A citation-based method for searching scientific literature

Elke Braems, Paraskevi Tziortzouda, Ludo Van Den Bosch. Neurosci Lett 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Profilin enhances Cdc42-induced nucleation of actin polymerization.
C Yang, M Huang, J DeBiasio, M Pring, M Joyce, H Miki, T Takenawa, S H Zigmond. J Cell Biol 2000
100
100

Amyotrophic lateral sclerosis-associated mutant profilin 1 increases dendritic arborisation and spine formation in primary hippocampal neurons.
Merryn Brettle, Alexandra K Suchowerska, Sook W Chua, Lars M Ittner, Thomas Fath. Neurosci Lett 2015
13
100

Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts.
Nicholas J Kramer, Yari Carlomagno, Yong-Jie Zhang, Sandra Almeida, Casey N Cook, Tania F Gendron, Mercedes Prudencio, Marka Van Blitterswijk, Veronique Belzil, Julien Couthouis,[...]. Science 2016
82
100

Nuclear localization sequence of FUS and induction of stress granules by ALS mutants.
Jozsef Gal, Jiayu Zhang, David M Kwinter, Jianjun Zhai, Hongge Jia, Jianhang Jia, Haining Zhu. Neurobiol Aging 2011
143
100

Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury.
A G Reaume, J L Elliott, E K Hoffman, N W Kowall, R J Ferrante, D F Siwek, H M Wilcox, D G Flood, M F Beal, R H Brown,[...]. Nat Genet 1996
911
100

Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation.
Hidefumi Ito, Masataka Nakamura, Osamu Komure, Takashi Ayaki, Reika Wate, Hirofumi Maruyama, Yoshimi Nakamura, Kengo Fujita, Satoshi Kaneko, Yoko Okamoto,[...]. Acta Neuropathol 2011
48
100

The Redox Activity of Protein Disulfide Isomerase Inhibits ALS Phenotypes in Cellular and Zebrafish Models.
Sonam Parakh, Sina Shadfar, Emma R Perri, Audrey M G Ragagnin, Claudia V Piattoni, Mariela B Fogolín, Kristy C Yuan, Hamideh Shahheydari, Emily K Don, Collen J Thomas,[...]. iScience 2020
12
100


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
155
100


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
178
100

CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts.
Ricardos Tabet, Laure Schaeffer, Fernande Freyermuth, Melanie Jambeau, Michael Workman, Chao-Zong Lee, Chun-Chia Lin, Jie Jiang, Karen Jansen-West, Hussein Abou-Hamdan,[...]. Nat Commun 2018
66
100

Optineurin in neurodegenerative diseases.
Tenshi Osawa, Yuji Mizuno, Yukio Fujita, Masamitsu Takatama, Yoichi Nakazato, Koichi Okamoto. Neuropathology 2011
78
100

Early death of ALS-linked CHCHD10-R15L transgenic mice with central nervous system, skeletal muscle, and cardiac pathology.
Éanna B Ryan, Jianhua Yan, Nimrod Miller, Sudarshan Dayanidhi, Yongchao C Ma, Han-Xiang Deng, Teepu Siddique. iScience 2021
3
100

Human SOD1 ALS Mutations in a Drosophila Knock-In Model Cause Severe Phenotypes and Reveal Dosage-Sensitive Gain- and Loss-of-Function Components.
Aslı Şahin, Aaron Held, Kirsten Bredvik, Paxton Major, Toni-Marie Achilli, Abigail G Kerson, Kristi Wharton, Geoff Stilwell, Robert Reenan. Genetics 2017
29
100

Stable transgenic C9orf72 zebrafish model key aspects of the ALS/FTD phenotype and reveal novel pathological features.
Matthew P Shaw, Adrian Higginbottom, Alexander McGown, Lydia M Castelli, Evlyn James, Guillaume M Hautbergue, Pamela J Shaw, Tennore M Ramesh. Acta Neuropathol Commun 2018
26
100

