A citation-based method for searching scientific literature

Chaitali Misra, Feikai Lin, Auinash Kalsotra. Adv Neurobiol 2018
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Non-ATG-initiated translation directed by microsatellite expansions.
Tao Zu, Brian Gibbens, Noelle S Doty, Mário Gomes-Pereira, Aline Huguet, Matthew D Stone, Jamie Margolis, Mark Peterson, Todd W Markowski, Melissa A C Ingram,[...]. Proc Natl Acad Sci U S A 2011
524
75

Polyglutamine-Expanded Huntingtin Exacerbates Age-Related Disruption of Nuclear Integrity and Nucleocytoplasmic Transport.
Fatima Gasset-Rosa, Carlos Chillon-Marinas, Alexander Goginashvili, Ranjit Singh Atwal, Jonathan W Artates, Ricardos Tabet, Vanessa C Wheeler, Anne G Bang, Don W Cleveland, Clotilde Lagier-Tourenne. Neuron 2017
98
50

Mutant Huntingtin Disrupts the Nuclear Pore Complex.
Jonathan C Grima, J Gavin Daigle, Nicolas Arbez, Kathleen C Cunningham, Ke Zhang, Joseph Ochaba, Charlene Geater, Eva Morozko, Jennifer Stocksdale, Jenna C Glatzer,[...]. Neuron 2017
136
50

Antisense Oligonucleotide-Mediated Removal of the Polyglutamine Repeat in Spinocerebellar Ataxia Type 3 Mice.
Lodewijk J A Toonen, Frank Rigo, Haico van Attikum, Willeke M C van Roon-Mom. Mol Ther Nucleic Acids 2017
49
50

RNA toxicity and foci formation in microsatellite expansion diseases.
Nan Zhang, Tetsuo Ashizawa. Curr Opin Genet Dev 2017
46
50


Repeat expansion diseases.
Henry Paulson. Handb Clin Neurol 2018
97
50

Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31.
Taro Ishiguro, Nozomu Sato, Morio Ueyama, Nobuhiro Fujikake, Chantal Sellier, Akemi Kanegami, Eiichi Tokuda, Bita Zamiri, Terence Gall-Duncan, Mila Mirceta,[...]. Neuron 2017
57
50

Design of a bioactive small molecule that targets r(AUUCU) repeats in spinocerebellar ataxia 10.
Wang-Yong Yang, Rui Gao, Mark Southern, Partha S Sarkar, Matthew D Disney. Nat Commun 2016
30
50

Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.
Majid Fardaei, Mark T Rogers, Helena M Thorpe, Kenneth Larkin, Marion G Hamshere, Peter S Harper, J David Brook. Hum Mol Genet 2002
317
50


Compromised mitochondrial complex II in models of Machado-Joseph disease.
Mário N Laço, Catarina R Oliveira, Henry L Paulson, A Cristina Rego. Biochim Biophys Acta 2012
28
25

Presymptomatic testing for neurogenetic diseases in Brazil: assessing who seeks and who follows through with testing.
Caroline Santa Maria Rodrigues, Viviane Ziebell de Oliveira, Gabriela Camargo, Claudio Maria da Silva Osório, Raphael Machado de Castilhos, Maria Luiza Saraiva-Pereira, Lavínia Schuler-Faccini, Laura Bannach Jardim. J Genet Couns 2012
24
25

Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms.
T Schmitz-Hübsch, M Coudert, P Bauer, P Giunti, C Globas, L Baliko, A Filla, C Mariotti, M Rakowicz, P Charles,[...]. Neurology 2008
167
25

Effectiveness and safety of treatments for degenerative ataxias: a systematic review.
M Mar Trujillo-Martín, Pedro Serrano-Aguilar, Fernando Monton-Alvarez, Romen Carrillo-Fumero. Mov Disord 2009
40
25

Disruption of axonal transport by loss of huntingtin or expression of pathogenic polyQ proteins in Drosophila.
Shermali Gunawardena, Lu-Shiun Her, Richard G Brusch, Robert A Laymon, Ingrid R Niesman, Beth Gordesky-Gold, Louis Sintasath, Nancy M Bonini, Lawrence S B Goldstein. Neuron 2003
462
25

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.
Anna Duarri, Justyna Jezierska, Michiel Fokkens, Michel Meijer, Helenius J Schelhaas, Wilfred F A den Dunnen, Freerk van Dijk, Corien Verschuuren-Bemelmans, Gerard Hageman, Pieter van de Vlies,[...]. Ann Neurol 2012
86
25

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
107
25

Polyglutamines placed into context.
Albert R La Spada, J Paul Taylor. Neuron 2003
102
25


The cerebellar cognitive affective syndrome.
J D Schmahmann, J C Sherman. Brain 1998
25

An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
K Lindblad, M L Savontaus, G Stevanin, M Holmberg, K Digre, C Zander, H Ehrsson, G David, A Benomar, E Nikoskelainen,[...]. Genome Res 1996
86
25


Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
907
25


Spinocerebellar ataxia type 12: clues to pathogenesis.
Rachael L Cohen, Russell L Margolis. Curr Opin Neurol 2016
10
25

Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells.
Zhanhui Ou, Min Luo, Xiaohua Niu, Yuchang Chen, Yingjun Xie, Wenyin He, Bing Song, Yexing Xian, Di Fan, Shuming OuYang,[...]. Biomed Res Int 2016
23
25

Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegia.
Sophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, Cecilia Marelli, Pascale Ribai, Carlo Vincitorio, Mathieu Anheim, Lucie Guyant-Maréchal, Alice Le Bayon, Nadia Vandenberghe,[...]. Arch Neurol 2012
39
25

