A citation-based method for searching scientific literature

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
Times Cited: 1236







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



Times Cited
  Times     Co-cited
Similarity


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
77

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
72

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
836
30

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
644
27


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
529
23

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
366
18


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
106
18

Myotonic dystrophy.
Charles A Thornton. Neurol Clin 2014
165
18

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
502
17

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
460
16

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
462
15

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
562
14


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
210
14

Electrocardiographic abnormalities and sudden death in myotonic dystrophy type 1.
William J Groh, Miriam R Groh, Chandan Saha, John C Kincaid, Zachary Simmons, Emma Ciafaloni, Rahman Pourmand, Richard F Otten, Deepak Bhakta, Girish V Nair,[...]. N Engl J Med 2008
305
14

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
176
14

Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy.
J Mathieu, H Boivin, D Meunier, M Gaudreault, P Bégin. Neurology 2001
276
14

Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.
A Mankodi, C R Urbinati, Q P Yuan, R T Moxley, V Sansone, M Krym, D Henderson, M Schalling, M S Swanson, C A Thornton. Hum Mol Genet 2001
316
13


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
108
12


Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity.
Fernando Morales, Jillian M Couto, Catherine F Higham, Grant Hogg, Patricia Cuenca, Claudia Braida, Richard H Wilson, Berit Adam, Gerardo del Valle, Roberto Brian,[...]. Hum Mol Genet 2012
105
12


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
332
11

Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy.
Rahul N Kanadia, Jihae Shin, Yuan Yuan, Stuart G Beattie, Thurman M Wheeler, Charles A Thornton, Maurice S Swanson. Proc Natl Acad Sci U S A 2006
247
11


Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing.
Nicolas Charlet-B, Rajesh S Savkur, Gopal Singh, Anne V Philips, Elizabeth A Grice, Thomas A Cooper. Mol Cell 2002
427
11

Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
Claudia Braida, Rhoda K A Stefanatos, Berit Adam, Navdeep Mahajan, Hubert J M Smeets, Florence Niel, Cyril Goizet, Benoit Arveiler, Michel Koenig, Clotilde Lagier-Tourenne,[...]. Hum Mol Genet 2010
103
11

Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene.
Zuzana Musova, Radim Mazanec, Anna Krepelova, Edvard Ehler, Jiri Vales, Radka Jaklova, Tomas Prochazka, Petr Koukal, Tatana Marikova, Josef Kraus,[...]. Am J Med Genet A 2009
99
11

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
205
11

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.
Fernande Freyermuth, Frédérique Rau, Yosuke Kokunai, Thomas Linke, Chantal Sellier, Masayuki Nakamori, Yoshihiro Kino, Ludovic Arandel, Arnaud Jollet, Christelle Thibault,[...]. Nat Commun 2016
90
11

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
339
10

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
237
10

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
328
10

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
322
10


Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism.
Stéphanie Tomé, Elodie Dandelot, Céline Dogan, Alexis Bertrand, David Geneviève, Yann Péréon, Marie Simon, Jean-Paul Bonnefont, Guillaume Bassez, Geneviève Gourdon. Hum Mutat 2018
22
45


Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.
H G Harley, S A Rundle, J C MacMillan, J Myring, J D Brook, S Crow, W Reardon, I Fenton, D J Shaw, P S Harper. Am J Hum Genet 1993
309
10

Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.
Celine Dogan, Marie De Antonio, Dalil Hamroun, Hugo Varet, Marianne Fabbro, Felix Rougier, Khadija Amarof, Marie-Christine Arne Bes, Anne-Laure Bedat-Millet, Anthony Behin,[...]. PLoS One 2016
77
12

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
9

A 10-year study of mortality in a cohort of patients with myotonic dystrophy.
J Mathieu, P Allard, L Potvin, C Prévost, P Bégin. Neurology 1999
239
9

Splicing biomarkers of disease severity in myotonic dystrophy.
Masayuki Nakamori, Krzysztof Sobczak, Araya Puwanant, Steve Welle, Katy Eichinger, Shree Pandya, Jeannne Dekdebrun, Chad R Heatwole, Michael P McDermott, Tian Chen,[...]. Ann Neurol 2013
137
9

Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy.
Guey-Shin Wang, Debra L Kearney, Mariella De Biasi, George Taffet, Thomas A Cooper. J Clin Invest 2007
141
9

A postnatal switch of CELF and MBNL proteins reprograms alternative splicing in the developing heart.
Auinash Kalsotra, Xinshu Xiao, Amanda J Ward, John C Castle, Jason M Johnson, Christopher B Burge, Thomas A Cooper. Proc Natl Acad Sci U S A 2008
344
9

Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.
J W Day, K Ricker, J F Jacobsen, L J Rasmussen, K A Dick, W Kress, C Schneider, M C Koch, G J Beilman, A R Harrison,[...]. Neurology 2003
267
9

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
52
17



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.