, Nathan P Staff. Mayo Clin Proc 2018
75
100

Design of amidobenzimidazole STING receptor agonists with systemic activity.
Joshi M Ramanjulu, G Scott Pesiridis, Jingsong Yang, Nestor Concha, Robert Singhaus, Shu-Yun Zhang, Jean-Luc Tran, Patrick Moore, Stephanie Lehmann, H Christian Eberl,[...]. Nature 2018
183
100


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
564
100

Parkin and PINK1 mitigate STING-induced inflammation.
Danielle A Sliter, Jennifer Martinez, Ling Hao, Xi Chen, Nuo Sun, Tara D Fischer, Jonathon L Burman, Yan Li, Zhe Zhang, Derek P Narendra,[...]. Nature 2018
399
100

Mitochondrial bioenergetic deficits in C9orf72 amyotrophic lateral sclerosis motor neurons cause dysfunctional axonal homeostasis.
Arpan R Mehta, Jenna M Gregory, Owen Dando, Roderick N Carter, Karen Burr, Jyoti Nanda, David Story, Karina McDade, Colin Smith, Nicholas M Morton,[...]. Acta Neuropathol 2021
10
100

A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis.
Amr Al-Saif, Futwan Al-Mohanna, Saeed Bohlega. Ann Neurol 2011
272
100

ALS-Related Mutant SOD1 Aggregates Interfere with Mitophagy by Sequestering the Autophagy Receptor Optineurin.
Yeong Jin Tak, Ju-Hwang Park, Hyangshuk Rhim, Seongman Kang. Int J Mol Sci 2020
6
100

Exome sequencing reveals VCP mutations as a cause of familial ALS.
Janel O Johnson, Jessica Mandrioli, Michael Benatar, Yevgeniya Abramzon, Vivianna M Van Deerlin, John Q Trojanowski, J Raphael Gibbs, Maura Brunetti, Susan Gronka, Joanne Wuu,[...]. Neuron 2010
838
100


C9orf72 regulates energy homeostasis by stabilizing mitochondrial complex I assembly.
Tao Wang, Honghe Liu, Kie Itoh, Sungtaek Oh, Liang Zhao, Daisuke Murata, Hiromi Sesaki, Thomas Hartung, Chan Hyun Na, Jiou Wang. Cell Metab 2021
8
100

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
30
100

A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS.
Carina Lehmer, Martin H Schludi, Linnea Ransom, Johanna Greiling, Michaela Junghänel, Nicole Exner, Henrick Riemenschneider, Julie van der Zee, Christine Van Broeckhoven, Patrick Weydt,[...]. EMBO Mol Med 2018
22
100

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome.
Kiichi Nakahira, Jeffrey Adam Haspel, Vijay A K Rathinam, Seon-Jin Lee, Tamas Dolinay, Hilaire C Lam, Joshua A Englert, Marlene Rabinovitch, Manuela Cernadas, Hong Pyo Kim,[...]. Nat Immunol 2011
100

Amyotrophic Lateral Sclerosis Descriptive Epidemiology: The Origin of Geographic Difference.
Giancarlo Logroscino, Marco Piccininni. Neuroepidemiology 2019
29
100

Mutations of optineurin in amyotrophic lateral sclerosis.
Hirofumi Maruyama, Hiroyuki Morino, Hidefumi Ito, Yuishin Izumi, Hidemasa Kato, Yasuhito Watanabe, Yoshimi Kinoshita, Masaki Kamada, Hiroyuki Nodera, Hidenori Suzuki,[...]. Nature 2010
835
100

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
64
100

Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.
Shahram Saberi, Jennifer E Stauffer, Derek J Schulte, John Ravits. Neurol Clin 2015
112
100


Spatially Stable Mitochondrial Compartments Fuel Local Translation during Plasticity.
Vidhya Rangaraju, Marcel Lauterbach, Erin M Schuman. Cell 2019
89
100

ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs.
Yueh-Lin Tsai, Tristan H Coady, Lei Lu, Dinghai Zheng, Isabel Alland, Bin Tian, Neil A Shneider, James L Manley. Genes Dev 2020
8
100

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
S Hadano, C K Hand, H Osuga, Y Yanagisawa, A Otomo, R S Devon, N Miyamoto, J Showguchi-Miyata, Y Okada, R Singaraja,[...]. Nat Genet 2001
484
100

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
373
100

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
Y Yang, A Hentati, H X Deng, O Dabbagh, T Sasaki, M Hirano, W Y Hung, K Ouahchi, J Yan, A C Azim,[...]. Nat Genet 2001
547
100

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.
Tobias B Haack, Erika Ignatius, Javier Calvo-Garrido, Arcangela Iuso, Pirjo Isohanni, Camilla Maffezzini, Tuula Lönnqvist, Anu Suomalainen, Matteo Gorza, Laura S Kremer,[...]. Am J Hum Genet 2016
58
100

Pathomechanisms of ALS8: altered autophagy and defective RNA binding protein (RBP) homeostasis due to the VAPB P56S mutation.
Priyanka Tripathi, Haihong Guo, Alice Dreser, Alfred Yamoah, Antonio Sechi, Christopher Marvin Jesse, Istvan Katona, Panagiotis Doukas, Stefan Nikolin, Sabrina Ernst,[...]. Cell Death Dis 2021
1
100

Enhanced Bulbar Function in Amyotrophic Lateral Sclerosis: The Nuedexta Treatment Trial.
Richard Smith, Erik Pioro, Kathleen Myers, Michael Sirdofsky, Kimberly Goslin, Gregg Meekins, Hong Yu, James Wymer, Merit Cudkowicz, Eric A Macklin,[...]. Neurotherapeutics 2017
36
100