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.
T Ikeuchi, R Koide, H Tanaka, O Onodera, S Igarashi, H Takahashi, R Kondo, A Ishikawa, A Tomoda, T Miike. Ann Neurol 1995
140
25

Fragile X syndrome and fragile X-associated tremor ataxia syndrome.
Deborah A Hall, Elizabeth Berry-Kravis. Handb Clin Neurol 2018
14
25

Hsp104 suppresses polyglutamine-induced degeneration post onset in a drosophila MJD/SCA3 model.
Mimi Cushman-Nick, Nancy M Bonini, James Shorter. PLoS Genet 2013
56
25

Dose-Dependent Lowering of Mutant Huntingtin Using Antisense Oligonucleotides in Huntington Disease Patients.
Willeke M C van Roon-Mom, Raymund A C Roos, Susanne T de Bot. Nucleic Acid Ther 2018
22
25

Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology.
Theresa A Zesiewicz, George Wilmot, Sheng-Han Kuo, Susan Perlman, Patricia E Greenstein, Sarah H Ying, Tetsuo Ashizawa, S H Subramony, Jeremy D Schmahmann, K P Figueroa,[...]. Neurology 2018
39
25

A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.
Kenichi Yasui, Ichiro Yabe, Kunihiro Yoshida, Kazuaki Kanai, Kimihito Arai, Mizuki Ito, Osamu Onodera, Shigeru Koyano, Eiji Isozaki, Setsu Sawai,[...]. Orphanet J Rare Dis 2014
20
25


The neuropathology of the adult cerebellum.
Arnulf H Koeppen. Handb Clin Neurol 2018
16
25

Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity.
Cecilia Mancini, Eriola Hoxha, Luisa Iommarini, Alessandro Brussino, Uwe Richter, Francesca Montarolo, Claudia Cagnoli, Roberta Parolisi, Diana Iulia Gondor Morosini, Valentina Nicolò,[...]. Neurobiol Dis 2019
10
25

An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron.
Yu Miyazaki, Xiaofei Du, Shin-Ichi Muramatsu, Christopher M Gomez. Sci Transl Med 2016
35
25


Long-read sequencing across the C9orf72 'GGGGCC' repeat expansion: implications for clinical use and genetic discovery efforts in human disease.
Mark T W Ebbert, Stefan L Farrugia, Jonathon P Sens, Karen Jansen-West, Tania F Gendron, Mercedes Prudencio, Ian J McLaughlin, Brett Bowman, Matthew Seetin, Mariely DeJesus-Hernandez,[...]. Mol Neurodegener 2018
41
25

Targeting potassium channels to treat cerebellar ataxia.
David D Bushart, Ravi Chopra, Vikrant Singh, Geoffrey G Murphy, Heike Wulff, Vikram G Shakkottai. Ann Clin Transl Neurol 2018
28
25

Studying polyglutamine aggregation in Caenorhabditis elegans using an analytical ultracentrifuge equipped with fluorescence detection.
Bashkim Kokona, Carrie A May, Nicole R Cunningham, Lynn Richmond, F Jay Garcia, Julia C Durante, Kathleen M Ulrich, Christine M Roberts, Christopher D Link, Walter F Stafford,[...]. Protein Sci 2016
8
25

Rehabilitation for Individuals With Genetic Degenerative Ataxia: A Systematic Review.
Sarah C Milne, Louise A Corben, Nellie Georgiou-Karistianis, Martin B Delatycki, Eppie M Yiu. Neurorehabil Neural Repair 2017
22
25

Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
L Guerrini, F Lolli, A Ginestroni, G Belli, R Della Nave, C Tessa, S Foresti, M Cosottini, S Piacentini, F Salvi,[...]. Brain 2004
78
25

Antisense Oligonucleotides Reduce RNA Foci in Spinocerebellar Ataxia 36 Patient iPSCs.
Kosuke Matsuzono, Keiko Imamura, Nagahisa Murakami, Kayoko Tsukita, Takuya Yamamoto, Yuishin Izumi, Ryuji Kaji, Yasuyuki Ohta, Toru Yamashita, Koji Abe,[...]. Mol Ther Nucleic Acids 2017
14
25

Mutations in TGM6 induce the unfolded protein response in SCA35.
Debasmita Tripathy, Beatrice Vignoli, Nandini Ramesh, Maria Jose Polanco, Marie Coutelier, Christopher D Stephen, Marco Canossa, Marie-Lorraine Monin, Pascale Aeschlimann, Shannon Turberville,[...]. Hum Mol Genet 2017
19
25


Current concepts in the treatment of hereditary ataxias.
Pedro Braga Neto, José Luiz Pedroso, Sheng-Han Kuo, C França Marcondes Junior, Hélio Afonso Ghizoni Teive, Orlando Graziani Povoas Barsottini. Arq Neuropsiquiatr 2016
11
25

The natural history of degenerative ataxia: a retrospective study in 466 patients.
T Klockgether, R Lüdtke, B Kramer, M Abele, K Bürk, L Schöls, O Riess, F Laccone, S Boesch, I Lopes-Cendes,[...]. Brain 1998
223
25

Spinal cord atrophy in spinocerebellar ataxia type 3 and 6 : impact on clinical disability.
Carsten Lukas, Horst K Hahn, Barbara Bellenberg, Kerstin Hellwig, Christoph Globas, Sebastian K Schimrigk, Odo Köster, Ludger Schöls. J Neurol 2008
29
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.