A citation-based method for searching scientific literature

Guillaume M Hautbergue, John D Cleary, Shu Guo, Laura P W Ranum. Curr Opin Neurol 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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
75

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
75

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
50

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.
Manuela Neumann, Eva Bentmann, Dorothee Dormann, Ali Jawaid, Mariely DeJesus-Hernandez, Olaf Ansorge, Sigrun Roeber, Hans A Kretzschmar, David G Munoz, Hirofumi Kusaka,[...]. Brain 2011
202
50

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
50

Haploinsufficiency leads to neurodegeneration in C9ORF72 ALS/FTD human induced motor neurons.
Yingxiao Shi, Shaoyu Lin, Kim A Staats, Yichen Li, Wen-Hsuan Chang, Shu-Ting Hung, Eric Hendricks, Gabriel R Linares, Yaoming Wang, Esther Y Son,[...]. Nat Med 2018
261
50

Mechanisms of repeat-associated non-AUG translation in neurological microsatellite expansion disorders.
Lydia M Castelli, Wan-Ping Huang, Ya-Hui Lin, Kung-Yao Chang, Guillaume M Hautbergue. Biochem Soc Trans 2021
5
50

Relationship between C9orf72 repeat size and clinical phenotype.
Sara Van Mossevelde, Julie van der Zee, Marc Cruts, Christine Van Broeckhoven. Curr Opin Genet Dev 2017
71
50

Emerging Perspectives on Dipeptide Repeat Proteins in C9ORF72 ALS/FTD.
Alexander Schmitz, João Pinheiro Marques, Irina Oertig, Niran Maharjan, Smita Saxena. Front Cell Neurosci 2021
10
50

Molecular mechanisms underlying nucleotide repeat expansion disorders.
Indranil Malik, Chase P Kelley, Eric T Wang, Peter K Todd. Nat Rev Mol Cell Biol 2021
22
50

Poly-dipeptides encoded by the C9orf72 repeats bind nucleoli, impede RNA biogenesis, and kill cells.
Ilmin Kwon, Siheng Xiang, Masato Kato, Leeju Wu, Pano Theodoropoulos, Tao Wang, Jiwoong Kim, Jonghyun Yun, Yang Xie, Steven L McKnight. Science 2014
394
50

Gain of Toxicity from ALS/FTD-Linked Repeat Expansions in C9ORF72 Is Alleviated by Antisense Oligonucleotides Targeting GGGGCC-Containing RNAs.
Jie Jiang, Qiang Zhu, Tania F Gendron, Shahram Saberi, Melissa McAlonis-Downes, Amanda Seelman, Jennifer E Stauffer, Paymaan Jafar-Nejad, Kevin Drenner, Derek Schulte,[...]. Neuron 2016
309
50

Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72-associated amyotrophic lateral sclerosis.
Tania F Gendron, Jeannie Chew, Jeannette N Stankowski, Lindsey R Hayes, Yong-Jie Zhang, Mercedes Prudencio, Yari Carlomagno, Lillian M Daughrity, Karen Jansen-West, Emilie A Perkerson,[...]. Sci Transl Med 2017
129
50

Motor-Coordinative and Cognitive Dysfunction Caused by Mutant TDP-43 Could Be Reversed by Inhibiting Its Mitochondrial Localization.
Wenzhang Wang, Hiroyuki Arakawa, Luwen Wang, Ogoegbunam Okolo, Sandra L Siedlak, Yinfei Jiang, Ju Gao, Fei Xie, Robert B Petersen, Xinglong Wang. Mol Ther 2017
42
25

Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
Sara Van Mossevelde, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Anne Sieben, Tim Van Langenhove, Jan De Bleecker, Jonathan Baets, Mathieu Vandenbulcke, Koen Van Laere,[...]. Brain 2016
70
25

Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria.
Han-Xiang Deng, Yong Shi, Yoshiaki Furukawa, Hong Zhai, Ronggen Fu, Erdong Liu, George H Gorrie, Mohammad S Khan, Wu-Yen Hung, Eileen H Bigio,[...]. Proc Natl Acad Sci U S A 2006
326
25

