A citation-based method for searching scientific literature

Joana R Loureiro, Ana F Castro, Ana S Figueiredo, Isabel Silveira. Cells 2022
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Evidence against haploinsuffiency of human ataxin 10 as a cause of spinocerebellar ataxia type 10.
Boris Keren, Aurélia Jacquette, Christel Depienne, Patricia Leite, Alexandra Durr, Wassila Carpentier, Baya Benyahia, Gerard Ponsot, Florent Soubrier, Alexis Brice,[...]. Neurogenetics 2010
12
100


Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From Drosophila Model.
Taro Ishiguro, Yoshitaka Nagai, Kinya Ishikawa. Front Neurosci 2021
3
100

Mutant CAG repeats of Huntingtin transcript fold into hairpins, form nuclear foci and are targets for RNA interference.
Mateusz de Mezer, Marzena Wojciechowska, Marek Napierala, Krzysztof Sobczak, Wlodzimierz J Krzyzosiak. Nucleic Acids Res 2011
128
100

Transcriptional activation modulated by homopolymeric glutamine and proline stretches.
H P Gerber, K Seipel, O Georgiev, M Höfferer, M Hug, S Rusconi, W Schaffner. Science 1994
497
100

Dorsal root ganglionopathy is responsible for the sensory impairment in CANVAS.
David J Szmulewicz, Catriona A McLean, Michael L Rodriguez, Andrew M Chancellor, Stuart Mossman, Duncan Lamont, Leslie Roberts, Elsdon Storey, G Michael Halmagyi. Neurology 2014
64
100

A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele.
Sarah J Beecroft, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Zoe Dyer, Teddy Y Wu, Eoin Mulroy, Luciana Pelosi, Miriam Rodrigues, Rachael Taylor,[...]. Brain 2020
21
100


CRISPR-Cas9 In Vivo Gene Editing for Transthyretin Amyloidosis.
Julian D Gillmore, Ed Gane, Jorg Taubel, Justin Kao, Marianna Fontana, Michael L Maitland, Jessica Seitzer, Daniel O'Connell, Kathryn R Walsh, Kristy Wood,[...]. N Engl J Med 2021
293
100

Bioinformatics-Based Identification of Expanded Repeats: A Non-reference Intronic Pentamer Expansion in RFC1 Causes CANVAS.
Haloom Rafehi, David J Szmulewicz, Mark F Bennett, Nara L M Sobreira, Kate Pope, Katherine R Smith, Greta Gillies, Peter Diakumis, Egor Dolzhenko, Michael A Eberle,[...]. Am J Hum Genet 2019
86
100

Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice.
Dominic Jauvin, Jessina Chrétien, Sanjay K Pandey, Laurie Martineau, Lucille Revillod, Guillaume Bassez, Aline Lachon, A Robert MacLeod, Geneviève Gourdon, Thurman M Wheeler,[...]. Mol Ther Nucleic Acids 2017
49
100

SCA31 is rare in the Chinese population on Taiwan.
Yi-Chung Lee, Chin-San Liu, Tzu-Ying Lee, Yang-Chung Lo, Yi-Chun Lu, Bing-Wen Soong. Neurobiol Aging 2012
8
100

New CRISPR-Cas systems from uncultivated microbes.
David Burstein, Lucas B Harrington, Steven C Strutt, Alexander J Probst, Karthik Anantharaman, Brian C Thomas, Jennifer A Doudna, Jillian F Banfield. Nature 2017
281
100

Transcription of Satellite III non-coding RNAs is a general stress response in human cells.
Rut Valgardsdottir, Ilaria Chiodi, Manuela Giordano, Antonio Rossi, Silvia Bazzini, Claudia Ghigna, Silvano Riva, Giuseppe Biamonti. Nucleic Acids Res 2008
144
100

Inhibition of TDP-43 aggregation by nucleic acid binding.
Yi-Chen Huang, Ku-Feng Lin, Ruei-Yu He, Pang-Hsien Tu, Jiri Koubek, Yin-Chih Hsu, Joseph Jen-Tse Huang. PLoS One 2013
49
100

