A citation-based method for searching scientific literature

Agnieszka Mykowska, Krzysztof Sobczak, Marzena Wojciechowska, Piotr Kozlowski, Wlodzimierz J Krzyzosiak. Nucleic Acids Res 2011
Times Cited: 116







List of co-cited articles
1368 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
531
40

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
118
38

RNA toxicity is a component of ataxin-3 degeneration in Drosophila.
Ling-Bo Li, Zhenming Yu, Xiuyin Teng, Nancy M Bonini. Nature 2008
218
37

A pathogenic mechanism in Huntington's disease involves small CAG-repeated RNAs with neurotoxic activity.
Mónica Bañez-Coronel, Silvia Porta, Birgit Kagerbauer, Elisabet Mateu-Huertas, Lorena Pantano, Isidre Ferrer, Manuel Guzmán, Xavier Estivill, Eulàlia Martí. PLoS Genet 2012
109
33


Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
966
29

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy.
J W Miller, C R Urbinati, P Teng-Umnuay, M G Stenberg, B J Byrne, C A Thornton, M S Swanson. EMBO J 2000
626
27

Ribonuclease dicer cleaves triplet repeat hairpins into shorter repeats that silence specific targets.
Jacek Krol, Agnieszka Fiszer, Agnieszka Mykowska, Krzysztof Sobczak, Mateusz de Mezer, Wlodzimierz J Krzyzosiak. Mol Cell 2007
129
26

Triplet repeat RNA structure and its role as pathogenic agent and therapeutic target.
Wlodzimierz J Krzyzosiak, Krzysztof Sobczak, Marzena Wojciechowska, Agnieszka Fiszer, Agnieszka Mykowska, Piotr Kozlowski. Nucleic Acids Res 2012
105
25

Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease.
Kirupa Sathasivam, Andreas Neueder, Theresa A Gipson, Christian Landles, Agnesska C Benjamin, Marie K Bondulich, Donna L Smith, Richard L M Faull, Raymund A C Roos, David Howland,[...]. Proc Natl Acad Sci U S A 2013
257
25

CAG expansion induces nucleolar stress in polyglutamine diseases.
Ho Tsoi, Terrence Chi-Kong Lau, Suk-Ying Tsang, Kwok-Fai Lau, Ho Yin Edwin Chan. Proc Natl Acad Sci U S A 2012
86
27

Muscleblind-like 1 interacts with RNA hairpins in splicing target and pathogenic RNAs.
Yuan Yuan, Sarah A Compton, Krzysztof Sobczak, Myrna G Stenberg, Charles A Thornton, Jack D Griffith, Maurice S Swanson. Nucleic Acids Res 2007
156
23

Cellular toxicity of expanded RNA repeats: focus on RNA foci.
Marzena Wojciechowska, Wlodzimierz J Krzyzosiak. Hum Mol Genet 2011
153
23

Mechanisms of RNA-induced toxicity in CAG repeat disorders.
R Nalavade, N Griesche, D P Ryan, S Hildebrand, S Krauss. Cell Death Dis 2013
80
28

Chemical correction of pre-mRNA splicing defects associated with sequestration of muscleblind-like 1 protein by expanded r(CAG)-containing transcripts.
Amit Kumar, Raman Parkesh, Lukasz J Sznajder, Jessica L Childs-Disney, Krzysztof Sobczak, Matthew D Disney. ACS Chem Biol 2012
59
35

Long tract of untranslated CAG repeats is deleterious in transgenic mice.
Ren-Jun Hsu, Kuang-Ming Hsiao, Min-Jon Lin, Chui-Yen Li, Li-Chun Wang, Luen-Kui Chen, Huichin Pan. PLoS One 2011
53
39

Structural diversity of triplet repeat RNAs.
Krzysztof Sobczak, Gracjan Michlewski, Mateusz de Mezer, Elzbieta Kierzek, Jacek Krol, Marta Olejniczak, Ryszard Kierzek, Wlodzimierz J Krzyzosiak. J Biol Chem 2010
82
24

Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
Thai H Ho, Rajesh S Savkur, Michael G Poulos, Michael A Mancini, Maurice S Swanson, Thomas A Cooper. J Cell Sci 2005
141
20

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
Melinda L Moseley, Tao Zu, Yoshio Ikeda, Wangcai Gao, Anne K Mosemiller, Randy S Daughters, Gang Chen, Marcy R Weatherspoon, H Brent Clark, Timothy J Ebner,[...]. Nat Genet 2006
301
20

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
J D Brook, M E McCurrach, H G Harley, A J Buckler, D Church, H Aburatani, K Hunter, V P Stanton, J P Thirion, T Hudson. Cell 1992
20

RNA structure of trinucleotide repeats associated with human neurological diseases.
Krzysztof Sobczak, Mateusz de Mezer, Gracjan Michlewski, Jacek Krol, Wlodzimierz J Krzyzosiak. Nucleic Acids Res 2003
152
19

A natural antisense transcript at the Huntington's disease repeat locus regulates HTT expression.
Daniel W Chung, Dobrila D Rudnicki, Lan Yu, Russell L Margolis. Hum Mol Genet 2011
127
19