Expression of mutant TDP-43 induces neuronal dysfunction in transgenic mice.
Ya-Fei Xu, Yong-Jie Zhang, Wen-Lang Lin, Xiangkun Cao, Caroline Stetler, Dennis W Dickson, Jada Lewis, Leonard Petrucelli. Mol Neurodegener 2011
105
100

Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.
Christopher Hewitt, Janine Kirby, J Robin Highley, Judith A Hartley, Rachael Hibberd, Hannah C Hollinger, Tim L Williams, Paul G Ince, Christopher J McDermott, Pamela J Shaw. Arch Neurol 2010
93
100

Motor neuron apoptosis and neuromuscular junction perturbation are prominent features in a Drosophila model of Fus-mediated ALS.
Ruohan Xia, Yajuan Liu, Liuqing Yang, Jozsef Gal, Haining Zhu, Jianhang Jia. Mol Neurodegener 2012
57
100

Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS.
Helene Tran, Sandra Almeida, Jill Moore, Tania F Gendron, UmaDevi Chalasani, Yubing Lu, Xing Du, Jeffrey A Nickerson, Leonard Petrucelli, Zhiping Weng,[...]. Neuron 2015
134
100

Drosophila as an In Vivo Model for Human Neurodegenerative Disease.
Leeanne McGurk, Amit Berson, Nancy M Bonini. Genetics 2015
135
100

Yeast genetic screen reveals novel therapeutic strategy for ALS.
Matthew D Figley, Aaron D Gitler. Rare Dis 2013
18
100

Nuclear import factor transportin and arginine methyltransferase 1 modify FUS neurotoxicity in Drosophila.
Sandra Jäckel, Anna K Summerer, Catherine M Thömmes, Xia Pan, Aaron Voigt, Jörg B Schulz, Tobias M Rasse, Dorothee Dormann, Christian Haass, Philipp J Kahle. Neurobiol Dis 2015
29
100

Hexanucleotide repeats in ALS/FTD form length-dependent RNA foci, sequester RNA binding proteins, and are neurotoxic.
Youn-Bok Lee, Han-Jou Chen, João N Peres, Jorge Gomez-Deza, Jan Attig, Maja Stalekar, Claire Troakes, Agnes L Nishimura, Emma L Scotter, Caroline Vance,[...]. Cell Rep 2013
302
100

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
100

Expression of C9orf72-related dipeptides impairs motor function in a vertebrate model.
Amrutha Swaminathan, Marilou Bouffard, Meijiang Liao, Sarah Ryan, Janis Bennion Callister, Stuart M Pickering-Brown, Gary Alan Barclay Armstrong, Pierre Drapeau. Hum Mol Genet 2018
29
100

C9orf72 is required for proper macrophage and microglial function in mice.
J G O'Rourke, L Bogdanik, A Yáñez, D Lall, A J Wolf, A K M G Muhammad, R Ho, S Carmona, J P Vit, J Zarrow,[...]. Science 2016
289
100

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
Janel O Johnson, Erik P Pioro, Ashley Boehringer, Ruth Chia, Howard Feit, Alan E Renton, Hannah A Pliner, Yevgeniya Abramzon, Giuseppe Marangi, Brett J Winborn,[...]. Nat Neurosci 2014
292
100

Glycine-alanine dipeptide repeat protein contributes to toxicity in a zebrafish model of C9orf72 associated neurodegeneration.
Yu Ohki, Andrea Wenninger-Weinzierl, Alexander Hruscha, Kazuhide Asakawa, Koichi Kawakami, Christian Haass, Dieter Edbauer, Bettina Schmid. Mol Neurodegener 2017
40
100

Null mutation of copper/zinc superoxide dismutase in Drosophila confers hypersensitivity to paraquat and reduced longevity.
J P Phillips, S D Campbell, D Michaud, M Charbonneau, A J Hilliker. Proc Natl Acad Sci U S A 1989
301
100

Proteome Homeostasis Dysfunction: A Unifying Principle in ALS Pathogenesis.
Justin J Yerbury, Natalie E Farrawell, Luke McAlary. Trends Neurosci 2020
18
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
488
100

