A citation-based method for searching scientific literature

Marisa Cappella, Pierre-François Pradat, Giorgia Querin, Maria Grazia Biferi. J Neuromuscul Dis 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Gene Therapy for ALS-A Perspective.
Marisa Cappella, Chiara Ciotti, Mathilde Cohen-Tannoudji, Maria Grazia Biferi. Int J Mol Sci 2019
41
80

Targeting RNA-Mediated Toxicity in C9orf72 ALS and/or FTD by RNAi-Based Gene Therapy.
Raygene Martier, Jolanda M Liefhebber, Ana García-Osta, Jana Miniarikova, Mar Cuadrado-Tejedor, Maria Espelosin, Susana Ursua, Harald Petry, Sander J van Deventer, Melvin M Evers,[...]. Mol Ther Nucleic Acids 2019
40
80

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
60

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
580
60

Amyotrophic Lateral Sclerosis: An Update for 2018.
Björn Oskarsson, Tania F Gendron, Nathan P Staff. Mayo Clin Proc 2018
85
40

C9orf72-mediated ALS and FTD: multiple pathways to disease.
Rubika Balendra, Adrian M Isaacs. Nat Rev Neurol 2018
210
40

Emerging Issues in AAV-Mediated In Vivo Gene Therapy.
Pasqualina Colella, Giuseppe Ronzitti, Federico Mingozzi. Mol Ther Methods Clin Dev 2017
306
40

C9orf72 BAC Mouse Model with Motor Deficits and Neurodegenerative Features of ALS/FTD.
Yuanjing Liu, Amrutha Pattamatta, Tao Zu, Tammy Reid, Olgert Bardhi, David R Borchelt, Anthony T Yachnis, Laura P W Ranum. Neuron 2016
191
40

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
280
40

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Elisa Majounie, Alan E Renton, Kin Mok, Elise G P Dopper, Adrian Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simon-Sanchez,[...]. Lancet Neurol 2012
752
40

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
40


Clinical trials in amyotrophic lateral sclerosis: why so many negative trials and how can trials be improved?
Hiroshi Mitsumoto, Benjamin R Brooks, Vincenzo Silani. Lancet Neurol 2014
167
40


Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice.
Lindsay A Becker, Brenda Huang, Gregor Bieri, Rosanna Ma, David A Knowles, Paymaan Jafar-Nejad, James Messing, Hong Joo Kim, Armand Soriano, Georg Auburger,[...]. Nature 2017
233
40


SOD1 Suppression with Adeno-Associated Virus and MicroRNA in Familial ALS.
Christian Mueller, James D Berry, Diane M McKenna-Yasek, Gwladys Gernoux, Margaret A Owegi, Lindsay M Pothier, Catherine L Douthwright, Dario Gelevski, Sarah D Luppino, Meghan Blackwood,[...]. N Engl J Med 2020
35
40

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy.
Jerry R Mendell, Samiah Al-Zaidy, Richard Shell, W Dave Arnold, Louise R Rodino-Klapac, Thomas W Prior, Linda Lowes, Lindsay Alfano, Katherine Berry, Kathleen Church,[...]. N Engl J Med 2017
862
40

A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model.
Maria Grazia Biferi, Mathilde Cohen-Tannoudji, Ambra Cappelletto, Benoit Giroux, Marianne Roda, Stéphanie Astord, Thibaut Marais, Corinne Bos, Thomas Voit, Arnaud Ferry,[...]. Mol Ther 2017
42
40

Stress Granule Assembly Disrupts Nucleocytoplasmic Transport.
Ke Zhang, J Gavin Daigle, Kathleen M Cunningham, Alyssa N Coyne, Kai Ruan, Jonathan C Grima, Kelly E Bowen, Harsh Wadhwa, Peiguo Yang, Frank Rigo,[...]. Cell 2018
158
40

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
40

Artificial MicroRNAs Targeting C9orf72 Can Reduce Accumulation of Intra-nuclear Transcripts in ALS and FTD Patients.
Raygene Martier, Jolanda M Liefhebber, Jana Miniarikova, Tom van der Zon, Jolanda Snapper, Iris Kolder, Harald Petry, Sander J van Deventer, Melvin M Evers, Pavlina Konstantinova. Mol Ther Nucleic Acids 2019
21
40

Phase 1-2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS.
Timothy Miller, Merit Cudkowicz, Pamela J Shaw, Peter M Andersen, Nazem Atassi, Robert C Bucelli, Angela Genge, Jonathan Glass, Shafeeq Ladha, Albert L Ludolph,[...]. N Engl J Med 2020
90
40

Cre-dependent selection yields AAV variants for widespread gene transfer to the adult brain.
Benjamin E Deverman, Piers L Pravdo, Bryan P Simpson, Sripriya Ravindra Kumar, Ken Y Chan, Abhik Banerjee, Wei-Li Wu, Bin Yang, Nina Huber, Sergiu P Pasca,[...]. Nat Biotechnol 2016
412
40