Programmed DNA destruction by miniature CRISPR-Cas14 enzymes.
Lucas B Harrington, David Burstein, Janice S Chen, David Paez-Espino, Enbo Ma, Isaac P Witte, Joshua C Cofsky, Nikos C Kyrpides, Jillian F Banfield, Jennifer A Doudna. Science 2018
383
100

Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast.
Nicole Cherng, Alexander A Shishkin, Lucas I Schlager, Ryan H Tuck, Laura Sloan, Robert Matera, Partha S Sarkar, Tetsuo Ashizawa, Catherine H Freudenreich, Sergei M Mirkin. Proc Natl Acad Sci U S A 2011
40
100

Repeat-associated non-ATG (RAN) translation.
John Douglas Cleary, Amrutha Pattamatta, Laura P W Ranum. J Biol Chem 2018
54
100

The CRISPR-Cas13a Gene-Editing System Induces Collateral Cleavage of RNA in Glioma Cells.
Qixue Wang, Xing Liu, Junhu Zhou, Chao Yang, Guangxiu Wang, Yanli Tan, Ye Wu, Sijing Zhang, Kaikai Yi, Chunsheng Kang. Adv Sci (Weinh) 2019
46
100

CRISPR-Cas9 In Vivo Gene Editing for Transthyretin Amyloidosis. Reply.
Julian D Gillmore, Michael L Maitland, David Lebwohl. N Engl J Med 2021
5
100

Reversal of RNA dominance by displacement of protein sequestered on triplet repeat RNA.
Thurman M Wheeler, Krzysztof Sobczak, John D Lueck, Robert J Osborne, Xiaoyan Lin, Robert T Dirksen, Charles A Thornton. Science 2009
288
100

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome: genetic and clinical insights.
Roisin Sullivan, Rauan Kaiyrzhanov, Henry Houlden. Curr Opin Neurol 2021
2
100

DNAzyme Cleavage of CAG Repeat RNA in Polyglutamine Diseases.
Nan Zhang, Brittani Bewick, Jason Schultz, Anjana Tiwari, Robert Krencik, Aijun Zhang, Kaho Adachi, Guangbin Xia, Kyuson Yun, Partha Sarkar,[...]. Neurotherapeutics 2021
3
100

The roles of RNA processing in translating genotype to phenotype.
Kassie S Manning, Thomas A Cooper. Nat Rev Mol Cell Biol 2017
103
100


Pathogenesis of SCA3 and implications for other polyglutamine diseases.
Hayley S McLoughlin, Lauren R Moore, Henry L Paulson. Neurobiol Dis 2020
60
100

Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10.
Misti C White, Rui Gao, Weidong Xu, Santi M Mandal, Jung G Lim, Tapas K Hazra, Maki Wakamiya, Sharon F Edwards, Salmo Raskin, Hélio A G Teive,[...]. PLoS Genet 2010
84
100

The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
M Wakamiya, T Matsuura, Y Liu, G C Schuster, R Gao, W Xu, P S Sarkar, X Lin, T Ashizawa. Neurology 2006
53
100

CRISPR/Cas9 Editing of the Mutant Huntingtin Allele In Vitro and In Vivo.
Alex Mas Monteys, Shauna A Ebanks, Megan S Keiser, Beverly L Davidson. Mol Ther 2017
172
100

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion.
Andrea Cortese, Stefano Tozza, Wai Yan Yau, Salvatore Rossi, Sarah J Beecroft, Zane Jaunmuktane, Zoe Dyer, Gianina Ravenscroft, Phillipa J Lamont, Stuart Mossman,[...]. Brain 2020
81
100

A CRISPR-Cas13a system for efficient and specific therapeutic targeting of mutant KRAS for pancreatic cancer treatment.
Xiao Zhao, Liang Liu, Jiayan Lang, Keman Cheng, Yongwei Wang, Xueyan Li, Jian Shi, Yanli Wang, Guangjun Nie. Cancer Lett 2018
61
100

Motor neuron involvement expands the neuropathological phenotype of late-onset ataxia in RFC1 mutation (CANVAS).
David Reyes-Leiva, Iban Aldecoa, Ellen Gelpi, Ricard Rojas-García. Brain Pathol 2022
3
100

