A citation-based method for searching scientific literature

Łukasz J Sznajder, Maurice S Swanson. Int J Mol Sci 2019
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity


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
38

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
666
30

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.
M Mahadevan, C Tsilfidis, L Sabourin, G Shutler, C Amemiya, G Jansen, C Neville, M Narang, J Barceló, K O'Hoy. Science 1992
28

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
849
28

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
592
28

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
374
25

Loss of MBNL leads to disruption of developmentally regulated alternative polyadenylation in RNA-mediated disease.
Ranjan Batra, Konstantinos Charizanis, Mini Manchanda, Apoorva Mohan, Moyi Li, Dustin J Finn, Marianne Goodwin, Chaolin Zhang, Krzysztof Sobczak, Charles A Thornton,[...]. Mol Cell 2014
188
23

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
Y H Fu, A Pizzuti, R G Fenwick, J King, S Rajnarayan, P W Dunne, J Dubel, G A Nasser, T Ashizawa, P de Jong. Science 1992
20

Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
Jun Sone, Satomi Mitsuhashi, Atsushi Fujita, Takeshi Mizuguchi, Kohei Hamanaka, Keiko Mori, Haruki Koike, Akihiro Hashiguchi, Hiroshi Takashima, Hiroshi Sugiyama,[...]. Nat Genet 2019
190
20

rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences.
Chantal Sellier, Estefanía Cerro-Herreros, Markus Blatter, Fernande Freyermuth, Angeline Gaucherot, Frank Ruffenach, Partha Sarkar, Jack Puymirat, Bjarne Udd, John W Day,[...]. Nat Commun 2018
38
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
335
17

Transcriptome alterations in myotonic dystrophy skeletal muscle and heart.
Eric T Wang, Daniel Treacy, Katy Eichinger, Adam Struck, Joseph Estabrook, Hailey Olafson, Thomas T Wang, Kirti Bhatt, Tony Westbrook, Sam Sedehizadeh,[...]. Hum Mol Genet 2019
58
17

Antagonistic regulation of mRNA expression and splicing by CELF and MBNL proteins.
Eric T Wang, Amanda J Ward, Jennifer M Cherone, Jimena Giudice, Thomas T Wang, Daniel J Treacy, Nicole J Lambert, Peter Freese, Tanvi Saxena, Thomas A Cooper,[...]. Genome Res 2015
122
17

Transcriptome alterations in myotonic dystrophy frontal cortex.
Brittney A Otero, Kiril Poukalov, Ryan P Hildebrandt, Charles A Thornton, Kenji Jinnai, Harutoshi Fujimura, Takashi Kimura, Katharine A Hagerman, Jacinda B Sampson, John W Day,[...]. Cell Rep 2021
23
30


A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophy.
Eric D Wieben, Ross A Aleff, Nirubol Tosakulwong, Malinda L Butz, W Edward Highsmith, Albert O Edwards, Keith H Baratz. PLoS One 2012
149
15

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
B Brais, J P Bouchard, Y G Xie, D L Rochefort, N Chrétien, F M Tomé, R G Lafrenière, J M Rommens, E Uyama, O Nohira,[...]. Nat Genet 1998
572
15

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
15

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
15

RNA phase transitions in repeat expansion disorders.
Ankur Jain, Ronald D Vale. Nature 2017
395
15

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
542
15


Muscleblind-like 2-mediated alternative splicing in the developing brain and dysregulation in myotonic dystrophy.
Konstantinos Charizanis, Kuang-Yung Lee, Ranjan Batra, Marianne Goodwin, Chaolin Zhang, Yuan Yuan, Lily Shiue, Melissa Cline, Marina M Scotti, Guangbin Xia,[...]. Neuron 2012
222
15

Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy.
James D Thomas, Łukasz J Sznajder, Olgert Bardhi, Faaiq N Aslam, Zacharias P Anastasiadis, Marina M Scotti, Ichizo Nishino, Masayuki Nakamori, Eric T Wang, Maurice S Swanson. Genes Dev 2017
58
15

Compound loss of muscleblind-like function in myotonic dystrophy.
Kuang-Yung Lee, Moyi Li, Mini Manchanda, Ranjan Batra, Konstantinos Charizanis, Apoorva Mohan, Sonisha A Warren, Christopher M Chamberlain, Dustin Finn, Hannah Hong,[...]. EMBO Mol Med 2013
116
15