The spliceosome: a self-organized macromolecular machine in the nucleus?
José Rino, Maria Carmo-Fonseca. Trends Cell Biol 2009
54
25

TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97.
Gillian P Ritson, Sara K Custer, Brian D Freibaum, Jake B Guinto, Dyanna Geffel, Jennifer Moore, Waixing Tang, Matthew J Winton, Manuela Neumann, John Q Trojanowski,[...]. J Neurosci 2010
188
25

Immunoreactivities of p62, an ubiqutin-binding protein, in the spinal anterior horn cells of patients with amyotrophic lateral sclerosis.
Yuji Mizuno, Masakuni Amari, Masamitsu Takatama, Hitoshi Aizawa, Ban Mihara, Koichi Okamoto. J Neurol Sci 2006
115
25

Poly(ADP-Ribose) Prevents Pathological Phase Separation of TDP-43 by Promoting Liquid Demixing and Stress Granule Localization.
Leeanne McGurk, Edward Gomes, Lin Guo, Jelena Mojsilovic-Petrovic, Van Tran, Robert G Kalb, James Shorter, Nancy M Bonini. Mol Cell 2018
186
25

Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).
Laura E Cox, Laura Ferraiuolo, Emily F Goodall, Paul R Heath, Adrian Higginbottom, Heather Mortiboys, Hannah C Hollinger, Judith A Hartley, Alice Brockington, Christine E Burness,[...]. PLoS One 2010
168
25

The role of insulin-like growth factor 1 in ALS cell and mouse models: A mitochondrial protector.
Di Wen, Can Cui, Weisong Duan, Wan Wang, Ying Wang, Yakun Liu, Zhongyao Li, Chunyan Li. Brain Res Bull 2019
19
25

The clinical spectrum of multisystem proteinopathy: Data from a neurodegenerative cohort.
Veria Vacchiano, Nicola Mometto, Anna Bartoletti-Stella, Giovanni Rizzo, Samir Abu-Rumeileh, Fabrizio Salvi, Piero Parchi, Rocco Liguori, Sabina Capellari. J Neurol Sci 2021
1
100

The wide-ranging clinical and genetic features in Japanese families with valosin-containing protein proteinopathy.
Takashi Ando, Ryoichi Nakamura, Satoshi Kuru, Daichi Yokoi, Naoki Atsuta, Haruki Koike, Masashi Suzuki, Kazuhiro Hara, Yohei Iguchi, Yumiko Harada,[...]. Neurobiol Aging 2021
3
33

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
25

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
Elisa Rubino, Innocenzo Rainero, Adriano Chiò, Ekaterina Rogaeva, Daniela Galimberti, Pierpaola Fenoglio, Yakov Grinberg, Giancarlo Isaia, Andrea Calvo, Salvatore Gentile,[...]. Neurology 2012
206
25

Partial Failure of Proteostasis Systems Counteracting TDP-43 Aggregates in Neurodegenerative Diseases.
Roberta Cascella, Giulia Fani, Alessandra Bigi, Fabrizio Chiti, Cristina Cecchi. Int J Mol Sci 2019
14
25

Optineurin in amyotrophic lateral sclerosis: Multifunctional adaptor protein at the crossroads of different neuroprotective mechanisms.
Andrea Markovinovic, Raffaello Cimbro, Tereza Ljutic, Jasna Kriz, Boris Rogelj, Ivana Munitic. Prog Neurobiol 2017
52
25

Neuronal and glial inclusions in frontotemporal dementia with or without motor neuron disease are immunopositive for p62.
Tetsuaki Arai, Takashi Nonaka, Masato Hasegawa, Haruhiko Akiyama, Mari Yoshida, Yosio Hashizume, Kuniaki Tsuchiya, Tatsuro Oda, Kenji Ikeda. Neurosci Lett 2003
69
25

Defective mitochondrial dynamics is an early event in skeletal muscle of an amyotrophic lateral sclerosis mouse model.
Guo Luo, Jianxun Yi, Changling Ma, Yajuan Xiao, Frank Yi, Tian Yu, Jingsong Zhou. PLoS One 2013
69
25