Small molecule targeting r(UGGAA)n disrupts RNA foci and alleviates disease phenotype in Drosophila model.
Tomonori Shibata, Konami Nagano, Morio Ueyama, Kensuke Ninomiya, Tetsuro Hirose, Yoshitaka Nagai, Kinya Ishikawa, Gota Kawai, Kazuhiko Nakatani. Nat Commun 2021
14
100


The atlas of RNase H antisense oligonucleotide distribution and activity in the CNS of rodents and non-human primates following central administration.
Paymaan Jafar-Nejad, Berit Powers, Armand Soriano, Hien Zhao, Daniel A Norris, John Matson, Beatrice DeBrosse-Serra, Jamie Watson, Padmakumar Narayanan, Seung J Chun,[...]. Nucleic Acids Res 2021
22
100

Spinocerebellar ataxia type 31 exists in northeast China.
Yi Ouyang, Zhiyi He, Lei Li, Xue Qin, Yinan Zhao, Liying Yuan. J Neurol Sci 2012
11
100

Targeting nuclear RNA for in vivo correction of myotonic dystrophy.
Thurman M Wheeler, Andrew J Leger, Sanjay K Pandey, A Robert MacLeod, Masayuki Nakamori, Seng H Cheng, Bruce M Wentworth, C Frank Bennett, Charles A Thornton. Nature 2012
349
100

Lives that introns lead after splicing.
Jay R Hesselberth. Wiley Interdiscip Rev RNA 2013
44
100

Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.
J F Baizabal-Carvallo, G Xia, P Botros, J Laguna, T Ashizawa, J Jankovic. Acta Neurol Scand 2015
9
100

Contracting CAG/CTG repeats using the CRISPR-Cas9 nickase.
Cinzia Cinesi, Lorène Aeschbach, Bin Yang, Vincent Dion. Nat Commun 2016
49
100


Midbrain atrophy related to parkinsonism in a non-coding repeat expansion disorder: five cases of spinocerebellar ataxia type 31 with nigrostriatal dopaminergic dysfunction.
Ryohei Norioka, Keizo Sugaya, Aki Murayama, Tomoya Kawazoe, Shinsuke Tobisawa, Akihiro Kawata, Kazushi Takahashi. Cerebellum Ataxias 2021
1
100

When should we test patients with familial ataxias for SCA31? A misdiagnosed condition outside Japan?
José Luiz Pedroso, Agessandro Abrahao, Kinya Ishikawa, Salmo Raskin, Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, Pedro Braga-Neto, Marcus Vinicius Cristino de Albuquerque, Hidehiro Mizusawa, Orlando G P Barsottini. J Neurol Sci 2015
9
100

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.
L Zu, K P Figueroa, R Grewal, S M Pulst. Am J Hum Genet 1999
95
100

The AUUCU repeats responsible for spinocerebellar ataxia type 10 form unusual RNA hairpins.
Vaishali Handa, Herman J C Yeh, Peter McPhie, Karen Usdin. J Biol Chem 2005
25
100

An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics.
Sanjog R Chintalaphani, Sandy S Pineda, Ira W Deveson, Kishore R Kumar. Acta Neuropathol Commun 2021
25
100

A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.
K Owada, K Ishikawa, S Toru, G Ishida, M Gomyoda, O Tao, Y Noguchi, K Kitamura, I Kondo, E Noguchi,[...]. Neurology 2005
55
100

Microsatellite repeat instability and neurological disease.
Judith R Brouwer, Rob Willemsen, Ben A Oostra. Bioessays 2009
87
100

The Genetic Diagnosis of Neurodegenerative Diseases and Therapeutic Perspectives.
Julio-César García, Rosa-Helena Bustos. Brain Sci 2018
14
100

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.
Raji P Grewal, Madhureeta Achari, Tohru Matsuura, Alberto Durazo, Emilio Tayag, Lan Zu, Stefan M Pulst, Tetsuo Ashizawa. Arch Neurol 2002
50
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.