MicroRNA-Based Therapeutic Perspectives in Myotonic Dystrophy.
Arturo López Castel, Sarah Joann Overby, Rubén Artero. Int J Mol Sci 2019
20
30


Myotonic Dystrophies: State of the Art of New Therapeutic Developments for the CNS.
Genevieve Gourdon, Giovanni Meola. Front Cell Neurosci 2017
59
15

MBNL proteins and their target RNAs, interaction and splicing regulation.
Patryk Konieczny, Ewa Stepniak-Konieczna, Krzysztof Sobczak. Nucleic Acids Res 2014
108
15

Repeat expansion diseases.
Henry Paulson. Handb Clin Neurol 2018
153
15

The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.
Kohji Mori, Shih-Ming Weng, Thomas Arzberger, Stephanie May, Kristin Rentzsch, Elisabeth Kremmer, Bettina Schmid, Hans A Kretzschmar, Marc Cruts, Christine Van Broeckhoven,[...]. Science 2013
855
12

Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia.
Andrea Cortese, Roberto Simone, Roisin Sullivan, Jana Vandrovcova, Huma Tariq, Wai Yan Yau, Jack Humphrey, Zane Jaunmuktane, Prasanth Sivakumar, James Polke,[...]. Nat Genet 2019
183
12

Alternative splicing as a regulator of development and tissue identity.
Francisco E Baralle, Jimena Giudice. Nat Rev Mol Cell Biol 2017
526
12

RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia.
Tao Zu, Yuanjing Liu, Monica Bañez-Coronel, Tammy Reid, Olga Pletnikova, Jada Lewis, Timothy M Miller, Matthew B Harms, Annet E Falchook, S H Subramony,[...]. Proc Natl Acad Sci U S A 2013
526
12

Repeat-Associated Non-ATG Translation: Molecular Mechanisms and Contribution to Neurological Disease.
Lien Nguyen, John Douglas Cleary, Laura P W Ranum. Annu Rev Neurosci 2019
41
12


Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification.
M De Antonio, C Dogan, D Hamroun, M Mati, S Zerrouki, B Eymard, S Katsahian, G Bassez. Rev Neurol (Paris) 2016
121
12

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
347
12

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat.
A Mankodi, E Logigian, L Callahan, C McClain, R White, D Henderson, M Krym, C A Thornton. Science 2000
512
12

Loss of muscleblind-like 1 results in cardiac pathology and persistence of embryonic splice isoforms.
Donald M Dixon, Jongkyu Choi, Ayea El-Ghazali, Sun Young Park, Kenneth P Roos, Maria C Jordan, Michael C Fishbein, Lucio Comai, Sita Reddy. Sci Rep 2015
51
12

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.
Oscar Hernández-Hernández, Céline Guiraud-Dogan, Géraldine Sicot, Aline Huguet, Sabrina Luilier, Esther Steidl, Stefanie Saenger, Elodie Marciniak, Hélène Obriot, Caroline Chevarin,[...]. Brain 2013
53
12

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.
Yun Tian, Jun-Ling Wang, Wen Huang, Sheng Zeng, Bin Jiao, Zhen Liu, Zhao Chen, Yujing Li, Ying Wang, Hao-Xuan Min,[...]. Am J Hum Genet 2019
129
12

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.
Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, Yuta Suzuki, Wei Qu, Koichiro Doi, M Asem Almansour, Junko Kanda Kikuchi, Makiko Taira, Jun Mitsui,[...]. Nat Genet 2019
148
12

Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy.
Thurman M Wheeler, John D Lueck, Maurice S Swanson, Robert T Dirksen, Charles A Thornton. J Clin Invest 2007
188
10


Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.
Charlotte Fugier, Arnaud F Klein, Caroline Hammer, Stéphane Vassilopoulos, Ylva Ivarsson, Anne Toussaint, Valérie Tosch, Alban Vignaud, Arnaud Ferry, Nadia Messaddeq,[...]. Nat Med 2011
222
10

Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy.
Ami Mankodi, Masanori P Takahashi, Hong Jiang, Carol L Beck, William J Bowers, Richard T Moxley, Stephen C Cannon, Charles A Thornton. Mol Cell 2002
470
10


Myotonic dystrophy.
Charles A Thornton. Neurol Clin 2014
188
10

Mitigating RNA Toxicity in Myotonic Dystrophy using Small Molecules.
Kaalak Reddy, Jana R Jenquin, John D Cleary, J Andrew Berglund. Int J Mol Sci 2019
14
28


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.