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
446
40

Engineered AAVs for efficient noninvasive gene delivery to the central and peripheral nervous systems.
Ken Y Chan, Min J Jang, Bryan B Yoo, Alon Greenbaum, Namita Ravi, Wei-Li Wu, Luis Sánchez-Guardado, Carlos Lois, Sarkis K Mazmanian, Benjamin E Deverman,[...]. Nat Neurosci 2017
360
40

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
401
40

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
24
40

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
107
40

The phenotypic variability of amyotrophic lateral sclerosis.
Bart Swinnen, Wim Robberecht. Nat Rev Neurol 2014
288
40

Recognition of c9orf72 Mutant RNA by Single-Stranded Silencing RNAs.
Jiaxin Hu, Frank Rigo, Thazha P Prakash, David R Corey. Nucleic Acid Ther 2017
12
20

Intravenous scAAV9 delivery of a codon-optimized SMN1 sequence rescues SMA mice.
Elisa Dominguez, Thibaut Marais, Nicolas Chatauret, Sofia Benkhelifa-Ziyyat, Sandra Duque, Philippe Ravassard, Romain Carcenac, Stéphanie Astord, Aurélie Pereira de Moura, Thomas Voit,[...]. Hum Mol Genet 2011
204
20

In vivo genome editing improves motor function and extends survival in a mouse model of ALS.
Thomas Gaj, David S Ojala, Freja K Ekman, Leah C Byrne, Prajit Limsirichai, David V Schaffer. Sci Adv 2017
68
20

Intramuscular delivery of HGF-expressing recombinant AAV improves muscle integrity and alleviates neurological symptoms in the nerve crush and SOD1-G93A transgenic mouse models.
Sang Hwan Lee, Nayeon Lee, Subin Kim, Junghun Lee, Wooshik Choi, Seung Shin Yu, Jin Hong Kim, Sunyoung Kim. Biochem Biophys Res Commun 2019
1
100



Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN.
Kevin D Foust, Xueyong Wang, Vicki L McGovern, Lyndsey Braun, Adam K Bevan, Amanda M Haidet, Thanh T Le, Pablo R Morales, Mark M Rich, Arthur H M Burghes,[...]. Nat Biotechnol 2010
507
20

CRISPR/Cas9-Targeted Deletion of Polyglutamine in Spinocerebellar Ataxia Type 3-Derived Induced Pluripotent Stem Cells.
Shuming Ouyang, Yingjun Xie, Zeyu Xiong, Yi Yang, Yexing Xian, Zhanhui Ou, Bing Song, Yuchang Chen, Yuhuan Xie, Haoxian Li,[...]. Stem Cells Dev 2018
29
20

RNA metabolism in neurodegenerative disease.
Elaine Y Liu, Christopher P Cali, Edward B Lee. Dis Model Mech 2017
64
20

Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors.
Andrew V Anzalone, Luke W Koblan, David R Liu. Nat Biotechnol 2020
285
20

Intramuscular Delivery of scAAV9-hIGF1 Prolongs Survival in the hSOD1G93A ALS Mouse Model via Upregulation of D-Amino Acid Oxidase.
HuiQian Lin, HaoJie Hu, WeiSong Duan, YaLing Liu, GuoJun Tan, ZhongYao Li, YaKun Liu, BinBin Deng, XueQin Song, Wan Wang,[...]. Mol Neurobiol 2018
22
20



Global analysis of TDP-43 interacting proteins reveals strong association with RNA splicing and translation machinery.
Brian D Freibaum, Raghu K Chitta, Anthony A High, J Paul Taylor. J Proteome Res 2010
293
20

Intralingual and Intrapleural AAV Gene Therapy Prolongs Survival in a SOD1 ALS Mouse Model.
Allison M Keeler, Marina Zieger, Carson Semple, Logan Pucci, Alessandra Veinbachs, Robert H Brown, Christian Mueller, Mai K ElMallah. Mol Ther Methods Clin Dev 2019
10
20

Taking a risk: a therapeutic focus on ataxin-2 in amyotrophic lateral sclerosis?
Dianne M A van den Heuvel, Oliver Harschnitz, Leonard H van den Berg, R Jeroen Pasterkamp. Trends Mol Med 2014
23
20

ALS Clinical Trials Review: 20 Years of Failure. Are We Any Closer to Registering a New Treatment?
Dmitry Petrov, Colin Mansfield, Alain Moussy, Olivier Hermine. Front Aging Neurosci 2017
180
20

Muscle-derived but not centrally derived transgene GDNF is neuroprotective in G93A-SOD1 mouse model of ALS.
Wen Li, Danielle Brakefield, Yanchun Pan, Dan Hunter, Terence M Myckatyn, Alexander Parsadanian. Exp Neurol 2007
89
20

Silencing mutant ataxin-3 rescues motor deficits and neuropathology in Machado-Joseph disease transgenic mice.
Clévio Nóbrega, Isabel Nascimento-Ferreira, Isabel Onofre, David Albuquerque, Hirokazu Hirai, Nicole Déglon, Luís Pereira de Almeida. PLoS One 2013
82
20

P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.
Amelia Conte, Serena Lattante, Marcella Zollino, Giuseppe Marangi, Marco Luigetti, Alessandra Del Grande, Serenella Servidei, Federica Trombetta, Mario Sabatelli. Neuromuscul Disord 2012
77
20


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.