A citation-based method for searching scientific literature

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
Times Cited: 1962







List of co-cited articles
953 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
45

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
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
619
21

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
806
18

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
350
17




Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort.
Sarah A Cumming, Cecilia Jimenez-Moreno, Kees Okkersen, Stephan Wenninger, Ferroudja Daidj, Fiona Hogarth, Roberta Littleford, Gráinne Gorman, Guillaume Bassez, Benedikt Schoser,[...]. Neurology 2019
26
57

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
521
15

Myotonic dystrophy.
Charles A Thornton. Neurol Clin 2014
143
14


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
447
12

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
124
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
484
12


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
192
12

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
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
83
13

Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy.
J Mathieu, H Boivin, D Meunier, M Gaudreault, P Bégin. Neurology 2001
268
11



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
94
11

De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1.
Sarah A Cumming, Mark J Hamilton, Yvonne Robb, Helen Gregory, Catherine McWilliam, Anneli Cooper, Berit Adam, Josephine McGhie, Graham Hamilton, Pawel Herzyk,[...]. Eur J Hum Genet 2018
33
30

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
75
13

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
307
10

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
329
10

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
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
66
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
510
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
450
10


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
31
32

Precise small-molecule cleavage of an r(CUG) repeat expansion in a myotonic dystrophy mouse model.
Alicia J Angelbello, Suzanne G Rzuczek, Kendra K Mckee, Jonathan L Chen, Hailey Olafson, Michael D Cameron, Walter N Moss, Eric T Wang, Matthew D Disney. Proc Natl Acad Sci U S A 2019
42
21

Precise small-molecule recognition of a toxic CUG RNA repeat expansion.
Suzanne G Rzuczek, Lesley A Colgan, Yoshio Nakai, Michael D Cameron, Denis Furling, Ryohei Yasuda, Matthew D Disney. Nat Chem Biol 2017
100
9

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
409
9


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
153
9

A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.
Marc Ciosi, Alastair Maxwell, Sarah A Cumming, Davina J Hensman Moss, Asma M Alshammari, Michael D Flower, Alexandra Durr, Blair R Leavitt, Raymund A C Roos, Peter Holmans,[...]. EBioMedicine 2019
44
20


Disease-associated repeat instability and mismatch repair.
Monika H M Schmidt, Christopher E Pearson. DNA Repair (Amst) 2016
113
9


MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
Michael Flower, Vilija Lomeikaite, Marc Ciosi, Sarah Cumming, Fernando Morales, Kitty Lo, Davina Hensman Moss, Lesley Jones, Peter Holmans, Darren G Monckton,[...]. Brain 2019
38
23

Muscle wasting in myotonic dystrophies: a model of premature aging.
Alba Judith Mateos-Aierdi, Maria Goicoechea, Ana Aiastui, Roberto Fernández-Torrón, Mikel Garcia-Puga, Ander Matheu, Adolfo López de Munain. Front Aging Neurosci 2015
44
18

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
E J Kremer, M Pritchard, M Lynch, S Yu, K Holman, E Baker, S T Warren, D Schlessinger, G R Sutherland, R I Richards. Science 1991
798
8


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
44
18

Pathogenic mechanisms of myotonic dystrophy.
Johanna E Lee, Thomas A Cooper. Biochem Soc Trans 2009
173
8

Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
Walther J A A van den Broek, Marcel R Nelen, Derick G Wansink, Marga M Coerwinkel, Hein te Riele, Patricia J T A Groenen, Bé Wieringa. Hum Mol Genet 2002
209
8


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.