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
N Parkinson, P G Ince, M O Smith, R Highley, G Skibinski, P M Andersen, K E Morrison, H S Pall, O Hardiman, J Collinge,[...]. Neurology 2006
293
25


Translation repressors, an RNA helicase, and developmental cues control RNP phase transitions during early development.
Arnaud Hubstenberger, Scott L Noble, Cristiana Cameron, Thomas C Evans. Dev Cell 2013
95
25

Antioxidant and bioenergetic coupling between neurons and astrocytes.
Seila Fernandez-Fernandez, Angeles Almeida, Juan P Bolaños. Biochem J 2012
162
25

FUS and TDP-43 Phases in Health and Disease.
Bede Portz, Bo Lim Lee, James Shorter. Trends Biochem Sci 2021
39
25

Increased oxidative damage to DNA in ALS patients.
M Bogdanov, R H Brown, W Matson, R Smart, D Hayden, H O'Donnell, M Flint Beal, M Cudkowicz. Free Radic Biol Med 2000
225
25

Therapeutic news in ALS.
P Corcia, S Beltran, S E Bakkouche, P Couratier. Rev Neurol (Paris) 2021
5
25

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
25

Novel tankyrase inhibitors suppress TDP-43 aggregate formation.
Kunikazu Tanji, Fumiaki Mori, Fumiyuki Shirai, Takehiro Fukami, Hiroyuki Seimiya, Jun Utsumi, Akiyoshi Kakita, Koichi Wakabayashi. Biochem Biophys Res Commun 2021
3
33

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis.
Bradley N Smith, Simon D Topp, Claudia Fallini, Hideki Shibata, Han-Jou Chen, Claire Troakes, Andrew King, Nicola Ticozzi, Kevin P Kenna, Athina Soragia-Gkazi,[...]. Sci Transl Med 2017
70
25


Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.
Colin J Mahoney, Jon Beck, Jonathan D Rohrer, Tammaryn Lashley, Kin Mok, Tim Shakespeare, Tom Yeatman, Elizabeth K Warrington, Jonathan M Schott, Nick C Fox,[...]. Brain 2012
305
25

Alternative polyadenylation diversifies post-transcriptional regulation by selective RNA-protein interactions.
Ishaan Gupta, Sandra Clauder-Münster, Bernd Klaus, Aino I Järvelin, Raeka S Aiyar, Vladimir Benes, Stefan Wilkening, Wolfgang Huber, Vicent Pelechano, Lars M Steinmetz. Mol Syst Biol 2014
64
25

RNA Binding Proteins and Genome Integrity.
Kensei Nishida, Yuki Kuwano, Tatsuya Nishikawa, Kiyoshi Masuda, Kazuhito Rokutan. Int J Mol Sci 2017
31
25

Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.
Shuo-Chien Ling, Magdalini Polymenidou, Don W Cleveland. Neuron 2013
985
25

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology.
Elisa Teyssou, Takahiro Takeda, Vincent Lebon, Séverine Boillée, Brahima Doukouré, Guillaume Bataillon, Véronique Sazdovitch, Cécile Cazeneuve, Vincent Meininger, Eric LeGuern,[...]. Acta Neuropathol 2013
154
25

RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations.
J Gavin Daigle, Nicholas A Lanson, Rebecca B Smith, Ian Casci, Astha Maltare, John Monaghan, Charles D Nichols, Dmitri Kryndushkin, Frank Shewmaker, Udai Bhan Pandey. Hum Mol Genet 2013
142
25


Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
Ian R A Mackenzie, Eileen H Bigio, Paul G Ince, Felix Geser, Manuela Neumann, Nigel J Cairns, Linda K Kwong, Mark S Forman, John Ravits, Heather Stewart,[...]. Ann Neurol 2007
666
25

Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS.
Joanna J Bury, J Robin Highley, Johnathan Cooper-Knock, Emily F Goodall, Adrian Higginbottom, Christopher J McDermott, Paul G Ince, Pamela J Shaw, Janine Kirby. Neuropathology 2016
27
25


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.