RAN Translation in Huntington Disease.
Monica Bañez-Coronel, Fatma Ayhan, Alex D Tarabochia, Tao Zu, Barbara A Perez, Solaleh Khoramian Tusi, Olga Pletnikova, David R Borchelt, Christopher A Ross, Russell L Margolis,[...]. Neuron 2015
167
19

Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients.
Chantal Sellier, Frédérique Rau, Yilei Liu, Flora Tassone, Renate K Hukema, Renata Gattoni, Anne Schneider, Stéphane Richard, Rob Willemsen, David J Elliott,[...]. EMBO J 2010
246
18

RNA gain-of-function in spinocerebellar ataxia type 8.
Randy S Daughters, Daniel L Tuttle, Wangcai Gao, Yoshio Ikeda, Melinda L Moseley, Timothy J Ebner, Maurice S Swanson, Laura P W Ranum. PLoS Genet 2009
190
18

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.
C L Liquori, K Ricker, M L Moseley, J F Jacobsen, W Kress, S L Naylor, J W Day, L P Ranum. Science 2001
813
18


Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins.
Eric T Wang, Neal A L Cody, Sonali Jog, Michela Biancolella, Thomas T Wang, Daniel J Treacy, Shujun Luo, Gary P Schroth, David E Housman, Sita Reddy,[...]. Cell 2012
307
18

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues.
K L Taneja, M McCurrach, M Schalling, D Housman, R H Singer. J Cell Biol 1995
451
17

Muscleblind participates in RNA toxicity of expanded CAG and CUG repeats in Caenorhabditis elegans.
Li-Chun Wang, Kuan-Yu Chen, Huichin Pan, Chia-Chieh Wu, Po-Hsuan Chen, Yuan-Ting Liao, Chin Li, Min-Lang Huang, Kuang-Ming Hsiao. Cell Mol Life Sci 2011
51
33


RNA toxicity in polyglutamine disorders: concepts, models, and progress of research.
Agnieszka Fiszer, Wlodzimierz J Krzyzosiak. J Mol Med (Berl) 2013
40
42

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
16

Huntington's disease--like 2 is associated with CUG repeat-containing RNA foci.
Dobrila D Rudnicki, Susan E Holmes, Mark W Lin, Charles A Thornton, Christopher A Ross, Russell L Margolis. Ann Neurol 2007
106
16

Triplet repeats in transcripts: structural insights into RNA toxicity.
Paulina Galka-Marciniak, Martyna O Urbanek, Wlodzimierz J Krzyzosiak. Biol Chem 2012
53
30

Atomic resolution structure of CAG RNA repeats: structural insights and implications for the trinucleotide repeat expansion diseases.
Agnieszka Kiliszek, Ryszard Kierzek, Wlodzimierz J Krzyzosiak, Wojciech Rypniewski. Nucleic Acids Res 2010
59
25

RNA-mediated neuromuscular disorders.
Laura P W Ranum, Thomas A Cooper. Annu Rev Neurosci 2006
342
15


An antisense CAG repeat transcript at JPH3 locus mediates expanded polyglutamine protein toxicity in Huntington's disease-like 2 mice.
Brian Wilburn, Dobrila D Rudnicki, Jing Zhao, Tara Murphy Weitz, Yin Cheng, Xiaofeng Gu, Erin Greiner, Chang Sin Park, Nan Wang, Bryce L Sopher,[...]. Neuron 2011
102
15

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.
Xiaoyan Lin, Jill W Miller, Ami Mankodi, Rahul N Kanadia, Yuan Yuan, Richard T Moxley, Maurice S Swanson, Charles A Thornton. Hum Mol Genet 2006
358
15


Sustained therapeutic reversal of Huntington's disease by transient repression of huntingtin synthesis.
Holly B Kordasiewicz, Lisa M Stanek, Edward V Wancewicz, Curt Mazur, Melissa M McAlonis, Kimberly A Pytel, Jonathan W Artates, Andreas Weiss, Seng H Cheng, Lamya S Shihabuddin,[...]. Neuron 2012
442
15

Muscleblind proteins regulate alternative splicing.
Thai H Ho, Nicolas Charlet-B, Michael G Poulos, Gopal Singh, Maurice S Swanson, Thomas A Cooper. EMBO J 2004
334
14

Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy.
Frédérique Rau, Fernande Freyermuth, Charlotte Fugier, Jean-Philippe Villemin, Marie-Christine Fischer, Bernard Jost, Doulaye Dembele, Geneviève Gourdon, Annie Nicole, Denis Duboc,[...]. Nat Struct Mol Biol 2011
188
14



A muscleblind knockout model for myotonic dystrophy.
Rahul N Kanadia, Karen A Johnstone, Ami Mankodi, Codrin Lungu, Charles A Thornton, Douglas Esson, Adrian M Timmers, William W Hauswirth, Maurice S Swanson. Science 2003
516
13

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy.
Hongqing Du, Melissa S Cline, Robert J Osborne, Daniel L Tuttle, Tyson A Clark, John Paul Donohue, Megan P Hall, Lily Shiue, Maurice S Swanson, Charles A Thornton,[...]. Nat Struct Mol Biol 2010
232
13

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
13

Repeat instability as the basis for human diseases and as a potential target for therapy.
Arturo López Castel, John D Cleary, Christopher E Pearson. Nat Rev Mol Cell Biol 2010
292
13


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.