Advances in porcine genomics and proteomics--a toolbox for developing the pig as a model organism for molecular biomedical research.
Emøke Bendixen, Marianne Danielsen, Knud Larsen, Christian Bendixen. Brief Funct Genomics 2010
100
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
551
100


Oxidative Stress, Neuroinflammation and Mitochondria in the Pathophysiology of Amyotrophic Lateral Sclerosis.
Elena Obrador, Rosario Salvador, Rafael López-Blanch, Ali Jihad-Jebbar, Soraya L Vallés, José M Estrela. Antioxidants (Basel) 2020
15
100

Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2.
George H Gorrie, Faisal Fecto, Daniel Radzicki, Craig Weiss, Yong Shi, Hongxin Dong, Hong Zhai, Ronggen Fu, Erdong Liu, Sisi Li,[...]. Proc Natl Acad Sci U S A 2014
47
100

Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS.
Paola Crociara, Maria Novella Chieppa, Elena Vallino Costassa, Elena Berrone, Marina Gallo, Monica Lo Faro, Maria Domenica Pintore, Barbara Iulini, Antonio D'Angelo, Giovanni Perona,[...]. Neurobiol Dis 2019
6
100

Energy Homeostasis and Abnormal RNA Metabolism in Amyotrophic Lateral Sclerosis.
Yu-Ju Liu, Po-Yi Tsai, Yijuang Chern. Front Cell Neurosci 2017
9
100


C9ORF72: What It Is, What It Does, and Why It Matters.
Julie Smeyers, Elena-Gaia Banchi, Morwena Latouche. Front Cell Neurosci 2021
4
100

Profilin1 biology and its mutation, actin(g) in disease.
Duah Alkam, Ezra Z Feldman, Awantika Singh, Mahmoud Kiaei. Cell Mol Life Sci 2017
42
100

New links between SOD1 and metabolic dysfunction from a yeast model of amyotrophic lateral sclerosis.
Emma L Bastow, Amber R Peswani, Daniel S J Tarrant, Daniel R Pentland, Xi Chen, Alan Morgan, Gemma L Staniforth, Jennifer M Tullet, Michelle L Rowe, Mark J Howard,[...]. J Cell Sci 2016
30
100

Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders.
Tibor Hortobágyi, Claire Troakes, Agnes L Nishimura, Caroline Vance, John C van Swieten, Harro Seelaar, Andrew King, Safa Al-Sarraj, Boris Rogelj, Christopher E Shaw. Acta Neuropathol 2011
60
100

Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).
David S Howland, Jian Liu, Yijin She, Beth Goad, Nicholas J Maragakis, Benjamin Kim, Jamie Erickson, John Kulik, Lisa DeVito, George Psaltis,[...]. Proc Natl Acad Sci U S A 2002
610
100

Intravenously Administered, Retinoid Activating Nanoparticles Increase Lifespan and Reduce Neurodegeneration in the SOD1G93A Mouse Model of ALS.
David X Medina, Eugene P Chung, Collin D Teague, Robert Bowser, Rachael W Sirianni. Front Bioeng Biotechnol 2020
4
100

Modelling amyotrophic lateral sclerosis: progress and possibilities.
Philip Van Damme, Wim Robberecht, Ludo Van Den Bosch. Dis Model Mech 2017
88
100

Over-expression of N-type calcium channels in cortical neurons from a mouse model of Amyotrophic Lateral Sclerosis.
Massimo Pieri, Silvia Caioli, Nadia Canu, Nicola B Mercuri, Ezia Guatteo, Cristina Zona. Exp Neurol 2013
15
100

A systematic analysis of human disease-associated gene sequences in Drosophila melanogaster.
L T Reiter, L Potocki, S Chien, M Gribskov, E Bier. Genome Res 2001
480
100

Amyotrophic lateral sclerosis (ALS)-associated VAPB-P56S inclusions represent an ER quality control compartment.
Marijn Kuijpers, Vera van Dis, Elize D Haasdijk, Martin Harterink, Karin Vocking, Jan A Post, Wiep Scheper, Casper C Hoogenraad, Dick Jaarsma. Acta Neuropathol Commun 2013
33
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.