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
100

Long non-coding and coding RNAs characterization in Peripheral Blood Mononuclear Cells and Spinal Cord from Amyotrophic Lateral Sclerosis patients.
Stella Gagliardi, Susanna Zucca, Cecilia Pandini, Luca Diamanti, Matteo Bordoni, Daisy Sproviero, Maddalena Arigoni, Martina Olivero, Orietta Pansarasa, Mauro Ceroni,[...]. Sci Rep 2018
36
100

Dysfunction in nonsense-mediated decay, protein homeostasis, mitochondrial function, and brain connectivity in ALS-FUS mice with cognitive deficits.
Wan Yun Ho, Ira Agrawal, Sheue-Houy Tyan, Emma Sanford, Wei-Tang Chang, Kenneth Lim, Jolynn Ong, Bernice Siu Yan Tan, Aung Aung Kywe Moe, Regina Yu,[...]. Acta Neuropathol Commun 2021
4
100

The sex ratio in amyotrophic lateral sclerosis: A population based study.
Zita R Manjaly, Kirsten M Scott, Kumar Abhinav, Lokesh Wijesekera, Jeban Ganesalingam, Laura H Goldstein, Anna Janssen, Andrew Dougherty, Emma Willey, Biba R Stanton,[...]. Amyotroph Lateral Scler 2010
89
100

Olesoxime delays muscle denervation, astrogliosis, microglial activation and motoneuron death in an ALS mouse model.
C Sunyach, M Michaud, T Arnoux, N Bernard-Marissal, J Aebischer, V Latyszenok, C Gouarné, C Raoul, R M Pruss, T Bordet,[...]. Neuropharmacology 2012
54
100

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
168
100

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
100

GNX-4728, a novel small molecule drug inhibitor of mitochondrial permeability transition, is therapeutic in a mouse model of amyotrophic lateral sclerosis.
Lee J Martin, Daniele Fancelli, Margaret Wong, Mark Niedzwiecki, Marco Ballarini, Simon Plyte, Qing Chang. Front Cell Neurosci 2014
40
100

Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis.
Andrea Stoccoro, Adam R Smith, Lorena Mosca, Alessandro Marocchi, Francesca Gerardi, Christian Lunetta, Cristina Cereda, Stella Gagliardi, Katie Lunnon, Lucia Migliore,[...]. Clin Epigenetics 2020
6
100

Edaravone protects PC12 cells from ischemic-like injury via attenuating the damage to mitochondria.
Ying Song, Meng Li, Ji-cheng Li, Er-qing Wei. J Zhejiang Univ Sci B 2006
20
100

Mitochondrial DNA Integrity: Role in Health and Disease.
Priyanka Sharma, Harini Sampath. Cells 2019
50
100

Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis.
Aaron P Russell, Shogo Wada, Lodovica Vergani, M Benjamin Hock, Séverine Lamon, Bertrand Léger, Takashi Ushida, Romain Cartoni, Glenn D Wadley, Peter Hespel,[...]. Neurobiol Dis 2013
136
100

Hot-spot KIF5A mutations cause familial ALS.
David Brenner, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl, Susanne Petri, Thomas Meyer, Julian Grosskreutz, Patrick Weydt, Wolfgang Ruf, Christoph Neuwirth,[...]. Brain 2018
88
100

Mitochondrial DNA stress primes the antiviral innate immune response.
A Phillip West, William Khoury-Hanold, Matthew Staron, Michal C Tal, Cristiana M Pineda, Sabine M Lang, Megan Bestwick, Brett A Duguay, Nuno Raimundo, Donna A MacDuff,[...]. Nature 2015
676
100

SOD1 Function and Its Implications for Amyotrophic Lateral Sclerosis Pathology: New and Renascent Themes.
Rosie K A Bunton-Stasyshyn, Rachele A Saccon, Pietro Fratta, Elizabeth M C Fisher. Neuroscientist 2015
55
100

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
465
100

A phase II-III trial of olesoxime in subjects with amyotrophic lateral sclerosis.
T Lenglet, L Lacomblez, J L Abitbol, A Ludolph, J S Mora, W Robberecht, P J Shaw, R M Pruss, V Cuvier, V Meininger. Eur J Neurol 2014
77
100

SQSTM1 and Paget's disease of bone.
R Layfield, L J Hocking. Calcif Tissue Int 2004
51
100

Impairment of Mitochondrial Calcium Buffering Links Mutations in C9ORF72 and TARDBP in iPS-Derived Motor Neurons from Patients with ALS/FTD.
Ruxandra Dafinca, Paola Barbagallo, Lucy Farrimond, Ana Candalija, Jakub Scaber, Nida'a A Ababneh, Chaitra Sathyaprakash, Jane Vowles, Sally A Cowley, Kevin Talbot. Stem Cell Reports 2020
20
100

Loss of function CHCHD10 mutations in cytoplasmic TDP-43 accumulation and synaptic integrity.
Jung-A A Woo, Tian Liu, Courtney Trotter, Cenxiao C Fang, Emillio De Narvaez, Patrick LePochat, Drew Maslar, Anusha Bukhari, Xingyu Zhao, Andrew Deonarine,[...]. Nat Commun 2017
51
100

Identification and characterization of cholest-4-en-3-one, oxime (TRO19622), a novel drug candidate for amyotrophic lateral sclerosis.
Thierry Bordet, Bruno Buisson, Magali Michaud, Cyrille Drouot, Pascale Galéa, Pierre Delaage, Natalia P Akentieva, Alex S Evers, Douglas F Covey, Mariano A Ostuni,[...]. J Pharmacol Exp Ther 2007
183
100



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.